Page last updated: 2024-09-28

Idiopathic Parkinson Disease

Synonyms(10)

Synonym
Paralysis Agitans
Lewy Body Parkinson's Disease
Parkinson Disease, Idiopathic
Parkinson's Disease, Idiopathic
Idiopathic Parkinson Disease
Lewy Body Parkinson Disease
Primary Parkinsonism
Idiopathic Parkinson's Disease
Parkinson's Disease, Lewy Body
Parkinson's Disease

Research Excerpts

Overview

ExcerptReference
"Parkinson's disease is characterised by an imbalance between acetylcholine and dopamine which probably results from the degeneration of a dopaminergic nigrostriatal pathway."( Spehlmann, R; Stahl, SM, 1976)
"The treatment of Parkinson's disease is discussed."( Godwin-Austen, RB, 1977)
"Patients with Parkinson's disease are unable to adjust the firing rate of motor units that initiate contraction from zero to higher rates; the frequency modulation of motor units is not normal, but motor units recruit normally as effort is increased."( Jarcho, LW; Petajan, JH, 1975)
"Parkinson's disease is characterized by the loss of midbrain dopamine neurons that innervate the caudate and the putamen."( Bunney, BS; Gjedde, A; Leranth, C; Marek, KL; Naftolin, F; Price, LH; Robbins, RJ; Roth, RH; Spencer, DD; Vollmer, T, 1992)
"Parkinson's disease is a neurodegenerative disorder characterized mainly by a loss of the dopaminergic neurons of the nigrostriatal pathway."( Levivier, M; Przedborski, S, 1992)
"Parkinson's disease is associated with degeneration of the dopaminergic component of the nigrostriatal pathway."( Abercrombie, ED; Berger, TW; Grace, AA; Stricker, EM; Zigmond, MJ, 1990)
"Their mechanism in Parkinson's disease is discussed."( Bathien, N; Feve, AP; Rondot, P, 1991)
"We conclude that Parkinson's disease is a systemic disorder of Oxphos, probably of a complex genetic etiology."( Juncos, JL; Shoffner, JM; Torroni, A; Wallace, DC; Watts, RL, 1991)
"Parkinson's disease is associated with a massive loss in melanized dopaminergic neurons in the substantia nigra resulting in a severe striatal dopaminergic denervation."( Agid, Y; Dumas, S; Duyckaerts, C; Hirsch, EC; Javoy-Agid, F; Mallet, J, 1990)
"Parkinson's disease is associated with degeneration of the nigrostriatal bundle."( Abercrombie, ED; Stricker, EM; Zigmond, MJ, 1990)
"Parkinson's disease is a neurological condition associated with neuronal degeneration in the corpora nigra with a drop in the level of dopamine in the striatum."( Allain, H; Giraud, JR; Jacquemard, F; Palaric, JC, 1990)
"My knowledge of Parkinson's disease is minimal, but I am a trained observer and I have attempted to present a brief study of the condition from 'inside looking out' in the hope that it will assist in expanding clinical rapport."( Cowan, A, 1990)
"Two patients with Parkinson's disease are reported, in whom painful sensory phenomena preceded or accompanied the disease process."( Sandyk, R, 1986)
"For this reason, Parkinson's disease is a very good model for the study of such interactions."( Dubois, B, 1989)
"Parkinson's disease is characterized especially by a degeneration of pigmented brain regions, like substantia nigra."( Brücke, T; Riederer, P, 1986)
"1."( Hassan, MN; Thakar, JH, 1988)
"Parkinson's disease is an illness with neuropathological and neuroanatomical abnormalities in many areas of the central nervous system."( Perlow, MJ, 1987)
"Treatment of Parkinson's disease is not difficult in the early stages of the disease; a therapeutic regimen of carbidopa-levodopa or possibly, a combination of carbidopa-levodopa and bromocriptine, provides the best therapeutic results."( Muenter, MD, 1986)
"This approach to Parkinson's disease is useful, safe, and at least as effective as levodopa alone."( Barbeau, A; Botez, MI; Joubert, M; Mars, H, 1972)
"The diagnosis of Parkinson's disease is not as easy as previously claimed, and presents a number of pitfalls."( Barbeau, A, 1984)
"Parkinson's disease is characterized by a deficiency of dopamine in the nigrostriatal system."( Laakso, K; Lönnberg, P; Rinne, JK; Rinne, JO; Rinne, UK, 1984)
"Parkinson's disease is associated with a variety of neurotransmitter disturbances which may be further altered by its treatment with dopamine agonists."( Lang, AE, 1984)
"Juvenile Parkinson's disease is rare."( Clough, CG; Mendoza, M; Yahr, MD, 1981)
"Management of Parkinson's disease is dominated by the desire to prevent the development of fluctuations, dyskinesia, and psychiatric complications, and to treat effectively these effects when they appear."( Nutt, JG, 1995)
"Parkinson's disease is one of the most common movement disorders and is related to destruction of neurons in the substantia nigra pars compacta (SNpc) of the basal ganglia."( Montgomery, EB, 1995)
"Parkinson's disease is a neurodegenerative disorder of older persons that eventually leads to disability."( Cutson, TM; Laub, KC; Schenkman, M, 1995)
"Early diagnosis of Parkinson's disease is often difficult."( Bakheit, AM, 1995)
"Parkinson's disease is a prevalent neurological disease characterized by profound and incapacitating movement disorders."( Armanini, M; Berkemeier, L; Hynes, MA; Phillips, H; Poulsen, K; Rosenthal, A, 1994)
"Parkinson's disease is a progressive neurodegenerative condition of unknown cause and with no known cure."( Mahler, ME; Scharre, DW, 1994)
"Because Parkinson's disease is characterized by a decrease in dopaminergic neurotransmission in the basal ganglia, the selective inhibition of MAO-B should lead to diminished metabolism of dopamine in the nigrostriatal system and a significant increase in the concentration of the neurotransmitter."( Lange, KW; Riederer, P; Youdim, MB, 1994)
"Parkinson's disease is one of the most common neurologic disorders."( Standaert, DG; Stern, MB, 1993)
"Parkinson's disease is characterized by massive degeneration of the melanized dopaminergic neurons in the substantia nigra."( Agid, Y; Herrero, MT; Hirsch, EC; Javoy-Agid, F; Kastner, A, 1993)
"The etiology of Parkinson's disease is mainly unknown."( Fiszer, U; Fredrikson, S; Kostulas, V; Link, H; Mix, E; Olsson, T, 1994)
"Parkinson's disease is a neurodegenerative disorder characterized by a selective loss of nerve cells which die slowly, but more rapidly than similar effects due to aging."( Agid, Y, 1993)
"Parkinson's disease is a specific disorder of central dopaminergic systems."( Blin, O; Masson, G; Mestre, D, 1993)
"Parkinson's disease is characterized by a massive neuronal loss in several cell groups of the midbrain."( Hirsch, EC, 1993)
"The treatment of Parkinson's disease is reviewed."( Lieberman, A, 1993)
"Parkinson's disease is treated with a number of medications, but levodopa, a dopamine precursor, is considered most effective."( Brownlee, HJ; Stacy, M, 1996)
"Parkinson's disease is characterized by the loss of dopaminergic neurons in the substantia nigra and, to a lesser extent, the ventral tegmental area and catecholaminergic cell group A8."( Agid, Y; Hirsch, EC; Karlsson, JO; Mouatt-Prigent, A, 1996)
"Parkinson's disease is treated in relation to its symptoms and stage in any individual plan of therapy."( Fischer, PA, 1995)
"Parkinson's disease is characterized by chronic progression of dopaminergic neuronal death, the mechanism of which is still unknown."( Akaike, A; Kawamura, T; Kimura, J; Sawada, H; Shimohama, S; Tamura, Y, 1996)
"Parkinson's disease is a progressive neurodegenerative disorder that is associated with the loss of nerve terminals from specific brain areas, particularly in the caudate and putamen, which contains the highest concentrations of dopamine transporter sites."( Byon, C; Elmaleh, DR; Fischman, AJ; Hanson, RN; Liang, AY; Madras, BK; Meltzer, PC; Shoup, TM, 1996)
"Parkinson's disease is characterized by degeneration of dopamine (DA) neurons and their terminals."( Babich, JW; Barrow, SA; Elmaleh, DR; Fischman, AJ; Hanson, RN; Madras, BK; Meltzer, P, 1997)
"Although Parkinson's disease is characterized by a loss of dopaminergic neurons in the substantia nigra not all dopaminergic neurons degenerate in this disease."( Agid, Y; Damier, P; Faucheux, B; Hirsch, EC; Mouatt-Prigent, A, 1997)
"Parkinson's disease is a common disabling disease of old age."( Playfer, JR, 1997)
"Idiopathic Parkinson's disease is a common neurodegenerative disease that is difficult to distinguish from other parkinsonian syndromes such as multiple-system atrophy (MSA)."( Kimber, JR; Mathias, CJ; Watson, L, 1997)
"Hallucinosis in idiopathic Parkinson's disease is heterogeneous, falling into two groups."( Graham, JM; Grünewald, RA; Sagar, HJ, 1997)
"Parkinson's disease is a common neurodegenerative disorder of unknown aetiology."( Schapira, AH; Warner, TT, 1998)
"Parkinson's disease is a chronic and disabling illness and there is currently wide variation in its management."( Bhatia, K; Brooks, DJ; Burn, DJ; Clarke, CE; Playfer, J; Sawle, GV; Schapira, AH; Stewart, D; Williams, AC, 1998)
"Parkinson's disease is found to cause a consistent deficit in simple reaction time."( Brown, VJ; Gauntlett-Gilbert, J, 1998)
"Three patients with Parkinson's disease are described who developed pericardial, retroperitoneal, and pleural fibrosis associated with pergolide treatment."( Dick, DJ; Pilling, JB; Shaunak, S; Wilkins, A, 1999)
"Parkinson's disease is characterized by degeneration of dopaminergic neurons, resulting in loss of dopamine transporters in the striatum."( Booij, J; de Bruin, K; Hemelaar, TG; Janssen, AG; Speelman, JD; van Royen, EA, 1999)
"Parkinson's disease is characterized by a massive loss of nigral dopamine neurons that results in a reduction of dopamine concentrations in the striatum."( Abrous, DN; Agid, Y; Bernard, V; Bloch, B; Hirsch, EC; Laribi, O; Levey, AI; Muriel, MP, 1999)
"Parkinson's disease is characterized by massive degeneration of dopamine-containing neurons in the midbrain."( Agid, Y; Damier, P; Graybiel, AM; Hirsch, EC, 1999)
"The cause of Parkinson's disease is still an enigma."( Booij, J; Drukarch, B; Groenewegen, HJ; Stoof, JC; van Muiswinkel, FL; Voorn, P; Winogrodzka, A; Wolters, EC, 1999)
"Parkinson's disease is a readily recognized clinical syndrome, characterized by resting tremor, rigidity, bradykinesia and loss of postural reflexes."( King, DB, 1999)
"Parkinson's disease is a progressive neurodegenerative disorder characterized by striatal dopaminergic loss."( Stacy, M, 1999)
"Parkinson's disease is a neurodegenerative disorder which is mainly characterized by degeneration of the dopaminergic cells in the nigro-striatal system."( Amicarelli, F; Carlucci, G; Gasbarri, A; Masciocco, L; Miranda, M; Pacitti, C; Palumbo, G; Pompili, A, 1999)
"Parkinson's disease is a neurodegenerative disease that is consequent to the loss of brain dopamine (DA) cells."( Cadet, JL; Harrington, B; Ordonez, S, 2000)
"Parkinson's disease is characterized by a selective loss of dopaminergic neurons in the nigrostriatal pathway."( Agid, Y; Hirsch, EC; Karlsson, JO; Mouatt-Prigent, A; Yelnik, J, 2000)
"Parkinson's disease is a common neurodegenerative syndrome characterized by loss of dopaminergic neurons in the substantia nigra, formation of filamentous intraneuronal inclusions (Lewy bodies) and an extrapyramidal movement disorder."( Bender, WW; Feany, MB, 2000)
"Parkinson's disease is characterized by the loss of dopamine (DA) neurons, which leads to overactivity of the surviving DA neurons and an increase in neurotransmitter release and turnover."( Cohen, G, 2000)
"The etiology of Parkinson's disease is not known."( Grünblatt, E; Mandel, S; Youdim, MB, 2000)
"Parkinson's disease is a neurodegenerative disorder that manifests clinically with variable degrees of tremor, muscle rigidity, bradykinesia and postural instability."( Koller, W; Marjama-Lyons, J, 2000)
"The pathogenesis of Parkinson's disease is still an enigma."( Maruyama, W; Naoi, M; Strolin-Benedetti, M, 2000)
"Parkinson's disease is thought to be caused by an interaction of polygenic predisposition with environmental factors."( Kitada, T; Mizuno, Y, 2000)
"Parkinson's disease is a progressive neurodegenerative disorder."( Fujimoto, K; Nakano, I, 2000)
"Parkinson's disease is a major neurological disorder that primarily affects the nigral dopaminergic cells."( Anichtchik, OV; Haycock, JW; Huotari, M; Männistö, PT; Panula, P; Peitsaro, N, 2000)
"Parkinson's disease is a common neurodegenerative disorder in which familial-linked genes have provided novel insights into the pathogenesis of this disorder."( Chung, KK; Dawson, TM; Dawson, VL; Gao, J; Huang, H; Zhang, Y, 2000)
"Parkinson's disease is the second most common neurodegenerative disease, after Alzheimer's disease."( Goedert, M; Spillantini, MG, 2000)
"L-DOPA therapy for Parkinson's disease is one of the major achievements of twentieth century neurology; Parkinson's disease was the first in which specific neurochemical deficits in defined brain regions were identified, and thus for which a rational, chemical therapy could be developed, ushering in the era of clinical neurochemistry."( Foley, P, 2000)
"Although Parkinson's disease is typically characterised by bradykinesia, rigidity, and rest tremor, the possibility that two additional motor deficits are manifest during small hand muscle activity was explored-namely, weakness and abnormal physiological tremor."( Corcos, DM; Marsden, CD; McAuley, JH; Quinn, NP; Rothwell, JC, 2001)
"The etiology of Parkinson's disease is still unknown, though current investigations support the notion of the pivotal involvement of oxidative stress in the process of neurodegeneration in the substantia nigra (SN)."( Barzilai, A; Daily, D; Melamed, E; Offen, D; Panet, H, 2001)
"Parkinson's disease is the most common neurodegenerative disease in which the chemical pathology is known and effective symptomatic treatment, levodopa, is available."( Gálvez-Jiménez, N; Hanson, MR, 2001)
"Parkinson's disease is one of the commonest neurodegenerative diseases of the elderly."( Tan, AK, 2001)
"Parkinson's disease is the most common movement disorder and the second most common neurodegenerative disease."( Goedert, M, 2001)
"Parkinson's disease is a common neurodegenerative disorder characterized by the progressive loss of the dopaminergic neurons in the substantia nigra pars compacta."( Choi, DK; Guégan, C; Jackson-Lewis, V; Przedborski, S; Teismann, P; Tieu, K; Vila, M; Wu, DC, 2001)
"Secondly, Parkinson's disease is a cause of primary autonomic failure with an involvement of the peripheral autonomic system as shown by the ubiquitous distribution of Lewy bodies and reduced iobenguane [metaiodobenzylguanidine (MIBG)] cardiac uptake."( Brefel-Courbon, C; Montastruc, JL; Rascol, O; Senard, JM, 2001)
"Parkinson's disease is one of the major neurodegenerative diseases."( Ektessabi, A; Fujisawa, S; Yoshida, S, 2001)
"Parkinson's disease is a progressive neurological disease caused by rather selective degeneration of the dopaminergic neurons in the substantia nigra."( Barzilai, A; Melamed, E; Shirvan, A, 2001)
"Parkinson's disease is a nosological entity of unknown origin for which, in some cases, a possible pathogenetic role for mitochondrial dysfunction has been postulated."( Bonuccelli, U; Ceravolo, R; Iudice, A; Lombardi, V; Mancuso, M; Siciliano, G, 2001)
"Parkinson's disease is typically characterised by loss of function and previous abilities, often accompanied by complications of treatment in later stages of the disease."( Schrag, A; Trimble, M, 2001)
"Parkinson's disease is the second most common neurodegenerative disease and results from loss of dopaminergic neurons in the substantia nigra."( Cohlberg, JA; Fink, AL; Li, J; Uversky, VN, 2002)
"Parkinson's disease is a movement disorder characterized by degeneration of dopaminergic neurons in the substantia nigra pars compacta."( Auluck, PK; Bonini, NM; Chan, HY; Lee, VM; Trojanowski, JQ, 2002)
"Parkinson's disease is also characterized by decreases in midbrain levels of total glutathione which could impact on E1 enzyme activity via oxidation of the active site sulfhydryl."( Andersen, JK; Boonplueang, R; Jha, N; Kumar, MJ, 2002)
"Parkinson's disease is characterized by a loss of dopaminergic nigrostriatal neurons."( Bilsland, J; Grimm, E; Han, Y; Harper, SJ; Hefti, F; Nicholson, DW; Roy, S; Xanthoudakis, S, 2002)
"Parkinson's disease is caused by a dopamine deficiency state in the fore brain area."( Klopman, G; Sedykh, A, 2002)
"Parkinson's disease is the second most common age-related neurodegenerative disease, resulting from loss of dopaminergic neurons in the substantia nigra."( Bower, KS; Fink, AL; Li, J; M Cooper, E; Uversky, VN, 2002)
"Parkinson's disease is a widespread condition caused by the loss of midbrain neurons that synthesize the neurotransmitter dopamine."( Auerbach, JM; Bankiewicz, K; Gavin, D; Kim, JH; Lee, SH; Lumelsky, N; McKay, R; Nguyen, J; Rodríguez-Gómez, JA; Sánchez-Pernaute, R; Velasco, I, 2002)
"Alzheimer's and Parkinson's diseases are associated with the formation in the brain of amyloid fibrils from beta-amyloid and alpha-synuclein proteins, respectively."( Hartley, D; Lansbury, PT; Lashuel, HA; Petre, BM; Walz, T, 2002)
"Parkinson's disease is a neurodegenerative disorder characterized by the progressive degeneration of the dopaminergic nigrostriatal pathway, and the presence of Lewy bodies."( Brice, A; Corti, O, 2002)
"1."( Froberg, J, 2002)
"Parkinson's disease is an increasingly common disease of elderly patients who present a particular anaesthetic challenge."( Hall, GM; Nicholson, G; Pereira, AC, 2002)
"The diagnosis of Parkinson's disease is based on clinical features with pathological verification."( Friberg, L; Løkkegaard, A; Werdelin, LM, 2002)
"While Parkinson's disease is undoubtedly a disorder with a primary pathology of dopamine neuronal loss, that loss of dopamine and subsequent dopamine replacement therapy leads to imbalances in many non-dopaminergic transmitter systems, including 5-hydroxytryptamine (5-HT)."( Brotchie, JM; Nicholson, SL, 2002)
"Tertiary Parkinson's disease care center and sleep laboratory at university hospital neurology department."( Brandauer, E; Frauscher, B; Glatzl, S; Högl, B; Poewe, W; Saletu, M; Seppi, K; Ulmer, H; Wenning, G, 2002)
"Parkinson's disease is the most prevalent neurodegenerative movement disorder and research into its pathogenesis recently accelerated following the identification of a number of causal genetic mutations."( Halliday, GM; Orr, CF; Rowe, DB, 2002)
"Parkinson's disease is associated with slowness, especially of sequential movements, and is characterized pathologically by degeneration of dopaminergic neurons, particularly targeting nigrostriatal projections."( Brooks, DJ; Goerendt, IK; Grasby, PM; Lawrence, AD; Messa, C; Piccini, P, 2003)
"Parkinson's disease is considered to offer only a limited view of basal ganglia function due to partial striatal depletion of dopamine and the potential involvement of other structures and transmitters in its pathology."( Saint-Cyr, JA, 2003)
"Parkinson's disease is the most frequent movement disorder caused by loss of dopaminergic neurons in the midbrain."( Eulitz, D; Karschin, A; Prüss, H; Thomzig, A; Veh, RW; Wenzel, M, 2003)
"Parkinson's disease is the second most common neurodegenerative disorder, and the cause is unknown; however, substantial evidence implicates the aggregation of alpha-synuclein as a critical factor in the etiology of the disease."( Fink, AL; Zhu, M, 2003)
"Parkinson's disease is a progressive neurodegenerative disorder that demands a holistic approach to treatment."( Martin, WR; Wieler, M, 2003)
"Parkinson's disease is one of the most common neurodegenerative diseases, and affects approximately 1% of the population over 65 years of age."( Brundin, P; Lotharius, J; Smith, R, 2003)
"Parkinson's disease is a neurodegenerative disorder associated with selective loss of the dopaminergic neurons in the substantia nigra."( Choi, HJ; Hwang, O; Kim, SW; Lee, SY; Moon, YW, 2003)
"Parkinson's disease is a neurodegenerative disorder associated with selective loss of dopaminergic neurons in the substantia nigra."( Choi, HJ; Hwang, O; Kim, SW; Lee, SY, 2003)
"Parkinson's disease is a neurodegenerative disorder associated with the selective death of dopaminergic neurons."( Klann, E; Lin, E; Perez, RG; Ugarte, SD; Zigmond, MJ, 2003)
"Parkinson's disease is characterized by the progressive and selective loss of the dopaminergic neurons in the substantia nigra and the presence of ubiquitinated protein inclusions termed Lewy bodies."( Brice, A; Corti, O, 2003)
"Parkinson's disease is a focal degeneration of dopaminergic neurons in the brain with progressive loss of ability to produce the neurotransmitter dopamine."( Arya, SK; Bankiewicz, KS; Brady, RO; D'Costa, J; Davis-Warren, A; Harvey-White, J; Kaneski, CR; Limaye, A; Major, EO; Qasba, P, 2003)
"Parkinson's disease is a neurodegenerative disorder of unknown pathogenesis."( Ischiropoulos, H; Przedborski, S; Tieu, K, 2003)
"Parkinson's disease is a cause of primary autonomic failure with involvement of the peripheral nervous system."( Senard, JM, 2003)
"Parkinson's disease is neural degenerative disease, and the influence of paclitaxel administration on patients with Parkinson's disease is unknown."( Date, K; Egawa, M; Fujitoh, N; Fujiwara, H; Furukawa, M; Mizunoe, T; Sakashita, T; Ueda, K; Urabe, S; Urabe, T, 2003)
"Levodopa-treated Parkinson's disease is often complicated by the occurrence of motor fluctuations, which can be predictable ('wearing-off') or unpredictable ('on-off')."( Calne, DB; de la Fuente-Fernández, R; Mak, E; Schulzer, M; Stoessl, AJ, 2004)
"Freezing in Parkinson's disease is a severe and disabling problem of unknown aetiology."( De Weerdt, W; Desloovere, K; Dom, R; Janssens, L; Nieuwboer, A; Stijn, V, 2004)
"Parkinson's disease is a common age-related neurodegenerative disease characterized pathologically by a loss of dopaminergic neurons in the substantia nigra with resultant depletion of striatal dopamine and presence of Lewy bodies in the remaining neurons."( Goodlett, DR; Zhang, J, 2004)
"Parkinson's disease is a progressive neurodegenerative disorder whose main histopathological feature is the loss of dopaminergic neurons in the pars compacta of the substantia nigra with secondary striatal dopaminergic insufficiency."( Fraix, V, 2004)
"Parkinson's disease is a chronic, progressive, neurodegenerative disease with a reduction of dopamine levels causing the typical symptoms tremor, hypokinesia, rigidity, and postural disturbance."( Lökk, J, 2004)
"Dementia in Parkinson's disease is increasingly being recognized."( Emre, M, 2004)
"Parkinson's disease is associated with the deposition and accumulation of alpha-synuclein fibrils in the brain."( Gray, HB; Hummel, PA; Langen, R; Lee, JC; Winkler, JR, 2004)
"Parkinson's disease is a common neurodegenerative disease characterized by the loss of dopaminergic neurons in the substantia nigra pars compacta and the accumulation of the protein alpha-synuclein into aggregates called Lewy bodies and Lewy neurites."( Auluck, PK; Bonini, NM; Meulener, MC, 2005)
"Psychosis in Parkinson's disease is a serious disorder that is often difficult to treat."( Diraoui, S; Jansen, PA; van Melick, EJ, 2004)
"Parkinson's disease is due to the selective loss of nigrostriatal dopaminergic neurons."( Gao, Q; Geller, AI; Goldstein, DS; Holmes, C; Kong, L; Pfeilschifter, J; Sun, M; Wang, X; Zhang, GR, 2004)
"Parkinson's disease is a neurodegenerative disorder associated with progressive loss of dopaminergic cells in the substantia nigra."( Cho, Y; Choi, HJ; Hwang, O; Lee, SY, 2005)
"Although Parkinson's disease is a common neurodegenerative disorder characterised by its motoric symptoms, there is an increasing recognition of accompanying impairments in cognition that have a profound impact on the quality of life of these patients."( Barker, RA; Lewis, SJ; Owen, AM; Robbins, TW; Slabosz, A, 2005)
"Whereas Parkinson's disease is a neurodegenerative disorder that typically onsets after 60 years of age, the possibility that it could result from insults sustained during development has been proposed."( Barlow, BK; Brooks, AI; Cory-Slechta, DA; Richfield, EK; Thiruchelvam, M, 2005)
"Parkinson's disease is characterized by a progressive loss of dopaminergic neurons in the substantia nigra zona compacta, and in other sub-cortical nuclei associated with a widespread occurrence of Lewy bodies."( Brown-Borg, H; Ebadi, M; El Refaey, H; Garrett, S; Sharma, SK; Shavali, S; Singh, BB, 2005)
"Resting tremor in Parkinson's disease is usually not the primary disabling feature, and in most cases, levodopa/carbidopa is satisfactory for many years."( Charles, PD; Duffis, EI; Schadt, CR, 2005)
"Parkinson's disease is a progressive neurodegenerative disorder caused by the loss of midbrain dopaminergic neurons."( Minger, SL; Taylor, H, 2005)
"Idiopathic Parkinson's disease is most confidently clinically diagnosed if we follow the United Kingdom Parkinson's Disease Society Brain Bank Diagnostic Criteria for Parkinson's disease."( Ghosh, B; Mishra, A; Sengupta, P, 2005)
"Parkinson's disease is a neurodegenerative movement disorder characterized by a progressive degeneration of the nigrostriatal system."( McIntosh, JM; Quik, M, 2006)
"The pathogenesis of idiopathic Parkinson's disease is unknown, but nigral degeneration and depigmentation are associated with microglial inflammation and anti-inflammatory medications appear to protect against the disease."( Halliday, GM; Mizuno, Y; Mori, H; Orr, CF; Rowe, DB, 2005)
"Parkinson's disease is a common neurodegenerative disorder with a mainly sporadic aetiology, although a number of monogenic familiar forms are known."( Bergamasco, B; Fasano, M; Lopiano, L, 2006)
"Parkinson's disease is a neurodegenerative disorder affecting the dopaminergic neurons in the substantia nigra."( Baekelandt, V; Bequé, D; Bockstael, O; Bormans, G; Casteels, C; Debyser, Z; Lauwers, E; Mortelmans, L; Nuttin, B; Nuyts, J; Van Laere, K; Vercammen, L, 2007)
"Pharmacotherapy for Parkinson's disease is focused on dopaminergic drugs, mainly the dopamine precursor levodopa and dopamine receptor agonists."( Nyholm, D, 2006)
"Parkinson's disease is a chronic neurodegenerative disorder of unknown etiology."( Bhat, V; Shulman, LM, 2006)
"Parkinson's disease is associated with a progressive loss of substantia nigra pars compacta dopaminergic neurons."( Garris, BL; Garris, DR; Lau, YS; Novikova, L, 2006)
"Parkinson's disease is a neurodegenerative disorder which is in most cases of unknown etiology."( Casarejos, MJ; García de Yébenes, J; Mena, MA; Menéndez, J; Rodríguez-Navarro, JA; Solano, RM, 2006)
"Parkinson's disease is a movement disorder that results from a loss of dopaminergic neurons in the substantia nigra."( Mirzaei, H; Regnier, F; Rochet, JC; Schieler, JL, 2006)
"Parkinson's disease is the second most common neurodegenerative disorder and is characterized by the degeneration of dopaminergic neurons in the substantia nigra."( Cao, JH; Clark, IE; Dodson, MW; Guo, M; Hay, BA; Huh, JR; Jiang, C; Seol, JH; Yoo, SJ, 2006)
"Parkinson's disease is a neurological disorder associated with disfunction of dopaminergic pathways of the basal ganglia."( Colonnese, C; Garreffa, G; Giove, F; Giulietti, G; Macrì, MA; Maraviglia, B; Modugno, N; Moraschi, M, 2006)
"Parkinson's disease is a common incurable neurodegenerative disease whose molecular aetiology remains unclear."( Abou-Sleiman, PM; Gandhi, S; Ganguly, M; Hargreaves, I; Heales, S; Healy, DG; Holton, JL; Latchman, DS; Lees, AJ; Muqit, MM; Parsons, L; Revesz, T; Stanyer, L; Wood, NW, 2006)
"L-dopa treatment of Parkinson's disease is complicated in the long term by the appearance of dyskinesia."( Corvol, JC; Girault, JA; Hervé, D, 2006)
"Parkinson's disease is a progressive neurological disorder characterized by tremor, bradykinesia, rigidity, gait and postural instability and a variety of nonmotor symptoms."( Diamond, A; Jankovic, J, 2006)
"Parkinson's disease is characterized by progressive slowness in activities of daily living and is the most common cause of parkinsonism, whose symptoms include resting tremor, cogwheel rigidity, and bradykinesia."( Weiner, WJ, 2006)
"Parkinson's disease is classically characterised as a motor neurodegenerative disorder."( Calabresi, P; Di Filippo, M; Parnetti, L; Picconi, B, 2006)
"Parkinson's disease is a common neurodegenerative disorder."( Chen, S; Deng, X; Ding, X; Dong, H; Li, W; Li, X; Ma, G; Wu, T; Yao, J; Zeng, Y; Zhang, X, 2006)
"Parkinson's disease is also characterised by various vegetative symptoms, impairment of olfaction, anxiety, depression, and with increasing age also by cognitive deficits and dementia."( Ransmayr, G, 2007)
"Parkinson's disease is no longer regarded a pure motor disorder, but a complex disease with motor as well as non-motor symptoms, the latter having a major impact on the quality of life of the patient as well as the caregiver."( Waldvogel, D, 2007)
"Parkinson's disease is a neurodegenerative movement disorder that is characterized by a loss of nigrostriatal dopamine-containing neurons."( O'Neill, M; Perez, XA; Quik, M, 2007)
"Parkinson's disease is the neurodegenerative disorder characterized by dopaminergic cell loss in the compact part of substantia nigra."( Dabek, J; Jabłońska, B; Lepich, T, 2006)
"Parkinson's disease is the second most common neurodegenerative disease."( Björklund, T; Carlsson, T; Kirik, D, 2007)
"Parkinson's disease is a neurodegenerative disorder, related to the loss of dopamine (DA)-containing neurons in the substantia nigra."( Elliott, CJ; Hernádi, L; Hiripi, L; Szabó, H; Vehovszky, A, 2007)
"Parkinson's disease is associated with profound alterations in the central control of energy metabolism."( Arnaud, P; Bannier, S; Boirie, Y; Brandolini-Bunlon, M; Derost, P; Durif, F; Giraudet, C; Montaurier, C; Morio, B, 2007)
"Clinical Parkinson's disease is most likely to be identified if the orbito-frontal cortex is affected, while the diagnosis is less likely if the pathology is restricted to the olfactory bulb or tract."( Esiri, MM; Hubbard, PS; McShane, R; Nagy, Z; Reading, M, 2007)
"Parkinson's disease is associated with both swallowing and respiratory dysfunction, increasing the risk of aspiration and pneumonia."( Anderson, T; Frampton, C; Huckabee, ML; Leow, L; Lim, A, 2008)
"Parkinson's disease is associated with dementia in about 40% of cases, and in time up to 80% of patients will develop dementia."( Wesnes, K, 2007)
"Parkinson's disease is the second most common age-related neurodegenerative disorder and is characterized clinically by classical parkinsonism and pathologically by selective loss of dopaminergic neurons in the substantia nigra and Lewy bodies."( Klein, C; Lohmann-Hedrich, K, 2007)
"Parkinson's disease is a neurodegenerative disorder that affects approximately 1% of people over the age of 60 years."( Jankovic, J; Stacy, M, 2007)
"Parkinson's disease is a debilitating neurodegenerative movement disorder characterized by damage to the nigrostriatal dopaminergic system."( Bordia, T; O'Leary, K; Quik, M, 2007)
"Parkinson's disease is a neurodegenerative disorder of the substantia nigra accompanied by the depletion of dopamine levels."( Dohi, T; Kitayama, T; Morioka, N; Morita, K; Onitsuka, Y; Song, L, 2007)
"AA key feature in Parkinson's disease is the deposition of Lewy bodies."( Beyer, K, 2007)
"Parkinson's disease is a common neurodegenerative disorder of unknown cause."( Surmeier, DJ, 2007)
"Parkinson's disease is one of the most common neurological conditions associated with visual hallucinations."( Aydemir, T; Cetin, S; Erol, C; Hanoglu, L; Meral, H; Ozben, S; Ozer, F; Ozkayran, T; Ozturk, O; Yilsen, M, 2007)
"Parkinson's disease is characterized by the progressive degeneration of midbrain dopaminergic neurons."( Li, Q; Li, YY; Lu, JH; Pu, XP; Zhao, YY, 2008)
"Since Parkinson's disease is a progressive disorder, adjustments to pharmacotherapy must be expected over time."( Chen, JJ; Swope, DM, 2007)
"Parkinson's disease is a neurodegenerative disorder characterized by a progressive neuronal loss affecting preferentially the dopaminergic neurons of the nigrostriatal projection."( Arias-Carrión, O; Freundlieb, N; Höglinger, GU; Oertel, WH, 2007)
"Parkinson's disease is an environmentally influenced, neurodegenerative disease of unknown origin that is characterized by the progressive loss of dopaminergic neurons in the substantia nigra pars compacta of the brain."( Sens, DA; Shavali, S, 2008)
"Parkinson's disease is associated with small, bradykinetic postural weight shifts while standing but it is unclear whether this is due to reduced limits of stability and/or to the selection of abnormal strategies for leaning."( Chiari, L; Horak, FB; Mancini, M; Rocchi, L, 2008)
"Parkinson's disease is a common disorder that becomes more prevalent with advanced age."( Stoessl, J, 2008)
"Drug treatment for Parkinson's disease is largely symptomatic and relies primarily on levodopa (L-dopa) and adjuvant therapies including dopamine agonists and catechol-O-methyltransferase (COMT) inhibitors."( Chan, DK; Cordato, DJ; O'Rourke, F, 2008)
"Parkinson's disease is one of the most common neurodegenerative disorders and still remains incurable."( Latchman, DS; Yang, YX, 2008)
"Parkinson's disease is a neurodegenerative disorder with uncertain aetiology and ill-defined pathophysiology."( Ferrari, CC; Pitossi, FJ; Pott Godoy, MC; Sarchi, MI; Tarelli, R, 2008)
"Parkinson's disease is a complex disorder characterized by degeneration of dopaminergic neurons in the substantia nigra in the brain."( Bianco, J; Burne, T; Donnellan, M; Féron, F; Kesby, J; Mackay-Sim, A; Meedeniya, A; Murrell, W; Perry, C; Silburn, P; Wetzig, A, 2008)
"Parkinson's disease is treated pharmacologically with dopamine replacement medication and, more recently, by stimulating basal-ganglia nuclei such as the subthalamic nucleus (STN)."( Aziz, T; Brittain, JS; Holland, P; Jenkinson, N; Joint, C; Ray, NJ; Stein, JF; Wang, S, 2008)
"Parkinson's disease is a neurodegenerative disorder characterized by the formation of Lewy bodies containing aggregated alpha-synuclein."( Bammens, T; Bastiaens, I; De Virgilio, C; Delay, C; Ghillebert, R; Pellens, K; Van Leuven, F; Winderickx, J; Zabrocki, P, 2008)
"Parkinson's disease is more frequent in males than in females, and more prevalent in females with short reproductive life."( Casarejos, MJ; de Yébenes, JG; Gomez, A; Mena, MA; Perucho, J; Rodríguez-Navarro, JA; Solano, RM, 2008)
"Parkinson's disease is a neurodegenerative disorder characterized by bradykinesia, rigidity, postural instability, and resting tremor."( Ferrara, JM; Stacy, M, 2008)
"Parkinson's disease is to some degree caused by lipid peroxidation due to phospholipases activation."( Adibhatla, RM; Hatcher, JF, 2008)
"Parkinson's disease is a primarily sporadic occurring neurodegenerative disorder of advanced age."( Schulz, JB, 2008)
"Parkinson's disease is a progressive neurodegenerative disorder, associated with the selective loss of dopaminergic neurons in the substantia nigra pars compacta."( Chetsawang, B; Ebadi, M; Govitrapong, P; Kooncumchoo, P, 2008)
"Early Parkinson's disease is dominated by a motor syndrome called parkinsonism, but as the disease develops motor complications and non-motor problems may occur as well."( Aasly, JO; Beiske, AG; Bekkelund, SI; Dietrichs, E; Larsen, JP; Tysnes, OB; Vilming, ST, 2008)
"Parkinson's disease is caused by a progressive loss of the midbrain dopamine (DA) neurons in the substantia nigra pars compacta."( Andersen, SL; Benes, FM; Brown, LT; Krichevsky, AM; Macey, L; Simunovic, F; Sonntag, KC; Stephens, RM; Wang, Y; Yi, M, 2009)
"Parkinson's disease is a neurodegenerative process characterized by progressive degeneration of the substantia nigra and concurrent loss of neuromelanin in these structures."( Halabe Bucay, A, 2008)
"Parkinson's disease is a neurodegenerative, slowly progressive, age-related disorder."( Kubo, M; Moritoyo, H; Moritoyo, T; Nagai, M; Nakatsuka, A; Nishikawa, N; Nomoto, M; Yabe, H, 2009)
"Parkinson's disease is the second most common neurodegenerative disorder and remains incurable."( Latchman, DS; Wood, NW; Yang, YX, 2009)
"Parkinson's disease is the second most common neurodegenerative disease following Alzheimer's disease."( Frei, K; Truong, DD; Wolters, E, 2008)
"Parkinson's disease is associated with increased oscillatory firing patterns in basal ganglia output, which are thought to disrupt thalamocortical activity."( Bergstrom, DA; Parr-Brownlie, LC; Poloskey, SL; Walters, JR, 2009)
"Parkinson's disease is a common condition with a broad clinical diversity suggesting the existence of distinct subgroups of patients."( Barker, RA; Lewis, SJ, 2009)
"Parkinson's disease is characterised by a slow and progressive degeneration of dopaminergic neurons in the substantia nigra."( Hirsch, EC; Hunot, S, 2009)
"Parkinson's disease is a common neurodegenerative disorder with both motor symptoms and cognitive deficits such as executive dysfunction."( Abe, N; Fujii, T; Fukuda, H; Hirayama, K; Hosokai, Y; Ishioka, T; Itoyama, Y; Mori, E; Nishio, Y; Suzuki, K; Takahashi, S; Takeda, A, 2009)
"Parkinson's disease is characterized by the degeneration of dopaminergic pathways projecting to the striatum."( Bereczki, D; Bódi, N; Daw, N; Dibó, G; Gluck, MA; Kéri, S; Moustafa, A; Myers, CE; Nagy, H; Takáts, A, 2009)
"Parkinson's disease is a common neurodegenerative disease in the elderly."( Cai, ZL; Cao, BY; Huang, JZ; Liu, CF; Mao, CJ; Shi, JJ; Yang, F; Yang, YP; Zhang, P, 2009)
"Parkinson's disease is a common progressive bradykinetic disorder that can be accurately diagnosed."( Hardy, J; Lees, AJ; Revesz, T, 2009)
"Parkinson's disease is a hypokinetic movement disorder with cardinal motor features of bradykinesia, resting tremor and rigidity."( Park, A; Stacy, M, 2009)
"Parkinson's disease is a disorder of the extrapyramidal system resulting from the deficiency of dopamine in the basal ganglia."( Kato, S; Mizuno, J; Morita, S; Watada, M, 2009)
"Parkinson's disease is characterized by selective loss of dopaminergic neurons in the substantia nigra and by the appearance of Lewy bodies."( Akaike, A; Izumi, Y; Kume, T; Sawada, H; Shimohama, S; Takahashi, R; Takeuchi, H; Yamakawa, K; Yamamoto, N, 2010)
"Parkinson's disease is an archetypal disorder of dopamine dysfunction characterised by motor, cognitive, behavioural, and autonomic symptoms."( Baunez, C; Bezard, E; Fernagut, PO; Juncos, JL; Obeso, JA; Pavon, N; Rodriguez, M; Voon, V; Wickens, J, 2009)
"Parkinson's disease is caused by a deficiency of the neurotransmitter dopamine."( Min, K; Park, DH; Yoo, YJ, 2010)
"The diagnosis of idiopathic Parkinson's disease is based on a thorough clinical examination with demonstration of the presence of bradykinesia, as well as tremor, rigidity, postural instability and hyposmia."( Reichmann, H, 2006)
"Parkinson's disease is characterized by a progressive and selective loss of dopaminergic neurons in the substantia nigra."( Corona, G; Spencer, JP; Vauzour, D, 2010)
"Parkinson's disease is the second most common neurological condition, behind dementia, for which there is currently no cure."( Thomas, M, 2010)
"Parkinson's disease is a complex disease characterized by a progressive degeneration of nigrostriatal dopaminergic neurons."( Limborska, SA; Shadrina, MI; Slominsky, PA, 2010)
"Parkinson's disease is a neurodegenerative disorder that is caused by mutation of alpha-synuclein or other genes."( Kamitani, T; Matsuo, Y, 2010)
"Parkinson's disease is the second most common neurodegenerative disease, after Alzheimer's disease, among the aging human population."( Darios, F; Davletov, B; Ruipérez, V, 2010)
"Parkinson's disease is a multifactorial, neurodegenerative disease where etiopathogenetic mechanisms are not fully understood."( Glocker, MO; Haas, SJ; Kreutzer, M; Lessner, G; Mikkat, S; Schmitt, O; Wree, A, 2010)
"Parkinson's disease is characterized by the presence of intracellular aggregates composed primarily of the neuronal protein α-synuclein (αS)."( Middleton, ER; Rhoades, E, 2010)
"Parkinson's disease is a neurodegenerative disorder with selective and progressive loss of dopaminergic neurons in substantia nigra."( Huang, YM; Yin, ZQ, 2011)
"The development of Parkinson's disease is accompanied by concurrent activation of caspase-3 and apoptosis of dopaminergic neurons of human patients and rodent models."( Amutuhaire, W; Ichinose, F; Kaneki, M; Kida, K; Yamada, M, 2010)
"Parkinson's disease is a progressive neurodegenerative disease, which is initially well-treated with L-dopa."( Haahr, A; Hall, EO; Kirkevold, M; Ostergaard, K, 2011)
"Parkinson's disease is one of the major neurodegenerative disorders."( Ichinose, F; Kakinohana, M; Kaneki, M; Kida, K; Marutani, E; Tokuda, K; Yamada, M, 2011)
"Parkinson's disease is a pervasive, ageing-related neurodegenerative disease the cardinal motor symptoms of which reflect the loss of a small group of neurons, the dopaminergic neurons in the substantia nigra pars compacta (SNc)."( Guzman, JN; Ilijic, E; Kondapalli, J; Sanchez-Padilla, J; Schumacker, PT; Surmeier, DJ; Wokosin, D, 2010)
"Parkinson's disease is a common neurodegenerative disorder characterized by a profound motor disability that is traceable to the emergence of synchronous, rhythmic spiking in neurons of the external segment of the globus pallidus (GPe)."( Chan, CS; Chetkovich, DM; Fleming, SM; Gertler, TS; Glajch, KE; Goldberg, AB; Guzman, JN; Kita, H; Lewis, AS; Mercer, JN; Osten, P; Shigemoto, R; Surmeier, DJ; Tkatch, T, 2011)
"Parkinson's disease is characterized by preferential degeneration of the dopamine-producing neurons of the brain stem substantia nigra."( Dächsel, JC; Fjorback, AW; Jensen, PH; Sinning, S; Sundbye, S; Wiborg, O, 2011)
"Parkinson's disease is a complicated disease state that affects patients' quality of life."( Knudsen Gerber, DS, 2011)
"Parkinson's disease is characterized by a progressive loss of dopaminergic neurons in the substantia nigra."( Bachstetter, AD; Bickford, PC; Gemma, C; Hudson, CE; Pabon, MM, 2011)
"Parkinson's disease is a neurodegenerative disorder manifesting in debilitating motor symptoms."( Bar-Gad, I; Belelovsky, K; Erez, Y; Tischler, H, 2011)
"Parkinson's disease is a movement disorder whose principal symptoms are tremor, rigidity, bradykinesia and postural instability."( Alegría, MA; Armony, JL; Drucker-Colín, R; González-García, N; Soto, J; Trejo, D, 2011)
"Parkinson's disease is characterised not only by the classic triad of bradykinesia, rigidity and tremor, but also by the frequent occurrence of various non-motor symptoms such as the impulse control disorders (pathological gambling, hypersexuality, compulsive buying, binge eating, punding and dopamine dependency)."( Berendse, HW; Foncke, EM; Groenewegen, HJ; Van den Heuvel, OA; Van der Werf, YD, 2011)
"Pain sensitivity in Parkinson's disease is known to be altered in an L-dopa-dependent manner with increased spinal nociception and experimental pain perception in the medication-defined "off" state."( Brebbermann, J; Dohmann, H; Engau, I; Möller, JC; Mylius, V; Oertel, WH, 2011)
"PD (Parkinson's disease) is a neurodegenerative disorder, caused by a selective loss of dopaminergic neurons in the substantia nigra, which affects an increasing number of the elderly population worldwide."( Büttner, S; Franssens, V; Galas, MC; Madeo, F; Outeiro, TF; Swinnen, E; Winderickx, J, 2011)
"Parkinson's disease is a relentlessly progressive neurodegenerative disease."( Cragg, J; de la Fuente-Fernandez, R; Kuramoto, L; Mak, E; McCormick, S; McKenzie, J; Nandhagopal, R; Ruth, TJ; Schulzer, M; Sossi, V; Stoessl, AJ, 2011)
"Parkinson's disease is now recognized as a major form of α-synucleinopathy involving both the central and peripheral nervous systems."( Homma, T; Mizutani, T; Mochizuki, Y, 2012)
"The risk of Parkinson's disease is reduced by cigarette smoking, which raises some unanswered questions."( Cesaro, P; Fenelon, G; Grapin, F; Remy, P; Thiriez, C; Villafane, G, 2011)
"Parkinson's disease is the second most prevalent neurodegenerative disease, yet despite this, very little is known about the underlying cellular mechanisms."( Brundin, P; Dunning, CJ; Reyes, JF; Steiner, JA, 2012)
"As Parkinson's disease is histopathologically characterized by the selective, progressive, and chronic degeneration of the nigrostriatal and mesocorticolimbic dopamine systems, it can therefore serve as a model for assessing the functional role of these circuits in humans."( Dondaine, T; Grandjean, D; Le Jeune, F; Péron, J; Vérin, M, 2012)
"Parkinson's disease is a neurodegenerative disorder characterized by oxidative stress and CNS iron deposition."( Alessio, M; Barbariga, M; Campanella, A; Cannistraci, CV; Cappa, SF; Codazzi, F; Conti, A; Franciotta, D; Iannaccone, S; Magnani, G; Olivieri, S; Pelizzoni, I; Pesca, M, 2011)
"Parkinson's disease is a multisystem disorder involving dopaminergic, noradrenergic, serotoninergic and cholinergic systems, characterized by motor and non-motor symptoms."( Awad, RA, 2011)
"Parkinson's disease is the second most common neurodegenerative disease in the world."( Chen, J; Fan, JB; Liang, Y; Liao, JM; Zhang, P; Zhou, Z, 2011)
"Parkinson's disease is a neurodegenerative disorder characterized by the progressive loss of dopaminergic neurons in the substantia nigra."( Aebischer, P; Löw, K, 2012)
"Parkinson's disease is one of the most common neurodegenerative disorders associated with aging, reaching ∼ 2% of individuals over 65 years."( de Rosso, AL; José Silva, D; Junior, MC; Moura, KC; Nicaretta, DH; Pereira, JS; Pimentel, MM; Santos-Rebouças, CB, 2012)
"PD (Parkinson's disease) is characterized by the selective loss of DA (dopaminergic) neurons in the substantia nigra of the midbrain region, but not in the ventral tegmental area and other catecholaminergic cell group areas."( Bhonde, R; Datta, I, 2012)
"Parkinson's disease is a debilitating progressive neurodegenerative disorder that results from the loss of or damage to dopaminergic cells containing neuromelanin in the substantia nigra (SN)."( Caviedes, P; Cuevas, C; Huenchuguala, S; Muñoz, P; Paris, I; Segura-Aguilar, J; Tizabi, Y; Villa, M, 2012)
"Parkinson's disease is an age-related neurodegenerative disorder that is ameliorated with levodopa."( Martínez-Banaclocha, MA, 2012)
"Parkinson's disease is a major age-related neurodegenerative disorder."( Greig, NH; Kamal, MA; Nawaz, MS; Parveen, Z; Shakil, S, 2012)
"Parkinson's disease is a common neurodegenerative disease characterised by progressive loss of dopaminergic neurons, leading to dopamine depletion in the striatum."( Abramov, AY; Duchen, MR; Gandhi, S; Vaarmann, A; Wood, NW; Yao, Z, 2012)
"Parkinson's disease is characterized by toxicity of α-synuclein."( Miłowska, K; Szwed, A, 2012)
"Parkinson's disease is a high incidence neurodegenerative disease in elderly people, and oxidative stress plays an important role in the pathogenesis."( Chen, X; Huang, B; Xu, X; Ye, L; Ye, Q; Zhang, X; Zhu, Y, 2012)
"Parkinson's disease is a neurodegenerative disorder characterized by motor and nonmotor impairments, including constipation."( Brookes, SJ; de Vries, E; Sharrad, DF, 2013)
"Parkinson's disease is a common adult-onset neurodegenerative disorder whose pathogenesis remains essentially unknown."( Hirsch, EC; Jenner, P; Przedborski, S, 2013)
"Idiopathic Parkinson's disease is still a clinical diagnosis."( Barbe, MT; Eggers, C; Pauls, KA; Salimi Dafsari, H; Timmermann, L, 2012)
"Parkinson's disease is a degenerative disorder of the central nervous system caused by selective dopamine-generating cell death, and oxidative stress and mitochondrial dysfunction are thought to be responsible for the onset of Parkinson's disease."( Ariga, H; Iguchi-Ariga, S; Niki, T; Takahashi-Niki, K, 2012)
"Parkinson's disease is a promising target of applying personalized medicine."( Balicza, P; Balogh, I; Bereznai, B; Dibó, G; Hidasi, E; Klivényi, P; Molnár, MJ; Takáts, A, 2012)
"Parkinson's disease is a neurodegenerative disorder that can, at least partly, be mimicked by the neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine."( Berg, D; Fleckenstein, C; Itohara, S; Lang, JD; Maetzler, W; Martin, HL; Mounsey, RB; Mustafa, S; Sathe, K; Schulte, C; Synofzik, M; Teismann, P; Vukovic, Z, 2012)
"A key feature of Parkinson's disease is the dopaminergic neuronal cell loss in the substantia nigra pars compacta."( Arias-Carrión, O; El-Gamal, M; Ellaithy, A; Helmy, B; Mohamed, M; Salama, M; Sheashaa, H; Sobh, M; Tantawy, D, 2012)
"When patients with Parkinson's disease are placed on NPO (nil per os, or nothing by mouth) status for surgery, they may miss several doses of carbidopa-levodopa, possibly resulting in exacerbation of Parkinson's disease symptoms."( Anderson, LC; Fagerlund, K; Gurvich, O, 2013)
"Parkinson's disease is one of the most frequent progressive degenerative disorders with unknown origin of the nervous system."( Guseo, A, 2012)
"Parkinson's disease is the most common neurodegenerative movement disorder."( Arawaka, S; Kato, T; Sato, H, 2013)
"A key feature of Parkinson's disease is the dopaminergic neuronal cell loss in the substantia nigra pars compacta."( El-Gamal, A; El-Gamal, M; Ellaithy, A; Helmy, B; Mohamed, M; Reda, A; Salama, M; Sheashaa, H; Sobh, M; Tantawy, D, 2013)
"Parkinson's disease is the second most common neurodegenerative disorder."( Fang, JY; Tolleson, CM, 2013)
"Parkinson's disease is characterized by progressive degeneration of dopaminergic neurons."( Agari, T; Date, I; Kadota, T; Kameda, M; Kikuchi, Y; Liang, H; Shinko, A; Thomas Tayra, J; Vcelar, B; Wakamori, T; Wang, F; Weik, R; Yasuhara, T, 2013)
"Parkinson's disease is most common degenerative disorder."( Pandey, S, 2012)
"As Parkinson's disease is mainly characterized by a dysfunction of the sensorimotor pathways, which can be influenced by levodopa administration, the present study investigated the functional connectivity changes within the sensorimotor resting-state network in drug-naïve patients with Parkinson's disease after acute levodopa administration."( Annunziato, L; Conforti, R; De Micco, R; Esposito, F; Giordano, A; Paccone, A; Pignataro, G; Tedeschi, G; Tessitore, A, 2013)
"Parkinson's disease is a severe neurodegenerative disorder with a prevalence rate of approximately 1."( Bowers, J; Elkins, G; Encarnacion, E; Sliwinski, J, 2013)
"Parkinson's disease is the second most common neurodegenerative disorder and, at present, has no cure."( Beltramini, M; Bisaglia, M; Bubacco, L; Greggio, E, 2013)
"Although Parkinson's disease is a common neurodegenerative disorder its cause is still unknown."( Jang, IS; Oh, WK; Park, J; Ryu, HW, 2013)
"Parkinson's disease is characterized by neuronal death in the substantia nigra and the presence of intracellular inclusions of α-synuclein in the Lewy bodies."( Andersen, KJ; Febbraro, F; Romero-Ramos, M; Sanchez-Guajardo, V; Tentillier, N, 2013)
"Parkinson's disease is universal and the second most prevalent neurodegenerative disease among the elderly affecting between 0."( Chagas, MH; Crippa, JA; Marchi, KC; Miasso, AI; Tirapelli, CR; Tumas, V, 2013)
"Parkinson's disease is associated with alterations in nasal cycle, nasal mucosa pH and mucociliary clearance time."( Aygul, R; Kotan, D; Tatar, A; Ulvi, H, 2013)
"Parkinson's disease is a neurodegenerative disorder caused by loss of dopaminergic neurons in the substantia nigra."( Liu, Z; Song, L; Wu, N; Yang, X; Yuan, W, 2013)
"Parkinson's disease is characterized by α-synuclein pathology in the form of Lewy bodies and Lewy neurites."( Brundin, P; George, S; Reichenbach, N; Rey, NL; Steiner, JA, 2013)
"Parkinson's disease is characterized by the loss of dopamine neurons in the substantia nigra pars compacta, decreased striatal dopamine levels and consequent onset of extrapyramidal motor dysfunction."( Bel, ED; Lazzarini, M; Martin, S; Mitkovski, M; Stühmer, W; Vozari, RR, 2013)
"Parkinson's disease is characterized by intracellular proteinaceous depositions known as Lewy bodies."( Eisbach, SE; Outeiro, TF, 2013)
"Parkinson's disease is associated with gastrointestinal motility abnormalities favoring the occurrence of local infections."( Barbaro, F; Bentivoglio, AR; Bove, F; Campanale, M; Di Giacopo, R; Fasano, A; Fortuna, S; Gabrielli, M; Gasbarrini, A; Gigante, G; Lauritano, EC; Marconi, S; Navarra, P; Petracca, M; Piano, C; Ragazzoni, E; Tortora, A; Zocco, MA, 2013)
"Parkinson's disease is the second most common neurodegenerative disorder, in which both alpha-synuclein (α-syn) and dopamine (DA) have a critical role."( Dalton, CF; Illes-Toth, E; Smith, DP, 2013)
"Parkinson's disease is a common progressive neurodegenerative disease, of which the main neuropathological hallmark is dopaminergic neuronal loss."( Calabresi, P; Castrioto, A; Di Filippo, M; Picconi, B, 2013)
"Parkinson's disease is characterized by motor deficits caused by loss of midbrain dopaminergic neurons."( Andersson, A; Dannaeus, K; Delfani, K; Di Monte, DA; Haegerstrand, A; Häggblad, J; Hill, MP; Isacson, R; Janson Lang, AM; McCormack, AL; Nielsen, E; Palmer, T; Patrone, C; Rönnholm, H; Wikstrom, L; Zachrisson, O; Zhao, M, 2011)
"The hallmark of Parkinson's disease is the destruction of nigrostriatal dopaminergic neurons."( Artigas, F; Bortolozzi, A; Daws, LC; De Deurwaerdère, P; Hensler, JG; Koek, W; Milan, L; Navailles, S, 2013)
"Motor symptoms of Parkinson's disease are commonly treated using l-DOPA although long-term treatment usually causes debilitating motor side effects including dyskinesias."( Bishop, C; Dupre, KB; Eskow Jaunarajs, KL; Goldenberg, AA; Lindenbach, D; Ostock, CY, 2013)
"Parkinson's disease is a common neurodegenerative disease characterised by the loss of dopaminergic neurons in the substantia nigra pars compacta and the formation of α-synuclein aggregates found in Lewy bodies throughout the brain."( Danzer, KM; Eschbach, J, 2014)
"Parkinson's disease is an age-related disease whose pathogenesis is not completely known."( Büchel, F; Dräger, A; Hoffmann, S; Kahle, PJ; Saliger, S; Wrzodek, C; Zell, A, 2013)
"Parkinson's disease is characterised by the degeneration of the midbrain dopaminergic system and is associated with cognitive dysfunction, including slowed information processing."( Biernat, HB; Friberg, L; Jennum, PJ; Korbo, L; Nikolic, M; Zoetmulder, M, 2014)
"Parkinson's disease is characterised by excessive subcortical beta oscillations."( Anzak, A; Brown, P; Kühn, A; Little, S; Pogosyan, A; Tan, H, 2013)
"Parkinson's disease is typically treated with oral dopamine replacement therapies; however, long-term treatment leads to motor complications and, occasionally, impulse control disorders caused by intermittent stimulation of dopamine receptors and off-target effects, respectively."( Abhay, K; Barker, RA; Breen, DP; Brugières, P; Buttery, PC; Cesaro, P; Deeley, S; Dolphin, P; Drouot, X; Fenelon, G; Gabriel, I; Ghaleh, B; Gurruchaga, JM; Guzman, NV; Hantraye, P; Harrop, R; Iwamuro, H; Kas, A; Kelleher, M; Kingsman, SM; Lavisse, S; Le Corvoisier, P; Lefaucheur, JP; Lepetit, H; Lucas, C; Mason, S; Mazarakis, ND; Miskin, J; Mitrophanous, KA; Naylor, S; Palfi, S; Radcliffe, PA; Ralph, GS; Rascol, O; Remy, P; Tani, N; Thiriez, C; Watts, C, 2014)
"Parkinson's disease is a neurodegenerative disorder characterized by the loss of striatal dopaminergic neurons."( Dézsi, L; Vécsei, L, 2014)
"Parkinson's disease is the second most common neurodegenerative movement disorder; however, its etiology remains elusive."( Gaki, GS; Papavassiliou, AG, 2014)
"PD (Parkinson's disease) is characterized by some typical motor features that are caused by striatal dopamine depletion and respond well to dopamine-replacement therapy with L-dopa."( Cenci, MA, 2014)
"Parkinson's disease is a neurodegenerative disorder characterized by Lewy bodies, a pathological hallmark comprised mostly of aggregated alpha synuclein."( Dimant, H; Fan, Z; Hyman, BT; Kibuuka, LN; McLean, PJ; Zhu, L, 2014)
"Parkinson's disease is a frequent neurodegenerative disease, which typically occurs in older age."( Lettow, I; Röther, J, 2014)
"Parkinson's disease is one of the most common neurodegenerative disorders and mitochondrial dysfunction plays an important role in its pathogenesis."( Luo, H; Luo, M; Wang, J; Xiao, Y, 2014)
"Parkinson's disease is characterized by the progressive and selective loss of dopaminergic neurons in the substantia nigra."( Cooper, AJ; Pinto, JT; Spencer, JP; Vauzour, D, 2014)
"Parkinson's disease is a multifactorial neurodegenerative disorder, characterized by a reduction of dopamine (DA) levels."( Conte, C; Ianni, F; Lisanti, A; Natalini, B; Sardella, R; Scorzoni, S, 2014)
"PD (Parkinson's disease) is a complex disorder that is associated with neuronal loss or dysfunction caused by genetic risks, environmental factors and advanced aging."( Ding, JQ; Lou, J; Ma, J; Wu, JB; Wu, R; Yuan, Z; Zhang, Q; Zheng, Z, 2014)
"A major feature of Parkinson's disease is the formation of Lewy bodies in dopaminergic neurons which consist of misfolded α-synuclein."( Dmitriev, O; Kakish, J; Lee, JS; Nokhrin, S; Tavassoly, O, 2014)
"Parkinson's disease is a chronic neurodegenerative disorder characterized by the motor symptoms of bradykinesia, tremor, rigidity and postural instability."( Niccolini, F; Politis, M, 2015)
"Parkinson's disease is a neurodegenerative disorder that results from the degeneration of dopaminergic neurons in the central nervous system, primarily in the substantia nigra."( Ahmad, ST; Liao, J; Morin, LW, 2014)
"Parkinson's disease is a chronic, progressive neurodegenerative disorder with increased prevalence in the aging population."( Abdullah, R; Alves, G; Basak, I; Larsen, JP; Møller, SG; Patil, KS, 2015)
"While Parkinson's disease is a chronic and progressive movement disorder, no one can predict which symptoms will affect an individual patient."( Alexiou, A; Psiha, M; Vlamos, P, 2015)
"Parkinson's disease is one of several neurodegenerative diseases associated with a misfolded, aggregated and pathological protein."( Herva, ME; Spillantini, MG, 2015)
"Parkinson's disease is one of the most common neurologic disorder, affecting about 1-4% of persons older than 60 years."( Alecci, M; Antonosante, A; Benedetti, E; Cimini, A; Cristiano, L; Di Giacomo, E; Falcone, R; Fidoamore, A; Florio, TM; Giordano, A; Ippoliti, R; Massimi, M, 2015)
"Parkinson's disease is associated with early parasympathetic dysfunction leading to constipation and gastroparesis."( Borghammer, P; Brooks, DJ; Danielsen, EH; Fedorova, T; Gjerløff, T; Hansen, J; Jacobsen, S; Knudsen, K; Munk, OL; Nahimi, A; Pavese, N; Terkelsen, AJ, 2015)
"Parkinson's disease is primarily a movement disorder with predilection for the nigral dopaminergic neurons and is often associated with widespread neurodegeneration and diffuse Lewy body deposition."( Alexopoulou, Z; Perrett, RM; Tofaris, GK, 2015)
"Parkinson's disease is an incurable neurodegenerative disease."( Vanhauwaert, R; Verstreken, P, 2015)
"Parkinson's disease is a neurodegenerative disorder characterized by the loss of neurons in specific regions of the nervous system, notably in the substantia nigra pars compacta and, in most cases, by the deposition of intraneuronal inclusions named Lewy bodies."( Bobela, W; Schneider, BL; Zheng, L, 2014)
"Sleep disorders in Parkinson's disease are very common."( Alatriste-Booth, V; Camacho-Ordoñez, A; Cervantes-Arriaga, A; Rodríguez-Violante, M, 2015)
"Parkinson's disease is the second most common neurodegenerative disease which affects almost 1 percent of the population above the age of 60."( Sen, D; Varma, D, 2015)
"A key-feature of Parkinson's disease is the formation of Lewy bodies, which are cytoplasmic protein inclusions."( Braus, GH; Kleinknecht, A; Popova, B, 2015)
"Parkinson's disease is the second most common neurodegenerative disorder with selective and progressive decline of nigral dopaminergic neurons."( Baluchnejadmojarad, T; Kiasalari, Z; Roghani, M, 2016)
"Alzheimer's and Parkinson's diseases are the most prevalent neurodegenerative diseases that generate important health-related direct and indirect socio-economic costs."( Bezard, E; Bourdenx, M; Dehay, B; Koulakiotis, NS; Sanoudou, D; Tsarbopoulos, A, 2017)
"The diagnosis of Parkinson's disease is supported histologically by the findings of α-synuclein immunopositive Lewy bodies and neurites and severe substantia nigra cell loss."( Davey, K; Holton, JL; Kearney, S; Lees, AJ; Ling, H; Mok, KY; Polke, JM; Revesz, T; Silveira-Moriyama, L; Strand, C; Yip, HL, 2016)
"Parkinson's disease is primarily a disorder of response initiation characterized by an excessive motor inhibition, whereas levodopa-induced dyskinesias are clearly a clinical expression of disinhibition of movements."( Arabia, G; Augimeri, A; Cerasa, A; Donzuso, G; Mangone, G; Morelli, M; Passamonti, L; Quattrone, A; Salsone, M, 2015)
"Parkinson's disease is a progressive neurodegenerative disorder with multiple factors contributing to increasing severity of pathology in specific brain regions."( Cartwright, H; Halliday, GM; McCann, H, 2016)
"Parkinson's disease is characterised by three main symptoms: slowness and paucity of movements, rigidity, and resting tremor."( , 2015)
"Parkinson's disease is the most common movement disorder, characterized by a progressive and extensive loss of dopaminergic neurons in the substantia nigra pars compacta and their terminals in the striatum."( Moldzio, R; Radad, K; Rausch, WD, 2015)
"Parkinson's disease is a progressive neurodegenerative disorder associated with tremor, rigidity, and bradykinesia, as well as nonmotor symptoms including autonomic impairments, olfactory dysfunction, sleep disturbances, depression, and dementia."( Bordia, T; Perez, XA; Quik, M; Zhang, D, 2015)
"Parkinson's disease is the second most frequent neurodegenerative disorder."( Ransmayr, G, 2015)
"Parkinson's disease is a progressive neurological disorder that is characterized by the formation of intracellular protein inclusion bodies composed primarily of a misfolded and aggregated form of the protein α-synuclein."( Brundin, P; Steiner, JA; Tyson, T, 2016)
"Parkinson's disease is characterized by degeneration of dopaminergic neurons in the substantia nigra pars compacta along with the formation of intracellular fibrillar inclusions (Lewy bodies and Lewy neuritis), which are mainly composed of aggregated α-synuclein (ASYN)."( Atienzar, FA; Foerch, P; Marmolino, D; Michel, A; Scheller, D; Staelens, L, 2016)
"Parkinson's disease is the second most common neurodegenerative disorder around the world."( Bereczki, D; Nagy, H; Takáts, A; Toth, A; Wacha, J, 2015)
"Parkinson's disease is a neurodegenerative disorder characterized by a loss of nigrostriata dopaminergic neurons, which has been thought, at least in part, to result from oxidative stress."( Du, N; Guo, Z; Han, M; Huang, Y; Liu, J; Xu, S, 2016)
"Parkinson's disease is a motor dysfunction that has been widely studied but many of the reports on commercial drugs for the treatment of this disease have afforded some undesirable side effects that generate an extensive and unviable treatment by economic costs and due to the bioavailability of the assayed compounds."( Fazel Nabavi, S; Modak, B; Rastrelli, L; Sobarzo-Sánchez, E; Uriarte, E, 2016)
"Parkinson's disease is a common progressive neurodegenerative disorder presenting with characteristic motor symptoms."( Fülöp, F; Majláth, Z; Toldi, J; Vécsei, L, 2016)
"Parkinson's disease is a progressive brain disorder due to the degeneration of dopaminergic neurons in the substantia nigra."( Allsop, D; Aojula, H; Emamzadeh, FN; McHugh, PC, 2016)
"Parkinson's disease is a slowly progressing neurodegenerative disorder caused by loss of dopaminergic neurons in the substantia nigra (SN), leading to severe impairment in motor and non-motor functions."( Collmann, FM; Dollé, F; Faber, C; Faust, A; Fricke, IB; Hermann, S; Jacobs, AH; Kuhlmann, MT; Schäfers, K; Schwamborn, JC; Viel, T; Vrachimis, A; Wachsmuth, L; Worlitzer, MM, 2016)
"The dyskinesia of Parkinson's Disease is most likely due to excess levels of dopamine in the striatum."( Boon, WC; Chua, HK; Horne, M; Stanic, D; Tomas, D; White, K, 2016)
"Parkinson's disease is a common, progressive neurodegenerative disorder, affecting 3% of those older than 75 years of age."( Hernandez, DG; Reed, X; Singleton, AB, 2016)
"Parkinson's disease is a complex age-related neurodegenerative disorder."( Cook, AL; Dong, LF; Mackay-Sim, A; Matigian, N; Mellick, GD; Murtaza, M; Neuzil, J; Ravishankar, S; Shan, J; Silburn, P; Todorovic, M; Wood, SA, 2016)
"Parkinson's disease is characterized by progressive loss of dopaminergic neurons."( Audrain, H; Bender, D; Borghammer, P; Brooks, DJ; Fedorova, T; Hansen, AK; Knudsen, K; Landau, AM; Lillethorup, TP; Parbo, P; Østergaard, K, 2016)
"Parkinson's disease is primarily caused by dysfunction of dopaminergic neurons, however, nondopaminergic (ND) systems are also involved."( Fox, SH; Freitas, ME, 2016)
"Parkinson's disease is a progressive neurodegenerative disorder characterised by a loss of dopaminergic neurons in the substantia nigra pars compacta, which results in a significant decrease in dopamine levels and consequent functional motor impairment."( Canales-Aguirre, AA; Diaz, NF; Díaz-Martínez, NE; Gómez-Pinedo, U; Gutiérrez-Mercado, YK; Marquez-Aguirre, AL; Padilla-Camberos, E; Sandoval-Avila, S, 2019)
"Parkinson's disease is a neurodegenerative disorder which is primarily characterized by an abnormal basal ganglia activity."( Bokor, M; Gyorfi, O; Keri, S; Nagy, H, 2016)
"Parkinson's disease is a chronic neurodegenerative disorder characterized by a progressive loss of dopaminergic neurons."( Ashraghi, MR; Niccolini, F; Pagano, G; Politis, M; Polychronis, S, 2016)
"Parkinson's disease is a common neurodegenerative disorder, which is due to the loss of dopaminergic neurons in the substantia nigra pars compacta (SNpc) and for which no definitive cure is currently available."( Altarche-Xifro, W; Bortolozzi, A; Bové, J; Cosma, MP; di Vicino, U; Muñoz-Martin, MI; Vila, M, 2016)
"Parkinson's disease is characterized by the death of dopaminergic neurons, mainly in the substantia nigra, and causes serious locomotor dysfunctions."( Bordin, DL; Ellwanger, JH; Franke, SI; Henriques, JA; Prá, D, 2016)
"Parkinson's disease is a highly debilitating neurodegenerative condition whose pathological hallmark is the presence in nerve cells of proteinacious deposits, known as Lewy bodies, composed primarily of amyloid fibrils of α-synuclein."( Buell, AK; Dobson, CM; Flagmeier, P; Galvagnion, C; Knowles, TP; Meisl, G; Vendruscolo, M, 2016)
"Parkinson's disease is the second most prevalent neurodegenerative disorder."( Outeiro, TF; Paiva, I; Pavlou, MAS; Pinho, R, 2017)
"Parkinson's disease is a progressive neurological disorder, marked by the loss of dopaminergic neurons in the nigrostriatal pathway that leads to abnormal gait, rigidity, slowness of movement, and tremor."( Baldwin, HA; Harvey, BK; Koivula, PP; Necarsulmer, JC; Whitaker, KW, 2017)
"In fact, Parkinson's disease is characterized not only by unilateral motor symptoms that arise at the early stages, but has other non-motor symptoms such as autonomic or cognitive alterations that are also revealed asymmetrically."( Banegas, I; Prieto, I; Ramirez-Sanchez, M; Segarra, AB, 2016)
"Parkinson's disease is a disabling hypokinetic neurological movement disorder in which the aetiology is unknown in the majority of cases."( Hurley, MJ; Swart, T, 2016)
"Parkinson's disease is a debilitating, age-associated movement disorder."( Abeliovich, A; Gitler, AD, 2016)
"Parkinson's disease is a progressive neurodegenerative disorder characterized by the loss of dopaminergic neurons in the substantia nigra and the accumulation of α-synuclein (Lewy bodies)."( Doria, M; Lizard, G; Maugest, L; Moreau, T; Vejux, A, 2016)
"Parkinson's disease is the second most common neurodegenerative disorder, with only partial symptomatic therapy and no mechanism-based therapies."( Goedert, M; Spillantini, MG; Tofaris, GK, 2017)
"Parkinson's disease is accompanied by nonmotor symptoms including cognitive impairment, which precede the onset of motor symptoms in patients and are regulated by dopamine (DA) receptors and the mesocorticolimbic pathway."( Mishra, A; Shukla, R; Shukla, S; Singh, S; Srivastava, N, 2018)
"Parkinson's disease is a debilitating neurodegenerative disorder that is pathologically characterized by intracellular inclusions comprised primarily of alpha-synuclein (αSyn) that can also be transmitted from neuron to neuron."( Darley-Usmar, V; Redmann, M; Volpicelli-Daley, L; Wani, WY; Zhang, J, 2017)
"Although Parkinson's disease is characterized by dopamine depletion in the basal ganglia, the dopaminergic basis of resting tremor remains unclear: dopaminergic medication reduces tremor in some patients, but many patients have a dopamine-resistant tremor."( Aarts, E; Bloem, BR; den Ouden, HE; Dirkx, MF; Helmich, RC; Timmer, MH; Toni, I, 2017)
"The pathogenesis of Parkinson's disease is closely associated with the aggregation of the α-synuclein protein."( Ma, B; Nussinov, R; Thompson, D; Xu, L, 2017)
"Parkinson's disease is characterized by accumulation of intraneuronal cytoplasmic inclusions, Lewy bodies, which mainly consist of aggregated α-synuclein."( Bornefall, P; Eriksson, I; Giraldo, AM; Nath, S; Öllinger, K, 2017)
"Parkinson's disease is characterized by the progressive loss of dopaminergic neurons from the substantia nigra, a process that leads to a dopamine deficiency in the striatum."( Azevedo, BN; Calice da Silva, C; da Costa, JC; Machado, DC; Martins, LAM; Zimmer, ER, 2017)
"Parkinson's disease is characterized by a pure asymmetric parkinsonian syndrome, responsive to dopaminergic treatment."( Grabli, D, 2017)
"Parkinson's disease is characterized by the presence of insoluble and neurotoxic aggregates (amyloid fibrils) of an intrinsically disordered protein α-synuclein."( Batra, R; Chowdhury, PK; Gautam, S; Karmakar, S; Kundu, B; Pradhan, P; Sharma, P; Singh, J, 2017)
"The treatment of Parkinson's disease is symptomatic with the use of dopaminergic medications: levodopa, dopaminergic agonists and enzymatic inhibitors."( Defebvre, L; Moreau, C, 2017)
"Parkinson's disease is a growing threat to an ever-ageing population."( Styczyńska-Soczka, K; Zechini, L; Zografos, L, 2017)
"Parkinson's disease is neuropathologically characterised by loss of catecholamine neurons in vulnerable brain regions including substantia nigra pars compacta and locus coeruleus."( Liddell, JR; White, AR, 2018)
"Parkinson's disease is a multifactorial neurodegenerative disorder, the aetiology of which remains elusive."( Devedjian, JC; Devos, D; Duce, JA; Durham, H; Smith, DP; Wong, BX, 2017)
"Parkinson's disease is the second most common neurodegenerative disorder after Alzheimer's disease."( Azulay, JP; Blin, O; Guilhaumou, R; Marsot, A, 2017)
"Parkinson's disease is assumed to be caused by mitochondrial dysfunction in the affected dopaminergic neurons in the brain."( Fuchigami, T; Imamura, H; Kakizuka, A; Nakano, M; Sasaoka, N; Shudo, T; Takahashi, R; Uemura, N; Yamamoto, M, 2017)
"Parkinson's disease is characterized by progressively distributed Lewy pathology and neurodegeneration."( Halliday, GM; Simuni, T; Surmeier, DJ, 2017)
"Parkinson's disease is the second most common neurodegenerative illness after Alzheimer's disease."( Ceballos-Baumann, A; Honig, H; Jost, WH; Storch, A; Tönges, L, 2017)
"Parkinson's disease is characterized by a heterogeneous combination of motor and non motor symptoms."( Müller, T, 2017)
"Parkinson's disease is characterized by progressive decline in motor function due to degeneration of nigrostriatal dopaminergic neurons, as well as other deficits including cognitive impairment and behavioural abnormalities."( Boger, HA; Corum, D; Lynn, MK; Schnellmann, RG; Scholpa, NE, 2018)
"Parkinson's disease is a common, debilitating, neurodegenerative disorder for which the current gold standard treatment, levodopa (L-DOPA) is symptomatic."( Cronin, A; Grealy, M, 2017)
"Anxiety in Parkinson's disease is a comorbid non-motor symptom that alters the quality of life of patients."( Benazzouz, A; Faggiani, E; Janssen, MLF; Naudet, F; Temel, Y, 2018)
"Parkinson's disease is a progressive, age-related, neurodegenerative disorder, and oxidative stress is an important mediator in its pathogenesis."( Saito, Y, 2017)
"Parkinson's disease is the most common neurodegenerative disorder after Alzheimer's disease, with the majority of cases being sporadic or "idiopathic"."( Grünblatt, E; Mandel, SA; Monoranu, CM; Riederer, P; Ruder, J; Youdim, MB, 2018)
"Parkinson's disease is a growing concern as the longevity of the world's population steadily increases."( Bardien, S; Bossert, M; Buckle, C; Carr, J; du Plessis, S; Emsley, R; Seedat, S; van den Heuvel, L; Vink, M, 2018)
"Parkinson's disease is a chronic neurodegenerative disorder characterized by cardinal motor features, such as bradykinesia, but also vocal deficits (e."( Andreatini, R; Bruginski, E; Campos, FR; de Almeida Soares Hocayen, P; Kanazawa, LKS; Miyoshi, E; Schwarting, RKW; Stern, CAJ; Vecchia, DD; Vital, MABF; Wendler, E; Wöhr, M, 2018)
"Parkinson's disease is marked clinically by motor dysfunction and pathologically by dopaminergic cell loss in the substantia nigra and iron accumulation in the substantia nigra."( Connor, JR; Huang, X; Lamendella, R; Meadowcroft, MD; Nandar, W; Neely, EB; Nixon, AM; Purnell, CJ; Snyder, AM; Wright, J, 2018)
"Parkinson's disease is characterized by the loss of dopamine (DA) neurons in the substantia nigra pars compacta (SNc)."( Farino, ZJ; Freyberg, RJ; Freyberg, Z; Hnasko, TS; Lu, W; Przedborski, S; Sonders, MS; Steinkellner, T; Villeneuve, M; Zell, V, 2018)
"Parkinson's disease is a progressive neurodegenerative disease that affects millions of elderly individuals worldwide."( Blesa, J; Del Rey, NL; Trigo-Damas, I, 2018)
"Parkinson's disease is a neurodegenerative disease, associated with reactive gliosis, neuroinflammation, and oxidative stress."( Garrett, TJ; Gill, EL; Raman, S; Vedam-Mai, V; Yost, RA, 2018)
"Parkinson's disease is characterized by the progressive loss of midbrain dopamine neurons."( Bair-Marshall, CJ; Girasole, AE; Guenthner, CJ; Kreitzer, AC; Lum, MY; Luo, L; Nathaniel, D; Nelson, AB, 2018)
"Parkinson's disease is a neurodegenerative movement disorder caused by the loss of dopaminergic neurons from substantia nigra."( Alaimo, A; Coluccio Leskow, F; Fuentes, F; Gorojod, RM; Kotler, ML; Martinez, JH; Porte Alcon, S, 2018)
"Parkinson's disease is associated with intracellular α-synuclein accumulation and ventral midbrain dopaminergic neuronal death in the Substantia Nigra of brain patients."( Berkowitz, L; Calatayud, C; Caldwell, GA; Caldwell, KA; Carballo-Carbajal, I; Consiglio, A; Dalfo, E; Ezquerra, M; Fernández-Carasa, I; Fernández-Santiago, R; Guha, S; Kapahi, P; Kim, H; Lizcano, JM; Miranda-Vizuete, A; Raya, Á; Vila, M, 2018)
"Parkinson's disease is caused by complex interactions between environmental factors and a genetic predisposition."( Parr-Brownlie, LC; Smith, LM, 2019)
"Parkinson's disease is a heterogeneous disorder where genetic factors may underlie clinical variability."( Bjørnarå, KA; Dietrichs, E; Pihlstrøm, L; Toft, M, 2018)
"Parkinson's disease is affecting about 1% of the population above 65 years."( Gazzaz, M; Lucio, M; Michalke, B; Schmitt-Kopplin, P; Schroeter, M; Sigaroudi, A; Willkommen, D, 2018)
"Parkinson's disease is characterized by the loss of nigrostriatal dopaminergic signaling and the presence of alpha-synuclein aggregates (also called Lewy bodies and neurites) throughout the brain."( Brundin, P; Quansah, E; Steiner, JA, 2018)
"Parkinson's disease is a neurodegenerative disorder characterized by motor and non-motor symptoms."( D'Abreu, A, 2018)
"Parkinson's disease is a progressive neurodegenerative disease characterized by Lewy body pathology of which the primary constituent is aggregated misfolded alpha-synuclein protein."( Fowler, AJ; Moussa, CE, 2018)
"Parkinson's disease is a leading hypokinetic disorder characterized by selective loss of dopaminergic neurons in substantia nigra pars compacta (SNpc) region of mid-brain."( Deshmukh, R; Kumar, P; Sharma, S, 2018)
"Parkinson's disease is the second most common neurodegenerative disorder after Alzheimer's disease."( Ketterman, AJ; Kumrapich, B; Roytrakul, S; Saisawang, C; Wipasa, J; Wongtrakul, J, 2018)
"Parkinson's disease is the most common neurodegenerative movement disorder."( Kalia, LV; Kalia, SK; O'Hara, DM, 2018)
"Parkinson's disease is a chronic, neurodegenerative disease."( Möhr, JD; Müller, T, 2018)
"Parkinson's disease is a common neurodegenerative disorder presenting with a variety of motor and non-motor symptoms."( O'Keeffe, GW; Sullivan, AM, 2018)
"Parkinson's disease is a progressive neurodegenerative disease characterized by progressive and selective death of dopaminergic neurons."( Asadi-Shekaari, M; Eftekhar-Vaghefi, SH; Elyasi, L; Esmaeili-Mahani, S, 2019)
"Parkinson's disease is a progressive neuropathological disorder that belongs to the class of synucleinopathies, in which the protein alpha-synuclein is found at abnormally high concentrations in affected neurons."( Britschgi, M; Guerrero-Ferreira, R; Lauer, ME; Mona, D; Riek, R; Ringler, P; Stahlberg, H; Taylor, NM, 2018)
"Parkinson's disease is diagnosed upon the presentation of motor symptoms, resulting from substantial degeneration of dopaminergic neurons in the midbrain."( Barnham, KJ; Beauchamp, LC; Bush, AI; Chan, J; Coleman, B; Hill, AF; Hung, LW; Jacobson, L; Lazarou, M; Liu, XM; Padman, BS; Vella, LJ, 2018)
"Parkinson's disease is characterized by a progressive loss of substantia nigra (SN) dopaminergic neurons and the formation of Lewy bodies containing accumulated alpha-synuclein (α-syn)."( Alstrup, AKO; Brooks, DJ; Doudet, DJ; Glud, AN; Hinz, R; Jakobsen, S; Kirik, D; Landau, AM; Landeck, N; Lillethorup, TP; Sørensen, JC; Vang, K, 2018)
"Parkinson's disease is the second most common neurodegenerative disorder."( Barker, RA; Stoker, TB, 2018)
"Parkinson's disease is a neurodegenerative disorder involving the progressive loss of dopaminergic neurons (DNs), with currently available therapeutics, such as L-Dopa, only able to relieve some symptoms."( Foster, JD; Humphrey, KM; Ohm, JE; Pandey, S; Selvaraj, S; Singh, BB; Sun, Y; Watt, JA; Wu, M, 2018)
"Parkinson's disease is characterized by a loss of dopaminergic innervation in the basal ganglia leading to complex motor and non-motor symptoms."( de Almeida Marcelino, AL; Ewert, S; Hamker, F; Horn, A; Irmen, F; Krause, P; Kühn, AA; Neumann, WJ; Schneider, GH; Schroll, H, 2018)
"Parkinson's disease is a common neurodegenerative disease characterized by a widely variety of motor and non-motor symptoms."( Di Giovanni, G; Galati, S; Grandi, LC, 2018)
"Parkinson's disease is a progressive neurodegenerative disease increasingly affecting our aging population."( Choudhury, GR; Daadi, MM, 2018)
"Parkinson's disease is caused by dopamine deficiency in the striatum, which is a result of loss of dopamine neurons from the substantia nigra pars compacta."( Inoue, KI; Minamimoto, T; Miyachi, S; Nagai, Y; Nambu, A; Nishi, K; Okado, H; Takada, M, 2019)
"Parkinson's disease is pathologically characterized by the degeneration of dopaminergic neurons in the substantia nigra and the accumulation of neuronal cytoplasmic inclusions known as Lewy bodies, which are primarily composed of α-synuclein."( Chen, S; He, Y; Yu, Z, 2019)
"Parkinson's disease is characterized by neurodegeneration of the dopaminergic neurons in the substantia nigra pars compacta."( Butler, B; Felfli, M; Lambert, J; Lehéricy, S; Perlbarg, V; Petiet, A; Privat, AL; Valabrègue, R, 2018)
"Parkinson's disease is a widespread neurodegenerative disorder which affects brain metabolism."( Supandi, F; van Beek, JHGM, 2018)
"Parkinson's disease is a chronic multi-system disease that can cause motor and non-motor symptoms, cognitive changes and variably effective medications."( Brock, P; Fisher, JM; Hand, A; Walker, RW, 2019)
"Parkinson's disease is characterized by progressive death of dopaminergic neurons, leading to motor and cognitive dysfunction."( Bender, CA; Francisco, AB; Glorioso, C; Libert, S; Lugay, FJ; Nicholatos, JW; Salazar, JE; Yeh, T, 2018)
"Parkinson's disease is characterized by the progressive loss of dopamine neurons in the substantia nigra, leading to severe motor deficits."( Beckstead, MJ; Branch, SY; Chen, C; Ge, G; Li, S; Lynch, WB; Sharpe, AL; Tschumi, CW, 2018)
"Parkinson's disease is a prevalent and debilitating neurological disorder, where the severity of motor symptoms are frequently monitored using clinical tests that include a hand pronation and supination task."( Hernandez, ME; Hu, Y; Ziegelmanl, L, 2018)
"Parkinson's disease is a neurodegenerative disease resulting in degeneration of midbrain dopaminergic neurons."( Hey, SM; Jensen, P; Kristensen, BW; Martínez Serrano, A; Meyer, M; Ryding, M, 2019)
"Parkinson's disease is a neurodegenerative disorder, and recent studies suggested that oxidative stress contributes to the degeneration of dopamine cell in Parkinson's disease."( Li, J; Liu, Z; Lu, G; Wang, Q; Wang, Y; Zhao, Y, 2019)
"Parkinson's disease is the second most common neurodegenerative disorder in adults over the age of 65."( Korkmaz, OT; Tunçel, N, 2018)
"Parkinson's disease is the second most common neurodegenerative disease without cure."( Szabo, A; Tofaris, GK, 2019)
"Parkinson's disease is the second most common neurodegenerative disorder, leading to the progressive decline of motor control due to the loss of dopaminergic neurons in the substantia nigra pars compacta."( Gonzalez, C; Hetz, C; Lopez, N; Martinez, A, 2019)
"Parkinson's disease is primarily characterized by diminished dopaminergic function; however, the impact of these impairments on large-scale brain dynamics remains unclear."( Bell, PT; Halliday, GM; Lewis, SJG; Matar, E; O'Callaghan, C; Poldrack, RA; Shine, JM, 2019)
"Parkinson's disease is characterized by the deterioration of dopaminergic neurons of substantia nigra pars compacta along with a substantial loss of noradrenergic neurons of the locus coeruleus, which is the major source of noradrenaline (NA) in the brain."( Bhat, R; Singh, P, 2019)
"Parkinson's disease is characterized by a proteinopathy that includes aggregates of α-synuclein."( Flores-Cuadrado, A; Martinez-Marcos, A; Mohedano-Moriano, A; Saiz-Sanchez, D; Ubeda-Bañon, I, 2019)
"Parkinson's disease is characterized by multiple motor and non-motor symptoms that are difficult to diagnose at early stages of the pathogenesis."( Cheng, WH; Liu, RP; Zhang, X; Zhu, JH, 2019)
"Dystonia and Parkinson's disease are closely linked disorders sharing many pathophysiological overlaps."( Bhatia, KP; Lang, AE; Shetty, AS, 2019)
"Parkinson's disease is the second most common neurodegenerative disease."( Boros, FA; Klivényi, P; Pesei, ZG; Török, R; Vágvölgyi-Sümegi, E; Vécsei, L, 2019)
"Parkinson's disease is the second most common neurodegenerative disorder worldwide."( Arcos-López, T; Fernández, CO; González, N; König, A; Menacho Márquez, M; Outeiro, TF; Quintanar, L, 2019)
"Parkinson's disease is an intractable disorder with heterogeneous clinical presentation that may reflect different underlying pathogenic mechanisms."( Figini, S; Galvani, M; Marinus, J; Mastroberardino, PG; Milanese, C; Molano González, N; Nait Abdellah, S; Payán-Gómez, C; Tresini, M; van Hilten, JJ; van Roon-Mom, WMC, 2019)
"Parkinson's disease is the second most common neurodegenerative disease caused by degeneration of dopamine neurons in the substantia nigra."( Af Bjerkén, S; Dudka, I; Laterveer, R; Virel, A, 2019)
"Pain in Parkinson's disease is not simply a consequence of motor complainants."( Buhidma, Y; Duty, S; Leta, V; Malcangio, M; Ray Chaudhuri, K; Rukavina, K; Sportelli, C, 2019)
"Parkinson's disease is the second most common neurodegenerative disorder after Alzheimer's disease and is estimated to affect approximately 1-4% of individuals aged over 60 years old."( El-Agnaf, OMA; Erskine, D; Fayyad, M; Majbour, N; Mollenhauer, B; Salim, S; Stoops, E, 2019)
"Parkinson's disease is a neurodegenerative disorder with motor symptoms linked to the loss of dopaminergic neurons in the substantia nigra compacta."( Bourque, MJ; Cannon, T; Cayrol, R; Desjardins, M; Ducrot, C; Fahmy, AM; Gruenheid, S; Laplante, A; Le Campion, A; Matheoud, D; McBride, HM; Penttinen, AM; Ramet, L; Trudeau, LE; Voisin, A; Zhu, L, 2019)
"Parkinson's disease is a neurodegenerative movement disorder; however, peripheral symptoms can arise decades prior."( Giasson, BI; Sorrentino, ZA, 2019)
"Parkinson's disease is characterized by a loss of dopaminergic neurons in the ventral midbrain."( Alonso-Gil, S; Morales-Garcia, JA; Perez-Castillo, A; Santos, Á, 2020)
"Parkinson's disease is characterized by motor symptoms (akinesia, rigidity, etc."( Castro-Zaballa, S; Cavelli, M; Costa, G; Gonzalez, J; Lima, MMS; Prunell, G; Torterolo, P; Velásquez, N, 2019)
"Parkinson's disease is a progressive neurodegenerative disorder resulting from the degeneration of pigmented dopaminergic neurons in the substantia nigra pars compacta."( Fu, P; Ko, JK; Lin, K; Yung, KK; Zhang, S; Zhang, Z, 2019)
"Rest tremor in Parkinson's disease is related to cerebral activity in both the basal ganglia and a cerebello-thalamo-cortical circuit."( Bloem, BR; Dirkx, MF; Helmich, RC; Toni, I; van Nuland, A; Zach, H, 2019)
"Parkinson's disease is considered to be due to an increase in the catabolism of dopamine by the action of monoamine oxidase (MAO) enzymes which leads to an increase in reactive oxygen species (ROS) and loss of dopaminergic neurons."( Avila-Acevedo, JG; Garcia-Jimenez, S; Monroy-Noyola, A; Montes, S; Perez-Barron, GA; Rios, LC; Rubio-Osornio, M, 2020)
"Parkinson's disease is the second most common neurodegenerative disorder, and a significant increase in its prevalence in the past three decades has been documented."( Cabreira, V; Massano, J, 2019)
"Parkinson's disease is the second most common neurodegenerative disease."( Bi, K; Fan, K; Gong, G; Jia, Y; Li, Y; Sun, Y; Wu, B; Yan, T, 2019)
"Parkinson's disease is characterized by the aggregation of the presynaptic protein α-synuclein and its deposition into pathologic Lewy bodies."( Chandra, SS; Fenton, WA; Gorenberg, EL; Horwich, AL; Nagy, M; Taguchi, YV; Thrasher, D; Volpicelli-Daley, L, 2019)
"Parkinson's disease is characterized by neurodegeneration and learning deficiency."( Alaei, H; Esfarjani, F; Marandi, SM; Rezaee, Z, 2019)
"Parkinson's disease is characterized by bradykinesia, rigidity, and tremor."( Cools, R; den Ouden, HEM; Dirkx, MFM; Helmich, RC; Scheenen, TWJ; Toni, I; van Asten, JJA; van Nuland, AJM; Zach, H, 2020)
"Parkinson's disease is the second most common neurodegenerative disease in the elderly after Alzheimer's disease."( Cheng, Z; Haacke, EM; He, N; Jiao, Y; Shi, F; Wang, Q; Xiao, B; Yan, F, 2019)
"Parkinson's disease is a neurodegenerative disease characterized by a loss of dopaminergic substantia nigra neurons and depletion of dopamine."( Abd-Elrahman, KS; Bureau, SC; Derksen, A; Dwyer, Z; Farmer, K; Ferguson, SSG; Fortin, T; Hayley, S; Prowse, NA; Rowe, EM; Rudyk, CA; Thompson, AM, 2020)
"Parkinson's disease is a genetically complex disorder."( Ahmed, S; Albert, MS; Alcalay, RN; Bandres-Ciga, S; Blauwendraat, C; Bonet-Ponce, L; Brice, A; Brockmann, K; Cannon, P; Cookson, MR; Corvol, JC; Dawson, TM; Eerola-Rautio, J; Ferrucci, L; Gan-Or, Z; Gasser, T; Gibbs, JR; Greenbaum, L; Grenn, FP; Grosset, D; Hardy, J; Hassin-Baer, S; Heilbron, K; Hernandez, DG; Heutink, P; Hillis, AE; Iwaki, H; Jankovic, J; Krohn, L; Kumaran, R; Langston, R; Leonard, HL; Lesage, S; Majamaa, K; Makarious, MB; Marinus, J; Masliah, E; Morris, CM; Morris, H; Nalls, MA; Noyce, AJ; Pantelyat, A; Pihlstrøm, L; Pletnikova, O; Reed, X; Resnick, SM; Rosenthal, LS; Ruskey, JA; Sabir, M; Scholz, SW; Schulte, C; Sharma, M; Shulman, JM; Shulman, LM; Siitonen, A; Singleton, AB; Tan, M; Tienari, PJ; Toft, M; Troncoso, J; van Hilten, JJ; Wood, N, 2020)
"Parkinson's disease is one of the most common movement disorders and is characterized by dopaminergic cell loss and the accumulation of pathological α-synuclein, but its precise pathogenetic mechanisms remain elusive."( Ayaki, T; El-Agnaf, OMA; Hara, J; Hatanaka, Y; Hondo, M; Ikuno, M; Koike, M; Matsuzawa, S; Nakanishi, E; Okuda, S; Parajuli, LK; Sawamura, M; Taguchi, K; Taguchi, T; Takahashi, R; Tanaka, M; Ueda, J; Uemura, MT; Uemura, N; Yamakado, H; Yanagisawa, M, 2020)
"Parkinson's disease is a very complex public health problem with different etiologies and a wide range of clinical features including motor and non-motor symptoms."( Aimrane, A; Draoui, A; El Hiba, O; El Khiat, A; Gamrani, H, 2020)
"Parkinson's disease is a progressive neurodegenerative disease characterized by striatal dopaminergic loss."( Brevard, J; Fonseca, KR; Gray, DL; Kozak, R; Popiolek, M; Trapa, P; Young, D, 2020)
"Parkinson's disease is one of the most severe progressive neurodegenerative disorders, having a mortifying effect on the health of millions of people around the globe."( Fayaz, F; Kumar, B; Pandey, M; Pottoo, FH; Sahoo, PK; Sharma, A, 2020)
"Parkinson's disease is a progressive nervous system disorder characterized by motor, cognitive, sensory, psychiatric, and autonomic disturbances."( López, WOC; Rondón-Villarreal, P, 2020)
"Parkinson's disease is a progressive neurodegenerative disorder of dopaminergic striatal neurons in basal ganglia."( Elango, P; Ghanta, MK; L V K S, B, 2020)
"Parkinson's disease is a neurodegenerative disorder partly caused by the loss of the dopamine neurons of the nigrostriatal pathway."( Barrot, M; Bezard, E; Bido, S; Dovero, S; Faivre, F; Joshi, A; Sánchez-Catalán, MJ, 2020)
"Parkinson's disease is a common neurodegenerative disorder that presents with nonmotor and motor symptoms."( Elfil, M; Kamel, S; Kandil, M; Koo, BB; Schaefer, SM, 2020)
"Parkinson's disease is one of the most common neurodegenerative diseases."( Byeon, JJ; Choi, JM; Kim, N; Lee, BI; Lim, JH; Na, YG; Park, MH; Park, MJ; Park, SJ; Park, Y; Shin, SH; Shin, YG, 2020)
"Parkinson's disease is one of the most common neurodegenerative disorders and although its aetiology is not yet fully understood, neuroinflammation has been identified as a key factor in the progression of the disease."( de Souza, FRO; Lima, PMD; Ribeiro, FM, 2021)
"A hallmark of Parkinson's disease is the death of neuromelanin-pigmented neurons, but the role of neuromelanin is unclear."( Banerjee, S; Brooks, J; Collingwood, JF; Everett, J; Lermyte, F; Morris, CM; O'Connor, PB; Sadler, PJ; Telling, ND; Tjhin, VT, 2020)
"Parkinson's disease is a neurodegenerative disorder that affects the central nervous system and is mainly characterized by the loss of dopaminergic neurons and pro-oxidant mechanisms."( Aragão Catunda Junior, FE; Basto Souza, R; da Cunha Ferreira, NM; de Sousa Dos Reis, TD; Hardy Lima Pontes, N; Maranguape Silva da Cunha, R; Moreira Vasconcelos, CF; Vasconcelos Aguiar, LM, 2020)
"Parkinson's disease is associated with aggregation of pathological α-synuclein (αSyn) proteins."( Tripathi, T, 2020)
"Parkinson's disease is a progressive and debilitating disorder that has so far eluded attempts to develop disease-modifying treatment."( Hirsch, EC; Standaert, DG, 2021)
"Parkinson's disease is a neurodegenerative disorder that manifests as motor deficits, tremors, rigidity, and postural instability."( Hattori, N; Nagai, M, 2020)
"Parkinson's disease is defined by neuronal degeneration and neuroinflammation and it is reported that the presence of the neurofibrillary aggregates such as Lewy bodies is considered as the marker."( Das, R; Dhanawat, M; Gupta, S; Mehta, DK, 2020)
"Parkinson's disease is a neurodegenerative disorder characterized by the transmission and accumulation of toxic species of α-synuclein (α-syn)."( Aro, P; Bercow, M; Khrisat, T; Li, N; Liu, Z; Matsumoto, J; Peskind, E; Quinn, JF; Sheng, L; Shi, M; Soltys, D; Stewart, T; Thorland, E; Tian, C; Xie, Z; Yang, D; Zabetian, CP; Zhang, J, 2020)
"Parkinson's disease is the second most common neurodegenerative disease after Alzheimer's disease."( Aubignat, M; Krystkowiak, P; Tir, M, 2021)
"Parkinson's disease is associated with severe nigro-striatal dopamine depletion, leading to motor dysfunction and altered reward processing."( Bloem, BR; Buhmann, C; Helmich, RC; Hulme, OJ; Madsen, KH; Münchau, A; Siebner, HR; van der Vegt, JPM, 2020)
"Parkinson's disease is characterized by the presence of abnormal, intraneuronal α-synuclein aggregates, which may propagate from cell-to-cell in a prion-like manner."( Andersen, KB; Bech, E; Berg, D; Bonkat, SK; Borghammer, P; Brooks, DJ; Danielsen, EH; Fedorova, TD; Geday, J; Göder, R; Hansen, SD; Horsager, J; Knudsen, K; Kraft, J; Munk, OL; Okkels, N; Otto, M; Pavese, N; Schaeffer, E; Skjærbæk, C; Sommerauer, M, 2020)
"Parkinson's disease is one of the most common neurodegenerative disorders in elderly age."( Adornato, I; De Luca, L; Gitto, R; Peña-Díaz, S; Ventura, S; Vittorio, S, 2020)
"Parkinson's disease is one of the most common adult-onset, a chronic disorder involving neurodegeneration, which progressively leads to deprivation of dopaminergic neurons in substantia nigra, causing a subsequent reduction of dopamine levels in the striatum resulting in tremor, myotonia, and dyskinesia."( Agarwal, T; He, X; Shen, B; Singla, RK, 2021)
"Parkinson's disease is a progressive neurodegenerative disease for which prevention and effective treatments are lacking."( Kawahara, M; Kobayashi, N; Kubota, M; Shimoda, M; Sugizaki, T; Tanaka, KI, 2020)
"Parkinson's disease is a neurodegenerative disorder mainly characterized by the degeneration of dopaminergic neurons in the substantia nigra."( Castonguay, AM; Gravel, C; Lévesque, M, 2021)
"Parkinson's disease is clinically defined by bradykinesia, along with rigidity and tremor."( Cools, R; den Ouden, HEM; Dirkx, MF; Helmich, RC; Toni, I; van Nuland, AJ; Zach, H, 2020)
"Parkinson's disease is an increasingly prevalent and currently incurable neurodegenerative disorder."( Jayaram, AK; Knowles, TPJ; Krainer, G; Musteikytė, G; Vendruscolo, M; Xu, CK, 2021)
"Parkinson's disease is a common neurodegenerative disease."( Huang, T; Ji, L; Shi, H; Xu, Y, 2021)
"Parkinson's disease is an age-associated neurodegenerative disorder characterized by the progressive loss of dopaminergic neurons from the midbrain."( Ciesla, L; Harding, T; Liang, Q; Maitra, U, 2021)
"Parkinson's disease is the second major neurodegenerative diseases secondarily to Alzheimer's disease."( Chen, X; He, Y; Luo, H; Luo, Z; Tian, F; Wang, M; Yin, L; Yu, X; Zhang, G, 2021)
"Parkinson's disease is a degenerative brain disorder distinguished by growing motor & non-motor failure due to the degeneration of medium-sized spiked neurons in the striatum region."( Kumar, P; Kumar, S, 2021)
"Parkinson's disease is one of the commonest neurodegenerative disorders, particularly in those over 60 years of age."( Paton, DM, 2021)
"Parkinson's disease is a neurodegenerative disorder characterized by accumulation of misfolded α-synuclein within the central nervous system (CNS)."( Baron, T; Greenlee, JJ; Greenlee, MHW; Mammadova, N; Verchère, J, 2021)
"Parkinson's disease is the most common neurodegenerative movement disorder with unclear etiology and only symptomatic treatment to date."( Angelopoulou, E; Paudel, YN; Piperi, C, 2021)
"Parkinson's disease is a multifactorial neurodegenerative disease."( Alrashidi, H; Eaton, S; Heales, S, 2021)
"Thus, sporadic Parkinson's disease is caused by multifactorial trigger factors and metabolic disturbances, which need to be considered for the development of potential drugs in the disorder."( Riederer, P; Sian-Hulsmann, J, 2021)
"Parkinson's disease is characterized by accumulation of α-synuclein (αSyn)."( Ambasudhan, R; Dolatabadi, N; Eisele, YS; Golde, TE; Goodwin, MS; Grabauskas, T; Karin, M; Kelly, JW; Levites, Y; Lipton, SA; Nazor, KL; Parker, J; Schork, NJ; Sierks, MR; Sultan, A; Trudler, D; Zhong, Z, 2021)
"Parkinson's disease is a recognisable clinical syndrome with a range of causes and clinical presentations."( Bloem, BR; Klein, C; Okun, MS, 2021)
"Advanced Parkinson's disease is inconsistently defined, and evidence is lacking in relation to device-aided therapies."( Fukae, J; Hatano, T; Hattori, N; Oyama, G; Saiki, S; Shimo, Y; Tsunemi, T, 2021)
"Parkinson's disease is characterized by motor dysfunctions including bradykinesia."( Jensen, BR; Malling, ASB; Meyer, M; Morberg, BM; Schmidt, SI; Wermuth, L, 2021)
"Parkinson's disease is characterized by nonmotor/motor dysfunction, midbrain dopaminergic neuronal death, and α-synuclein (aSN) deposits."( Lerner, A, 2022)
"Parkinson's disease is the second most common neurodegenerative disease."( Cheng, Y; Hu, Y; Li, H; Liu, C; Liu, J; Qin, X; Wang, W; Wei, Y; Zhang, P, 2021)
"Parkinson's disease is considered a multifactorial disease and evidence from multiple patient studies and animal models has shown a significant immune component during the course of the disease, highlighting immunomodulation as a potential treatment strategy."( Svenningsson, P; Wallin, J, 2021)
"The treatment of Parkinson's disease is adversely affected by several factors: the disease progresses relentlessly, the symptoms and rate of progression, other concomitant non-motor symptoms, and the appearance of complications caused by treatment show great heterogeneity."( Nagy, F, 2021)
"Parkinson's disease is a progressive neurodegenerative disorder in which dopaminergic neurons located in the substantia nigra are gradually lost."( Dehghani Ashkezari, M; Seifati, SM; Zarrin, P, 2021)
"Alzheimer's and Parkinson's disease are the most prevalent neurodegenerative diseases and the leading causes of dementia worldwide."( Matos, MJ, 2021)
"Parkinson's disease is most highly recognised by tremors of the hands that occur in those afflicted with the disease."( Kmanzi, S; Masoumi, M; Mohammadi, H; Wang, H, 2021)
"Parkinson's disease is a common neurodegenerative disease."( Dey, A; Maulik, U; Sen, S, 2021)
"Parkinson's disease is a neurodegenerative disease caused by the death of neurons, ie, cells critical to the production of dopamine, an important neurotransmitter in the brain."( Akram, M; Ali Shariati, M; Ashiq, M; Azam Ansari, M; Bouyahya, A; El Allam, A; Garipova, L; Ghaffar, A; Jahangeer, M; Latif, S; Maknoon Razia, D; Thiruvengadam, M, 2021)
"Idiopathic Parkinson's disease is the second most common neurodegenerative disease and is estimated to be approximately 30% heritable."( Feany, MB; Olsen, AL, 2021)
"Parkinson's disease is the second most prevalent neurodegenerative disease."( Bhatia, D; Gadhavi, J; Gupta, S; Patel, M, 2022)
"Parkinson's disease is characterized by typical motor symptoms, loss of dopamine neurons in the substantia nigra, and accumulation of Lewy body composed of mutated α-synuclein."( Maruyama, W; Naoi, M; Shamoto-Nagai, M, 2022)
"Parkinson's disease is characterized by a variety of motor and non-motor symptoms."( Iakovleva, OV; Levin, OS, 2021)
"Parkinson's disease is a progressive neurodegenerative disorder characterized by the intracellular accumulation of insoluble alpha-synuclein aggregates into Lewy bodies and neurites."( Abbasi, N; Abdelgawad, A; Caputo, A; Dagher, A; Kehm, V; Kozak, M; Liu, ZQ; Lo, A; Luk, KC; Mišić, B; Rahayel, S; Yoo, HS; Zhang, B; Zheng, YQ, 2022)
"Parkinson's disease is the second most common neurological disorder marked by characteristic poverty and dysfunction in movement."( Sian-Hülsmann, J, 2022)
"Parkinson's disease is a gradually progressive neurodegenerative disorder characterized by a selective loss of dopaminergic neurons in the midbrain area called the substantia nigra pars compacta and cytoplasmic alpha-synuclein-rich inclusions termed Lewy bodies."( Exarchos, T; Krokidis, MG; Vlamos, P, 2021)
"Parkinson's disease is a progressive neurodegenerative disorder characterized by the accumulation of misfolded alpha-synuclein in intraneuronal inclusions known as Lewy bodies and Lewy neurites."( Al-Azzani, M; Dominguez-Meijide, A; Flores-León, M; Kanellidi, A; Melki, R; Outeiro, TF; Stefanis, L; Vasili, E, 2022)
"Parkinson's disease is a neurodegenerative disease characterized by the formation of neuronal inclusions of α-synuclein in patient brains."( Aguirre, C; Baba, K; Choong, CJ; Doi, J; Goto, Y; Hideshima, M; Ikenaka, K; Kakuda, K; Kimura, Y; Mochizuki, H; Nabekura, K; Nagai, Y; Nagano, S; Nakajima, K; Takeuchi, T; Yamaguchi, K, 2022)
"Parkinson's disease is associated with the accumulation of α-synuclein (AS) aggregates that include polymorphic AS oligomers and polymorphic fibrils."( Lan-Mark, S; Miller, Y, 2022)
"Parkinson's disease is a progressive neurodegenerative disease characterized by motor and non-motor symptoms."( Gencler, OS; Oztekin, MF; Oztekin, N, 2022)
"Parkinson's disease is a progressive neurodegenerative disorder that is characterized by pathological protein inclusions that form in the brains of patients, leading to neuron loss and the observed clinical symptoms."( Lee, VM; Marotta, NP, 2022)
"The etiology of Parkinson's disease is poorly understood and is most commonly associated with advancing age, genetic predisposition, or environmental toxins."( Bernis, ME; Grigoletto, J; Lohmann, S; Ma, L; Pesch, V; Reithofer, S; Tamgüney, G, 2022)
"Animal models of Parkinson's disease are useful to evaluate new treatments and to elucidate the etiology of the disease."( Avendaño-Estrada, A; Ávila-Rodríguez, MA; Verdugo-Díaz, L, 2022)
"Parkinson's disease is a chronic and gradually progressive neurodegenerative disorder triggered due to the loss of dopamine-releasing neurons in the region of substantia nigra pars compacta characterized by the motor symptoms, such as tremor, bradykinesia, akinesia, and postural instability."( Garabadu, D; Gopika, S; Goyal, A; Kumar, A, 2022)
"Parkinson's disease is a progressive neurodegenerative disease, which significantly impacts patients' quality of life and is associated with high treatment and direct healthcare costs."( Alobaidi, A; Bao, Y; Chaudhuri, KR; Jalundhwala, YJ; Jones, G; Kandukuri, PL; Madin-Warburton, M; Najle-Rahim, S; Oddsdottir, J; Pickard, AS; Ridley, C; Schrag, A; Sus, J; Xu, W, 2022)
"Parkinson's disease is a neurodegenerative disease characterized by progressive dopaminergic neuronal loss."( Choe, HK; Choe, Y; Choi, JW; Choi, M; Jang, S; Kim, D; Kim, J; Kim, K; Moon, C; Park, I; Park, SH; Sun, W, 2022)
"Parkinson's disease is a degenerative disease of the nervous system, which is more common in middle-aged and elderly people."( Chen, Y; Gao, X; Kong, Q; Zhang, J, 2022)
"Parkinson's disease is a neurodegenerative disorder characterized by the loss of dopaminergic neurons in the substantia nigra, as well as the accumulation of intraneuronal proteinaceous inclusions known as Lewy bodies and Lewy neurites."( Manglano-Artuñedo, Z; Outeiro, TF; Peña-Díaz, S; Pinheiro, F; Pujols, J; Santos, J; Vasili, E; Ventura, S, 2022)
"Parkinson's disease is characterized by the deposition of α-synuclein, which leads to synaptic dysfunction, the loss of neuronal connections and ultimately progressive neurodegeneration."( Facey, PD; Hirth, F; Kocinaj, A; Parsons, AE; Parsons, RB; Prendergast, SA; Ruiz Pulido, G, 2022)
"Parkinson's disease is one of the progressive neurodegenerative diseases from which people suffer for years."( Abuleil, A; Ajagbe, AO; Alhendawi, BHM; Badri, R; Chaaya, C; Chalhoub, E; Korkusuz, AK; Onyeaka, H; Uwishema, O; Yücel, AN, 2022)
"Parkinson's disease is the most common movement disorder worldwide because of the loss of dopaminergic neurons in the substantia nigra."( Abuleil, A; Ajagbe, AO; Alhendawi, BHM; Badri, R; Chaaya, C; Chalhoub, E; Korkusuz, AK; Onyeaka, H; Uwishema, O; Yücel, AN, 2022)
"Parkinson's disease is a common progressive neurodegenerative disease, and presently has no curative agent."( Botchway, BOA; Fan, R; Jin, T; Liu, X; Zhang, J; Zhang, Y, 2022)
"Parkinson's disease is a neurodegenerative disorder that causes motor and nonmotor symptoms due to the loss of dopaminergic nerves and is characterized by the presence of Lewy bodies, which are mainly composed of α-synuclein."( Kodera, K; Matsui, H; Matsui, N; Saitoh, A, 2022)
"Parkinson's disease is mainly caused by aggregation of α-synuclein (α-syn) in the brain."( Alam, P; Brewer, JR; Holst, MR; Jensen, PH; Lauritsen, L; Nielsen, J; Nielsen, MS; Nielsen, SSE; Otzen, DE, 2022)
"Parkinson's disease is a neurodegenerative disease characterized by the loss of dopaminergic neurons in the substantia nigra with no effective cure available."( Abreu, R; Barão, M; Bernardino, L; Cristóvão, AC; Esteves, M; Fernandes, H; Ferreira, L; Ferreira, R; Martins, PAT; Saraiva, C; Serra-Almeida, C, 2022)
"Parkinson's disease is a neurodegenerative condition initially characterized by the presence of tremor, muscle stiffness and impaired balance, with the deposition of insoluble protein aggregates in Lewy's Bodies the histopathological hallmark of the disease."( Ceña, V; Pérez-Carrión, MD; Posadas, I; Solera, J, 2022)
"Parkinson's disease is characterized by the gradual appearance of intraneuronal inclusions that are primarily composed of misfolded α-synuclein protein, leading to cytotoxicity and neural death."( Djaldetti, R; Herman, S; Mollenhauer, B; Offen, D, 2023)
"Introduction: Parkinson's disease is a neurodegenerative disease, the symptoms of which can be treated reasonably well; however, therapeutic recommendations need to be refined based on the observations from everyday practice."( Baróti, B; Constantin, V; Forró, T; Frigy, A; Kelemen, K; Metz, J; Mihály, I; Orbán-Kis, K; Szász, JA; Szász, RM; Szatmári, S; Török, Á, 2022)
"Parkinson's disease is associated with α-synuclein and Lewy body dementia, a secondary tauopathy related to hyperphosphorylation of tau protein, and tauopathy is among several pathophysiological pathways shared between Parkinson's disease and diabetes."( Brown, RB, 2022)
"Idiopathic Parkinson's disease is a slowly progressive neurodegenerative disease."( Fung, VS; Griffith, J; Qiu, J; Tsui, D; Waller, S; Williams, L, 2022)
"Parkinson's disease is a neurodegenerative disorder that involves the death of the dopaminergic neurons of the nigrostriatal pathway and, consequently, the progressive loss of control of voluntary movements."( Catenaccio, A; Chovar, O; Court, F; Elgueta, D; Pacheco, R; Sánchez-Guajardo, V; Ugalde, V, 2022)
"Parkinson's disease is the second most common neurodegenerative disease."( Alayli, A; Borlongan, CV; Choudhary, H; Gordon, J; Lockard, G; Monsour, M, 2022)
"Advanced Parkinson's disease is characterized by motor and non-motor fluctuations to oral dopamine replacement therapy."( Arlt, C; Ebersbach, G; Eggert, K; Fritz, B; Möller, JC; Schwarz, J; Sensken, SC; Weiss, D, 2022)
"Parkinson's disease is a neurodegenerative disease, the etiology of which remains unknown, but some likely causes include oxidative stress, mitochondrial dysfunction and neuroinflammation."( Barbiero, JK; Bassani, T; Boschen, S; Da Cunha, C; Ramos, DC; Vital, MABF, 2022)
"Parkinson's disease is the second most prevalent neurodegenerative disease after Alzheimer's disease, mostly happened in the elder population and the prevalence gradually increased with age."( Liu, X; Ming, D; Moussian, B; Pang, M; Peng, R; Su, Y; Wang, P; Wang, Y; Zhu, Y, 2022)
"Parkinson's disease is the second most common age-related, neurodegenerative disease."( Olivas, WM; Snoderly-Foster, LJ, 2022)
"Parkinson's disease is a universally progressive neurodegenerative disease."( Fung, VSC; Griffith, J; Qiu, J; Tsui, D; Waller, S; Williams, L, 2022)
"Parkinson's disease is a progressive neurodegenerative movement disorder."( Boracı, H; Gergin, S; Kirazlı, Ö; Şehirli, ÜS; Yananlı, HR; Yıldız, SD, 2023)
"Parkinson's disease is characterized by locomotion deficits, dopaminergic neuronal loss and alpha-synuclein (SYN) aggregates; the Tubulin Polymerization Promoting Protein (TPPP/p25 or TPPP1) is also implicated in these processes."( Berki, T; Lehotzky, A; Oláh, J; Ovádi, J; Szénási, T, 2022)
"Parkinson's disease is one of the most common neurodegenerative diseases affecting the ageing population, with a prevalence that has doubled over the last 30 years."( Chien, CT; Dewadas, HD; Foo, CN; Lim, YM; Lin, YE; Ravinther, AI; Tong, SR, 2022)
"Parkinson's disease is the second most common neurodegenerative disease."( Blanco-Prieto, MJ; Del Campo-Montoya, R; Garbayo, E; Luquin, MR; Puerta, E, 2022)
"Parkinson's disease is a progressive neurodegenerative disorder characterized by the preferential loss of tyrosine hydroxylase (TH)-expressing dopaminergic neurons in the substantia nigra."( Ayaki, T; Chiba, S; Hirai, H; Hirotsune, S; Ishida, R; Jin, M; Komai, S; Konno, A; Matsumoto, S; Nakajima, H; Taguchi, T; Takahashi, R; Takao, T; Togawa, N; Yamakado, H, 2022)
"Parkinson's disease is both a motor and non-motor disorder."( Adeyeye, TA; Babatunde, BR; Johnson, VF; Shallie, PD, 2023)
"Parkinson's disease is characterized by the aggregation of the presynaptic protein α-synuclein (αSyn), and its co-assembly with lipids and other cellular matter in the brain."( Bernfur, K; Fridolf, S; Linse, S; Pallbo, J; Pham, QD; Sparr, E; Topgaard, D, 2023)
"Parkinson's disease is characterized by the aggregation of the presynaptic protein α-synuclein (αSyn), and its co-assembly with lipids and other cellular matter in the brain."( Bernfur, K; Fridolf, S; Linse, S; Pallbo, J; Pham, QD; Sparr, E; Topgaard, D, 2023)
"Parkinson's disease is the second most common neurodegenerative disorder and is characterized by progressive cell death caused by the formation of Lewy bodies containing misfolded and aggregated α-synuclein."( Jeong, J; Kim, H; Lee, C, 2022)
"Parkinson's disease is the second most common neurodegenerative disorder and is characterized by progressive cell death caused by the formation of Lewy bodies containing misfolded and aggregated α-synuclein."( Jeong, J; Kim, H; Lee, C, 2022)
"Parkinson's disease is a neurodegenerative disorder which is characterised mostly by loss of dopaminergic nerve cells throughout the nigral area mainly as a consequence of oxidative stress."( Albratty, M; Behl, T; Jain, V; Makeen, HA; Meraya, AM; Najmi, A; Sehgal, A; Sharma, N; Singh, S, 2023)
"Parkinson's disease is the second most common neurodegenerative pathology."( Belozertseva, IV; Dorotenko, A; Efimova, EV; Fesenko, Z; Gainetdinov, RR; Mor, MS; Savchenko, A; Sotnikova, TD; Sukhanov, I, 2022)
"Parkinson's Disease is the most common neurodegenerative movement disorder globally, with prevalence increasing."( Aasly, J; Bandmann, O; Cameron, SA; Clemmens, H; Furneaux, RH; Harris, LD; Hastings, C; Luxenburger, A; Mortiboys, H; Ure, EM; Weymouth-Wilson, A, 2022)
"Parkinson's disease is a health-threatening neurodegenerative disease of the elderly with clinical manifestations of motor and non-motor deficits such as tremor palsy and loss of smell."( Chen, ML; Li, CL; Li, JY; Li, YB; Liu, JM; Pang, SC; Wang, R; Wang, YM, 2023)
"Parkinson's disease is the second most prevalent neurological disease after Alzheimer's."( Dubey, SK; Kumari, S; Taliyan, R, 2023)
"Parkinson's disease is among the most common forms of neurodegenerative illness, with present treatment being primarily symptomatic and frequently coming with substantial adverse effects."( Agrawal, A; Behl, T; Dubey, N; Goyal, A; Kumar, A; Verma, A, 2023)
"Parkinson's disease is a progressive neurodegenerative disorder that is associated with motor and nonmotor symptoms."( Chu, Y; Hirst, WD; Kordower, JH, 2023)
"Parkinson's disease is a movement disorder caused by dopamine depletion in the basal ganglia."( Kitano, K, 2023)
"Parkinson's disease is one such disease that is linked with environmental toxin exposure."( Ali, SA; Khan, Z, 2023)
"Parkinson's disease is a severe neurodegenerative disease."( Barouki, R; Birman, S; Coumoul, X; Dairou, J; Galardon, E; Gonis, E; Larigot, L; Laurent, C; Le-Grand, B; Mansuy, D; Mathas, N; Nioche, P; Poncet, G; Sari, MA; Tiouaini, M, 2023)
"Parkinson's disease is a progressive neurodegenerative disorder caused by the degeneration of dopaminergic neurons."( Farhadi, K; Hosseini, N; Mehrabi, S; Mohtasham Kia, Y; Noori, A, 2023)
"Parkinson's disease is the second most common neurodegenerative disease and yet the early pathophysiological events of the condition and sequences of dysfunction remain unclear."( Beccano-Kelly, D; Cragg, SJ; Cramb, KML; Wade-Martins, R, 2023)
"Parkinson's disease is a complex age-related progressive dopaminergic neurodegenerative disease consistently viewed as a disorder of movement and is characterized by its cardinal motor symptoms."( Dhanabal, SP; Dhanasekaran, M; J, JB; Justin, A; Palathoti, N; Ponnusankar, S; Sankar, V; Sivasamy, R, 2023)
"Parkinson's disease is a neurodegenerative disease and depends on the dopamine system's dysregulation."( Algul, O; Ozcelik, I; Yucel, MA, 2023)
"Parkinson's disease is the second most common neurodegenerative disease."( Aleksandrova, Y; Ardashov, O; Chaprov, K; Neganova, M; Podturkina, A; Salakhutdinov, N; Volcho, K; Yandulova, E, 2023)
"Parkinson's disease is one of the neurodegenerative diseases that have no cure."( Chang, CH; Cheng, KC; Chok, D; Ho, CT; Koh, YC; Nagabhushanam, K; Pan, MH; Wei, CC; Wu, CT, 2023)
"Parkinson's disease is characterized by the selective death of dopaminergic neurons in the midbrain and accumulation of amyloid fibrils composed of α-synuclein (αSyn)."( Borisova, T; Galkin, M; Priss, A; Shvadchak, VV; Topcheva, O, 2023)
"The pathogenesis of Parkinson's disease is complex and not yet fully clarified and the heterogeneity of the disease, with diverse genetic susceptibility and risk factors and different clinical courses, adds further complexity."( Calabresi, P; Campanelli, F; Di Lazzaro, G; Ghiglieri, V; Marino, G, 2023)
"Parkinson's disease is a neurodegenerative disease affecting mainly the elderly population."( Bhatt, LK; Siddiqui, T, 2023)
"Older adults with Parkinson's disease are sensitive to adverse effects of psychotropic agents, including SSRIs, which are not recommended first-line agents for behavioral symptoms in PDD."( Albalawi, A, 2023)
"The pathogenesis of Parkinson's disease is complex, and abnormal lipid metabolism resulting in ferroptosis due to the excessive accumulation of free radicals from oxidative stress in the substantia nigra of the brain was thought to be one of the factors causing the disease."( Feng, X; Jiang, L; Li, M; Liu, M; Wang, W; Yang, D; Zhang, J, 2023)
"Parkinson's disease is accompanied by the presence of amyloids in the brain that are formed of α-synuclein chains."( Chesney, AD; Hansmann, UHE; Maiti, B, 2023)
"Parkinson's disease is one of the most common neurodegenerative diseases."( Jin, H; Li, S; Liu, X; Ma, T; Peng, Y; Shen, Z; Wang, J; Yao, J; Zeng, M, 2023)
"Parkinson's disease is a neurodegenerative disorder characterized by oxidative stress and immune activation in the nigro-striatal pathway."( León, CTG; Monroy, A; Montes, S; Morales-Montor, J; Ríos, C; Rubio, C; Rubio-Osornio, M, 2023)
"Advanced Parkinson's disease is characterized by periods of poor mobility, dyskinesia and progressive decline in functional independence of the affected person despite the manipulation of levodopa doses and the introduction of supplemental therapies such as catechol-O-methyl transferase inhibitors, monoamine oxidase-B inhibitors and dopamine agonists."( Antonini, A; D'Onofrio, V; Guerra, A, 2023)
"The pathogenesis of Parkinson's disease is closely linked to impaired mitochondrial function and abnormal mitophagy."( Du, M; Li, H; Xia, X; Xu, X; Zhao, G, 2023)
"Similarly, Parkinson's disease is characterized by the loss of dopaminergic neurons in the substantia nigra, resulting in motor symptoms."( Geelhand de Merxem, R; Hanak, C; Launay, S, 2023)
"Parkinson's disease is a chronic neurodegenerative condition that has no cure, characterized by the progressive degeneration of specific brain cells responsible for producing dopamine, a crucial neurotransmitter for controlling movement and muscle coordination."( Costa, EV; Costa, RA; Mary, YS; S Al-Otaibi, J; Tananta, VL, 2023)
"Parkinson's disease is associated with increased inflammation, but this is insufficient to underpin dyskinesia."( Egan, T; Kuriakose, A; Rentsch, P; Stayte, S; Vissel, B, 2023)

Context

ExcerptReference
"Parkinson's disease has been associated with defects in oxidative phosphorylation (Oxphos)."( Juncos, JL; Shoffner, JM; Torroni, A; Wallace, DC; Watts, RL, 1991)
"Patients with Parkinson's disease have been suspected to have a low incidence of DIC, and this may be the first case report on successful treatment of levodopa-induced NMS with DIC in the patient with Parkinson's disease."( Ogawa, N; Yamawaki, Y, 1991)
"Edema in Parkinson's disease has been considered to be caused by autonomic nervous system dysfunctions, however little is still known about the exact pathophysiological mechanism involved."( Maki, T; Sonoda, Y; Sugita, K, 1990)
"Idiopathic Parkinson's disease has been postulated to result from exposure to environmental toxins similar to the parkinsonism-causing neurotoxin MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine)."( Das, NP; Lee, EJ; Moochhala, SM; Shahi, GS, 1989)
"Patients with Parkinson's disease have a decrement in homovanillic acid that is reversed by treatment with L-3,4-dihydroxyphenylalanine."( Aguado, EG; de Yebenes, JG; Mena, MA, 1984)
"This suggests that Parkinson's disease has a widely variable rate of progression, and is most compatible with a short preclinical period."( Brooks, DJ; Morrish, PK; Sawle, GV, 1995)
"The treatment of idiopathic Parkinson's disease has been divided in 3 different phases."( Ludin, HP, 1995)
"Mortality due to Parkinson's disease has decreased significantly after the introduction of L-dopa treatment."( Kuno, S, 1994)
"Some patients with Parkinson's disease have shown improvement in tremor and other abnormal movements when given clozapine."( Pfeiffer, C; Wagner, ML, 1994)
"Research on Parkinson's disease has led to new hypotheses concerning the mechanisms of neurodegeneration and to the development of neuroprotective agents."( Gsell, W; Lange, KW; Naumann, M; Oestreicher, E; Rausch, WD; Riederer, P, 1994)
"The advance of Parkinson's disease has been suspected to be an outcome of oxidative stresses related to the metabolism of dopamine."( LeWitt, PA, 1993)
"2."( Deveaugh-Geiss, J; Doraiswamy, M; Martin, W; Metz, A, 1995)
"Treatment of Parkinson's disease has progressed steadily for the last decades after introduction of levodopa."( Yanagisawa, N, 1997)
"Progression of Parkinson's disease has been associated with several biochemical changes in the substantia nigra including increased oxidative challenge, catechol oxidation, and inhibition of mitochondrial complex I activity."( Amarnath, V; Graham, DG; Montine, TJ; Picklo, MJ; Whetsell, WO, 1997)
"Subjects with Parkinson's disease have abnormal postural sway in stance."( Chiari, L; Horak, FB; Rocchi, L, 2002)
"Patients with Parkinson's disease have been known to have sleep disturbances of various types."( Abe, K; Hikita, T; Sakoda, S, 2005)
"Increasingly, Parkinson's disease has been associated with a broad spectrum of non-motor symptoms, such as olfactory loss, sleep disorders, autonomic dysfunction, cognitive impairment, psychosis, depression, anxiety, and apathy."( Ferrara, JM; Stacy, M, 2008)
"Animal models of Parkinson's disease have been widely used for investigating the mechanisms of neurodegenerative process and for discovering alternative strategies for treating the disease."( Kurz, MJ; Lau, YS; Pothakos, K, 2009)
"Treatment of Parkinson's disease has traditionally focused on the management of motor disability while behavioural disturbances have received less attention."( Antonini, A; Cilia, R, 2009)
"Parkinson's disease has now evolved beyond what was considered to be a traditional motor disorder."( Chitnis, S; Rao, J, 2009)
"Typical Parkinson's disease has an initial rapid loss of midbrain dopamine neurons with a slow progression of Lewy body infiltration into the brain (over decades)."( Halliday, GM; McCann, H, 2010)
"Parkinson's disease has been found to be caused by both, genetic and environmental factors."( Bayersdorfer, F; Botella, JA; Schneuwly, S; Voigt, A, 2010)
"Patients with Parkinson's disease have great difficulty in performing bimanual movements; this problem is more obvious when they perform bimanual anti-phase movements."( Chan, P; Hallett, M; Li, K; Wang, L; Wu, T, 2010)
"Parkinson's disease has been so far commonly treated with medication therapy."( Morizane, A; Takahashi, J, 2012)
"Parkinson's disease has a long presymptomatic stage, which indicates a substantial capacity of the human brain to compensate for dopaminergic nerve degeneration before clinical manifestation of the disease."( Anders, S; Binkofski, F; Klein, C; Münte, T; Pohl, A; Pramstaller, P; Sack, B, 2012)
"Parkinson's disease has long been associated with neurodegeneration of the dopaminergic neurons located in the substantia nigra."( De Deurwaerdère, P; Navailles, S, 2012)
"Several people with Parkinson's disease have been treated with intrastriatal grafts of fetal dopaminergic neurons."( Angot, E; Björklund, A; Brundin, P; Ekström, P; Lema Tomé, CM; Mattsson, B; Steiner, JA, 2012)
"Many patients with Parkinson's disease have mild cognitive impairment (MCI)."( Ekman, U; Eriksson, J; Forsgren, L; Mo, SJ; Nyberg, L; Riklund, K, 2012)
"Patients with Parkinson's disease have an elevated risk of pneumonia and randomized trials suggest that this risk may be increased with the dopamine agonist pramipexole."( Dell'Aniello, S; Ernst, P; Renoux, C; Suissa, S, 2012)
"Patients with Parkinson's disease have reduced gray matter volume and fractional anisotropy in both cortical and sub-cortical structures, yet changes in the pre-motor phase of the disease are unknown."( Artzi, M; Ben Bashat, D; Bloem, BR; Bressman, S; Giladi, N; Gurevich, T; Helmich, RC; Hendler, T; Jacob, Y; Marder, K; Mirelman, A; Orr-Urtreger, A; Thaler, A; van Nuenen, BF, 2014)
"Many patients with Parkinson's disease have motor fluctuations despite treatment with available drugs."( Bandak, S; Docu-Axelerad, A; Hauser, RA; Kenney, C; Kieburtz, KD; Kozyolkin, O; Lew, M; Meya, U; Neale, A; Olanow, CW; Pourcher, E; Resburg, C, 2014)
"Patients with Parkinson's disease have better functional status and motor performance under on-drug conditions."( Bonnet, CT; Defebvre, L; Delval, A; Szaffarczyk, S, 2017)
"Both ageing and Parkinson's disease have an impact on dopamine neurotransmission."( Bardien, S; Bossert, M; Buckle, C; Carr, J; du Plessis, S; Emsley, R; Seedat, S; van den Heuvel, L; Vink, M, 2018)
"Common forms of Parkinson's disease have long been described as idiopathic, with no single penetrant genetic factor capable of influencing disease aetiology."( Klein, AD; Mazzulli, JR, 2018)
"Symptoms of Parkinson's disease have been controlled with levodopa for many years; however, motor complications consisting of wearing off of medication effect and dyskinesias tend to occur within a few years of starting levodopa."( Frei, K; Tran, TN; Truong, DD; Vo, TNN, 2018)
"Many patients with Parkinson's disease have potentially disabling off episodes that are not predictably responsive to levodopa."( Bhargava, P; Blum, D; Espay, AJ; Factor, SA; Hauser, RA; Isaacson, S; Leinonen, M; Navia, B; Olanow, CW; Pahwa, R; Sciarappa, K; Shill, HA, 2020)
"The pathogenesis of Parkinson's disease has not been fully clarified yet but its cause is known to be multifactorial."( Araujo, SM; Bortolotto, VC; Dahleh, MMM; de Freitas Couto, S; Jardim, EF; Meichtry, LB; Musachio, EAS; Petri Guerra, G; Poetini, MR; Prigol, M; Ramborger, BP; Roehrs, R, 2020)
"Parkinson's disease has been considered as a motor neuron disease with dopamine (DA) deficit caused by neuronal loss in the substantia nigra, but now proposed as a multi-system disorder associated with α-synuclein accumulation in neuronal and non-neuronal systems."( Maruyama, W; Naoi, M; Shamoto-Nagai, M, 2020)
"Parkinson's disease has become one of the most common neurodegenerative diseases."( Cao, X; Chen, C; Peng, Q; Tan, Y; Wang, J; Wu, Y; Xu, Y; Yang, X; Zeng, W, 2020)
"Patients with Parkinson's disease have reduced reward sensitivity related to dopaminergic neuron loss, which is associated with impairments in reinforcement learning."( Duncan, K; Foerde, K; Sharp, ME; Shohamy, D, 2020)
"Patients with Parkinson's disease have a high dislocation rate after total hip arthroplasty (THA)."( Horiba, M; Imamura, A; Kuroyanagi, G; Matsukawa, N; Murakami, H; Sakai, H; Sato, T; Takahashi, A; Ueki, Y; Usami, T, 2023)

Actions

ExcerptReference
"Parkinson's disease affects thousands of Americans, men and women equally and apparently with little regard to race."( Jacobs, MB; Varon, J, 1991)
"Parkinson's disease affects the central programming of functionally related muscles involved in voluntary and rhythmic jaw movements and levodopa replacement influences only certain aspects of jaw movement, most likely those requiring sensory feedback."( Hammerstad, JP; Robertson, LT, 1996)
"Parkinson's disease affects one out of every 100 people above the age of 55."( Hastings, TG; Zigmond, MJ, 1997)
"Parkinson's disease affects various neurotransmitter systems."( Barthel, H; Becker, T; Müller, U; Murai, T; Reuter, M; Sorger, D; von Cramon, DY; Werheid, K, 2001)
"To examine whether Parkinson's disease affects men and women differently, relative to age-matched controls, in manual tracking."( Carey, JR; Deskin, KA; Josephson, KT; Wichmann, RL, 2002)
"Parkinson's disease affects men and women disproportionately in manual tracking."( Carey, JR; Deskin, KA; Josephson, KT; Wichmann, RL, 2002)
"Parkinson's disease affects up to 1 million people in the US, most of them elderly."( Chen, JJ; Fernandez, HH, 2007)
"Parkinson's disease affects 5 million people worldwide, but the molecular mechanisms underlying its pathogenesis are still unclear."( Adler, CH; Beach, TG; Cantuti-Castelvetri, I; Davis, RL; Eklund, AC; Federoff, HJ; Graeber, MB; Grünblatt, E; Hauser, MA; Hedreen, JC; Kim, PD; Lesniak, KA; Liao, Z; Locascio, JJ; Mandel, SA; Middleton, FA; Miller, RM; Moran, LB; Papapetropoulos, S; Riederer, P; Rochet, JC; Roderick, SS; Scherzer, CR; Vance, JM; Watt, ML; Wüllner, U; Youdim, MB; Young, AB; Zhang-James, Y; Zheng, B, 2010)
"Parkinson's disease affects several neuronal structures outside the substantia nigra, among which is the enteric nervous system."( Awad, RA, 2011)
"Parkinson's disease affects a growing number of people."( Magyar, K; Szökő, E; Tábi, T; Vécsei, L, 2013)
"Parkinson's disease affects more than 6,3 million people worldwide."( Csóka, M; Domján, G; Kellős, É; Molnár, S, 2016)
"Parkinson's disease is affecting about 1% of the population above 65 years."( Gazzaz, M; Lucio, M; Michalke, B; Schmitt-Kopplin, P; Schroeter, M; Sigaroudi, A; Willkommen, D, 2018)
"And Parkinson's disease, affecting the health of 1-2% of people over 60 years old throughout the world, is the second largest neurodegenerative disease in the brain."( Xu, J; Yang, X; Zhang, Z; Zhao, H; Zhou, Y, 2022)

Treatment

ExcerptReference
"Sixty cases of Parkinson's disease were treated with piribedil alone (dose : 274 mg/day, duration : 20,4 months)."( Bastard, J; Chanelet, J; Emile, J; Six, P; Truelle, JL, 1977)
"Patients with Parkinson's disease showed a relatively high incidence to psychoses during drug treatment (51."( Danielczyk, W, 1979)
"In eight subjects with Parkinson's disease under an optimal daily dose of L-dopa, acute administration of MIF-I (200 mg i."( Caraceni, T; Celano, I; Cocchi, D; Frigerio, C; Girotti, F; Müller, EE; Parati, EA, 1979)
"Like the diabetic, the patients with Parkinson's disease may run into problems during long-term treatment."( Marsden, CD; Parkes, JD, 1977)
"Six patients with Parkinson's disease developed nocturnal myoclonic attacks after prolongued treatment with L-Dopa which were electroencephalographically recorded."( Glaubman, H; Rabey, JM; Streifler, M; Vardi, J, 1978)
"In 13 elderly patients, 12 of whom had Parkinson's disease, visual hallucinations and delirium developed as a side effect of amantadine hydrochloride (Symmetrel) therapy."( Postma, JU; Van Tilburg, W, 1975)
"In 13 patients with Parkinson's disease treated with lergotrile (up to 12 mg a day), overall improvement was observed in five."( Battista, AF; Goldstein, M; Lieberman, A; Miyamoto, T, 1975)
"The treatment of Parkinson's disease is discussed."( Godwin-Austen, RB, 1977)
"Four women with Parkinson's disease undergoing prolonged levodopa therapy had daily episodes of dystonic posturing, affecting one lower extremity, several years after initiation of treatment."( Melamed, E, 1979)
"Nine patients 55 to 74 years old with Parkinson's disease were tested before and after treatment with 50 to 225 mg dimepramine fumarate (CIBA G-31406) for about three weeks daily in order to determine the drug's effects on electrodermal responsiveness to a series of unpredictably occurring loud sounds."( Feldman, RG; Gade, A; Oscar-Berman, M; Saavedra, MA, 1979)
"Twenty-six patients affected by Parkinson's disease were treated with a 2-Br-alpha-ergocriptine (CB 154): 14 cases were given CB 154 alone, and 12 were given CB 154 along with L-dopa plus benserazide (Madopar)."( Caraceni, TA; Celano, I; Girotti, F; Parati, E, 1977)
"Of 88 patients with idiopathic Parkinson's disease, without prior psychotic symptoms, and without significant dementia, nearly half had experienced vivid dreams, hallucinations, illusions, and nonconfusional as well as confusional psychoses as side effects of chronic levodopa therapy within the previous year of treatment."( Klawans, HL; Moses, H; Moskovitz, C, 1978)
"Thirteen patients with Parkinson's disease, whose disability was increasing and on long-term levodopa therapy (both with and without carbidopa), had the levodopa fully replaced by bromocriptine."( Gilligan, B; Stark, R; Wodak, J, 1978)
"Patients who had had Parkinson's disease for more than 4 years appeared to do less well than those with recently diagnosed disease, but many patients responded well even when treatment was initiated 10 years after the onset of symptoms."( Bladin, PF; Donnan, GA; Vajda, FJ, 1978)
"Fifteen patients with early or mild Parkinson's disease were studied clinically and electroencephalographically while receiving L-dopa or placebo treatment."( Ferriss, GS; Martinez, RD; Paddison, RM, 1976)
"Thirty-one patients with Parkinson's disease were treated with the ergot alkaloid bromocriptine, a drug which stimulates dopamine receptors."( Asselman, P; Donaldson, I; Galea-Debono, A; Kennedy, G; Marsden, CD; Parkes, JD; Walters, J, 1976)
"The treatment of Parkinson's disease today is complex, time-consuming, but rewarding."( Marsden, CD, 1976)
"Twenty-three patients with Parkinson's disease participated in long-term, double-blind evaluations of the effectiveness and side effects of amantadine in combination with levodopa therapy."( Fahn, S; Isgreen, WP, 1975)
"Eleven patients with Parkinson's disease were treated with bromocriptine (mean dose, 26."( Battista, A; Boal, D; Fuxe, K; Goldstein, M; Hassouri, H; Lieberman, A; Vogel, B; Zolfaghari, M, 1976)
"It is characteristic of Parkinson's disease and responds to treatment with L-dopa either alone or in combination with a decarboxylase inhibitor."( McKinney, AS, 1977)
"A patient with Parkinson's disease, in whom polycythemia vera was known to be present for several years prior to the onset of parkinsonian symptoms, received treatment with a preparation consisting of L-dopa plus a decarboxylase inhibitor (Madopar)."( Herishanu, Y; Rosenberg, P, 1977)
"The "On-Off Effect" in levodopa treated Parkinson's disease began in a few patients during the first year of treatment."( Clark, EC; Feinstein, B, 1977)
"Six patients with Parkinson's disease and five controls were premedicated with probenecid and the peripheral decarboxylase inhibitor alpha-methyldopathydrazine (Carbidopa) before intravenous administration of 50 muc of 14C-L-dopa in tracer quantity."( Bowers, MB; Extein, I; Roth, RH; Van Woert, M, 1976)
"Two patients with severe Parkinson's disease were treated with electroconvulsive therapy for a supervening depression."( Jenkins, RB; Lebensohn, ZM, 1975)
"A group of 71 patients with Parkinson's disease were treated with L-Dopa and benserazide during periods ranging from 27 to 60 months."( Chouza, C; Gomensoro, JB; Romero, S, 1975)
"92 patients with Parkinson's disease not previously treated with levodopa were considered as eligible for this triple-blind trial."( Birket-Smith, E; Dupont, E; Hansen, E; Mikkelsen, B; Pakkenberg, H; Presthus, J; Rautakorpi, I; Riman, E; Rinne, UK, 1976)
"After 9 years of treatment for Parkinson's disease, a 68-year-old woman developed the complications of neuroleptic malignant syndrome (NMS) and disseminated intravascular coagulation (DIC) while she was still receiving levodopa, bromocriptine and amantadine hydrochloride."( Ogawa, N; Yamawaki, Y, 1992)
"The clinical management of Parkinson's disease has been revolutionized by the introduction of levodopa therapy."( Asanuma, M; Hirata, H; Kondo, Y; Ogawa, N, 1992)
"Amantadine is used in the treatment of Parkinson's disease without a well established mechanism of action."( Booij, J; Drukarch, B; Stoof, JC, 1992)
"In the patients with Parkinson's disease measurements were made in both the untreated state and after an injection of the dopamine agonist apomorphine (treated state)."( Cox, M; Markus, HS; Tomkins, AM, 1992)
"Treatment of Parkinson's disease (PD) can be divided into two categories: symptomatic therapy (restoring dopamine levels toward normal and reversing functional disability) and preventive therapy (interfering with the pathophysiologic mechanism of PD to prevent or decrease the rate of progression of the disease)."( Koller, WC, 1992)
"A patient with Parkinson's disease, initially treated with bromocriptine and subsequently with cabergoline, developed progressive pleuropulmonary abnormalities during the latter therapy."( Demedts, M; Dom, R; Frans, E, 1992)
"The treatment of Parkinson's disease seems to be moving slowly from mere symptomatic therapy to the one which is aiming the protection of nigral cells."( Mizuno, Y, 1992)
"The management of patients with early Parkinson's disease should now take into account the possibility that MAO-B inhibitors may provide neuroprotective therapy, that dopamine undergoes oxidative metabolism and has the potential to generate cytotoxic free radicals, and that the early employment of drugs which provide sustained central dopamine agonism may delay the development of adverse effects associated with chronic levodopa therapy."( Olanow, CW, 1992)
"In the brains of subjects with Parkinson's disease (PD) treated with levodopa, a significant reduction of PST activities was observed in hypothalamus, frontal and temporal cortex, amygdaloid nucleus, occipital and parietal cortex (between 20 and 38."( Baran, H; Jellinger, K, 1992)
"Twenty-nine patients with advanced Parkinson's disease were treated with subcutaneous lisuride infusion in addition to a basic therapy consisting of levodopa + PDI in all, and deprenyl in some patients."( Heinz, A; Klewin, I; Klotz, P; Kuhn, W; Przuntek, H; Suchy, I, 1992)
"215 Chinese Parkinson's disease (PD) patients on levodopa therapy were followed up between 1982 and 1991."( Chia, LG; Liu, LH, 1992)
"Patients with Parkinson's disease tend to have a reduced response to levodopa after 5 to 20 years of therapy, with "on-off" fluctuations consisting of dyskinesia alternating with immobility."( Breeze, RE; Freed, CR; Kriek, E; Lone, T; Qi, JX; Rosenberg, NL; Schneck, SA; Snyder, JA; Wells, TH; Zhang, YB, 1992)
"50 de novo patients with Parkinson's disease were investigated in a retrospective study after selegiline (-)deprenyl monotherapy and a combination of (-)deprenyl and levodopa."( Málly, J, 1992)
"20 patients with Parkinson's disease and a fluctuating response to chronic treatment with conventional L-dopa preparations participated in an open randomized trial comparing two sustained-release L-dopa preparations (Madopar HBS, Sinemet CR4)."( Kleedorfer, B; Poewe, W, 1992)
"Since Parkinson's disease was first described by James Parkinson in 1817, the natural history has been confounded by various treatment modalities: the replenishment of deficient dopamine, the addition of the dopamine agonists, and the more recent addition of drugs whose putative action may slow the natural history of the disease."( Hoehn, MM, 1992)
"Although not significant, more severe Parkinson's disease was associated with greater IRI, timekeeper and motor delay variance, while administration of levodopa resulted in reduction of the three types of variance."( Artieda, J; Jahanshahi, M; Obeso, JA; Pastor, MA, 1992)
"Newly diagnosed Parkinson's disease patients maintained on (-)deprenyl need levodopa significantly later than their placebo-treated peers."( Knoll, J, 1992)
"Akathisia improved in 4 patients with idiopathic Parkinson's disease after low dose propranolol treatment."( Adler, LA; Angrist, B; Rotrosen, J; Weinreb, H, 1991)
"administration to 13 patients with Parkinson's disease."( Agnoli, A; Baronti, F; Horowski, R; Lucarelli, C; Ruggieri, S; Stocchi, F; Viselli, F, 1991)
"Among Parkinson's disease (PD) patients complaining of pain, 10 with pain not associated with a motor fluctuation or L-dopa therapy were evaluated."( Matsushima, E; Nishikawa, S; Sano, K; Takahashi, K; Takao, T; Urakami, K, 1990)
"Eighteen patients with Parkinson's disease were treated with placebo for 4 weeks and with the MAO-B inhibitor selegiline for 8 weeks without levodopa in a randomized double-blind clinical study."( Hietanen, MH, 1991)
"The case of a 60 year old patient with Parkinson's disease is reported, who, following 2 years of treatment with bromocriptine, presented a left pleural effusion in which chronic constrictive pericarditis was demonstrated."( Aguilar, M; Alió, J; Saura, J, 1991)
"Current long-term treatment of Parkinson's disease is inadequate, and improved symptomatic and neuroprotective therapies are needed."( Greenamyre, JT; O'Brien, CF, 1991)
"Chronic L-DOPA treatment of Parkinson's disease frequently leads to the development of motoric overstimulation and hyperkinetic movements."( Carey, RJ, 1991)
"We treated 20 early Parkinson's disease subjects with the dopamine agonist lisuride in combination with the MAO-B inhibitor selegiline (L-deprenyl)."( Bruggi, P; Horowski, R; Martignoni, E; Nappi, G; Pacchetti, C; Rainer, E; Runge, I, 1991)
"Nine levodopa treated patients with Parkinson's disease and severe on-off syndrome received apomorphine."( Christensen, PB; Dupont, E; Jensen, NB, 1991)
"The influence of age of onset of Parkinson's disease on the severity and the pattern of motor symptoms was investigated by comparing the motor scores with and without levodopa therapy in two groups of patients divided according to age of onset (early less than 50, late greater than 60 years) and matched for disease duration (n = 69 in each group, Study I)."( Agid, Y; Blin, J; Bonnet, AM; Brandabur, M; Dubois, B; Vidailhet, M, 1991)
"The current study on 36 patients with Parkinson's disease under long-term treatment with levodopa/dopadecarboxylase inhibitor showed, however, that the erythrocyte-COMT was unaffected by additional (-)-deprenyl medication."( Dettner, O; Gerlach, M; Kuhn, W; Przuntek, H; Russ, H, 1991)
"Long-term treatment of human Parkinson's disease with levodopa or dopamine agonists is often complicated by the appearance of abnormal involuntary movements (dyskinesias) that are extremely difficult to control."( Crossman, AR, 1990)
"Patients with Parkinson's disease have been suspected to have a low incidence of DIC, and this may be the first case report on successful treatment of levodopa-induced NMS with DIC in the patient with Parkinson's disease."( Ogawa, N; Yamawaki, Y, 1991)
"Six patients with Parkinson's disease (PD) and therapeutic response fluctuations (RF) on levodopa treatment participated in an open-label trial of L-deprenyl (Eldepryl) in conjunction with Sinemet."( Cedarbaum, JM; Clark, M; Harts, A; Kutt, H; Silvestri, M, 1990)
"Fifty Thai patients with Parkinson's disease of all staging were allocated for 10 mg/day L-deprenyl therapy as the monotherapy (6 patients) and adjunctive therapy for at least two months."( Poungvarin, N; Viriyavejakul, A, 1990)
"When used to treat patients with Parkinson's disease pergolide acts at dopamine receptors in the corpus striatum to improve locomotor activity, reducing the tremor, gait disturbances, bradykinesia or akinesia and rigidity experienced by such patients."( Clissold, SP; Langtry, HD, 1990)
"Abnormalities of foot strike in idiopathic Parkinson's disease may be amenable to therapy: objective measurements may reveal response which is not clinically apparent."( Bowes, SG; Deshmukh, AA; Dobbs, RJ; Dobbs, SM; Hughes, JR; Leeman, AL; Nicholson, PW; O'Neill, CJ, 1990)
"Fifty four patients with idiopathic Parkinson's disease receiving levodopa therapy were studied."( Berger, HJ; Horstink, MW; Pasman, JW; van't Hof, MA; Zijlmans, JC, 1990)
"For patients with Parkinson's disease there was no correlation between the change in their peak BP negativity (N1) after L-DOPA and their change in clinical mobility; in addition, there was no difference in the peak BP negativity of patients OFF therapy and that of age-matched normals, though there was a slight decrease in the amplitude of the early part of the BP for the patients with Parkinson's disease; this was the same part that had been enlarged by L-DOPA therapy."( Benecke, R; Buruma, O; Cantello, R; Day, BL; Dick, JP; Gioux, M; Marsden, CD; Rothwell, JC; Thompson, PD, 1987)
"Eleven patients with severe Parkinson's disease and on-off-phenomena were included in a controlled double-blind study on the effect of electroconvulsive therapy (ECT)."( Andersen, K; Balldin, J; Gottfries, CG; Granérus, AK; Modigh, K; Svennerholm, L; Wallin, A, 1987)
"Two patients with Parkinson's disease were treated with 1 g tetrahydrobiopterin (BH4) for 5 days."( Dissing, IC; Gerdes, AM; Güttler, F; Lou, H; Lykkelund, C; Pakkenberg, H; Rasmussen, V, 1989)
"Twelve patients with Parkinson's disease on treatment with L-dopa who showed evidence of wearing-off effects or motor oscillation were studied in a double-blind, placebo-controlled, crossover trial to compare conventional doses of deprenyl with higher doses (up to 40 mg/day) and placebo."( Eatough, VM; Frankel, JP; Kempster, PA; Lees, AJ; Nathanson, M; Stern, GM; Stibe, CM, 1989)
"Treating psychosis in patients with Parkinson's disease (PD) is one of the more difficult problems in clinical psychiatry."( Dean, RC; Roberts, HE; Stoudemire, A, 1989)
"The treatment of Parkinson's disease can be demanding, rewarding and sometimes frustrating, but it remains a most challenging exercise in pharmacotherapy."( Calne, DB; Wolters, EC, 1989)
"The latest improvements in Parkinson's disease therapy are reviewed with particular emphasis on the management of long-term treatment syndrome, which has become the chief problem for Parkinson patients since the introduction of levodopa."( Caraceni, T; Geminiani, G; Tamma, F, 1989)
"Unified Parkinson's disease, Hoehn and Yahr, Schwab and England scores, number of hours on per day, number of hours of dyskinesia per day, daily dose of levodopa, and number of doses per day were monitored at the end of each treatment period and the results compared."( Factor, SA; Ingenito, AM; Sanchez-Ramos, JR; Weiner, WJ, 1989)
"Ten patients with Parkinson's disease (PD) with motor fluctuations under levodopa treatment were given repeated equal subcutaneous injections of apomorphine [minimal effective dose (MED)] in 1 day."( Grandas, F; Obeso, JA, 1989)
"101 patients with Parkinson's disease were analyzed in a retrospective study to evaluate the influence of L-Dopa monotherapy, duration of the disease and age at onset on the clinical course of the syndrome."( Emskötter, T; Heidenreich, C; Lachenmayer, L, 1989)
"We studied whether Parkinson's disease patients who had lost efficacy from pergolide (PERG) could benefit if transferred to bromocriptine (BCT) therapy."( Carroll, VS; Goetz, CG; Klawans, HL; Shannon, KM; Tanner, CM, 1989)
"Patients were selected with idiopathic Parkinson's disease without other associated neurological disease or dementia; 20 had never received antiparkinsonian drugs and in 25 such treatment had been stopped for at least 2 days."( Clanet, M; Doyon, B; Montastruc, JL; Rascol, A; Rascol, O; Simonetta, M; Soulier-Esteve, MJ, 1989)
"Two L-dopa-treated patients with Parkinson's disease who developed distressing belching during "off" periods are reported."( Crichton, P; Frankel, JP; Kempster, PA; Lees, AJ; Shorvon, P, 1989)
"28 patients with Parkinson's disease showing complex "on-off" fluctuations in response to chronic levodopa plus dopa decarboxylase inhibitor (po) were treated with subcutaneous lisuride using a portable infusion pump."( Luquin, MR; Martînez Lage, JM; Obeso, JA; Vaamonde, J, 1988)
"Thirteen patients with idiopathic Parkinson's disease and "on-off" fluctuations on oral levodopa plus dopa decarboxylase inhibitor (DDI) were treated with continuous (24 hour) subcutaneous lisuride infusions together with a reduced dose of levodopa (plus DDI)."( Critchley, PH; Grandas Perez, F; Marsden, CD; Parkes, JD; Quinn, NP, 1988)
"Four patients with Parkinson's disease and severe fluctuating responses to levodopa and oral dopamine agonists were treated with continuous administration of lisuride infusions, administered by means of an externally worn pump."( Fernandez Pardal, M; Gatto, M; Micheli, F; Perez y Gonzalez, N, 1988)
"Thirty patients with Parkinson's disease, treated with levodopa for the past few years, concomitantly received 500 mg of cytidine diphosphate choline (CDPC) daily for 30 days."( Cubells, JM; Hernando, C, 1988)
"In experimental Parkinson's disease, we studied the effects of chronic administration (30 days), withdrawal, and reinstitution of bromocriptine."( Baden, DR; Kenny, AM; Murrin, LC; Pfeiffer, RF; Schneider, MB, 1986)
"A series of 203 patients with primary Parkinson's disease treated with L-DOPA, with adequate neurological documentation of mental status at serial intervals during their illness, constitutes the study population."( Elizan, TS; Maker, H; Smith, H; Sroka, H; Yahr, MD, 1986)
"In addition the time from the onset of Parkinson's disease to significantly longer in the group of patients which were treated with Madopar and (-)deprenyl in combination."( Birkmayer, GD; Birkmayer, W, 1986)
"The classical treatment of Parkinson's disease (PD) using L-dopa plus a peripheral decarboxylase inhibitor (DI) often leads after 3-5 years to the onset of the so-called long-term L-dopa syndrome (LTS)."( Agnoli, A; Baronti, F; Denaro, A; Ruggieri, S; Stocchi, F, 1986)
"28 patients with Parkinson's disease and long-term levodopa therapy have received additional selegiline (10 mg/d) over the past 3 years and been followed up for a mean period of 18."( Gerstenbrand, F; Poewe, W; Ransmayr, G, 1987)
"To simulate an animal model of Parkinson's disease, MPTP (1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine) was administered to five monkeys."( Imai, H; Itakura, T; Kamei, I; Komai, N; Naka, Y; Nakai, K; Nakakita, K, 1988)
"In 22 patients with idiopathic Parkinson's disease, we tested spatial orientation with the rod orientation test, before and after levodopa substitution therapy was started."( De Jong, GJ; Hovestadt, A; Meerwaldt, JD, 1988)
"We postulated that in certain types of Parkinson's disease, the generalized defect of 5HT and enzyme metabolism might primarily exist, and might influence the efficacy of L-dopa therapy and the prognosis of the disease."( Ishizaki, F; Nishikawa, S, 1988)
"A patient with recent-onset Parkinson's disease was tested for mood, physical disability, and cognition, before treatment and then during and after a period of levodopa-induced hypersexuality."( Harvey, NS, 1988)
"Patients with Parkinson's disease and the "on-off" syndrome studied during an "on" phase (under levodopa therapy) and on another occasion after withdrawal of levodopa ("off") demonstrated a significant change in the uptake of [99mTc]-d,l-HM-PAO in the caudate nucleus (lower on "off") and thalamus (higher on "off")."( Burns, A; Costa, DC; Ell, PJ; Levy, R; Philpot, M, 1988)
"Sixty-three patients with Parkinson's disease who failed bromocriptine therapy for various reasons were treated in an open-label trial of pergolide."( Factor, SA; Sanchez-Ramos, JR; Weiner, WJ, 1988)
"Sixteen patients with advanced Parkinson's disease (PD) and motor fluctuations were evaluated throughout 12 months of open label therapy on CR4-Sinemet."( Carroll, VS; Carvey, PM; Gilley, D; Goetz, CG; Klawans, HL; Shannon, KM; Tanner, CM, 1988)
"Results obtained in 22 patients with Parkinson's disease in whom treatment with standard Madopar was replaced by Madopar HBS, a CR formulation of the same product, are presented."( D'Andrea, G; Durisotti, C; Ferro-Milone, F; Lion, P; Lorizio, A; Nordera, GP, 1987)
"In 23 patients with idiopathic Parkinson's disease presenting with severe fluctuations in motor performance and 'on-off' phenomena after long-term treatment with levodopa, the standard form of Madopar was replaced by the controlled-release form Madopar HBS."( Heersema, T; Jansen, EN; Meerwaldt, JD; Speelman, JD; van Manen, J, 1987)
"In 3 patients with longstanding Parkinson's disease treated with Madopar or Nacom, who were not included in the study, the doses of the above drugs could be maintained or reduced by addition of deprenyl."( Grundmann, M; Schimrigk, K, 1987)
"Thirty-eight patients with Parkinson's disease were treated with a protein-restricted diet in addition to their usual drug regime."( Lang, AE; Riley, D, 1988)
"In a 39-year-old man with Parkinson's disease and a history of anxiety disorders, anxiety-provoking situations such as group psychotherapy precipitated panic attacks and caused pronounced worsening of the parkinsonian symptoms."( Ahlskog, JE; Black, JL; Routh, LC, 1987)
"A group of 19 patients with Parkinson's disease, who began dopa therapy 1 to 3 years after onset of symptoms, were followed for 12 years."( Diamond, SG; Markham, CH, 1986)
"Treatment of Parkinson's disease is not difficult in the early stages of the disease; a therapeutic regimen of carbidopa-levodopa or possibly, a combination of carbidopa-levodopa and bromocriptine, provides the best therapeutic results."( Muenter, MD, 1986)
"In 47 patients with Parkinson's disease, we studied the visual evoked potential (VEP) using the pattern-reversal checkerboard (CBVEP) and the grating (GVEP) stimuli before and after 3 months of L-dopa therapy."( Bhaskar, EA; Bhaskar, PA; Devaprabhu, A; Ganesan, RA; Vanchilingam, S, 1986)
"Thirty-five patients with early mild Parkinson's disease were treated from the outset with small doses of L-dopa (mean dose, 396 to 454 mg daily) and a peripheral decarboxylase inhibitor, for a mean of 6 years."( Lees, AJ; Poewe, WH; Stern, GM, 1986)
"Ten patients with idiopathic Parkinson's disease and severe motor-fluctuations participated in an open inpatient trial comparing the efficacy of standard L-Dopa/benserazide (Madopar) treatment with that of an oral sustained-release preparation (Madopar HBS) combined with the standard drug."( Lees, AJ; Poewe, WH; Stern, GM, 1986)
"Nine patients with idiopathic Parkinson's disease were treated with pergolide to a daily maintenance dose of 2."( Hamill, R; Kurlan, R; Levy, R; Macik, B; Miller, C; Shoulson, I, 1985)
"Twenty patients with Parkinson's disease were treated with the 8-alpha-ergoline derivative mesulergine."( Glaeske, C; Pfeiffer, RF; Wilken, K, 1985)
"We treated 12 patients with Parkinson's disease with an 8-alpha-amino-ergoline derivative, CU 32-085."( Hietanen, M; Huttunen, J; Teräväinen, H, 1985)
"In 18 patients with Parkinson's disease, the effects of pergolide after 28 months of treatment were compared with the response after the initial 10-week therapy."( Jankovic, J, 1985)
"Studies performed on 18 patients with Parkinson's disease and 6 control subjects have shown that acute administration of L-DOPA in clinically effective doses gives rise to a diffuse increase in regional cerebral blood flow without accompanying stimulation of regional oxygen utilization."( Causon, R; Gibbs, JM; Jones, T; Leenders, KL; Legg, NJ; Wise, RJ; Wolfson, L, 1985)
"Twenty Parkinson's disease patients, who had not yet received levodopa, were treated with low-dose bromocriptine."( Delgado, MR; Grimes, JD, 1985)
"15 years' experience with Parkinson's disease treated with levodopa was compared to the 15 years before the advent of levodopa."( Hoehn, MM, 1985)
"The literature on the association of Parkinson's disease, levodopa therapy and melanoma is reviewed."( Rampen, FH, 1985)
"Each patient had a long history of Parkinson's disease treated with a carbidopa-levodopa combination."( Feinberg, SS; Feldman, RG; Friedman, JH, 1985)
"Sixty patients suffering from Parkinson's disease, irrespective of previous treatment, were recruited and treated with benserazide/l-dopa or carbidopa/l-dopa, randomly allocated, in a double-blind comparative study."( Admani, AK; Cordingley, GJ; Harris, RI; Verma, S, 1985)
"Thirty-four patients with advanced Parkinson's disease showing intolerance to therapeutic doses of L-DOPA were treated with L-DOPA plus carbidopa at two different proportions."( Bermejo Pareja, F; de Yébenes, JG; Martinez-Martin, P; Muradas, V, 1985)
"Forty-seven patients with Parkinson's disease were evaluated prior to and during levodopa treatment (at five weeks and at six months), to obtain quantitative measures of the effects of the disease and of levodopa on a variety of cognitive and psychomotor functions, by means of psychological tests and special apparatus."( Radbill, R; Rosenberg, G; Schwartz, A, 1974)
"Thirty patients with Parkinson's disease were treated for four weeks with levodopa combined with an inhibitor of extracerebral dopa decarboxylase, L-alpha-methyldopahydrazine (MK 486)."( Barry, PE; Marsden, CD; Parkes, JD; Zilkha, KJ, 1973)
"A small group of patients with Parkinson's disease were treated with oral l-dopa."( Hofmann, WW; Ryan, RL, 1970)
"Eighty-eight patients with Parkinson's disease were treated with levodopa."( Barbeau, A; Libman, I; Mars, H; Rosenberg, G; Schwartz, A; Spencer, A, 1972)
"One hundred patients with Parkinson's disease were treated with levodopa for more than a year at UCLA Medical Center."( Ansel, RD; Markham, CH; Treciokas, LJ, 1971)
"Twenty-two patients with Parkinson's disease were treated for the periods of up to six months with L-dopa."( Bianchine, JR; Peaston, MJ, 1970)
"Interest in l-dopa therapy for Parkinson's disease has been considerably enhanced since the recent release of this drug to all medical practitioners."( Kofman, O, 1971)
"With the exception of Parkinson's disease, there is little evidence that treatments which decrease DA function are potent inducers of depression, but it is argued that such a relationship might not necessarily be expected."( Willner, P, 1983)
"In 6 hypertensive patients with Parkinson's disease, chronic treatment with bromocriptine (46."( Chamontin, B; Montastruc, JL; Rascol, A, 1984)
"The approach to treatment of Parkinson's disease depends on the severity of symptoms at presentation and the response to previous therapy."( Burton, K; Calne, DB, 1984)
"Patients with Parkinson's disease have a decrement in homovanillic acid that is reversed by treatment with L-3,4-dihydroxyphenylalanine."( Aguado, EG; de Yebenes, JG; Mena, MA, 1984)
"Chronic high-dose levodopa therapy in Parkinson's disease is associated with an apparent loss of efficacy and an increased prevalence of side effects which limit its effectiveness."( Koller, WC, 1983)
"In the initial stage of Parkinson's disease deprenyl is only partially sufficient as monotherapy."( Csanda, E; Tárczy, M, 1983)
"A 77-year-old man with Parkinson's disease of long standing, under treatment with L-DOPA and benserazide, was administered DL-threo-3, 4-dihydroxyphenylserine (DL-threo-DOPS), a precursor of norepinephrine, for 10 days."( Kuroda, H; Nukina, I; Ogawa, N; Ota, Z; Yamamoto, M, 1984)
"The drug treatment of Parkinson's disease has progressed through 3 main stages: firstly, the use of anticholinergic drugs and amantadine; then the introduction of levodopa and its association with peripheral decarboxylase inhibitors; and finally the use of direct acting dopamine agonist drugs."( Quinn, NP, 1984)
"The drug treatment of Parkinson's disease should be tailored to the age of the patient, coexistence of dementia or postural hypotension, duration of the disease process and the emergence of side effects."( Morris, JG, 1984)
"Thirty-three patients with advanced Parkinson's disease complicated by end of dose deterioration were treated with bromocriptine."( Bouchard, S; Grimes, JD; King, DB; Kofman, OS; Molina-Negro, P; Wilson, AF, 1984)
"In patients with Parkinson's disease who had never previously been treated with any antiparkinsonism drug, we studied the effects of L-dopa on ballistic arm abduction movement in a step-tracking task."( Baroni, A; Benvenuti, F; Fantini, L; Pantaleo, T; Urbani, F, 1984)
"Patients with Parkinson's disease treated with levodopa over the past 15 years were compared, by parallel statistical methods, to a group of similar patients followed for 15 years before the levodopa era."( Maier Hoehn, MM, 1983)
"Low age at onset of Parkinson's disease, and at the commencement of levodopa therapy, the duration of levodopa treatment and a high dose of levodopa seem to be significant risk factors for the development of response fluctuations, but not the pretreatment duration of Parkinson's disease nor the disability of the patients."( Rinne, UK, 1983)
"In three patients with Parkinson's disease, treatment with pergolide also resulted in uniform 24-h suppression of PRL."( Greising, J; Kleinberg, DL; Kupersmith, M; Lieberman, A; Neophytides, A; Todd, J, 1980)
"The long-term responses of Parkinson's disease to levodopa therapy were studied in the patient material followed-up for 9 years."( Marttila, R; Rinne, UK; Siirtola, T; Sonninen, V, 1980)
"Forty patients with severe Parkinson's disease (23 men, 17 women) who had been treated for six years with L-dopa-decarboxylase inhibitor, were part of a placebo-controlled double-blind trial to test the effectiveness of bromocriptin."( Fischer, PA; Schneider, E, 1982)
"The authors studied 20 patients with Parkinson's disease and prominent hallucinations related to dopaminergic or anticholinergic therapy."( Goetz, CG; Klawans, HL; Tanner, CM, 1982)
"Thirty-seven patients with advanced Parkinson's disease who initially tolerated, and responded to bromocriptine therapy were followed for 12 to 50 (mean 28) months."( Grimes, JD; Hassan, MN, 1983)
"Twenty-three patients with idiopathic Parkinson disease with classic "on-off" phenomena were studied prospectively during treatment with bromocriptine (BCT)."( Glantz, R; Goetz, CG; Klawans, HL; Nausieda, PA; Weiner, WJ, 1981)
"In the untreated patients with Parkinson's disease, the CSF GABA level was 95 +/- 31 pmole/mL (n = 7) and in those who were treated with levodopa and carbidopa the level was 144 +/- 53 pmole/mL (n = 8)."( Manyam, BV, 1982)
"Bilateral vocal cord paralysis in Parkinson's disease may be seen more commonly in the future as therapy enables more patients to live longer."( Lieberman, AN; Plasse, HM, 1981)
"Patients with Parkinson's disease were treated with different antiparkinsonian drugs and the amino acid levels in serum and cerebrospinal fluid were determined."( Gerstenbrand, F; Gründig, E, 1980)
"In 14 patients with Parkinson's disease on long-term therapy the erythrocyte catechol-O-methyltransferase activity was found to correlate with the average plasma concentration ratio of 3-O-methyldopa to levodopa and with the fasting plasma concentration ratio of 3-O methyldopa to levodopa."( Reilly, DK; Rivera-Calimlim, L; Van Dyke, D, 1980)
"L-DOPA therapy (in Parkinson's disease) elevates urinary and tissue levels of the carboxylated THP derivatives, as well as of salsolinol and THP itself; hyperphenylalaninemia during PKU also increases tissue levels of a DA/phenylpyruvate-derived TIQ and an imine condensate of phenylethylamine and vitamin B6."( Collins, MA, 1980)
"The progress of 178 patients with Parkinson's disease who began treatment with levodopa between November 1969 and December 1972 is reviewed after six years."( Lees, AJ; Shaw, KM; Stern, GM, 1980)
"Ten patients with a diagnosis of idiopathic Parkinson's disease and motor fluctuations otherwise unresponsive to conventional therapy were selected."( Casas Parera, I; Diaz, S; Fernández Pardal, MM; Gatto, E; Micheli, F, 1991)
"Initiating treatment in a patient with Parkinson's disease requires consideration of age, degree of disease activity, and consequences of long-term treatment."( Ghika, J, 1995)
"Deterioration in Unified Parkinson's Disease Rating Score (UPDRS) between untreated baseline and final visits was used as an index of disease progression."( Bushenbark, K; Esterlitz, J; Gauger, L; Hauser, RA; Hubble, J; Koller, W; Lilienfeld, D; Malapira, T; Olanow, CW, 1995)
"Early stage Parkinson's disease may be better left untreated if it does not limit motor function."( Eadie, MJ, 1995)
"In untreated patients with Parkinson's disease (PD), the total (free and conjugated) serotonin (5-HT) and dopamine (DA) concentrations in the cerebrospinal fluid decreased significantly."( Abe, T; Hamato, H; Takahashi, J; Takahashi, S; Tohgi, H, 1993)
"Sixteen patients with Parkinson's disease and severe motor fluctuations were treated with subcutaneous injections of apomorphine and followed up prospectively for a year."( Leiguarda, R; Merello, M, 1995)
"The treatment of idiopathic Parkinson's disease has been divided in 3 different phases."( Ludin, HP, 1995)
"Management of Parkinson's disease is dominated by the desire to prevent the development of fluctuations, dyskinesia, and psychiatric complications, and to treat effectively these effects when they appear."( Nutt, JG, 1995)
"Twenty patients with Parkinson's disease were studied during the early phase of L-dopa treatment to clarify the development and progression of Parkinsonian motor fluctuations."( Kempster, PA; Shif, M, 1994)
"Three groups of patients with Parkinson's disease (PD) were studied: (1) PD patients treated medically with L-Dopa and anticholinergics, (2) PD patients treated with thalamo-subthalamotomies plus medical treatment, and (3) PD patients treated with autologous adrenal medullary transplantation to right caudate nucleus plus medical treatment."( Jimenez, F; Velasco, AL; Velasco, F; Velasco, M, 1994)
"Ten patients with idiopathic Parkinson's disease (PD) (3 men and 7 women, group A) who had received no treatment for the disease; 102 patients with PD (36 men and 66 women, group B) who had undergone treatment and 45 healthy volunteers (15 men and 30 women, control group) were subject to thyrotropin-releasing hormone (TRH) tests and levodopa tests."( Adachi, K; Hirooka, Y; Mitsuma, T; Oiso, Y; Otake, K, 1994)
"Studies examining the mortality from Parkinson's disease have been reviewed to assess the impact of levodopa therapy."( Clarke, CE, 1995)
"One therapeutic approach to treating Parkinson's disease is to convert endogenous striatal cells into levo-3,4-dihydroxyphenylalanine (L-dopa)-producing cells."( During, MJ; Geller, AI; Naegele, JR; O'Malley, KL, 1994)
"Two strategies of drug therapy for Parkinson's disease (PD) are neuroprotective and symptomatic."( Sweeney, PJ, 1995)
"Some treatments used for Parkinson's disease attenuate locomotor depression in rats treated with reserpine and alpha-methyl-p-tyrosine."( Danysz, W; Quack, G; Rogoz, Z; Skuza, G, 1994)
"Pharmacotherapy of Parkinson's disease (PD) has become so effective that patients with PD can enjoy a nearly normal life, including travel for several years."( Dodel, RC; Oertel, WH, 1995)
"The hypothesis that L-DOPA therapy in Parkinson's disease may augment neuronal damage and thus accelerate the progression of the disease remains controversial."( Walkinshaw, G; Waters, CM, 1995)
"Monotherapy of Parkinson's disease with glutamate antagonists appears impractical at the present time, due to their low efficacy and unacceptable side effects, but polypharmacy with L-DOPA and a glutamate antagonist as adjuvant is a more realistic prospect."( Starr, MS, 1995)
"Mortality due to Parkinson's disease has decreased significantly after the introduction of L-dopa treatment."( Kuno, S, 1994)
"For the treatment of Parkinson's disease, L-DOPA therapy has been applied to replace dopamine, and droxidopa (L-threo-3,4-dihydroxyphenylserine) therapy to supply noradrenaline (NA)."( Maruyama, W; Naoi, M; Narabayashi, H, 1994)
"It is used to treat Parkinson's disease at a dose of 5 mg twice a day."( Alexoff, D; Fowler, JS; Logan, J; MacGregor, RR; Pappas, N; Schyler, D; Shea, C; Volkow, ND; Wang, GJ; Wolf, AP, 1994)
"Two elderly patients with Parkinson's disease were treated with nicotine gum and patch."( Fagerström, KO; Giordani, B; Pomerleau, O; Stelson, F, 1994)
"Six patients with Parkinson's disease were treated for 3 months with s."( Gancher, ST; Nutt, JG; Woodward, WR, 1995)
"According to the Unified Parkinson's Disease Rating Scale a tendency to clinical improvement was seen after the iv infusions in both treatment and placebo groups."( Dizdar, N; Kågedal, B; Lindvall, B, 1994)
"In early untreated Parkinson's disease, cognitive performance appears to be stable and unrelated to either motor deterioration or treatment with deprenyl or tocopherol."( Brady, J; Carter, J; Como, P; Growdon, J; Huber, S; Kanigan, B; Kieburtz, K; Landow, E; McDermott, M; Rudolph, A, 1994)
"A 64-year-old man was diagnosed to have Parkinson's disease when aged 42 years and since then has been treated with levodopa and benserazide (up to 875 mg daily)."( Eberli, F; Greminger, P; Schmid, PA; Speich, R; Suter, T, 1994)
"All records were reviewed from a Parkinson's disease clinic to determine how many patients were treated simultaneously with selegiline and fluoxetine."( Waters, CH, 1994)
"Tremor at rest is a classic symptom of Parkinson's disease that causes significant disability and distress for the patient and is generally only weakly responsive to conventional treatment, like anticholinergic and dopaminergic medication."( Jansen, EN, 1994)
"Patients with Parkinson's disease generally have a smooth clinical response from levodopa therapy for the first 3 to 5 years."( Mark, MH; Sage, JI, 1994)
"149 previously untreated patients with Parkinson's disease were recruited over a three year period and randomly allocated to either low dose levodopa-carbidopa (< or = 600/150 mg/day) or low dose bromocriptine (< or = 30 mg/day)."( Broe, GA; Hely, MA; Margrie, S; Morris, JG; O'Sullivan, DJ; Rail, D; Reid, WG; Williamson, PM, 1994)
"This suggests that the change in GSH in Parkinson's disease is not solely due to nigral cell death, or entirely explained by drug therapy, for multiple-system atrophy patients were also treated with levodopa."( Agid, Y; Daniel, S; Dexter, DT; Javoy-Agid, F; Jenner, P; Lees, AJ; Marsden, CD; Sian, J, 1994)
"This article reviews the biology of Parkinson's disease, the diagnostic approach to patients with parkinsonism, pharmacologic treatments, and practical strategies for managing common clinical problems."( Standaert, DG; Stern, MB, 1993)
"We treated 17 patients with Parkinson's disease (PD) complicated by psychosis with the atypical antipsychotic drug, clozapine, for 6 to 24 months (mean, 15 months) in a prospective, open-label trial."( Brown, D; Factor, SA; Molho, ES; Podskalny, GD, 1994)
"Chronic levodopa administration in Parkinson's disease (PD) is associated with long-term motor side effects."( Quattrone, A; Zappia, M, 1993)
"Eighteen patients with advanced Parkinson's disease (n = 13) or dopamine-sensitive dystonia (n = 5) were treated with the dopaminergic agent, lisuride, applied as a long-term subcutaneous infusion."( Baier, JE; Gallati, H; Kovacs, S; Neumann, HA; Poehlau, D; Przuntek, H; Schmutz, T; Suchy, I; Will, C, 1994)
"The motor responses of 14 patients with Parkinson's disease (six previously untreated and eight chronically receiving levodopa) with pronounced asymmetry in the severity of motor signs between the left and right sides of the body were studied."( Lera, G; Luquin, MR; Obeso, JA; Rodriguez, M; Vaamonde, J, 1994)
"We report a patient with Parkinson's disease who developed orobuccal dyskinesia while being treated with trihexyphenidyl (Artane)."( Hauser, RA; Olanow, CW, 1993)
"More than 50% of all patients with Parkinson's disease who initially receive treatment with conventional levodopa will develop late complications, although the underlying mechanisms are not completely understood."( Poewe, W, 1993)
"Surgical treatment for Parkinson's disease began by blocking of the pyramidal system in early part of this era."( Komai, N, 1993)
"Patients (250) with Parkinson's disease, treated once daily with either 1 or 4 mg, together with L-Dopa and a decarboxylase inhibitor (MadoparR or SinemetR), saw significant improvements in symptoms compared with those on standard therapy without the inhibitor."( Bey, P; Cremer, G; Haegele, KD; McDonald, IA; Palfreyman, MG; Zreika, M, 1993)
"Presymptomatic detection of Parkinson's disease is necessary if neuroprotective therapies are to be utilized in its treatment."( Jenner, P, 1993)
"Seven patients with idiopathic Parkinson's disease, aged 62 to 76 years, average duration of the disease approximately eleven years, suffering from severe hallucinosis and paranoid delusions of different degree, in whom conventional therapeutic strategies (administration of benzodiazepines and mild neuroleptics) had no antipsychotic effect, received clozapine, a non-classical highly potent neuroleptic, while blood count was strictly monitored."( Helscher, RJ; Pinter, MM, 1993)
"Since the original description of Parkinson's disease (PD) more than 170 years ago, there have been major advances in the understanding and treatment of PD."( Poirier, J; Thiffault, C, 1993)
"782 patients with early Parkinson's disease who were not receiving dopaminergic treatment."( , 1993)
"The ratings for Parkinson's disease improved during the first three months of deprenyl treatment; the motor performance of deprenyl-treated patients worsened after the treatments were withdrawn."( , 1993)
"A series of 31 Parkinson's disease (PD) patients suffering from panic attacks (PA), late in the evolution of their disease, was analyzed from a group of 131 levodopa-treated PD patients."( García-Ruiz, P; García-Urra, D; Jiménez-Jiménez, FJ; Vázquez, A, 1993)
"The data indicate that in patients with Parkinson's disease treated long term, factors associated with age rather than duration of disease may have a stronger adverse influence on magnitude of response to levodopa."( Durso, R; Feldman, RG; Isaac, K; Perry, L; Saint-Hilaire, M, 1993)
"L-dopa, the major treatment for Parkinson's disease (PD), depletes S-adenosyl-L-methionine (SAM)."( Benson, R; Charlton, C; Crowell, B; Doonquah, K; Hill, B, 1993)
"Four patients with Parkinson's disease, optimally treated with levodopa/carbidopa (LD/CD) tablets but experiencing severe motor fluctuations, underwent an open trial of a levodopa/carbidopa/ascorbic acid solution (LCAS) orally at timed intervals."( Irwin, I; Kurth, MC; Langston, JW; Lyness, WH; Tetrud, JW, 1993)
"It was first used in the treatment of Parkinson's disease by Schwab in the 1950s but owing to its short duration of action, the need for parenteral administration, and adverse reactions including nausea, vomiting, postural hypotension and sedation, it was not widely prescribed."( Lees, AJ, 1993)
"The treatment of Parkinson's disease is reviewed."( Lieberman, A, 1993)
"We investigated a patient with Parkinson's disease accompanied by intellectual impairment induced by long-term AC therapy."( Momose, T; Nishiyama, K; Sakuta, M; Sugishita, M, 1995)
"Seven patients with idiopathic Parkinson's disease were enrolled in a ten week study to evaluate the efficacy of famotidine, an histamine H2-antagonist, in the treatment of bradyphrenia."( Di Rocco, A; Kaminski, R; Molinari, SP; Yahr, MD, 1995)
"In newly diagnosed cases of Parkinson's disease, administration of selegiline hydrochloride (Eldepryl) may slow symptom development and delay the need for levodopa therapy."( Silverstein, PM, 1996)
"In rodent models of Parkinson's disease such as reserpinized or 6-hydroxydopamine substantia nigra lesioned rats, blockade of glutamate receptors of the NMDA (N-methyl-D-aspartate) or the AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate) receptor subtypes and concomitant treatment with L-DOPA (L-3,4-dihydroxyphenylalanine) or direct dopamine agonists restores locomotor activity and induces rotations."( Eblen, F; Kockgether, T; Löschmann, PA; Wachtel, H; Wüllner, U, 1995)
"520 patients with early Parkinson's disease who were not receiving dopaminergic treatment."( Lees, AJ, 1995)
"To test the hypotheses that Parkinson's disease can differentially produce deficits in voluntary and rhythmic jaw movements, which involve different neuronal circuits, and that levodopa treatment improves specific components of the motor deficit."( Hammerstad, JP; Robertson, LT, 1996)
"In an open label study 63 patients with idiopathic Parkinson's disease suffering from end-of-dose akinesia were switched from a treatment with a L-DOPA standard formulation to a combined therapy of L-DOPA standard in the morning and L-DOPA slow release (levodopa, benserazide, Madopar Depot) at the remaining single doses."( Eichhorn, TE; Kohnen, R; Oertel, WH; Poewe, W; Schrag, A; Selzer, R; Trenkwalder, C, 1995)
"A 55-year-old woman with severe Parkinson's disease was treated by cografting adrenal medulla with pretransected peripheral nerve into the bilateral caudate nuclei."( Asari, S; Date, I; Imaoka, T; Miyoshi, Y; Ohmoto, T; Ono, T, 1996)
"The oxidant stress theory of Parkinson's disease (PD) hypothesizes that levodopa treatment may be potentially harmful and this is supported by studies demonstrating levodopa toxicity to cultured dopaminergic neurons."( Ahlskog, JE; Low, PA; Nickander, KK; O'Brien, JF; Tyce, GM; Uitti, RJ, 1996)
"Since 1985, treatment of idiopathic Parkinson's disease (PD) by surgical transfer of adult or fetal chromaffin tissue or of fetal central neural tissue to the brains of afflicted patients has been attempted, with variable clinical results."( Durso, R; Folkerth, RD, 1996)
"Eleven patients with Parkinson's disease (PD) were treated with individual doses of budipine added to stable conventional antiparkinsonian medication."( Boose, A; Dichgans, J; Jentgens, C; Klockgether, T; Löschmann, P; Spieker, S, 1995)
"We describe a 68-year-old patient with Parkinson's disease who developed retroperitoneal fibrosis during pergolide treatment."( Gutiérrez, F; Jiménez-Jiménez, FJ; López-Alvarez, J; Miquel, J; Montero, E; Sánchez-Chapado, M; Sierra, A, 1995)
"Forty two patients with Parkinson's disease (14 untreated, eight with a stable response to levodopa, and 20 with levodopa induced motor fluctuations) were challenged on two consecutive days with apomorphine and levodopa."( Colosimo, C; Hughes, AJ; Lees, AJ; Merello, M; Sieradzan, K, 1996)
"Seven patients suffering from Parkinson's disease (PD) with severely disabling dyskinesia received low-dose propranolol as an adjunct to the currently used medical treatment."( Agid, Y; Bonnet, AM; Carpentier, AF; Vidailhet, M, 1996)
"Drug holidays as treatment in Parkinson's disease (PD) to ameliorate the effects of chronic L-dopa use are a controversial method."( Corona, T; Otero, E; Rivera, C; Stopp, L, 1995)
"The patient with Parkinson's disease often needs concomitant treatment for disorders that accompany the disease, such as depression, insomnia or constipation, or for frequent concomitant alterations such as dizziness, high blood pressure or heart disease."( López de Munain, A; Martí Massó, JF; Poza, JJ, 1996)
"This article describes the pathology of Parkinson's disease, and how it can be managed through drug therapy and surgical intervention, particularly pallidotomy."( Roberts, J, 1996)
"Forty-six patients with Parkinson's disease experiencing motor fluctuations and not optimally controlled on levodopa received as adjunct therapy a new nonergoline dopamine agonist, ropinirole, in a 3-month randomized placebo-controlled trial."( Fuell, D; Lees, AJ; Montastruc, JL; Pirtosek, Z; Rascol, O; Senard, JM, 1996)
"We think that Parkinson's disease encompasses a heterogeneous group of patients of whom about 75% are well treated by bromocriptine alone at the early stages of the illness."( Akiguchi, I; Fukuyama, H; Imai, T; Kawamura, J; Kimura, J, 1996)
"Twenty de novo patients with Parkinson's disease (Hoehn-Yahr stages I, II, III) were studied in a double blind trial after introducing (--)-deprenyl monotherapy."( Kovacs, AB; Mally, J; Stone, TW, 1995)
"In 12 Parkinson's disease (PD) patients with motor fluctuations, cabergoline was added in an 8-week study to their usual L-dopa/carbidopa therapy."( Bonuccelli, U; Colzi, A; Del Dotto, P; Dubini, A; Grimaldi, R; Lucetti, C; Pardini, C, 1995)
"A 72-years old man with Parkinson's disease was treated with levodopa for 14 years."( Burg, G; Kleinhans, M; Schmid-Grendelmeier, P, 1996)
"The current symptomatic treatment of Parkinson's disease mainly relies on agents which are able to restore dopaminergic transmission in the nigrostriatal pathway, such as the dopamine precursor levodopa or direct agonists of dopamine receptors."( Albani, F; Baruzzi, A; Contin, M; Riva, R, 1996)
"Thirty Parkinson's disease patients (10 previously untreated, 10 with early disease, and 10 with motor fluctuations/dyskinesia) participated in a single-dose double-blind study."( Koller, WC; Lyons, K; Marjama, J; McGuire, D; Pahwa, R; Silverstein, P; Ward, R; Zwiebel, F, 1996)
"Furthermore, 6 of 15 untreated Parkinson's disease patients (40%) displayed markedly elevated plasma concentrations of the catecholamine MAO metabolites, DOPAC or DOPEG."( Ahlskog, JE; Kokmen, E; O'Brien, JF; Petersen, RC; Tyce, GM; Uitti, RJ, 1996)
"In advanced stages of Parkinson's disease treatment of concomitand mental symptoms and multifarious disorders of the autonomic nervous system are becoming of increasing significance."( Fischer, PA, 1995)
"Long-term levodopa treatment in Parkinson's disease is typically associated with "motor side effects" consisting in dyskinesias and/or fluctuations in motility referred to as the on-off phenomena."( Blümner, E; Danielczyk, W; Gerlach, M; Kaiser, HJ; Kraus, PH; Letzel, H; Przuntek, H; Riederer, P; Uberla, K; Welzel, D, 1996)
"The records of 49 patients with Parkinson's disease and psychosis who were treated with clozapine for up to 18 months were reviewed."( Defilippi, JL; Menza, MA; Sage, JI; Wagner, ML, 1996)
"Twenty patients with Parkinson's disease (PD), who developed delusions and psychotic behavior, underwent electroencephalogram (EEG) recordings before and during treatment with low-dose clozapine."( Korczyn, AD; Neufeld, MY; Orlov, E; Rabey, JM, 1996)
"Current treatments for Parkinson's disease (PD) rely on dopamine-replacing strategies, and centre around dopamine precursors (e."( Brotchie, JM; Henry, B, 1996)
"Fluorine-18-FDG was administered to 18 Parkinson's disease and 15 normal control subjects."( Giordani, B; Koeppe, RA; Kuhl, DE; Minoshima, S; Piert, M, 1996)
"Most patients with Parkinson's disease develop response fluctuations after several years of chronic treatment with levodopa."( Djaldetti, R; Melamed, E; Ziv, I, 1996)
"Treatment of Parkinson's disease has progressed steadily for the last decades after introduction of levodopa."( Yanagisawa, N, 1997)
"In this study, we randomized de novo Parkinson's disease (PD) patients to treatment with increasing doses of cabergoline (0."( Bracco, F; Chouza, C; Dubini, A; Dupont, E; Gershanik, O; Grimaldi, R; Marsden, CD; Marti Masso, JF; Montastruc, JL; Orlando, N; Rinne, UK, 1997)
"Patients with advanced Parkinson's disease often develop severe fluctuations and dyskinesias while receiving long-term levodopa therapy."( Marsden, CD; Nordera, G; Stocchi, F, 1997)
"Genetic intervention in Parkinson's disease may offer an entirely different method for treating this disease in the future, based not only on symptomatic therapy, but also on neuroprotective and/or neuroregenerative therapy which would alter the natural history of relentless progression."( Freese, A; Stern, MB, 1997)
"Many patients with Parkinson's disease develop both involuntary movements from and a critical dependency on, levodopa therapy as their disease progresses."( Kurth, MC, 1997)
"A recent study by the Parkinson's Disease Research Group of the United Kingdom revealed higher mortality in patients with Parkinson's disease who were treated with selegiline (deprenyl) compared with those who were not."( Kondo, T; Mizuno, Y, 1997)
"Twenty patients with idiopathic Parkinson's disease and disabling motor fluctuations were treated with intermittent subcutaneous (11 patients) or intranasal (nine patients) apomorphine for > 2 years."( Esteban Muñoz, J; Marín, C; Martí, MJ; Tolosa, E, 1997)
"For better treatment of Parkinson's disease, it is important to solve these problems."( Ogawa, N, 1997)
"The initial treatment of Parkinson's disease should be addressed to improve symptoms, slow down the progression of the illness and avoid long and short term complications."( Kulisevsky, J; López-Villegas, D, 1997)
"The progression of Parkinson's disease, and the increase in the time under therapy with levodopa of this disease, leds to development of several complications, including loss of efficacy of the therapy, motor fluctuations, dyskinesias, psychiatric disorders, etc."( Jiménez-Jiménez, FJ; Molina, JA, 1997)
"Dyskinesias are usually seen in Parkinson's disease (PD) patients after several years of L-dopa therapy."( Brooks, DJ; Lees, AJ; Turjanski, N, 1997)
"Parenteral apomorphine has been used in Parkinson's disease (PD) to replace levodopa after surgery or to treat the malignant syndrome brought about by sudden levodopa withdrawal."( Albanese, A; Colosimo, C; Merello, M, 1994)
"More than 50% of patients with Parkinson's disease develop motor response fluctuations (the "wearing off" phenomenon) after more than five years of levodopa therapy."( Baas, H; Beiske, AG; Ghika, J; Jackson, M; Oertel, WH; Poewe, W; Ransmayr, G, 1997)
"Investigations of gene therapy for Parkinson's disease have focused primarily on strategies that replace tyrosine hydroxylase."( Bencsics, C; Kang, UJ; Wachtel, SR, 1997)
"Most patients with Parkinson's disease who undergo levodopa therapy eventually develop fluctuations in the diurnal control of their symptoms."( Tolosa, E; Valldeoriola, F, 1994)
"Sixty patients with Parkinson's disease (46 male and 14 female) with a mean (+/- SD) age of 59 +/- 9 years were treated in an open study for 12 weeks."( , 1995)
"A patient with Parkinson's disease carried out the tests 12 hr after medication was withheld at a time when symptoms were evident ("off" stage), and after administration of medication when it had taken full effect ("on" stage)."( Giaschi, D; Lang, A; Regan, D, 1997)
"In two patients with severe Parkinson's disease (PD) whose response to levodopa had decreased, the parkinsonian motor symptoms responded to acute and maintenance unilateral electroconvulsive therapy (ECT)."( Aarsland, D; Langeveld, JH; Larsen, JP; Waage, O, 1997)
"Patients with early, untreated Parkinson's disease maintained on (-)deprenyl need levodopa significantly later than their placebo-treated peers, and when on levodopa plus (-)deprenyl, they live significantly longer than patients on levodopa alone."( Knoll, J, 1998)
"624 patients with early Parkinson's disease who were not receiving dopaminergic treatment and a subgroup fo 120 patients who died during the trial."( Ben-Shlomo, Y; Churchyard, A; Head, J; Hurwitz, B; Lees, AJ; Ockelford, J; Overstall, P, 1998)
"During the initial stages of Parkinson's disease, treatment with levodopa plus a decarboxylase inhibitor (carbidopa or benserazide) provides adequate control of symptoms."( Adler, CH; Kurth, MC, 1998)
"More than 50% of patients with Parkinson's disease develop motor response fluctuations (the 'wearing off" phenomenon) after more than five years of levodopa therapy."( Baas, H; Beiske, AG; Ghika, J; Jackson, M; Oertel, WH; Poewe, W; Ransmayr, G, 1998)
"Three cases of DMS in patients with Parkinson's disease and dementia, treated with dopaminergic medications, are presented."( Feinberg, TE; Roane, DM; Robinson, JH; Rogers, JD, 1998)
"Striatal dopamine deficiency in Parkinson's disease (PD), first described in 1960, was a key event that led to the era of levodopa therapy."( Martí, MJ; Molinuevo, JL; Tolosa, E; Valldeoriola, F, 1998)
"Studies in animal models of Parkinson's disease (PD) suggest that GM1 ganglioside treatment can restore neurologic and dopaminergic function."( Chapas-Crilly, J; Mancall, EL; Roeltgen, DP; Rothblat, DS; Schneider, JS; Tatarian, GT, 1998)
"It is approved as monotherapy in early Parkinson's disease and as adjunctive therapy to levodopa in patients with advanced disease experiencing motor effects because of diminished response to levodopa."( Dooley, M; Markham, A, 1998)
"Eight of the Parkinson's disease patients were on fludrocortisone (Florinef) therapy because of orthostatic hypotension."( Hakamäki, T; Lehtonen, A; Rajala, T, 1998)
"More than 50% of patients with Parkinson's disease (PD) develop response fluctuations following prolonged treatment with levodopa."( Djaldetti, R; Melamed, E, 1998)
"In many patients with idiopathic Parkinson's disease, treatment with levodopa is complicated by fluctuations between an "off" period, when the medication is not working and the motor symptoms of parkinsonism are present, and an "on" period, when the medication is causing improved mobility, often accompanied by debilitating dyskinesias."( Ardouin, C; Benabid, AL; Benazzouz, A; Hoffmann, D; Krack, P; Limousin, P; Pollak, P, 1998)
"Most Parkinson's disease (PD) treatments palliate symptoms by increasing nigrostriatal dopaminergic tone."( Swerdlow, RH, 1998)
"A new approach in the treatment of Parkinson's disease is the inhibition of catechol-O-methyltransferase (COMT) with new generation COMT inhibitors, entacapone and tolcapone."( Rinne, UK; Ruottinen, HM, 1998)
"Total Unified Parkinson's Disease Rating Scale motor "off" and motor "on" subscores all improved and the rapidity of action, magnitude, and duration of motor response to levodopa therapy were all maintained after pallidotomy."( Turk, MF; Uitti, RJ; Wharen, RE, 1998)
"Cerebrospinal fluid from L-dopa-treated Parkinson's disease patients and subjects without neurodegenerative diseases (controls) was explored in its trophic properties as culture medium on a variety of cells from neural origin."( Colombo, JA; Napp, MI, 1998)
"Three patients with Parkinson's disease are described who developed pericardial, retroperitoneal, and pleural fibrosis associated with pergolide treatment."( Dick, DJ; Pilling, JB; Shaunak, S; Wilkins, A, 1999)
"Thirty patients with Parkinson's disease not previously treated with dopamine agonists, of whom 28 produced evaluable pharmacokinetic data for ropinirole and 23 for L-dopa."( Beerahee, A; Burns, E; Citerone, DR; Cyronak, MJ; Fitzpatrick, KL; Leigh, TJ; Lennox, G; Lopez-Gil, A; Taylor, AC; Vakil, SD, 1999)
"Ten patients who had Parkinson's disease with disabling dyskinesia were included in this study to evaluate the role of mental (mental calculation) and motor (flexion/extension of right fingers, flexion/extension of left fingers, flexion/extension of the neck, speaking aloud) tasks on the worsening of peak-dose dyskinesia following administration of an effective single dose of apomorphine."( Agid, Y; Debilly, B; Durif, F; Vidailhet, M, 1999)
"Twenty-seven patients with idiopathic Parkinson's disease, treated with L-dopa but not sufficiently controlled, were included in this trial."( Malbezin, M; Montastruc, JL; Rascol, O; Ziegler, M, 1999)
"In both treated and de novo Parkinson's disease groups, decrease in ERD latency (1,000 to 1,250 ms before movement) was only observed when movements were performed with the akinetic hand and corresponded to a decrease in motor cortical activity."( Bourriez, JL; Defebvre, L; Derambure, P; Destée, A; Guieu, JD, 1999)
"Patients with Parkinson's disease were examined before and after L-dopa treatment."( Diószeghy, P; Hidasi, E; Mechler, F, 1999)
"It has been effective in early Parkinson's disease as monotherapy and as adjunctive therapy with L-dopa in advanced stages of the disease."( Galiano, ML; Grandas, F, 1999)
"As a potential treatment for Parkinson's disease, viral vector-mediated over-expression of striatal L-aromatic amino acid decarboxylase was tested in an attempt to facilitate the production of therapeutic levels of dopamine after peripheral L-dihydroxyphenylalanine administration."( Leff, SE; Mandel, RJ; Snyder, RO; Spratt, SK, 1999)
"Although hallucinations in Parkinson's disease (PD) are not unusual in the long-term treatment with anti-parkinsonian agents, their mechanism is not fully understood."( Kobayashi, S; Oguro, H; Okada, K; Suyama, N; Yamaguchi, S, 1999)
"In all, 71 grafts in 38 patients [24 Parkinson's disease (PD), 14 Huntington's disease (HD)] were examined, as well as 24 untreated PD and HD patients and 13 age-matched normal controls."( Blüml, S; Dubowitz, D; Hoang, TQ; Jacques, DB; Kopyov, OV; Lin, A; Ross, BD; Seymour, K; Tan, J, 1999)
"The early treatment of Parkinson's disease continues to be controversial as our understanding of the etiology of the disease remains incomplete."( Grimes, DA; Lang, AE, 1999)
"We report a 63-years old patient with Parkinson's disease, who experienced slight fluctuations 10 years after first signs of the disease and two years after initiation of levodopa/carbidopa and biperiden therapy."( Arnold, G; Kupsch, A, 1999)
"Patients with Parkinson's disease associated with NMS are considered to have a low incidence of DIC, status epilepticus, and in Japan this may be the first case report of the successful treatment of NMS with DIC and status epilepticus in a patient with Parkinson's disease."( Miyoshi, T; Motomura, S; Osoegawa, M; Tamura, K; Yamanaka, H, 1999)
"In the treatment of patients with Parkinson's disease, apomorphine has an established place as a back-up therapy if other antiparkinsonian drugs, such as levodopa and oral dopamine agonists, have not controlled the existing response fluctuations."( Neef, C; van Laar, T, 1999)
"The drug treatment of Parkinson's disease since the original description of the malady in 1817 is described."( Sourkes, TL, 1999)
"We enrolled 37 patients with advanced Parkinson's disease who had, despite optimum pharmacological treatment, at least one of the following symptoms: severe response fluctuations, dyskinesias, painful dystonias, or bradykinesia."( Beute, GN; Bosch, DA; de Bie, RM; de Haan, RJ; Haaxma, R; Nijssen, PC; Rutgers, AW; Schmand, B; Schuurman, PR; Speelman, JD; Staal, MJ, 1999)
"Treatment of Parkinson's disease with L-dopa is plagued in a majority of patients by dyskinesias."( Bédard, PJ; Doan, VD; Grondin, R; Hadj Tahar, A; Ladure, P, 2000)
"Ten patients treated for Parkinson's disease showed substantially increased tremor intensity, especially within the low-frequency window."( Biernat, H; Cleary, D; de Oliveira Santos, EC; Ellias, SA; Feldman, RG; Grandjean, P; Jørgensen, PJ; Wermuth, L, 1999)
"Some patients with idiopathic Parkinson's disease experience hallucinations as a result of treatment with levodopa and dopamine agonists."( Aitchison, KJ; Arranz, MJ; Forsyth, J; Graham, JM; Grünewald, RA; Li, T; Makoff, AJ; Shaikh, S, 2000)
"The blink rate is reduced in Parkinson's disease (PD) and increased with dopamine treatment."( Hallett, M, 2000)
"Early Parkinson's disease can be managed successfully for up to five years with a reduced risk of dyskinesia by initiating treatment with ropinirole alone and supplementing it with levodopa if necessary."( Brooks, DJ; Clarke, CE; De Deyn, PP; Korczyn, AD; Lang, AE; Rascol, O, 2000)
"Putative neuroprotective agents for Parkinson's disease can be assessed in untreated patients using progression of clinical disability as an index of disease progression."( Busenbark, K; Hauser, RA; Hubble, JP; Koller, WC; Malapira, T; Olanow, CW, 2000)
"Two patients with Parkinson's disease received treatment with ropinirole and/or pramipexole, during which both experienced sleep attacks."( Ryan, M; Slevin, JT; Wells, A, 2000)
"Four hundred twelve patients with Parkinson's disease with fluctuating and nonfluctuating responses to levodopa participated in three multicentered, parallel, double-blind, placebo-controlled dose-finding studies and received either placebo or tolcapone in addition to levodopa-decarboxylase inhibitor therapy."( Banken, L; Fotteler, B; Jorga, K; Snell, P; Steimer, JL, 2000)
"Her doctor initially diagnosed Parkinson's disease and administered amantadine and levodopa."( Kondo, M; Makino, M; Nakajima, K; Ueda, Y, 2000)
"In two patients with Parkinson's disease and L-Dopa induced dyskinesia we administered morphine orally to alleviate lumboradicular pain unresponsive to any other form of treatment."( Becker, G; Berg, D; Reiners, K, 1999)
"Long-term levodopa therapy for Parkinson's disease is complicated by the development of motor fluctuations and abnormal involuntary movements."( Clarke, CE; Deane, KH, 2000)
"Long-term levodopa therapy for Parkinson's disease is complicated by the development of motor fluctuations and abnormal involuntary movements."( Clarke, CE; Deane, KH, 2000)
"In the symptomatic treatment of early Parkinson's disease ropinirole monotherapy was significantly more effective than placebo in 2 multicentre, randomised, double-blind trials of 3 to 12 months duration as assessed by the Unified Parkinson's Disease Rating Scale (UPDRS) motor scores and Clinical Global Impression/Clinical Global Evaluation Scales."( Matheson, AJ; Spencer, CM, 2000)
"In patients with early Parkinson's disease, ropinirole monotherapy was more efficacious than bromocriptine with regard to improvement in activities of daily living, and need for supplemental levodopa."( Matheson, AJ; Spencer, CM, 2000)
"In the search for a therapy of Parkinson's disease, ionotropic, mainly NMDA, receptor antagonists were found to have moderately beneficial, yet also some undesirable side-effects."( Konieczny, J; Lorenc-Koci, E; Ossowska, K; Pilc, A; Wolfarth, S, 2000)
"The aim of current treatment of Parkinson's disease is to ameliorate the symptoms while seeking to lessen the potential development of late levodopa complications."( Fung, VS; Hely, MA; Morris, JG, 2000)
"The purpose of the new drugs for Parkinson's disease is control of the long-term levodopa treatment syndromes, especially wearing-off phenomenon and dyskinesia."( Hasegawa, K, 2000)
"A patient with severe Parkinson's disease presented with increasing dyspnea, bilateral pleural effusion and peripheral edema that were refractory to diuretic therapy and were first misdiagnosed as signs of right-sided heart failure."( Gershman, M; Hamaoui, E; Varsano, S, 2000)
"L-DOPA therapy for Parkinson's disease is one of the major achievements of twentieth century neurology; Parkinson's disease was the first in which specific neurochemical deficits in defined brain regions were identified, and thus for which a rational, chemical therapy could be developed, ushering in the era of clinical neurochemistry."( Foley, P, 2000)
"(-)-Deprenyl, used for the treatment of Parkinson's disease, was reported to possess neurorescuing/antiapoptotic effects independent of its MAO-B inhibiting properties."( Boulton, AA; Cools, AR; Kato, AC; Tatton, WG; Waldmeier, PC, 2000)
"Four patients affected by severe Parkinson's disease developed leucopenia (900-1200 WBC) during treatment of psychosis (3) or untreatable insomnia (1) with clozapine (37."( Bonanni, L; Gambi, F; Iacono, D; Onofrj, M; Thomas, A, 2000)
"Long-term levodopa therapy for Parkinson's disease is complicated by the development of motor fluctuations and abnormal involuntary movements."( Clarke, CE; Deane, KH, 2001)
"Long-term levodopa therapy for Parkinson's disease is complicated by the development of motor fluctuations and abnormal involuntary movements."( Clarke, CE; Deane, KH, 2001)
"Long term levodopa therapy in Parkinson's disease is associated with the development of motor complications including abnormal involuntary movements and a shortening response to each dose (wearing off phenomenon)."( Clarke, CE; Deane, KH, 2001)
"Long term levodopa therapy in Parkinson's disease is associated with the development of motor complications including abnormal involuntary movements and a shortening response to each dose (wearing off phenomenon)."( Clarke, CE; Deane, KD, 2001)
"In a 77-year-old male patient with Parkinson's disease and with acute pseudo-obstruction of the colon (Ogilvie's syndrome) conservative therapy was ineffective."( Klaver, NS; Koornstra, JJ; Limburg, AJ; ter Maaten, JC; van der Jagt, EJ; van der Werf, TS, 2001)
"When levodopa therapy is used in Parkinson's disease, degradation of the drug in the peripheral nervous system is associated with dyskinesias and motor fluctuations."( Najib, J, 2001)
"In levodopa-treated patients with Parkinson's disease who experience motor fluctuations, clinical trials have demonstrated entacapone's effectiveness in increasing "on" time (the period during which medications relieve the symptoms of Parkinson's disease) by up to 1."( Najib, J, 2001)
"Forty patients affected by severe Parkinson's disease (PD) were treated with tolcapone as an adjunctive therapy to L-DOPA, for 3-7 months, until this drug was discontinued because of side-effects (2 diarrhoea, one of them with orthostatic hypotension, 2 increments of liver enzymes) or because of mandatory indications of the European drugs authority."( Bonanni, L; Di Iorio, A; Iacono, D; Onofrj, M; Thomas, A, 2001)
"We studied the association of Parkinson's disease (PD) with type of menopause (natural or surgical), age at menopause, and postmenopausal estrogen replacement therapy using a case-control design."( Ahlskog, JE; Benedetti, MD; Bower, JH; Maraganore, DM; McDonnell, SK; Peterson, BJ; Rocca, WA; Schaid, DJ, 2001)
"Long-term dopaminergic treatment of Parkinson's disease is complicated by the occurrence of dyskinesia and motor fluctuations and is responsible for increasing the costs of treatment."( Arnold, G; Einhäupl, KM; Klaffke, S; Kühn, AA; Kupsch, A; Meissner, W; Paul, G; Trottenberg, T, 2001)
"Six patients with Parkinson's disease who had troublesome motor complications under levodopa/DCI and DA agonist combination therapy were compared in terms of the extent of motor complications and their satisfaction after changing their therapy from levodopa/DCI to levodopa without DCI."( Hironishi, M; Kondo, T; Miwa, H, 2002)
"Before the use of L-Dopa, Parkinson's disease (PD) was considered a disabling disease with no effective treatment."( García Ruiz, PJ; Meseguer, E, 2002)
"Drug treatment of idiopathic Parkinson's disease (IPD) is a difficult task, and comorbidity and comedication add to its complexity."( Calandrella, D; Cosentino, M; Frigo, G; Lecchini, S; Leoni, O; Martignoni, E; Michielotto, D; Nappi, G; Oria, C; Riboldazzi, G; Zangaglia, R, 2002)
"The treatment of Parkinson's disease unresponsive to dopaminergic substances and that associated with dementia remains problematical."( Ceballos-Baumann, AO, 2002)
"We studied 18 subjects with Parkinson's disease before they began levodopa therapy and after 6, 12, 24, and 48 months of long-term levodopa therapy."( Carter, JH; Lea, ES; Nutt, JG; Sexton, GJ, 2002)
"Levodopa-treated Parkinson's disease patients who had been treated with deprenyl for up to 7 years, compared with patients who were changed to a placebo after about 5 years, experienced slower motor decline and were more likely to develop dyskinesias but less likely to develop freezing of gait."( Fahn, S; Kieburtz, K; Lang, A; Langston, JW; LeWitt, P; Oakes, D; Olanow, CW; Penney, JB; Rudolph, A; Shoulson, I; Tanner, C, 2002)
"Treatments for Parkinson's disease based on replacement of lost dopamine have several problems."( Brotchie, JM; Nash, JE, 2002)
"Subjects with Parkinson's disease were tested in four treatment conditions: off both deep brain stimulation and levodopa (off condition); on deep brain stimulation; on levodopa; and on both deep brain stimulation and levodopa."( Chiari, L; Horak, FB; Rocchi, L, 2002)
"(1) The reference treatment for Parkinson's disease is levodopa plus a peripheral dopadecarboxylase inhibitor (benserazide or carbidopa)."( , 2002)
"Four hundred patients with early-stage Parkinson's disease (PD) who were participating in a multicenter clinical trial were evaluated using the UPDRS on two separate occasions (screening and baseline visits) prior to receiving treatment."( Blindauer, K; Kieburtz, K; McDermott, M; Plumb, S; Shoulson, I; Siderowf, A, 2002)
"The treatment of idiopathic Parkinson's disease becomes rather difficult if levodopa-induced late complications such as motor fluctuations or dyskinesias occur."( Cormann, K; Herting, B; Kohlert, F; Müller, A; Reichmann, H; Sommer, U, 2002)
"Excessive daytime sleepiness (EDS) in Parkinson's disease (PD) is due to either treatment-related factors or the disease itself."( Aurilia, C; Barbanti, P; Fabbrini, G; Meco, G; Pauletti, C; Vanacore, N, 2002)
"Chronically administered levodopa to Parkinson's disease (PD) patients ultimately produces alterations in motor response."( Chase, TN; Oh, JD, 2002)
"Patients with Parkinson's disease (PD) by definition benefit from treatment with the dopamine precursor levodopa."( Verhagen Metman, L, 2002)
"Seven Parkinson's disease cases experienced well-formed visual hallucinations many years after disease onset, while nine Parkinson's disease cases and three controls were treated for depression."( Halliday, GM; Harding, AJ; Henderson, JM; Stimson, E, 2002)
"Ten patients with Parkinson's disease were tested in an "on" state (on dopaminergic drug treatment) and a practical "off" state in two sessions held one week apart in counterbalanced order; 10 controls matched for age and education were studied at the same time points."( Manoach, DS; Mechanic, DJ; Press, DZ; Tarsy, D, 2002)
"While Parkinson's disease is undoubtedly a disorder with a primary pathology of dopamine neuronal loss, that loss of dopamine and subsequent dopamine replacement therapy leads to imbalances in many non-dopaminergic transmitter systems, including 5-hydroxytryptamine (5-HT)."( Brotchie, JM; Nicholson, SL, 2002)
"We report on 2 patients with idiopathic Parkinson's disease who experienced marked improvement in symptoms following the addition of itraconazole to current cabergoline treatment."( Christensen, J; Dupont, E; ØStergaard, K, 2002)
"To assess the patterns of drug use in Parkinson's disease in Spain, information about the clinical characteristics and current treatment of 1803 parkinsonian patients was obtained from a nationwide survey, involving 241 physicians with practice based on the different assistance levels of the Spanish National Healthcare System."( Grandas, F; Kulisevsky, J, 2003)
"In patients with advanced Parkinson's disease, previously reliant on apomorphine, bilateral STN DBS is an effective treatment to reduce motor fluctuations and enable a reduction in apomorphine use."( Byrne, P; Cameron, H; Eldridge, PR; Fletcher, N; Forster, A; Fox, SH; Littlechild, P; Marshall, A; McIver, K; Steiger, M; Varma, TR, 2003)
"This study evaluated the efficacy in Parkinson's disease (PD) of a new pharmacologic preparation of apomorphine included in microemulsions and administered by transdermal route, which provides a constant release of the drug for several hours (Apo-TD)."( Albani, G; Astolfi, V; Baudo, S; Bergamasco, B; Calderoni, S; Cavalli, R; Fraschini, F; Gasco, MR; Lopiano, L; Mauro, A; Priano, L; Rizzone, M, 2002)
"Three patients with advanced Parkinson's disease, all of whom developed excessive daytime sleepiness and 'sleep attacks' after the administration of entacapone, are described."( Bares, M; Kanovský, P; Rektor, I, 2003)
"Brain samples from 14 Parkinson's disease patients, 10 of whom developed motor complications (dyskinesias and/or wearing-off) on dopaminomimetic therapy, and 11 controls were analyzed."( Bédard, PJ; Calon, F; Di Paolo, T; Hornykiewicz, O; Morissette, M; Rajput, AH, 2003)
"Thirty-six patients with Parkinson's disease (PD) were randomized to either medical therapy (N = 18) or unilateral GPi pallidotomy (N = 18)."( Bakay, RA; Barnhart, H; Chockkan, V; DeLong, MR; Evatt, M; Freeman, A; Green, J; Haber, M; McDonald, W; Mewes, K; Triche, S; Vitek, JL; Wahlay, N; Zhang, JY, 2003)
"Long-term treatment with levodopa in Parkinson's disease results in the development of motor complications, including drug failure, reduced duration of antiparkinsonian action (wearing off phenomenon), sudden shifts between under-treated and over-treated states (on-off phenomenon), freezing and involuntary movements such as levodopainduced dyskinesia."( Calandrella, D; Martignoni, E; Riboldazzi, G; Riva, N, 2003)
"It did not appear that the Parkinson's disease patients on levodopa therapy were predisposed to melanoma, nor did levodopa therapy appear to exaggerate melanoma if it were previously present."( Fiala, KH; Manyam, BV; Whetteckey, J, 2003)
"The mainstay of treatment for Parkinson's disease remains medical therapy."( Betchen, SA; Kaplitt, M, 2003)
"Levodopa is the cornerstone of idiopathic Parkinson's disease (PD) treatment."( Borges, N, 2003)
"The symptoms of Parkinson's disease can become increasingly difficult to control as the disease advances, particularly with the development of motor complications, such as end-of-dose wearing-off and dyskinesias, following long-term therapy."( Stocchi, F, 2003)
"Along the years the treatment of Parkinson's disease with L-dopa has revealed unfavorable effects in general after 5-10 years."( Pantelie, CM; Schoenfeld, MA; Schwartz, B, 2003)
"In a review of 61 patients with Parkinson's disease who were treated by cryothalamectomy, the technique of freezing a surgical target as compared with destroying it by alcohol or thermal heat was found effective and to a degree safer than other techniques."( MARKHAM, CH; RAND, RW, 1964)
"The majority of Parkinson's disease patients undergoing levodopa therapy develop disabling motor complications (dyskinesias) within 10 years of treatment."( Asbrock, N; Ferrer, B; Giuffrida, A; Kathuria, S; Piomelli, D, 2003)
"Long-term treatment of Parkinson's disease with levodopa is compromised by the development of motor complications, including on-off fluctuations and involuntary movements termed dyskinesia."( Brotchie, JM; Crossman, AR; Duty, S; Fox, SH; Henry, B, 2003)
"A 74-year-old patient with idiopathic Parkinson's disease was evaluated for unintended sleep episodes that occurred after long-term treatment with 400 mg/day of L-dopa."( de la Llave, Y; Garcia de Yébenes, J; Garcia-Borreguero, D; Larrosa, O; Schwarz, C, 2003)
"A major goal of research in Parkinson's disease (PD) has been the development of treatments to slow the progressive degeneration of the nigrostriatal dopaminergic system and to reduce the functional decline of patients."( Brooks, DJ; Frey, KA; Marek, KL; Oakes, D; Paty, D; Prentice, R; Shults, CW; Stoessl, AJ, 2003)
"Patients with advanced Parkinson's disease who were treated with bilateral stimulation of the subthalamic nucleus had marked improvements over five years in motor function while off medication and in dyskinesia while on medication."( Ardouin, C; Batir, A; Benabid, AL; Benazzouz, A; Chabardes, S; Fraix, V; Koudsie, A; Krack, P; LeBas, JF; Limousin, PD; Pollak, P; Van Blercom, N, 2003)
"In schizophrenia and Parkinson's disease, cortical and subcortical motor organization is influenced by primary disease conditions and neuroleptic treatment."( Deuticke, C; Hajak, G; Müller, JL; Putzhammer, A; Röder, CH; Winkler, J, 2003)
"Long-term L-dopa treatment of Parkinson's disease can lose its effectiveness and cause development of motor complications such as dyskinesia."( Chen, JF, 2003)
"Untreated Parkinson's disease (PD) patients display speech abnormalities characterized by narrow range of fundamental frequency (Fo) variation and higher amplitude."( Azevedo, LL; Cardoso, F; Reis, C, 2003)
"Levodopa-treated Parkinson's disease is often complicated by the occurrence of motor fluctuations, which can be predictable ('wearing-off') or unpredictable ('on-off')."( Calne, DB; de la Fuente-Fernández, R; Mak, E; Schulzer, M; Stoessl, AJ, 2004)
"Fourteen levodopa-treated Parkinson's disease patients, of which seven developed dyskinesias and seven did not, were compared with nine controls."( Bédard, PJ; Calon, F; Di Paolo, T; Dridi, M; Hornykiewicz, O; Rajput, AH, 2004)
"We present two patients with Parkinson's disease in whom administration of quetiapine for drug-induced psychosis caused characteristic stereotyped behaviors or punding."( Kondo, T; Miwa, H; Morita, S; Nakanishi, I, 2004)
"Patients with advanced Parkinson's disease (PD) may develop a variety of motor complications associated with levodopa therapy."( Swope, DM, 2004)
"78 patients with Parkinson's disease treated with pergolide and 18 never treated with an ergot-derived dopamine agonist (controls) were evaluated by echocardiography."( Cosyns, B; De Sutter, J; Decoodt, P; Flamez, A; Moerman, C; Muyldermans, L; Santens, P; Schoors, D; Van Camp, G; Van Zandijcke, M; Weytjens, C, 2004)
"Among various neurological disorders, Parkinson's disease (PD) is one of the most appropriate candidates of gene therapy."( Ozawa, K, 2003)
"One experimental therapy for Parkinson's disease (PD) is the transplantation of embryonic ventral mesencephalic tissue."( Collier, TJ; Marchionini, DM; Pitzer, MR; Sortwell, CE, 2004)
"Current gene therapy models for Parkinson's disease have focused on two strategies."( Fraix, V, 2004)
"It only responds to an adjustment of Parkinson's disease therapy."( Avanzi, M; Bonfà, F; Uber, E, 2004)
"Dopamine replacement therapy in Parkinson's disease ameliorates motor symptoms."( Evans, AH; Lees, AJ, 2004)
"The unified Parkinson's disease rating scale (UPDRS), activities of daily living (ADL), Hamilton rating scale for depression (HRSD), Beck depression inventory (BDI), and mini-mental state examination (MMSE) were assessed by a rater blinded to treatment arm."( Barbosa, ER; Fregni, F; Gallucci-Neto, J; Marcolin, MA; Myczkowski, ML; Pascual-Leone, A; Rigolino, R; Santos, CM; Valente, KD, 2004)
"In the group with Parkinson's disease, gastric myoelectrical activity was recorded during both the "on" (with levodopa treatment) and the "wearing-off" (without levodopa for at least 12 hr) periods."( Chang, FY; Chen, CY; Chen, JD; Lee, SD; Lu, CL; Luo, JC; Shan, DE; Wu, HC, 2004)
"A conception of the approach to Parkinson's disease treatment at early stage, which could be realized in practice is suggested."( Aristova, RA; Belikova, LP; Gusev, EI; Piatnitskiĭ, AN; Selikhova, MV; Vialkova, AB, 2004)
"In clinical studies, individuals with Parkinson's disease have had higher concentrations of plasma homocysteine than did controls, and experimental evidence suggests that folate deficiency or focal administration of homocysteine sensitizes dopaminergic neurons to the neurotoxicity of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine."( Ascherio, A; Chen, H; Hernán, MA; Logroscino, G; Schwarzschild, MA; Willett, WC; Zhang, SM, 2004)
"Entacapone is a COMT inhibitor used in Parkinson's disease (PD) patients, as an adjunctive therapy to L-dopa in order to prolong its bioavailability and thus its clinical effect."( Bassi, A; Brusa, L; Fedele, E; Lunardi, G; Pasqualetti, P; Peppe, A; Pierantozzi, M; Stanzione, P; Stefani, A, 2004)
"A 79-year-old woman, with Parkinson's disease treated with cabergoline, was admitted to a hospital due to jaundice and weakness."( Johansen, SS; Karkov, J, 2004)
"Patients with Parkinson's disease may use Dopamine Replacement Therapy (DRT) in excess of therapeutic need."( Bearn, J; Evans, A; Kelleher, M; Lees, A; Turner, K, 2004)
"Phase III trials for the treatment of Parkinson's disease are underway in Germany and Europe, while phase II trials in patients with epilepsy are ongoing in Italy."( , 2004)
"In addition to Parkinson's disease, ropinirole is also used successfully in the treatment of restless legs syndrome."( Jost, WH, 2004)
"We report on a 78-year-old woman with Parkinson's disease who presented with hydroureteronephrosis and developed RPF and serosal fibrosis during treatment with pergolide."( Beger, T; Bilici, A; Cetinkaya, S; Doventas, A; Erdincler, DS; Karadag, B; Ogut, G; Tezcan, V, 2004)
"Both mean Unified Parkinson's Disease Rating Scale (UPDRS) total score and mean subset III of the UPDRS were significantly improved with dopaminergic treatment."( Benbir, G; Kaynak, D; Kaynak, H; Kiziltan, G; Uysal, O, 2005)
"The authors present here two cases of Parkinson's disease with depression refractory to SSRIs treatment, who experienced a complete remission after replacing the ongoing SSRIs with a serotonin-noradrenalin reuptake inhibitor (SNRI), milnacipran."( Higuchi, H; Kamata, M; Shimizu, T; Takahashi, H; Yoshida, K, 2005)
"In the 6-hydroxydopamine rat model of Parkinson's disease (PD), striatal synaptic plasticity has been shown to be impaired, although chronic treatment with levodopa was able to restore it."( Bernardi, G; Calabresi, P; Centonze, D; Pisani, A, 2005)
"We undertook a single-center study in Parkinson's disease (PD) using standardized questionnaires to score patient-perceived involvement in therapy decisions (score 4 = low to 25 = high) and satisfaction with the consultation (score 1 = low to 7 = high)."( Grosset, DG; Grosset, KA, 2005)
"When used as monotherapy in early Parkinson's disease, ropinirole improves signs and symptoms of the disorder."( Hauser, RA; Lyons, KE; Pahwa, R, 2004)
"A 58-year-old woman with Parkinson's disease was treated with high-dose pergolide for 10 years."( Bax, JJ; Jukema, JW; van Hilten, JJ; van Strater, AC, 2005)
"(1) If patients with Parkinson's disease treated with levodopa develop end-of-dose motor fluctuations, the standard therapy is to add bromocriptine, a dopamine receptor agonist, to their ongoing treatment."( , 2005)
"In advanced Parkinson's disease, the combination of disease progression and levodopa therapy leads to the development of motor problems complicating the therapeutic response, known as motor response complications."( Konitsiotis, S, 2005)
"Whereas, L-DOPA therapy in early Parkinson's disease is accepted to improve the motor symptoms, the effects on cognitive performance are more complex: both positive and negative effects have been observed."( Cools, R, 2006)
"The chronic treatment of Parkinson's disease with L-dopa is often associated with fluctuations of motor response and dyskinesias."( Bernardi, G; Mercuri, NB, 2005)
"Long-term disability in Parkinson's disease (PD) is related to progression of the underlying disease and the emergence of complications of chronic levodopa therapy."( Hauser, RA; Schwarzschild, MA, 2005)
"We report 69 Parkinson's disease patients treated with bilateral DBS of the subthalamic nucleus (STN, n = 49) or globus pallidus internus (GPi, n = 20) included in a multicentre study."( Agid, Y; Albanese, A; Benabid, AL; Bonnet, AM; Contarino, MF; Fraix, V; Gironell, A; Guridi, J; Hariz, MI; Houeto, JL; Kulisevsky, J; Lang, AE; Lozano, AM; Molet, J; Obeso, JA; Pascual-Sedano, B; Pidoux, B; Pollak, P; Quinn, NP; Rehncrona, S; Rodriguez-Oroz, MC; Romito, L; Saint-Cyr, J; Scerrati, M; Speelman, JD; Van Blercom, N; Volkmann, J; Xie, J; Zamarbide, I, 2005)
"Treating patients with Parkinson's disease is not an easy task for the physician who is facing a disease well responsive to symptomatic therapy, yet escaping any curative approaches."( Burkhard, PR; Villemure, JG; Vingerhoets, FJ, 2005)
"Fourteen male patients suffering from Parkinson's disease, each of whom had been treated with L-DOPA, and in whom additional treatment with oral dopamine agonist (DA) was needed, were followed for a period of one year."( Bares, M; Kanovský, P; Pohanka, M; Pulkrábek, J; Rektor, I, 2005)
"More than 50% of Parkinson's disease (PD) patients treated with L-dopa develop L-dopa-induced dyskinesias (LIDs) in the long term."( Linazasoro, G, 2005)
"Cell replacement therapy in Parkinson's disease depends on a reliable source of purified dopamine (DA) neurons (PDN) and the identification of factors relevant to their survival."( Donaldson, AE; Iacovitti, L; Marshall, CE; Suon, S; Yang, M, 2005)
"We evaluated the Unified Parkinson's Disease Rating Scale (UPDRS) and the Schwab England ADL score before and 6 months after this treatment in 6 patients with early-stage Parkinson's disease demonstrating predominantly unilateral parkinsonian symptoms."( Hamada, I; Okiyama, R; Shichi, T; Takahashi, H; Taniguchi, M; Yokochi, F, 2005)
"Cell replacement therapy in Parkinson's disease (PD) has so far been based on the use of primary dopaminergic (DA) neuroblasts obtained from the brain of aborted human fetuses."( Björklund, A, 2005)
"The treatment of patients suffering from idiopathic Parkinson's disease has become more and more complex."( Ludin, HP, 2005)
"In order to study the pathogenesis of Parkinson's disease (PD), and explore therapeutic drug or approaches, the accurate animal model of PD with inexpensive, biocompatible and convenient administration was necessary."( Gu, W; Huang, J; Li, Y; Liu, H; Xu, Z; Yan, Z; Yang, Y; Zhu, X, 2006)
"Patients with early Parkinson's disease receiving rotigotine monotherapy experienced significantly greater improvements in parkinsonian symptoms (as measured by Unified Parkinson's Disease Rating Scale scores) compared to placebo in two large, well designed clinical trials."( Easthope, SE; Reynolds, NA; Wellington, K, 2005)
"In general, therapy for Parkinson's disease is dominated by dopamine agonists (DA) in younger patients and levodopa in older patients with comorbidities."( Reichmann, H, 2005)
"Innovative drug delivery in Parkinson's disease (PD) has the potential to reduce or avoid many side effects of current treatment, such as wearing-off type fluctuations, dyskinesia, on-off phenomena or bouts of motor freezing."( Brotchie, JM; Fox, SH; Johnston, TH, 2005)
"The treatment of Parkinson's disease (PD) with l-DOPA leads to involuntary movements (dyskinesias)."( Berdeaux, G; Clarke, CE; Deschaseaux-Voinet, C; Khoshnood, B; Péchevis, M; Vieregge, P; Ziegler, M, 2005)
"Current treatments for Parkinson's disease (PD) rely on a dopamine replacement strategy and are reasonably effective, particularly in the early stages of the disease."( Dunnett, SB; Monville, C; Torres, EM, 2005)
"The poor survival of dopamine grafts in Parkinson's disease is one of the main obstacles to the widespread application of this therapy."( Castro, MG; Dunnett, SB; Lowenstein, PR; Monville, C; Torres, EM, 2005)
"Cabergoline is used in the treatment of Parkinson's disease (PD)."( Moritoyo, H; Moritoyo, T; Nagai, M; Nakatsuka, A; Nishikawa, N; Nomoto, M; Nomura, T; Yabe, H, 2006)
"In the treatment of Parkinson's disease, levodopa, DCI, MAO-B inhibitor, COMT inhibitors, dopamine receptor agonists, amantadine, anticholinergics have been applied and new drugs are being developed."( Moritoyo, H; Moritoyo, T; Nagai, M; Nakatsuka, A; Nisikawa, N; Nomoto, M; Yabe, H, 2005)
"Pharmacotherapy for Parkinson's disease is focused on dopaminergic drugs, mainly the dopamine precursor levodopa and dopamine receptor agonists."( Nyholm, D, 2006)
"Current gene therapy models for Parkinson's disease (PD) have adapted two treatment strategies."( Li, KR; Niu, DB; Wang, JJ; Wang, K; Wang, XM; Xue, B; Zhang, T, 2006)
"(1) When patients with Parkinson's disease who are taking levodopa develop motor fluctuations that do not respond to dose adjustments, the standard treatment is the addition of bromocriptine, a dopaminergic agonist."( , 2006)
"Nonhuman primate models of Parkinson's disease (PD) have been invaluable to our understanding of the human disease and in the advancement of novel therapies for its treatment."( Kordower, JH; O'Malley, J; Soderstrom, K; Steece-Collier, K, 2006)
"Visual hallucinations in Parkinson's disease are usually treatment-related and occur in at least 30% of patients."( Papapetropoulos, S, 2006)
"L-dopa treatment of Parkinson's disease is complicated in the long term by the appearance of dyskinesia."( Corvol, JC; Girault, JA; Hervé, D, 2006)
"The long-term treatment of Parkinson's disease with L-dopa is often associated with the appearance of involuntary movements called L-dopa-induced dyskinesias."( Bédard, PJ; Rouillard, C; Samadi, P, 2006)
"The authors treated 14 Parkinson's disease patients with major depression with escitalopram in an open-label study."( Duda, JE; Katz, IR; Morales, KH; Stern, MB; Taraborelli, D; Weintraub, D, 2006)
"The management of advancing Parkinson's disease (PD) is a daunting task, complicated by dynamic medication responses, side effects, and treatment-refractory symptoms in an aging patient population."( Goudreau, JL, 2006)
"Present Parkinson's disease treatment strategies are far from ideal for a variety of reasons; it has therefore been suggested that partial dopamine receptor agonism might be a potential therapeutic approach with potentially fewer side effects."( Feenstra, RW; Glennon, JC; Hesselink, MB; Long, SK; McCreary, AC; Reinders, JH; Ronken, E; Van Der Neut, M; Van Scharrenburg, G, 2006)
"Levodopa has been the gold standard for Parkinson's disease (PD) therapy since it was successfully introduced in 1967."( Fahn, S, 2006)
"The motor part of the Unified Parkinson's Disease Rating Scale, the Brief Psychiatric Rating Scale, the Mini-Mental State Examination, the Hamilton Rating Scale for Depression, the Epworth Sleepiness Score, and the Clinical Global Impression Scale were administered before and during the study."( Dobronevsky, E; Klein, C; Miniovitz, A; Prokhorov, T; Rabey, JM, 2007)
"We describe two patients with Parkinson's disease (PD) who developed clinical criteria of pathological gambling addiction in the setting of increased dopamine replacement therapy (levodopa and dopamine agonist medications)."( Bandini, F; Cocito, L; Pizzorno, M; Primavera, A, 2007)
"For decades, awareness of Parkinson's disease mainly focused on the presence and treatment of motor symptoms."( Mollenhauer, B; Trenkwalder, C; Wenzel, S, 2006)
"Treatment of patients with Parkinson's disease with levodopa has profound effects on both movement and the pattern of movement-related reactivity in the subthalamic nucleus (STN), as reflected in the local field potential (LFP)."( Androulidakis, AG; Blomstedt, P; Brown, P; Chen, CC; Dowsey-Limousin, P; Doyle, L; Hariz, MI; Kempf, F; Kühn, AA; Kupsch, A; Schneider, GH, 2007)
"In rodent models of Parkinson's disease (PD) blockade of these receptors increases locomotion and enhances the actions of dopamine (DA) replacement therapy."( Biedka, I; Brus, R; Drosik, M; Kostrzewa, RM; Nowak, P; Szczerbak, G, 2006)
"Because Parkinson's disease (PD) has multiple neurological symptoms and often complex treatments, the quality of PD care may be higher when a specialist is involved."( Cheng, EM; Eisa, MS; Jacob, E; Lee, M; Siderowf, AD; Swarztrauber, K; Vassar, S; Vickrey, BG, 2007)
"Psychotic symptoms (PS) in Parkinson's disease (PD) usually develop as a side effect of the dopaminergic therapy and consist of hallucinations and delusions."( Erginöz, E; Ertan, S; Ertan, T; Kiziltan, G; Ozekmekçi, S, 2007)
"Philadelphia Veterans Administration Parkinson's Disease Research, Education and Clinical Center (PADRECC)."( Fisman, DN; Kleiner-Fisman, G, 2007)
"A 61-year-old man with Parkinson's disease (PD) developed sudden-onset visual impairment after initiation of amantadine treatment."( Ebihara, N; Hattori, N; Iwatake, A; Kubo, S; Murakami, A, 2008)
"We report two male patients with Parkinson's disease who developed compulsive risk-seeking driving behaviour as a result of self-administering high doses of L-dopa despite an adequate therapeutic response at lower doses."( Avanzi, M; Baratti, M; Bonfà, F; Brighetti, G; Cabrini, S; Uber, E, 2008)
"The pathogenesis of Parkinson's disease (PD) is not understood and there are currently no accepted disease modifying, neuroprotective treatments."( Morris, HR, 2007)
"Thirteen treated patients with Parkinson's disease (PD) took one of the two tested LD formulations on two consecutive days under randomised, double blind, identical standardised conditions."( Ander, L; Kolf, K; Muhlack, S; Müller, T; Woitalla, D, 2007)
"Our findings show that levodopa-treated Parkinson's disease patients have low folate (p < 0."( Angelopoulos, E; Boufidou, F; Evangelopoulos, ME; Kararizou, E; Nikolaou, C; Triantafyllou, NI; Tsounis, S; Vassilopoulos, D, 2007)
"In the Parkinson's Disease on Estrogen Therapy Replacement in the Menopause Years (POETRY) study, participants were found to have improved scores on the Unified Parkinson Disease Rating Scale."( Shulman, LM, 2007)
"Treatment options for Parkinson's disease have greatly expanded in recent years."( Rezak, M, 2007)
"Recent pharmacotherapy trials in Parkinson's disease (PD) using dopaminergic neuroimaging as outcome parameter failed to show significant relationships between imaging and clinical results."( Bohnen, NI; Constantine, GM; Kuwabara, H; Mathis, CA; Moore, RY, 2007)
"(2) In patients with Parkinson's disease who have cognitive disorders, or in patients with Lewy body dementia, exacerbations of parkinsonism and tremor have been observed during treatment with cholinesterase inhibitors at normal doses."( , 2007)
"He had Parkinson's disease and had been treated with cabergoline during the preceding 4 years and 8 months."( Hanada, T; Higaki, Y; Hiroe, K; Inoue, S; Murakami, R; Oda, T; Okada, S; Ota, T; Shimizu, K, 2007)
"The unified Parkinson's disease rating scale (UP-DRS) score, TCM primary and secondary symptom scores were evaluated before treatment, every 3 months of treatment and at the end point."( Gao, JP; Li, WW; Zhao, H, 2007)
"Six patients with Parkinson's disease (PD) with severe motor complications were directly switched from their oral antiparkinsonian combination drug regime to nasoduodenal levodopa infusion without previously recommended transient treatment with levodopa alone."( Andrich, J; Meiler, B; Müller, T, 2008)
"Among various neurological disorders, Parkinson's disease (PD) is one of the most promising candidates of gene therapy."( Ozawa, K, 2007)
"Many Parkinson's disease (PD) patients treated with levodopa develop motor fluctuations and/or dyskinesia."( Haeger, DA; Hock, K; Mueller, T; Russ, H; Woitalla, D, 2007)
"Cardinal symptoms of Parkinson's disease (PD) respond well to treatment with levodopa and deep brain stimulation (DBS) of the subthalamic nucleus (STN)."( Braun, M; Groiss, S; Gross, J; Krause, H; Maarouf, M; Ostrowski, S; Ploner, M; Pollok, B; Schnitzler, A; Sturm, V; Südmeyer, M; Timmermann, L; Voges, J; Wojtecki, L, 2008)
"Many patients with advanced Parkinson's disease (PD) experience motor complications, which negatively impact quality of life, despite optimized oral therapy."( Silver, D; Stacy, M, 2008)
"Symptomatic treatment of Parkinson's disease (PD) is based on the dopamine precursor levodopa."( Lennernäs, H; Nyholm, D, 2008)
"Effective medical treatment for Parkinson's disease has been available for almost 40 years."( Sydow, O, 2008)
"To improve sleep in Parkinson's disease, it is important to achieve the critical balance of adequate dopaminergic therapy and control of symptoms."( Mehta, SH; Morgan, JC; Sethi, KD, 2008)
"Twenty-five patients with Parkinson's disease who used L-dopa (LD+) and 17 patients who did not use L-dopa (LD-) treatment were included in this study."( Apaydin, H; Ince, B; Oncel, C; Ozekmekçi, S; Uludüz, D, 2008)
"Dopamine replacement therapy in Parkinson's disease ameliorates motor symptoms."( Bayreuther, C; Borg, M, 2008)
"Drug treatment for Parkinson's disease is largely symptomatic and relies primarily on levodopa (L-dopa) and adjuvant therapies including dopamine agonists and catechol-O-methyltransferase (COMT) inhibitors."( Chan, DK; Cordato, DJ; O'Rourke, F, 2008)
"Early clinical trials designed to treat Parkinson's disease by transplantation of fetal tissue containing dopamine neuron precursors yielded promising results, but the approach retains several limitations."( Svendsen, C, 2008)
"Ten-year follow-up results from the Parkinson's Disease Research Group of the United Kingdom trial demonstrated that there were no long-term advantages to initiating treatment with bromocriptine compared with l-dopa in early Parkinson disease (PD)."( Ben-Shlomo, Y; Evans, A; Head, J; Katzenschlager, R; Lees, AJ; Schrag, A, 2008)
"Results achieved in treating the Parkinson's disease (PD) by the dopamine receptor agonist, ropinirole, have been hampered by its side effects."( Dikanovic, M; Jukic, I; Lusic, I; Titlic, M; Tonkic, A, 2008)
"To find effective agents for Parkinson's disease (PD) prevention and therapy, we examined the protective effects of the polyhydroxylated fullerene derivative C(60)(OH)(24) in a 1-methyl-4-phenylpyridinium (MPP(+)) -induced acute cellular PD model in human neuroblastoma cells and the free radical scavenging effects in this model with an electron spin resonance (ESR) spectrometer."( Cai, X; Feng, Z; Hou, B; Jia, H; Li, W; Liu, J; Liu, Z; Luo, C, 2008)
"Although motor symptoms of Parkinson's disease (PD) are initially responsive to dopamine replacement therapy, nonresponsive features develop over time, suggesting that impaired dopaminergic function alone may not be wholly responsible for all the motor features of the disease."( Camicioli, RM; Gee, M; Hanstock, CC; Martin, WR; Wieler, M, 2008)
"Long-term treatment for Parkinson's disease (PD) with the dopamine-precursor levodopa (l-DOPA) results in the development of motor fluctuations, including involuntary movements, termed l-DOPA-induced dyskinesia (LID)."( Brotchie, JM; Chuang, R; Fox, SH, 2008)
"Long term levodopa therapy in Parkinson's disease (PD) results in a range of problems."( Fox, SH; Lang, AE, 2008)
"Chronic levodopa treatment for Parkinson's disease patients is frequently associated with the development of motor complications such as end-of-dose wearing-off and dyskinesias."( Olanow, CW; Stocchi, F; Tagliati, M, 2008)
"Dopaminergic treatment of Parkinson's disease (PD) leads to significant improvement in Parkinsonian features; however, the treatment response is hampered by the appearance of motor complications, including dyskinesias and motor fluctuations."( Kieburtz, K, 2008)
"A total of 754 patients with Parkinson's disease were enrolled, 545 of the patients (63% male patients, mean age 68 years, mean duration of PD 6 years, Hoehn & Yahr stage II to III in 69% of the patients) started rasagiline 1 mg/day as adjunct therapy for up to 4 months."( Jost, WH; Klasser, M; Reichmann, H, 2008)
"Levodopa (L-dopa) treatment of Parkinson's disease (PD) is associated with elevated homocysteine (Hcy)."( Bouchard, TP; Camicioli, RM; Somerville, MJ, 2009)
"Stereotactic surgical interventions for Parkinson's disease (PD) can considerably improve appendicular motor signs, but their effect on axial motor signs--especially balance control under optimal drug therapy--remains unclear."( Allum, JH; Bloem, BR; Borm, GF; Carpenter, MG; Esselink, RA; Honegger, F; Limousin-Dowsey, P; Visser, JE, 2008)
"Sustained drug therapy in Parkinson's disease may alter the psychomotor responses to acute challenges with dopaminergic drugs, L-dopa and methylphenidate, and cause cross sensitisation."( Evans, AH; Lawrence, AD; Lees, AJ, 2009)
"Compared to controls, untreated Parkinson's disease patients showed reduced step length and velocity, and poor braking just prior to foot-contact, with a decrease in both soleus (S) and anterior tibialis (AT) muscle activity."( Agid, Y; Bardinet, E; Chastan, N; Do, MC; Welter, ML; Westby, GW; Yelnik, J, 2009)
"We studied 54 idiopathic Parkinson's disease (PD) patients with depressive disorders (DD) to compare the efficacy and the effect of treatment with sertraline in the usual formulation and in the liquid oral concentrate (LOC) formulation."( Alagna, A; Bramanti, P; Di Bella, P; Di Lorenzo, G; Digangi, G; Marino, S; Sessa, E, 2008)
"Current treatments for Parkinson's disease rely on a dopamine replacement strategy and are reasonably effective, particularly in the early stages of the disease."( Dunnett, SB; Lane, EL; Monville, C; Pekarik, V; Torres, EM, 2009)
"Functional models of Parkinson's disease (PD) have led to effective treatment for the motor symptoms."( Jenner, P, 2008)
"Treatment of Parkinson's disease (PD) is improving and we can choose a variety of drugs and surgical procedures for appropriate stages of the disease."( Fukuyama, H, 2009)
"Animal models of Parkinson's disease have been widely used for investigating the mechanisms of neurodegenerative process and for discovering alternative strategies for treating the disease."( Kurz, MJ; Lau, YS; Pothakos, K, 2009)
"Among the neuropsychiatric symptoms in Parkinson's disease (PD) patients, hallucination can result from the disease itself or medical treatment."( Hashiguchi, K; Kawaguchi, M; Kishimoto, J; Miyagi, Y; Morioka, T; Murakami, N; Sakae, N; Samura, K; Sasaki, T; Yamasaki, R; Yoshida, F, 2009)
"The management of early Parkinson's disease (PD) involves the treatment of motor symptoms and, increasingly, non-motor symptoms."( Comella, C; Elmer, L; Hauser, RA; Lyons, KE; Pahwa, R; Simuni, T; Weintraub, D, 2009)
"The management of early Parkinson's disease (PD) involves the treatment of motor symptoms, and, increasingly, non-motor symptoms."( Comella, C; Elmer, L; Hauser, RA; Lyons, KE; Pahwa, R; Simuni, T; Weintraub, D, 2009)
"The mainstay of treatment for Parkinson's Disease (PD) remains symptomatic despite the rapid expansion in knowledge of its neurodegenerative process."( Bhidayasiri, R; Ling, H, 2009)
"Dementia with Lewy bodies and Parkinson's disease with dementia should be treated with rivastigmine."( Hasselbalch, SG; Kampmann, JP, 2009)
"Current treatments for Parkinson's disease fail to modify disease progression, and the underlying pathogenic mechanisms remain elusive."( Sen, S; West, AB, 2009)
"Twenty-two consecutive patients with Parkinson's disease were included, 18 of them on cabergoline treatment."( Fujioka, S; Iwamoto, K; Kawamura, M; Nakajima, M; Ohno, H, 2009)
"Depth recordings in patients with Parkinson's disease on dopaminergic therapy have revealed a tendency for oscillatory activity in the basal ganglia that is sharply tuned to frequencies of approximately 70 Hz and increases with voluntary movement."( Altenmüller, DM; Brown, P; Brücke, C; Di Lazzaro, V; Doyle Gaynor, LM; Hoffmann, KT; Kempf, F; Krauss, JK; Kühn, AA; Kupsch, A; Mazzone, P; Salih, F; Schneider, GH; Trottenberg, T; Vesper, J; Wöhrle, J; Yelnik, J, 2009)
"Chronic L-DOPA pharmacotherapy in Parkinson's disease is often accompanied by the development of abnormal and excessive movements known as L-DOPA-induced dyskinesia."( Del-Bel, EA; Echeverry, MB; Padovan-Neto, FE; Tumas, V, 2009)
"Dopamine replacement therapy in Parkinson's disease improves motor symptoms, however some patients suffer from motor and behavioural disturbances attributable to taking doses of medication well beyond the dose required to treat their motor disabilities."( Grosset, D, 2008)
"Treatment of Parkinson's disease has traditionally focused on the management of motor disability while behavioural disturbances have received less attention."( Antonini, A; Cilia, R, 2009)
"New strategies for the treatment of Parkinson's disease (PD) are shifted from dopamine (DA) replacement to regeneration or restoration of the nigro-striatal system."( Chen, S; Fan, X; Gu, Q; Le, W; Li, L; Li, X; Ming, M; Yang, D, 2009)
"In a mouse model of Parkinson's disease, new evidence shows that l-DOPA, which is used to treat the symptoms of the disease but also causes dyskinesia, results in a persistent activation of the protein kinase mTOR (mammalian target of rapamycin) in a subset of striatal medium spiny neurons."( Klann, E, 2009)
"A total of 1176 subjects with untreated Parkinson's disease were randomly assigned to receive rasagiline (at a dose of either 1 mg or 2 mg per day) for 72 weeks (the early-start group) or placebo for 36 weeks followed by rasagiline (at a dose of either 1 mg or 2 mg per day) for 36 weeks (the delayed-start group)."( Feigin, PD; Hauser, R; Jankovic, J; Lang, A; Langston, W; Melamed, E; Olanow, CW; Poewe, W; Rascol, O; Stocchi, F; Tolosa, E, 2009)
"Available treatment for Parkinson's disease (PD) is mainly symptomatic instead of halting or reversing degenerative processes affecting the disease."( Castrén, E; Gyárfás, T; Knuuttila, J; Lindholm, P; Rantamäki, T, 2010)
"Pathological gambling (PG) in Parkinson's disease (PD) is a frequent impulse control disorder associated mainly with dopamine replacement therapy."( Cammarota, A; Cerquetti, D; de Achaval, D; Fahrer, R; Gerschcovich, ER; Inés Nouzeilles, M; Leiguarda, R; Merello, M; Perez-Lloret, S; Rossi, M, 2010)
"Physicians treating Parkinson's disease patients with dopamine replacement therapy should inquire about the development of any compulsive behaviours."( Khan, W; Rana, AQ, 2010)
"Patients with Parkinson's disease (PD) and chronically treated with L-DOPA exhibit, in a percentage of 10-30%, supra-physiological levels of plasma total homocysteinemia (tHcy)."( Belcastro, V; Calabresi, P; Castrioto, A; Gorgone, G; Ientile, R; Menichetti, C; Pierguidi, L; Pisani, F; Rossi, A; Tambasco, N, 2010)
"Despite the fact that Parkinson's disease (PD) was discovered almost 200 years ago, its treatment and management remain immense challenges because progressive loss of dopaminergic nigral neurons, motor complications experienced by the patients as the disease progresses and drawbacks of pharmacotherapeutic management still persist."( Choonara, Y; Du Toit, LC; Modi, G; Naidoo, D; Ndesendo, V; Ngwuluka, N; Pillay, V, 2010)
"In the majority of Parkinson's disease patients, chronic dopamine replacement therapy leads to involuntary aimless movements known as l-dopa-induced dyskinesia."( Berthet, A; Bezard, E, 2009)
"Clinical trials in Parkinson's disease using adeno-associated viral vector-based gene therapy have shown the safety of the approach."( Björklund, T; Carlsson, T; Carta, M; Cederfjäll, EA; Kirik, D, 2010)
"For the treatment of Parkinson's disease invasive therapies have a long tradition."( Deuschl, G, 2010)
"Treatment of early Parkinson's disease (PD) should pursue objectives like possible disease-modifying effect, more physiological dopaminergic stimulation, and avoidance of motor fluctuations."( Stocchi, F, 2010)
"Early treatment of Parkinson's disease (PD) affords an opportunity to forestall clinical progression."( Hauser, RA, 2010)
"To investigate gene therapy for Parkinson's disease, we simulated the disease in macaque monkeys by treating them with the complex I mitochondrial inhibitor 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, which induces selective degeneration of dopamine-producing neurons."( Azzouz, M; Bonvento, G; Boulet, S; Brouillet, E; Day, DM; Delzescaux, T; Drouot, X; Hantraye, P; Hérard, AS; Jan, C; Jarraya, B; Kingsman, SM; Mazarakis, ND; Miskin, JE; Mitrophanous, KA; Palfi, S; Ralph, GS; Shin, M, 2009)
"Timed tests of motor function in Parkinson's disease (PD) may be useful for the diagnosis of bradykinesia or to monitor disease progression or treatment response."( Counsell, CE; Macleod, AD, 2010)
"Both Parkinson's disease and its treatment can be associated with psychiatric symptoms."( Hol, WM; Hovestadt, A; van der Zwaard, R; van Megen, HJ, 2010)
"In the advanced stages of Parkinson's disease (PD), the conventional orally-administered pharmacological treatment can prove to be insufficient to control the motor complications associated with the disease."( Cámara, A; Valldeoriola, F, 2010)
"Previous research has indicated that in Parkinson's disease (PD) some motor speech characteristics are changed by levodopa administration, while others are not."( Boon, P; De Bodt, M; De Letter, M; Dhooge, I; Santens, P; Van Borsel, J, 2010)
"Psychotic features in patients with Parkinson's Disease usually present as visual hallucinations against a background of cognitive deterioration and dopaminomimetic therapy."( Bozi, M; Christodoulou, C; Douzenis, A; Gasparinatos, G; Stamboulis, E; Stefanis, C; Stefanis, L; Stefanis, N, 2010)
"Chronic levodopa treatment for Parkinson's disease often results in the development of abnormal involuntary movement, known as L-dopa-induced dyskinesia (LIDs)."( Belujon, P; Grace, AA; Lodge, DJ, 2010)
"In the mouse Parkinson's disease model, treatment with Yi-Gan San also significantly improved motor functioning and prevented dopaminergic loss related to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine challenge."( Cho, KH; Doo, AR; Eun-Kyung, K; Hong, J; Jung, JH; Jung, WS; Kim, SN; Lee, H; Moon, SK; Park, HJ; Park, JY, 2010)
"The incidence of dementia in Parkinson's Disease (PD) patients is higher than in the general population and plasma Homocysteine concentrations are increased in L-dopa treated PD patients."( Iliceto, G; Lamberti, P; Lamberti, SV; Logroscino, G; Santamato, A; Zoccolella, S, 2010)
"The treatment of Parkinson's disease with grafts of fetal ventral mesencephalic tissue has shown some success, but can result in graft-induced dyskinesias (GIDs)."( Barker, RA; Kuan, WL, 2010)
"Current therapy for Parkinson's disease (PD) is primarily directed at reversing the motor symptoms that are the consequence of dopamine deficiency and includes levodopa, dopamine agonists and monoamine oxidase (MAO) B inhibitors."( Schapira, AH, 2010)
"Current drugs used in the treatment of Parkinson's disease (PD), for example, L-DOPA and dopamine agonists, are very effective at reversing the motor symptoms of the disease."( Duty, S, 2010)
"Prolonged treatment of Parkinson's disease (PD) with levodopa leads to disabling side effects collectively referred to as 'dyskinesias'."( Kaczmarska, J; Konradi, C; Luksik, AS; Naydenov, AV; Vassoler, F, 2010)
"A 43-year-old male patient with idiopathic Parkinson disease, on dopaminergic therapy, was admitted with confusion and agitation, diaphoresis, and hyperkinesia after the commencement of the serotonin-noradrenaline reuptake inhibitor venlafaxine 2 weeks prior for depression."( Abeynaike, L; Rajapakse, S; Wickramarathne, T, 2010)
"For pramipexole in the treatment of Parkinson's disease, this means taking into account the available evidence regarding its symptomatic efficacy, effect on delaying long-term levodopa-related motor complications, beneficial effect on non-motor symptoms such as depression, and its safety and tolerability profile."( Abbruzzese, G; Antonini, A; Barone, P; Ceravolo, R; Fabbrini, G; Tinazzi, M, 2010)
"There is evidence that Parkinson's disease dementia is associated with a cholinergic deficit, supporting the therapeutic role of cholinesterase inhibitors, which are already first-line agents in the treatment of Alzheimer's disease."( Cus, A; Garasević, Z; Jensterle, J; Kramberger, MG; Meglic, NP; Pirtosek, Z; Repovs, G; Stukovnik, V; Tomse, P, 2010)
"Idiopathic Parkinson's disease (PD) is the only neurodegenerative disorder for which highly effective symptomatic therapy is available."( Gárdián, G; Vécsei, L, 2010)
"Dopamine replacement for Parkinson's disease (PD) have seen three major iterations of improvements since the introduction of l-3,4-dihydroxyphenylalanine (l-DOPA) pharmacotherapy: dopamine receptor agonists, ex vivo gene transfer for cell transplantation and most recently in vivo gene therapy."( Björklund, T; Cederfjäll, EA; Kirik, D, 2010)
"Following the diagnosis of Parkinson's disease, treatment may be initiated with MAO-B-inhibitor, even prior to the development of any functional deficit."( Atula, S; Heikkinen, E; Jaakkola, MR; Keränen, T; Martikainen, K; Pekka, J; Pekkonen, E; Reijo, M; Sotaniemi, K, 2010)
"Most medical treatments of Parkinson's disease (PD) are aimed at the reduction of motor symptoms."( Fiorlli, M; Iaconelli, S; Kusch, I; Lena, F; Mirabella, G; Modugno, N, 2010)
"Subjects included patients with Parkinson's disease who were treated with levodopa (L), carbidopa (C) and entacapone (E) either as separate tablets (LC + E) or as a single-tablet formulation (LCE)."( Delea, TE; Hagiwara, M; Thomas, SK, 2011)
"L-dopa therapy for Parkinson's disease leads to dyskinesias or abnormal involuntary movement (AIMs) for which there are few treatment options."( Campos, C; Huang, LZ; Ivy Carroll, F; Ly, J; Quik, M, 2011)
"A central problem in the treatment of Parkinson's disease (PD) is the development of motor disturbances like L: -DOPA-induced dyskinesia (LID) after long-term treatment."( Beck, J; Gerlach, M; Riederer, P; van den Buuse, M, 2011)
"Although Parkinson's disease (PD) is a well recognised risk factor for falls, how this disease and its therapy affect postural stability and leaning balance remains unclear."( Fung, VS; Latt, MD; Lord, SR; Menant, JC; Menz, HB, 2011)
"In animal models of Parkinson's disease, preladenant monotherapy improves motor function without causing dyskinesia and, as an adjunct to levodopa, it improves motor function without worsening dyskinesia."( Cantillon, M; Hauser, RA; Huyck, S; Micheli, F; Mok, V; Onofrj, M; Pourcher, E; Wolski, K, 2011)
"Two patients with Parkinson's disease (PD) treated successfully with subthalamic nucleus deep brain stimulation (STN-DBS) for 3-4 years are reported, who demonstrated a persistent improvement following removal of STN-DBS for late infection."( Duffy, A; Eldridge, PR; Fletcher, NA; Fox, SH; Varma, TR; Wong, SH, 2011)
"All patients with Parkinson's disease (PD) with motor fluctuations due to long-term levodopa therapy have at least one non-motor fluctuation symptom."( Ivanov, AK; Levin, OS; Shindriaeva, NN, 2011)
"Levodopa is the mainstay of Parkinson's disease (PD) treatment, but is often eventually associated with disabling motor complications in patients with advanced PD."( Fernandez, HH; Odin, P, 2011)
"Animal models of Parkinson's disease (PD) have proved highly effective in the discovery of novel treatments for motor symptoms of PD and in the search for clues to the underlying cause of the illness."( Duty, S; Jenner, P, 2011)
"Patients with Parkinson's disease receiving stable dopaminergic treatment were assigned to receive rasagiline 1 mg/day or placebo for 3 months."( Cakmur, R; Emre, M; Feyzioglu, A; Gunal, DI; Gurvit, H; Hanagasi, HA; Horozoglu, H; Sahin, HA; Tuncer, N; Unsalan, P; Yener, GG, 2011)
"We compared the number of Parkinson's disease cases in British Columbia derived from self-reports in the 2001 Canadian Community Health Survey to those obtained from administrative records of filled levodopa prescriptions and to Parkinson's disease diagnoses from physician visit billing and hospital discharge records in 1996 and 2005."( Harris, MA; Koehoorn, M; Teschke, K, 2011)
"Titration of therapy in Parkinson's disease is generally geared towards optimizing dorsal striatum-mediated motor symptoms, possibly at the expense of ventral striatum operations, a consequence that is only beginning to be recognized."( Ganjavi, H; MacDonald, AA; MacDonald, PA; Monchi, O; Provost, JS; Seergobin, KN; Tamjeedi, R, 2011)
"One patient with Parkinson's disease, treated with fetal grafts 14 years ago and deep brain stimulation 6 years ago, showed marked improvement of motor symptoms but continued to suffer from OFF-medication graft-induced dyskinesias."( Bjorklund, A; Brooks, DJ; Lindvall, O; Oertel, WH; Piccini, P; Pogarell, O; Politis, M; Quinn, NP; Wu, K, 2011)
"We evaluated 39-item Parkinson's disease Quality of Life Questionnaire Summary Index score (PDQ-39SI) changes analyzing its different domains in nine patients with advanced PD treated with DLI."( Carpintero, P; de la Fuente-Fernández, R; Llaneza, M; Macías, M; Sanjurjo, LF; Santos-García, D, 2012)
"In the mid-1980s, the treatment of Parkinson's disease was quite exclusively centered on dopatherapy and was focusing on dopamine systems and motor symptoms."( Lozano, A; Poewe, W; Rascol, O; Stern, M, 2011)
"Patients with advanced Parkinson's disease (PD) are known to develop motor complications after a few years of levodopa (L-dopa) therapy."( Konitsiotis, S; Maranis, S; Tsouli, S, 2011)
"Dopamine replacement therapy in Parkinson's disease (PD) improves the motor symptoms."( Bayard, S; Cochen De Cock, V; Dauvillers, Y, 2011)
"When young Parkinson's disease patients with a history of anxiety or depression are treated with high dose of DA, they are at risk of developing impulse control disorders."( Auyeung, M; Cheung, CM; Lee, CN; Li, R; Tang, WK; Tsoi, TH; Yeung, E, 2011)
"Levodopa treatment in Parkinson's disease (PD) increases in serum homocysteine levels due to its metabolism via catechol O-methyltransferase."( Choi, Y; Hong, JY; Kim, HO; Kim, HS; Lee, JE; Lee, PH; Nam, HS; Sohn, YH, 2011)
"Although the cardinal manifestations of Parkinson's disease (PD) are attributed to a decline in dopamine levels in the striatum, a breadth of non-motor features and treatment-related complications in which the serotonergic system plays a pivotal role are increasingly recognised."( Brotchie, JM; Fox, SH; Huot, P, 2011)
"Movement disability in advanced Parkinson's disease (PD) can be treated by high frequency stimulation (HFS) of the subthalamic nucleus (STN) but some patients experience psychiatric side-effects including depression, which is strongly linked to decreases in 5-hydroxytryptamine (5-HT)."( Hartung, H; Sharp, T; Steinbusch, HW; Tan, SK; Temel, Y; Visser-Vandewalle, V, 2012)
"In patients with advanced Parkinson's disease, the continuous delivery to the small intestine via a jejunal tube of levodopa/carbidopa, formulated as a gel suspension (Duodopa) represents a new treatment method."( Babiuc, RD; Bajenaru, OA; Ene, A; Negreanu, L; Popescu, BO; Smarandache, GC, 2011)
"L-Dopa is the mainstay of Parkinson's disease therapy; this drug is usually administered orally, but it is extensively metabolized in the gastrointestinal tract, so that relatively little arrives in the bloodstream as intact L-Dopa."( Cerasa, LS; Di Stefano, A; Iannitelli, A; Sozio, P, 2011)
"In early Parkinson's disease, compared with placebo, rotigotine monotherapy produced significantly greater improvements in the Unified Parkinson's Disease Rating Scale summed motor and activities of daily living (ADL) scores (primary endpoint), as well as significantly higher response rates."( Sanford, M; Scott, LJ, 2011)
"Impulse control disorders (ICDs) in Parkinson's disease (PD) are associated with dopamine agonist treatment."( Carrière, N; Defebvre, L; Destée, A; Dujardin, K; Kreisler, A, 2012)
"Levodopa has been the mainstay of Parkinson's disease (PD) therapy for over 40 years, with its efficacy surpassing that of other antiparkinsonian medications."( Emre, M; Reichmann, H, 2012)
"Treatment of Parkinson's disease with dopaminergic agents, such as l-DOPA, is frequently compromised by disabling side effects, particularly dyskinesia and a shortening in duration of antiparkinsonian action."( Brotchie, JM; Fox, SH; Gandy, MN; Gomez-Ramirez, J; Huot, P; Johnston, TH; Lee, J; Lewis, KD; Martin-Iverson, M; McIldowie, M; Millar, Z; Nash, JE; Piggott, MJ; Salomonczyk, D; Thiele, S; Wagg, K; Yong-Kee, CJ, 2012)
"It is indicated for the treatment of idiopathic Parkinson's disease as monotherapy or as adjunctive therapy to levodopa in patients [corrected]with end-of-dose fluctuations in the EU and for the treatment of adult patients with the signs and symptoms of idiopathic Parkinson's disease in the US."( Hoy, SM; Keating, GM, 2012)
"To evaluate the therapeutic effect of Parkinson's disease combined with overactive bladder syndrome (GAB) treated with combined therapy of oral administration of Tolterodine with low dose and electroacuponcture."( Chen, YL; Feng, WJ; Zhang, XL, 2012)
"Cell therapy studies in patients with Parkinson's disease (PD) have been confined to intrastriatal transplantation of dopamine-rich fetal mesencephalic tissue in efforts to improve motor performance."( Björklund, A; Brooks, DJ; Lindvall, O; Loane, C; Oertel, WH; Piccini, P; Politis, M; Quinn, NP; Wu, K, 2012)
"Current Parkinson's disease (PD) therapy is essentially symptomatic, and l-Dopa (LD), is the treatment of choice in more advanced stages of the disease."( Abbadessa, A; Cerasa, LS; Di Stefano, A; Sozio, P, 2012)
"  In chronic diseases including Parkinson's disease (PD), complex pharmacotherapy dosing schedules are reported to reduce adherence, perhaps leading to less-effective symptom control and, in PD, more erratic stimulation of dopamine receptors."( Barone, P; Busse, M; Debieuvre, C; Fraessdorf, M; Hauser, RA; Mizuno, Y; Poewe, W; Rascol, O; Schapira, AH, 2013)
"Postural disturbances in advanced Parkinson's disease are less responsive to therapy than other cardinal motor signs."( Colebatch, JG; Deuschl, G; Pötter-Nerger, M; Reich, MM; Volkmann, J, 2012)
"While Parkinson's disease (PD) phenotype in leucine-rich repeat kinase 2 gene (LRRK2)-associated and sporadic PD seems similar, there is paucity of data on the possible effect of mutations in LRRK2 on response to and complications of dopaminergic therapy."( Cohen, OS; Friedman, E; Hassin-Baer, S; Inzelberg, R; Kaplan, N; Korczyn, AD; Kozlova, E; Rosset, S; Vituri, A; Yahalom, G, 2012)
"The pharmacotherapy of Parkinson's disease (PD) is often challenging as clinicians have to find a favourable balance between the efficacy on motor symptoms and side effect profiles of different dopaminergic medications."( Alobaidi, H; Pall, H, 2013)
"Several people with Parkinson's disease have been treated with intrastriatal grafts of fetal dopaminergic neurons."( Angot, E; Björklund, A; Brundin, P; Ekström, P; Lema Tomé, CM; Mattsson, B; Steiner, JA, 2012)
"In patients with early Parkinson's disease, monotherapy with rasagiline 1 mg/day improved symptoms of the disease relative to placebo."( Hoy, SM; Keating, GM; Lyseng-Williamson, KA, 2012)
"Levodopa treatment of Parkinson's disease is very effective, but many types of adverse events can complicate the disease course, especially dyskinesias."( Daragon, A; Derrey, S; Lefaucheur, R; Maltête, D; Nicolau, J; Verdet, M, 2013)
"Drugs used for the treatment of Parkinson's disease and endocrine diseases, like hyperprolactinemia, may also induce VHD."( Cosyns, B; Droogmans, S; Lancellotti, P; Rosenhek, R, 2013)
"This suggests that cell death in Parkinson's disease is caused by a multifactorial cascade of pathogenic events and argues that effective neuroprotective therapy for Parkinson's disease may have to rely on multiple drug interventions."( Hirsch, EC; Jenner, P; Przedborski, S, 2013)
"Advances in the treatment of Parkinson's disease have led to significant improvement in many of the disabling motor symptoms of the disease, but often at the cost of neuropsychiatric side-effects."( Aarons, S; Peisah, C; Wijeratne, C, 2012)
"Levodopa therapy in Parkinson's disease (PD) is associated with non-motor complications resulting from sensitisation of the ventral striatum system."( Broussolle, E; Castrioto, A; Chabardès, S; Fraix, V; Kistner, A; Klinger, H; Krack, P; Lhommée, E; Mertens, P; Pollak, P; Quesada, JL; Schmitt, E; Thobois, SC, 2013)
"Levodopa on Motor complications in Parkinson's Disease (CALM-PD) study, a randomized clinical trial, we assessed the cross-sectional (baseline and 2 years) and longitudinal (change from baseline to 2 years) reliability of a modified motor UPDRS (removing rigidity and retropulsion items) compared to the standard motor UPDRS (all items) using intraclass correlation coefficients (ICC), stratified by treatment group."( Abdolahi, A; Biglan, KM; Dorsey, ER; Killoran, A; Scoglio, N, 2013)
"Motor complications of Parkinson's disease (PD) are a consequence of pulsatile dopaminergic stimulation from standard oral levodopa therapy."( Chatamra, K; Dutta, S; Johansson, A; Locke, C; Nyholm, D; Odin, P; Othman, AA, 2013)
"To explore a novel therapy against Parkinson's disease through enhancement of α7 nicotinic acetylcholine receptor (nAChR), we evaluated the neuroprotective effects of 3-[(2,4-dimethoxy)benzylidene]-anabaseine dihydrochloride (DMXBA; GTS-21), a functionally selective α7 nAChR agonist, in a rat 6-hydroxydopamine (6-OHDA)-induced hemiparkinsonian model."( Hisahara, S; Kawamata, J; Kem, W; Kitamura, Y; Matsumura, A; Matsushita, T; Shimohama, S; Suzuki, S; Takata, K, 2013)
"A small proportion of patients with Parkinson's disease (PD), chronically under dopamine replacement therapy, may undergo an addiction-like behavioral disturbance, named dopamine dysregulation syndrome (DDS)."( Cannas, A; Corona, M; Marrosu, F; Marrosu, MG; Solla, P, 2013)
"The long-term use of levodopa to treat Parkinson's disease (PD) is often limited by the development of motor complications (e."( Hashida, H; Hattori, N; Iijima, M; Kano, O; Kubo, S; Matsumura, M; Murakami, H; Nanri, K; Okuma, Y; Suzuki, M; Suzuki, Y; Tomimitsu, H; Utsumi, H, 2013)
"The comorbidity of schizophrenia and idiopathic Parkinson's disease (IPD) is illustrated by a case description of a schizophrenic patient who develops motor symptoms finally diagnosed and treated as comorbid IPD."( de Jong, MH; Van Gool, AR; Zemel, D, 2014)
"In advanced Parkinson's disease (PD) patients, continuous intra-duodenal infusion of levodopa/carbidopa intestinal gel (LCIG) is an established approach in the management of motor complications that cannot be further improved by conventional oral therapy."( Antonini, A; Cornblath, DR; Ebersbach, G; Grandas, FJ; Klostermann, F; Müller, T; Odin, P; Urban, PP; Valldeoriola, F; van Laar, T, 2013)
"'Off' periods increase as Parkinson's disease (PD) progresses and the benefits of standard therapy wane."( Grosset, DG; Grosset, KA; Malek, N; Morgan, F, 2013)
"The assay is applied in monitoring Parkinson's disease patients under different treatments."( Huisman, H; Kellermann, GH; Marc, DT; Nichkova, M; Wynveen, PM, 2013)
"Scores using the Unified Parkinson's Disease Rating Scale also improved during rasagiline treatment."( Chen, Y; Deng, L; Li, J; Qin, X; Sun, H; Tang, R; Yi, L; Zhang, C; Zhang, L; Zhang, Z; Zheng, J; Zhou, H, 2013)
"A subset of patients with Parkinson's disease (PD) develops behavioral addictions, which may be due to their dopamine replacement therapy."( Averbeck, BB; Djamshidian, A; Housden, CR; Lees, AJ; O'Sullivan, SS; Roiser, JP, 2013)
"In the 6-OHDA mouse model of Parkinson's disease, doxycycline administered at a dose that both induces/represses conditional transgene expression in the tetracycline system, mitigates the loss of dopaminergic neurons in the substantia nigra compacta and nerve terminals in the striatum."( Bel, ED; Lazzarini, M; Martin, S; Mitkovski, M; Stühmer, W; Vozari, RR, 2013)
"The treatment of Parkinson's disease (PD) in subjects over 70 years old is simpler than in younger subjects for correcting the consequences of dopamine deficiency, but more complex with regard to symptoms resulting from non-dopaminergic lesions (axial symptoms, cognitive decline)."( Damier, P; Derkinderen, P, 2006)
"describe a first in Parkinson's disease (PD) patient study using a drug previously approved for diabetes treatment."( Barker, RA; Brundin, P; Stacy, M, 2013)
"Sixty-eight patients with advanced Parkinson's disease were randomly assigned to have subthalamic nucleus-deep brain stimulation or best medical treatment for Parkinson's disease."( Daniels, C; Deuschl, G; Falk, D; Granert, O; van Eimeren, T; Volkmann, J; Witt, K, 2013)
"Current treatments for Parkinson's disease (PD) are aimed at addressing motor symptoms but there is no therapy focused on modifying the course of the disease."( Ansorena, E; Blanco-Prieto, MJ; Garbayo, E, 2013)
"Patients with Parkinson's disease and moderate-to-severe levodopa (l-dopa)-induced dyskinesia who were receiving stable l-dopa/anti-parkinsonian treatment and were not currently receiving amantadine were randomized to receive either AFQ056 (at doses of 20, 50, 100, 150, or 200 mg daily) or placebo (1:1:1:1:2:3 ratio) for 12 weeks."( Destee, A; Gao, H; Graf, A; Hattori, N; Hauser, RA; Kenney, C; Lang, AE; Merschhemke, M; Nagel, J; Poewe, W; Rascol, O; Stacy, M; Stocchi, F; Tolosa, E; Trenkwalder, C, 2013)
"The Unified Parkinson's Disease Rating Scale scores, TCM symptoms scores, quality of life, change of Madopar's dosage and the toxic and adverse effects of Madopar will be observed during a 3-month treatment period and through a further 6-month follow-up period."( Ma, YZ; Shen, XM; Zhang, J, 2013)
"Nonmotor symptoms (NMS) of Parkinson's disease (PD) are critical to identify and treat because of their impact on quality of life."( Nicholas, AP; Sung, VW, 2013)
"It is approved for the treatment of idiopathic Parkinson's disease (PD)."( Waters, C, 2013)
"In later stages of Parkinson's disease, treatment of 'off' periods with subcutaneous apomorphine is helpful but requires injection; inhaled apomorphine would be potentially more convenient."( Grosset, DG; Grosset, KA; Malek, N; Morgan, F, 2013)
"Chronic use of medication for treating Parkinson's disease (PD) can give rise to peak-dose dyskinesia."( Burack, MA; Giuffrida, JP; Mera, TO, 2013)
"Chronic pulsatile levodopa therapy for Parkinson's disease (PD) leads to the development of motor fluctuations and dyskinesia."( Hashim, HZ; Nafisah, WY; Norlinah, MI; Raymond, AA; Tamil, AM; Tan, HJ, 2014)
"Unmedicated Parkinson's disease patients tend to be risk-averse while dopaminergic treatment causes a tendency to take risks."( Appel-Cresswell, S; Barton, JJ; McKeown, MJ; Sharp, ME; Stoessl, AJ; Viswanathan, J, 2013)
"We performed the Unified Parkinson's Disease Rating Scale (UPDRS) and started a parenteral therapy with high doses of thiamine."( Colangeli, M; Compagnoni, L; Costantini, A; Pala, MI, 2013)
"We enrolled Parkinson's disease patients on dopamine agonist therapy with unsatisfactory control such as motor fluctuation, dyskinesia and sleep-related problems."( Jeon, BS; Kim, HJ; Kim, JM; Kim, JS; Kim, YE; Lee, JY; Yun, JY, 2013)
"In patients with Parkinson's disease (PD), dopamine-agonist (DA) therapy has been associated with increased impulsive behavior."( Antonelli, F; Houle, S; Ko, JH; Lang, AE; Miyasaki, J; Ray, NJ; Strafella, AP; Valzania, F, 2014)
"Motor symptoms of Parkinson's disease are commonly treated using l-DOPA although long-term treatment usually causes debilitating motor side effects including dyskinesias."( Bishop, C; Dupre, KB; Eskow Jaunarajs, KL; Goldenberg, AA; Lindenbach, D; Ostock, CY, 2013)
"Dopaminergic treatment of patients with Parkinson's disease can be associated with a finely tuned high-gamma (FTG) band oscillation between 60 and 90 Hz in the basal ganglia (BG) nuclei."( Brown, P; Cagnan, H; Kuhn, AA, 2014)
"Pimavanserin may benefit patients with Parkinson's disease psychosis for whom few other treatment options exist."( Ballard, C; Chi-Burris, K; Corbett, A; Cummings, J; Dhall, R; Isaacson, S; Mills, R; Williams, H, 2014)
"Younger age, female gender, Unified Parkinson's Disease Rating Scale (UPDRS) part II score and duration of anti-Parkinson treatment were found significantly associated with WO."( Abbruzzese, G; Albanese, A; Antonini, A; Attar, M; Barone, P; Bonuccelli, U; Colombo, D; Lopiano, L; Morgante, L; Onofrj, M; Posocco, V; Pramstaller, P; Ruggieri, S; Stocchi, F; Tinazzi, M; Zappia, M, 2014)
"The aim of stem cell therapy for Parkinson's disease (PD) is to reconstruct local synapse formation and/or induce the release of dopamine and cytokines from grafted cells in the putamen."( Takahashi, J, 2013)
"She had been treated for Parkinson's disease at the neurology department of another university hospital for 9 years."( Hisanaga, R; Nakamura, M; Nomoto, S; Sato, T, 2013)
"Levodopa is the gold standard in Parkinson's disease (PD) treatment but its use is associated with motor complications."( Antonini, A; Pilleri, M, 2014)
"To evaluate general knowledge on Parkinson's disease (PD) among patients with PD and current status and choices regarding diagnosis and treatment of PD among general neurologists from grassroots hospitals of Sichuan Province, China."( Cao, B; Chen, D; Chen, K; Huang, R; Li, J; Shang, H; Song, W; Yang, R, 2014)
"In an MPTP-treated animal model of Parkinson's disease, MSC administration significantly increased final maturation of late autophagic vacuoles, fusion with lysosomes."( Kim, HN; Lee, PH; Oh, SH; Park, HJ; Shin, JY, 2014)
"The initial pharmacological treatment of idiopathic Parkinson's disease (IPD) is symptomatic and remains based upon dopaminergic drugs."( Cesaro, P; Defebvre, L, 2014)
"Dysphagia in patients with Parkinson's disease, persisting despite dopaminergic treatment, affects intake of nutrients and medication, and reduces quality of life (QOL)."( Dick, J; Hamdy, S; Harris, M; Kellett, M; Michou, E; Rothwell, J; Vania, A, 2014)
"A total of 22 patients with Parkinson's disease and freezing while other symptoms had favorably responded to dopaminergic treatment."( Ceballos-Baumann, AO; Fietzek, UM; Schroeteler, FE; Ziegler, K; Zwosta, J, 2014)
"Thirteen idiopathic Parkinson's disease patients (iPD) with subthalamic deep brain stimulation (STN-DBS), 9 medically treated iPD, and 21 age-matched healthy controls were tested with a probabilistic classification task."( Breit, S; Gharabaghi, A; Krüger, R; Lam, JM; Luft, AR; Wächter, T; Weiss, D, 2014)
"Dopamine replacement therapy in Parkinson's disease is associated with several unwanted effects, of which dyskinesia is the most disabling."( Chakrabarty, K; Drucker-Colín, R; Garcia-Montes, JR; Herrero, MT; Heumann, R; Moratalla, R; Morelli, M; Simola, N, 2014)
"To embed the medication of Parkinson's disease into a complex treatment plan of a patient suffering from multimorbidity can be challenging."( Lettow, I; Röther, J, 2014)
"L-dopa was the mainstay of Parkinson's disease treatment between 2005 and 2010 in Japan."( Ikeda, S; Ishizaki, T; Nakaoka, S; Nakayama, T; Satoh, T; Urushihara, H; Yamamoto, M, 2014)
"The most effective treatment of Parkinson's disease (PD) L-DOPA is associated with major side effects, in particular L-DOPA-induced dyskinesia, which motivates development of new treatment strategies."( Alken, RG; Feltmann, K; Konradsson-Geuken, Å; Malmlöf, T; Schilström, B; Schneider, F; Svensson, TH, 2015)
"Whether initial treatment for Parkinson's disease should consist of levodopa, dopamine agonists, or monoamine oxidase type B inhibitors (MAOBI) is uncertain."( Clarke, CE; Gray, A; Gray, R; Ives, N; Jenkinson, C; McIntosh, E; Patel, S; Rick, C; Wheatley, K; Williams, A, 2014)
"A major unresolved issue in the Parkinson's disease (PD) treatment is the development of l-DOPA-induced dyskinesias (LIDs) as a side effect of chronic L-DOPA administration."( Auladell, C; Beas-Zarate, C; Camins, A; Canudas, AM; de Lemos, ML; Folch, J; Lazarowski, A; Pallàs, M; Pedros, I; Petrov, D, 2014)
"Rat models with 6-OHDA-induced Parkinson's disease were treated with curcumin, DFO, or both and the effect of different treatments on dopamine level was examined."( Cui, X; Jiang, F; Li, Z; Liu, J; Lv, H; Niu, Y; Wang, L; Wang, W; Yu, S; Yuan, J; Zhang, H, 2014)
"Many patients with Parkinson's disease have motor fluctuations despite treatment with available drugs."( Bandak, S; Docu-Axelerad, A; Hauser, RA; Kenney, C; Kieburtz, KD; Kozyolkin, O; Lew, M; Meya, U; Neale, A; Olanow, CW; Pourcher, E; Resburg, C, 2014)
"Current conventional treatments for Parkinson's disease (PD) are aimed at symptom management, as there is currently no known cure or treatment that can slow down its progression."( Brogan, B; Jansen, RL; Okello, EJ; Whitworth, AJ, 2014)
"Levodopa (l-dopa) therapy in Parkinson's disease (PD) increases serum homocysteine levels because of its metabolism via catechol O-methyltransferase, which may lead to endothelial dysfunction."( Hong, JM; Lee, JS; Lee, PH; Yong, SW; Yoon, JH, 2014)
"Patients with Parkinson's disease (PD) treated with oral levodopa have a higher prevalence of chronic, prevalently sensory, usually mild axonal polyneuropathy (PNP)."( Eleopra, R; Onofrj, M; Uncini, A, 2015)
"Treatment of Parkinson's disease (PD) with L-DOPA eventually causes abnormal involuntary movements known as dyskinesias in most patients."( Bishop, C; Conti, MM; Lindenbach, D; Ostock, CY; Palumbo, N; Vilceus, N, 2015)
"One problem with DOPA therapy for Parkinson's disease is its cardiovascular side effects including hypotension and syncope, the underlying mechanisms of which are largely unknown."( Chen, S; Goshima, Y; Koga, M; Masukawa, D; Nakamura, F, 2014)
"One potential complication of treating Parkinson's Disease (PD) with dopaminergic drugs is dopamine dysregulation syndrome, an addiction-like response to the drug therapy."( Campbell, JC; Chen, N; De La Cruz, P; Jeyamohan, SB; Pilitsis, JG; Shin, D, 2014)
"Several treatment guidelines for Parkinson's disease (PD) had been proposed in recent decades."( Chang, MH; Guo, YJ; Liao, YC; Lin, CH, 2014)
"Current treatment of Parkinson's disease (PD) is limited to symptomatic dopaminergic therapy, while no interventions have been shown to slow down disease progression."( Carta, AR; Simuni, T, 2015)
"Treatment for Parkinson's disease was used as a proxy for this condition and lack of such treatment as a proxy for severe mental illness (SMI)."( Pambrun, E; Verdoux, H, 2014)
"Psychotic symptoms in Parkinson's disease (PD) caused by dopamimetic treatment are a relevant clinical problem."( Altpass, D; Batra, A; Farger, G; Gasser, T; Karle, KN; Lutz, UC; Sirfy, A; Wiatr, G, 2014)
"The main pathochemical hallmark of Parkinson's disease (PD) is the loss of dopamine in the striatum of the brain, and the oral administration of levodopa (L-dopa) is a treatment that partially restores the dopaminergic transmission."( Ceci, R; Colamartino, M; Cozzi, R; Duranti, G; Padua, L; Sabatini, S; Santoro, M; Testa, A, 2015)
"For all its imperfections at treating Parkinson's disease (PD), orally-administered levodopa (l-dopa) can be regarded as the "platinum" standard of PD therapeutics for its impact on disability and discomfort and its cost-effectiveness."( LeWitt, PA, 2015)
"The effects of dopaminergic therapy in parkinson's disease (PD) can vary depending on the class of medication selected."( Aminoff, MJ; Bodis-Wollner, I; Boyd, JT; Christine, CW; Dhall, R; Fang, JY; Goudreau, JL; Leehey, M; Morgan, JC; Nicholas, AP; Pérez, A; Zweig, RM, 2015)
"Motor complications in Parkinson's disease (PD) are associated with long-term oral levodopa treatment and linked to pulsatile dopaminergic stimulation."( Benesh, JA; Chatamra, K; Chouinard, S; Dubow, J; Espay, AJ; Fernandez, HH; Fung, VS; Hall, CM; Hauser, RA; Klostermann, F; Lang, AE; Lew, MF; Odin, P; Robieson, WZ; Standaert, DG; Steiger, M; Suchowersky, O; Yakupov, EZ, 2015)
"Gait impairment in Parkinson's disease (PD) persists despite the use of dopaminergic therapy."( Burn, DJ; Galna, B; Lord, S; Rochester, L, 2015)
"Conventional symptomatic treatment for Parkinson's disease (PD) with long-term L-3,4-dihydroxyphenylalanine (DOPA) is complicated with development of drug-induced side effects."( Broom, L; Cederfjäll, E; Kirik, D, 2015)
"Additionally, patients with a Unified Parkinson's Disease Rating Scale score lower than 70 had a significantly higher chance of clinical improvement with doxazosin treatment than those with higher Unified Parkinson's Disease Rating Scale scores did (RR=3."( Barbosa, ER; Bessa Junior, Jd; Bruschini, H; Gomes, CM; Lopes, RI; Nitti, VW; Sallem, FS; Sammour, ZM; Srougi, M; Trigo-Rocha, FE, 2014)
"Late stages of Parkinson's disease (PD) are characterized by the development of motor fluctuations and dyskinesia which inevitably emerge during the disease due to long-term use of levodopa and hinder treatment."( Timofeeva, AA, 2014)
"In neurological diseases, such as Parkinson's disease and Alzheimer's disease, dual-target-directed drugs are expected to be advantageous over single-target treatments."( Petzer, A; Petzer, JP; Terre'Blanche, G; Van der Walt, MM, 2015)
"The cardinal motor symptoms of Parkinson's disease (PD) include resting tremor, akinesia, bradykinesia, and rigidity, and these motor abnormalities can be modeled in rodents by administration of the VMAT-2 (type-2 vesicular monoamine transporter) inhibitor tetrabenazine (9,10-dimethoxy-3-(2-methylpropyl)-1,3,4,6,7, 11b hexahydrobenzo[a]quinolizin-2-one; TBZ)."( Contreras-Mora, HM; Correa, M; Milligan, MN; Podurgiel, SJ; Purcell, LJ; Salamone, JD; Yohn, SE, 2015)
"After more than 50 years of treating Parkinson's disease with l-DOPA, there are still no guidelines on setting the optimal dose for a given patient."( Azulay, JP; Bardyn, T; Bordet, R; Brefel-Courbon, C; Corvol, JC; Debû, B; Defebvre, L; Delval, A; Destée, A; Devedjian, JC; Devos, D; Drapier, S; Duhamel, A; Dujardin, K; Durif, F; Eusebio, A; Faighel, M; Fraix, V; Giordana, C; Guehl, D; Houeto, JL; Labreuche, J; Lagha-Boukbiza, O; Maltête, D; Meguig, S; Moreau, C; Ory-Magne, F; Petyt, G; Rascol, O; Rouaix, N; Sablonnière, B; Saulnier, PJ; Tison, F; Tranchant, C; Vasseur, F; Vidailhet, M, 2015)
"Levodopa is first line treatment of Parkinson's disease (PD)."( Altmann, V; Callegari-Jacques, SM; Hutz, MH; Rieck, M; Rieder, CR; Schneider Medeiros, M; Schumacher-Schuh, AF, 2015)
"Whether the treatment of Parkinson's disease has to be initiated with levodopa or a D2 agonist like pramipexole remains debatable."( Fernández, E; Fresno, C; Gershanik, OS; Gomez, G; González, GA; Larramendy, C; Murer, MG; Saborido, MD; Spaans, F; Taravini, IR, 2016)
"Analysis of Parkinson's disease cases alone indicated that serpin-A5 and serpin-A13, and trypsin-2 expression in midbrain and cerebral cortex was different in cases with a high incidence of L-DOPA-induced dyskinesia and psychosis compared to those with low levels of these treatment-induced side effects."( Dexter, DT; Durrenberger, PF; Gentleman, SM; Hurley, MJ; Walls, AF, 2015)
"A marker for diagnosis of Parkinson's disease (PD), which reflects on the occurrence of peripheral pathogenic mechanisms, would potentially improve therapy."( Abd-Elhadi, S; Ben-Hur, T; Honig, A; Linetsky, E; Schechter, M; Sharon, R; Simhi-Haham, D, 2015)
"Levodopa treatment in Parkinson's disease (PD) causes motor fluctuations and dyskinesias, but few data describe their development or severity in unselected incident cohorts."( Counsell, CE; Macleod, AD; Scott, NW, 2016)
"Dopaminergic treatment in Parkinson's disease (PD) reduces the severity of motor symptoms of the disease."( de la Riva, P; Delgado-Alvarado, M; Gago, B; Jiménez-Urbieta, H; Marin, C; Rodriguez-Oroz, MC, 2015)
"The treatment of Parkinson's disease (PD) using stem cells has long been the focus of many researchers, but the ideal therapeutic strategy has not yet been developed."( Chang, KA; Choi, HS; Kim, HJ; Oh, JH; Park, HG; Ra, JC; Suh, YH, 2015)
"Most Parkinson's disease patients will receive levodopa therapy, and of these, the majority will develop some levodopa-induced complications."( Bajwa, JA; Bhidayasiri, R; Chen, RS; Hattori, N; Jamora, RD; Jeon, B; Lee, MK; Mok, VC; Pisarnpong, A; Poewe, W; Syamsudin, T; Tan, LC; Zhang, B, 2015)
"Levodopa therapy in Parkinson's disease (PD) is often associated with disabling motor and non-motor complications in patients with advanced disease due to the variable absorption of levodopa because of an irregular or erratic emptying of the gastric content."( Abou Al-Shaar, H; Al-Ajlan, F; Alkahtani, K; Alkhairallah, T; Bohlega, S; Hasan, N, 2015)
"The moderate and severe stages of Parkinson's disease (PD) are marked by motor and non-motor complications that still remain difficult to control with the currently available therapy."( Antonini, A; Vorovenci, RJ, 2015)
"We herein report three cases of Parkinson's disease associated with difficulty in eyelid opening, referred to as apraxia of eyelid opening (AEO), which improved after aripiprazole treatment."( Fukunaga, K; Nakanishi, R; Tokisato, K; Tokunaga, M; Watanabe, S; Yamanaga, H, 2015)
"The optimal treatment strategy for Parkinson's disease has been debated for decades."( Tan, LC; Zhang, J, 2016)
"The pharmacological treatment of Parkinson's disease (PD) is limited to dopamine agonists and anti-cholinergic drugs that do not stop the progress of disease."( Muñoz, P; Paris, I; Segura-Aguilar, J, 2016)
"Twenty-one patients with mild-moderate Parkinson's disease were studied twice, once after an overnight DRT washout and once after the administration of a standard dose of levodopa (Sinemet), and compared to 20 demographically-matched healthy control participants."( Dagher, A; Fellows, LK; Simioni, AC, 2016)
"In this study, ECG of 11 patients with Parkinson's disease was measured during levodopa challenge with pronounced dose of fast release levodopa to ensure the positive drug effect for deep brain stimulation treatment."( Karjalainen, PA; Pekkonen, E; Rissanen, SM; Ruonala, V; Tarvainen, MP, 2015)
"In patients with recently diagnosed Parkinson's disease, the advantage of first-line dopamine agonist therapy is uncertain."( , 2015)
"Building upon our expertise in Parkinson's disease translational research, the present study addressed this gap comparing plasma and cerebrospinal fluid bioavailability of l-3,4-dihydroxyphenylalanine, carbamazepine, quinidine, lovastatin, and simvastatin, in healthy and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-treated macaques, the gold standard model of Parkinson's disease."( Bezard, E; Contamin, H; Li, Q; Thiollier, T; Wu, C; Zhang, J, 2016)
"With an emphasis on Parkinson's disease, this chapter will discuss recent evidence supporting the assertion that vitamin D can be a useful therapeutic agent used as an intervention therapy to be combined with existing treatments; and the case for further development of novel treatments utilizing the potential of vitamin D."( Fricker, RA; Middleditch, C; Orme, RP; Waite, L, 2016)
"Cognitive impairment is common in Parkinson's disease (PD), but often not improved by dopaminergic treatment."( Borchert, RJ; Hughes, LE; Jones, SP; Nombela, C; Passamonti, L; Rae, CL; Rittman, T; Robbins, TW; Rowe, JB; Sami, S; Vatansever, D; Vázquez Rodríguez, P; Ye, Z, 2016)
"Studies in animal models of Parkinson's disease (PD) have suggested that the rate of exercise performance is important in treatment efficacy and neuroprotection."( Ahmed, A; Alberts, JL; Beall, EB; Feldman, M; Frankemolle, A; Lowe, MJ; Phillips, M; Ridgel, AL; Thota, A, 2016)
"For example, in Parkinson's disease, a placebo treatment induces a release of dopamine in the striatum and changes the activity of neurons in both thalamic and subthalamic nuclei."( Benedetti, F; Carlino, E; Frisaldi, E; Giudetti, L; Lanotte, M; Lopiano, L; Pampallona, A; Zibetti, M, 2016)
"Levodopa is the reference treatment for Parkinson's disease."( Azulay, JP; Boulamery, A; Eusebio, A; Gayraud, D; Simon, N; Viallet, F, 2016)
"Dyskinesias in Parkinson's disease (PD) patients are a common side effect of long-term dopaminergic therapy and are associated with motor dysfunctions, including gait and balance deficits."( Berg, D; Braatz, U; Ferreira, JJ; Graessner, H; Heger, T; Hobert, MA; Hucker, S; Maetzler, W; Manoli, Y; Meckler, S; Ramsperger, R; Serrano, JA; van Uem, J, 2016)
"No cure is currently available for Parkinson's disease patients; instead most medications are for treatment of symptoms."( Fraiwan, L; Khnouf, R; Mashagbeh, AR, 2016)
"L-Dopa continues to be the gold drug in Parkinson's disease (PD) treatment from 1967."( Abarca, J; Cardenas, C; Díaz-Veliz, G; Gysling, K; Herrera, A; Hultenby, K; Inzunza, J; Jaña, F; Mora, S; Muñoz, P; Paris, I; Raisman-Vozari, R; Segura-Aguilar, J; Steinbusch, HW, 2016)
"Levodopa is first-line treatment of Parkinson's disease motor symptoms but, dose response is highly variable."( Altmann, V; Callegari-Jacques, SM; Hutz, MH; Rieck, M; Rieder, CR; Schumacher-Schuh, AF, 2016)
"The treatment of Parkinson's disease may be initiated with dopamine agonist or MAO-B-inhibitor for people under 60-65 years of age."( Atula, S; Autere, J; Eerola-Rautio, J; Kaasinen, V; Kauppinen, M; Martikainen, K; Pekkonen, E; Ruottinen, H; Viljamaa, M, 2016)
"Patients with Parkinson's disease often have a good initial response to dopaminergic therapy but later usually develop motor fluctuations and dyskinesia."( Benita León, V; Campolongo Perillo, A; Fernández Díez, S; Mariscal Pérez, N; Martínez Castrillo, JC; Puente Périz, V; Santos García, D; Seoane Urgorri, A; Udaeta Baldivieso, B, 2016)
"A total of 73 patients diagnosed with Parkinson's disease and treated with a single dopamine agonist were included in the study after undergoing clinical assessment and completing the single-question screen for REM sleep behaviour disorder and the short version of the questionnaire for impulsive-compulsive behaviours in Parkinson's disease."( Bellosta Diago, E; Lopez Del Val, LJ; López Garcia, E; Santos Lasaosa, S; Viloria Alebesque, A, 2017)
"Clinically, Parkinson's disease (PD) is associated with resting tremor, postural instability, rigidity, bradykinesia, and a good response to levodopa therapy."( Hernandez, DG; Reed, X; Singleton, AB, 2016)
"Current pharmacological strategies for Parkinson's disease (PD), the most common neurological movement disorder worldwide, are predominantly symptom relieving and are often plagued with undesirable side effects after prolonged treatment."( Basil, AH; Hang, L; Lim, KL, 2016)
"The treatment of early Parkinson's disease with dopaminergic agents remains the mainstay of symptomatic therapy for this incurable neurodegenerative disorder."( Abler, V; Berkovich, E; Collinson, S; Eliaz, RE; Eyal, E; Fitzer-Attas, C; Freeman, N; Grossman, I; Hayden, MR; Kennedy, JL; Knight, J; Lang, AE; Levy, J; Masellis, M; Tampakeras, M; Tchelet, A; Tiwari, A, 2016)
"Up to 60 % of patients with Parkinson's disease may develop Parkinson's disease psychosis, which is associated with increased morbidity and mortality and has few treatment options."( Markham, A, 2016)
"Neuropsychiatric symptoms in Parkinson's disease usually require optimization of levodopa therapy as a first step."( Evans, AH; Looi, JC; Molina Ruiz, RM; Velakoulis, D, 2016)
"Impulse control disorders (ICDs) in Parkinson's disease (PD) are related to treatment with dopamine agonists, which is thought to deregulate the dopaminergic mesolimbic pathway and impair reward evaluation."( Bourriez, JL; Carriere, N; Defebvre, L; Delval, A; Derambure, P; Dujardin, K, 2016)
"Chronic treatment with levodopa in Parkinson's disease (PD) is associated with the risk of development of motor fluctuations and dyskinesias, i."( Fiszer, U; Michałowska, M; Szatanowski, T, 2016)
"Growing evidence demonstrates that in Parkinson's Disease (PD) sleep disturbances are frequent and difficult to treat."( Albanese, M; Imbriani, P; Liguori, C; Marciani, MG; Mercuri, NB; Pierantozzi, M; Placidi, F; Stanzione, P; Stefani, A, 2016)
"Patients with advanced Parkinson's disease and motor complications undergoing optimized oral therapy can significantly benefit from continuous intrajejunal levodopa/carbidopa infusion applied by means of a medication pump."( Ebersbach, G; Holtmann, M; Jost, W; Odin, P; Schrader, C; Südmeyer, M; Winkler, C, 2016)
"In advanced Parkinson's disease (PD), neurologists and patients face a complex decision for an advanced therapy."( Bloem, BR; Faber, MJ; Nijhuis, FA; Post, B; van Heek, J, 2016)
"Peripheral mononuclear cells from idiopathic Parkinson's disease patients and controls were treated ex vivo with two structurally distinct inhibitors of LRRK2, at four different doses, and immunoblotting was used to assess the reduction in LRRK2 phosphorylation at Ser910, Ser935, Ser955 and Ser973."( Dzamko, N; Halliday, GM; Perera, G; Ranola, M; Rowe, DB, 2016)
"The treatment of psychotic symptoms in Parkinson's disease is complicated due to the ability of antipsychotic medications to worsen motor symptoms."( Damjanović, A; Divac, N; Medić, B; Prostran, M; Savić Vujović, K; Stojanović, R, 2016)
"Cell replacement therapy in Parkinson's disease (PD) aims at re-establishing dopamine neurotransmission in the striatum by grafting dopamine-releasing cells."( Boronat-García, A; Drucker-Colín, R; Guerra-Crespo, M; Millán-Aldaco, D; Palomero-Rivero, M, 2016)
"Radboud Oral Motor Inventory for Parkinson's disease (ROMP) test was administered to all patients to evaluate speech, swallowing functions, and saliva control."( Ak, F; Cakmakli, GY; Gulunay, A; Karakoc, M; Oztekin, N; Ulusoy, EK; Yon, MI, 2016)
"A treatment for Parkinson's disease utilizing encapsulated porcine CP has been developed and is currently being evaluated in a Phase I clinical trial."( Emerich, DF; Sandrof, MA; Thanos, CG, 2017)
"Since Parkinson's disease (PD) provides a model for assessing dopaminergic dysfunctions in humans, our study was designed to investigate social interactions in PD patients receiving dopamine replacement therapy (Levodopa=l-Dopa) and in neurologically healthy controls."( Bulgheroni, M; Castiello, U; D'Amico, E; Scaravilli, T; Straulino, E, 2016)
"Patients with advanced Parkinson's disease (PD) and contraindications for subthalamic nucleus deep brain stimulation (DBS) could particularly benefit from subcutaneous infusion therapy with apomorphine."( Auffret, M; Drapier, S; Houvenaghel, JF; Le Jeune, F; Maurus, A; Robert, GH; Sauleau, P; Vérin, M, 2017)
"We report a long-term treatment of Parkinson's disease in out-patient clinics."( Mizuno, Y; Origasa, H; Shimoda, S, 2018)
"Current therapies for Parkinson's disease (PD) confer symptomatic relief and are particularly efficient in the treatment of motor symptoms in earlier disease stages."( Carboni, E; Koch, JC; Lingor, P, 2017)
"Currently, treatment of Parkinson's disease aims at alleviating its symptoms."( Hattori, N; Shimura, H, 2017)
"Sixty Parkinson's Disease (PD) specialists in Italy were invited to complete a survey covering issues on clinical and practical aspects of LCIG therapy."( Antonini, A; Cossu, G; Mancini, F; Modugno, N; Pilleri, M; Quatrale, R; Sensi, M; Tamma, F; Zibetti, M, 2017)
"In patients with Parkinson's disease (PD), the efficacy of L-dopa therapy depends on its ability to restore Dopamine (DA) neurotransmission in the striatum."( , 2016)
"The treatment of Parkinson's disease is symptomatic with the use of dopaminergic medications: levodopa, dopaminergic agonists and enzymatic inhibitors."( Defebvre, L; Moreau, C, 2017)
"Fluctuations in response to levodopa in Parkinson's disease (PD) are difficult to treat as tools to monitor temporal patterns of symptoms are hampered by several challenges."( Brokaw, EB; Burack, MA; Heldman, DA; Mari, ZK; Mera, TO; Pulliam, CL, 2018)
"Impulsive and compulsive behaviors in Parkinson's disease (PD) patients are most often attributed to dopamine agonist therapy; dysregulation of the mesocorticolimbic system accounts for this behavioral phenotype."( Claassen, DO; Lopez, AM; Weintraub, D, 2017)
"Prolonged treatment of Parkinson's disease (PD) with levodopa (L-DOPA) results in motor complications, including motor fluctuations and involuntary movements known as L-DOPA induced dyskinesias (LIDs)."( Blandini, F; Cerri, S; Siani, F, 2017)
"We reviewed the literature on Parkinson's disease, dopamine agonists, and hiccups, searching for specific treatment recommendations for hiccups in this disease."( Aguirre, C; Calvo, B; Del Pozo-Rodríguez, A; Domingo-Echaburu, S; García, M; Isla, A; Lertxundi, U; Marquínez, AC; Solinís, MÁ, 2017)
"Impulsive-compulsive disorders in Parkinson's disease patients have been described as behavioural or substance addictions including pathological gambling or compulsive medication use of dopamine replacement therapy."( Dardou, D; Durif, F; Fleurance, R; Gryshkova, V; Hafidi, A; Loiodice, S; McGhan, P; Nogueira da Costa, A, 2017)
"The phenomenon of sleep benefit (SB) in Parkinson's disease (PD), whereby waking motor function is improved despite no dopaminergic treatment overnight, is controversial."( Evans, A; Lee, W; Williams, DR, 2017)
"Dopamine as a drug for treating Parkinson's disease and metronidazole as an anti-inflammatory drug were encapsulated in the hydrogel."( Guo, B; Liang, X; Ma, PX; Ren, Y; Zhao, X, 2017)
"Mood disorders are very frequent in Parkinson's Disease (PD), and their effective treatment is still a major unresolved issue: growing evidence suggests that glutamatergic system dysfunction is directly involved."( Bonizzoni, E; Cattaneo, C; Keywood, C; Kottakis, I; Lazzeri, G; Müller, T, 2017)
"Patients with Parkinson's disease (PD) receiving long-term L-Dopa therapy eventually develop motor complications with unpredictable "on-off" response fluctuations and involuntary movements, leading to progressive disability."( D'Elia, A; Imbriani, P; Pisani, A; Schirinzi, T, 2017)
"A subgroup of Parkinson's disease (PD) patients treated with dopaminergic therapy develop compulsive reward-driven behaviors, which can result in life-altering morbidity."( Claassen, DO; Donahue, MJ; Kang, H; Kessler, R; Lin, YC; Petersen, K; Stark, A; Trujillo-Diaz, P; Van Wouwe, N; Zald, D, 2018)
"Early detection of Parkinson's disease (PD), as a dangerous neurodegenerative disease, is a key factor in the therapy or prevention of further development of this disease."( Aghili, Z; Divsalar, A; Nasirizadeh, N; Shoeibi, S; Yaghmaei, P, 2018)
"All current treatments of Parkinson's disease (PD) focus on enhancing the dopaminergic effects and providing symptomatic relief; however, they cannot delay the disease progression."( Azmy, MS; El-Naga, RN; Menze, ET; Tadros, MG, 2018)
"To induce Parkinson's disease-like phenotypes, we treated flies with the pesticide rotenone and isolated dopamine producing neurons of animals that were at an early disease stage."( Bruchhaus, I; El-Kholy, S; Fink, C; Hoffmann, J; Nolte, S; Roeder, T; Stephano, F; von Frieling, J, 2018)
"In a large cohort with Parkinson's disease and early motor complications, better overall behavioural outcomes were noted with bilateral subthalamic stimulation plus medical therapy compared with medical therapy alone."( Brefel-Courbon, C; Chabardès, S; Czernecki, V; Deuschl, G; Durif, F; Elben, S; Hälbig, TD; Houeto, JL; Krack, P; Krüger, R; Kupsch, A; Lhommée, E; Maier, F; Maltête, D; Mehdorn, M; Ory-Magne, F; Pineau, F; Pinsker, M; Rau, J; Regis, JM; Sauvaget, A; Schade-Brittinger, C; Schnitzler, A; Schüpbach, M; Sixel-Döring, F; Thobois, S; Timmermann, L; Tonder, L; Witjas, T; Witt, K; Wojtecki, L, 2018)
"In vivo, Parkinson's disease brain-derived α-synuclein/tau oligomers administered into Htau mouse brains accelerated endogenous tau oligomer formation concurrent with increasing cell loss."( Castillo-Carranza, DL; Gerson, JE; Guerrero-Muñoz, MJ; Kayed, R; Sengupta, U, 2018)
"The most commonly used Parkinson's disease (PD) treatment is the replacement of dopamine by its levodopa precursor (l-dopa)."( Asano, AGC; Asano, NMJ; Crovella, S; da Silva, RC; de Lima, GDC; de Souza, PRE; Dos Anjos, RSG; Dos Santos, EUD; Sampaio, TF, 2018)
"In a model of early-stage Parkinson's disease induced by a single intranasal administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) to Wistar rats, a neuroprotective effect of a new derivative of carnosine and α-lipoic acid (C/LA nanomicellar complex) was demonstrated."( Berezhnoy, DS; Fedorova, TN; Kulikova, OI; Lopachev, AV; Orlova, VS; Stvolinsky, SL, 2018)
"To determine if age and Parkinson's disease duration at therapy initiation influence the efficacy of levodopa-carbidopa intestinal gel (LCIG) on quality of life and activities of daily living."( Antonini, A; Bergmann, L; Poewe, W; Robieson, WZ; Yegin, A, 2018)
"The greatest unmet medical need in Parkinson's disease (PD) is treatments that slow the relentless progression of symptoms."( Brundin, P; Cedarbaum, JM; Sardi, SP, 2018)
"Technological solutions for quantifying Parkinson's disease (PD) symptoms may provide an objective means to track response to treatment, including side effects such as levodopa-induced dyskinesia."( Fox, SH; Li, MH; Mestre, TA; Taati, B, 2018)
"Long-term therapy of Parkinson's disease (PD) with levodopa (L-DOPA) is associated with a high risk of developing motor fluctuations and dyskinesia."( Foki, T; Hitzl, D; Lehrner, J; Novak, K; Pirker, W; Pusswald, G, 2018)
"The 39-item Parkinson's Disease Quality of Life Questionnaire (PDQ-39) is the most widely used self-administered questionnaire assessing the quality of life of Parkinson's disease (PD) patients."( Jamora, RDG; Saranza, GRM; Sumalapao, DEP; Suratos, CTR, 2018)
"Therefore, diagnosis of Parkinson's disease was made and a transdermal rotigotine patch was selected as a treatment."( Hattori, N; Ogawa, T; Oyama, G, 2018)
"The gold standard of treatment in Parkinson's disease (PD) is levodopa/carbidopa whose long-term use induces motor and non-motor fluctuations and dyskinesias."( Allone, C; Bonanno, L; Bramanti, P; Ciurleo, R; Corallo, F; Di Lorenzo, G; Lo Buono, V; Marino, S; Palmeri, R; Versaci, R, 2018)
"Among 657 patients with drug-naïve Parkinson's disease who met the study criteria, 90 were initially treated with dopamine agonists (levodopa-sparing group; levodopa supplementation after 2."( Chung, SJ; Jeong, HE; Kim, JS; Kim, SJ; Lee, HS; Lee, PH; Oh, JS; Sohn, YH; Yoo, HS, 2018)
"Pain in Parkinson's disease (PD) is a debilitating symptom with a prevalence of 68%, yet is untreated 50% of the time."( Akhter, S; Malik, SH; Qureshi, AR; Rana, AQ; Rana, R; Rizvi, SFH; Sarfraz, Z; Vannabouathong, C, 2018)
"This is the first case of Parkinson's disease patient with LCIG therapy by surgical gastrostomy in Japan."( Hirozawa, D; Ikenaka, K; Mochizuki, H; Nakano, T; Sasaki, T; Shimamura, M, 2018)
"The effects of dopaminergic therapy for Parkinson's disease (PD) on the brain functional architecture are still unclear."( Ballarini, T; Bezdicek, O; Jech, R; Mueller, K; Roth, J; Růžička, E; Růžička, F; Schroeter, ML; Villringer, A; Vymazal, J, 2018)
"In patients with Parkinson's disease (PD) treated with DBS of the subthalamic nucleus, we studied the effect of DBS on scanning eye movements."( Hamada, M; Hattori, N; Inomata-Terada, S; Matsuda, SI; Oyama, G; Sasaki, T; Shimo, Y; Terao, Y; Tokushige, SI; Tsuji, S; Ugawa, Y; Umemura, A; Yugeta, A, 2018)
"The greatest unmet therapeutic need in Parkinson's disease (PD) is a treatment that slows the relentless progression of the symptoms and the neurodegenerative process."( Brundin, P; Greenamyre, JT; Sardi, SP; Shihabuddin, LS; Stephenson, D, 2018)
"In 19 patients with Parkinson's disease (PD) and 18 age-matched controls, we found that dopaminergic therapy decreased the efficiency of stimulus-response learning, with corresponding attenuation of ventral striatum (VS) activation."( Ganjavi, H; Hiebert, NM; Jenkins, ME; MacDonald, PA; Mendonça, D; Owen, AM; Seergobin, KN, 2019)
"Treatment efficacy was assessed in 30 Parkinson's disease patients as motor symptoms improvement from unmedicated to medicated state as assessed by the Unified Parkinson's Disease Rating Scale score III."( Albrecht, F; Ballarini, T; Bezdicek, O; Jech, R; Mueller, K; Roth, J; Růžička, E; Růžička, F; Schroeter, ML; Vymazal, J, 2019)
"Patients with Parkinson's disease psychosis (PDP) are often treated with an atypical antipsychotic, especially quetiapine or clozapine, but side effects, lack of sufficient efficacy, or both may motivate a switch to pimavanserin, the first medication approved for management of PDP."( Adler, CH; Alva, G; Black, KJ; Cooney, JW; Isaacson, S; Kremens, D; Menza, MA; Meyer, JM; Morrissette, DA; Nasrallah, H; Pahwa, R; Patkar, AA; Simuni, T; Stacy, M; Stahl, SM, 2018)
"Impulse control disorders (ICDs) in Parkinson's disease (PD) are associated with dopaminergic dysfunction and treatment, but have no satisfactory therapeutic solution."( Ballanger, B; Boulinguez, P; Laurencin, C; Meyer, GM; Sescousse, G; Spay, C, 2019)
"Patients with Parkinson's disease chronically treated with levodopa commonly have delayed or unpredictable onset of its benefits after oral intake."( Batycky, R; Fernandez, HH; Hauser, RA; Isaacson, SH; Lew, M; LeWitt, PA; Lopez-Manzanares, L; Oh, C; Pahwa, R; Pourcher, E; Rudzínska, M; Saint-Hilaire, M; Sedkov, A; Waters, C, 2019)
"Among patients with early Parkinson's disease who were evaluated over the course of 80 weeks, treatment with levodopa in combination with carbidopa had no disease-modifying effect."( Bloem, BR; Boel, JA; de Bie, RMA; de Haan, RJ; Deuschl, G; Dijkgraaf, MGW; Lang, AE; Munts, AG; Post, B; Suwijn, SR; Tissingh, G; van Hilten, JJ; van Laar, T; Verschuur, CVM, 2019)
"Optimizing idiopathic Parkinson's disease treatment is a challenging, multifaceted and continuous process with direct impact on patients' quality of life."( Lees, AJ; Moro, A; Munhoz, RP; Pessoa, RR; Teive, HAG, 2018)
"For the treatment of advanced Parkinson's disease the deep brain stimulation (DBS) and the levodopa/carbidopa intestinal gel (LCIG) therapies are available in Hungary."( Aschermann, Z; Harmat, M; Janszky, J; Juhász, A; Kovács, N; Pintér, D, 2019)
"The treatment of Parkinson's disease remains symptomatic but allows, for many years, a good control of motor and non-motor signs."( Danaila, T; Laurencin, C; Thobois, S, 2018)
"Levodopa treatment does improve Parkinson's disease (PD) dysgraphia, but previous research is not in agreement about which aspects are most responsive."( Arjunan, SP; Kempster, P; Kumar, D; Nagao, KJ; Raghav, S; Viswanthan, R; Wong, K; Zham, P, 2019)
"Few studies have investigated if Parkinson's disease (PD), advancing age, or exogenous dopamine therapy affect the perceived timing of past events."( Goodale, MA; MacDonald, PA; Yabe, Y, 2019)
"Dementia is common in Parkinson's disease (PD), but treatment options are limited."( Cottam, V; Double, KL; Galli, E; Halliday, GM; Lindholm, P; Mathews, KJ; Rappou, E; Saarma, M; Shannon Weickert, C; Virachit, S; Werry, E, 2019)
"He also had advanced Parkinson's disease, treated with several dopamine agonists."( Del Yerro-Alvarez, MJ; Fernandez-Sotos, P; Garcia-Tercero, E; Lopez-Alvarez, J; Lopez-Arcas Calleja, P; Lozano-Vicario, L, 2019)
"In patients suffering from Parkinson's disease for more than 5 years, in 364 cases out of 653 a dopamine agonist was part of the therapy."( Biró, I; Mihály, I; Orbán-Kis, K; Péter, C; Szász, JA; Szatmári, S; Viorelia, C, 2019)
"Current pharmacotherapy of Parkinson's disease (PD) is palliative and unable to modify the progression of neurodegeneration."( Brum Junior, L; Campos, AC; Crippa, JA; Del-Bel, E; Ferreira-Junior, NC; Guimarães, FS; Hallak, JE; Zimmermann, PMDR; Zuardi, AW, 2020)
"The use of levodopa for treatment of Parkinson's disease is a well-established clinical practice."( Bougea, A; Katoulis, A; Spantideas, N; Stefanis, L, 2019)
"CONCLUSIONS SIP was downregulated in Parkinson's disease and it played a protective role in the development Parkinson's disease, thus may be a promising target for Parkinson's disease treatment."( Qu, M, 2019)
"Treatment patterns in Parkinson's disease (PD) have not been extensively studied for nearly two decades."( Boess, F; Constantinovici, N; Ding, Y; Freitas, R; Houghton, R; Ong, R; Verselis, L, 2019)
"LID is associated with Parkinson's disease (PD), emerging as a consequence of chronic therapy with levodopa, and may be either dystonic or choreiform."( Calabresi, P; Standaert, DG, 2019)
"Levodopa is widely used to treat Parkinson's disease (PD), and its long-term therapy may induce dyskinesia in a dose-dependent manner."( Chen, H; Feng, T; Jiang, Y; Liu, G; Ma, H; Su, D; Wang, D; Wang, X; Wang, Z; Yang, Y; Zhang, M, 2020)
"Impulse control disorders (ICDs) in Parkinson's disease (PD) have been associated with cognitive impulsivity and dopaminergic dysfunction and treatment."( Ballanger, B; Boulinguez, P; Cilia, R; Lio, G; Meyer, G; Pezzoli, G; Spay, C, 2019)
"Non-motor symptoms in Parkinson's Disease (PD) predate motor symptoms and substantially decrease quality of life; however, detection, monitoring, and treatments are unavailable for many of these symptoms."( Atashzar, SF; Bernardinis, M; Jog, MS; Patel, RV, 2019)
"Current pharmacological treatments for Parkinson's disease (PD) are focused on symptomatic relief, but not on disease modification, based on the strong belief that PD is caused by irreversible dopaminergic neuronal death."( Cho, IJ; Heo, JY; Huh, SH; Hwang, EM; Hwang, O; Hwang, YJ; Im, H; Jang, BK; Jang, DP; Jeon, SR; Jeong, JY; Jin, BK; Jo, S; Kim, HY; Kim, J; Kim, KI; Kim, S; Kim, Y; Kowall, NW; Kweon, GR; Lee, CJ; Lee, HJ; Lee, J; Lee, JA; Lee, MJ; Lee, SE; Nam, MH; Oh, SJ; Paek, SH; Park, HJ; Park, JH; Park, KD; Ryu, H; Shim, I; Shim, JE; Shin, H; Won, W; Woo, DH; Yoon, HH; Yoon, JH, 2020)
"The unified Parkinson's disease rating scale published by the Movement Disorder Society (MDS-UPDRS) is an validated instrument regularly administrated by trained physician to assess the severity of a PD patient's motor disorder."( Chang, CM; Chen, JC; Huang, YL; Lee, CC, 2019)
"Treatment of Parkinson's disease (PD) through dopamine replacement strategies may provide improvement in early stages and this treatment response is related to dopaminergic neuronal mass which decreases in advanced stages."( Elango, P; Ghanta, MK; L V K S, B, 2020)
"As patients suffering from Parkinson's disease (PD) are more prone to a movement disorder, the quantification of gait characteristics helps in personalizing the treatment."( Aich, S; Chakraborty, S; Jong Seong, S; Joo, MI; Kim, HC; Kim, HT; Kim, IH; Lee, HG; Park, J; Pradhan, PM, 2020)
"Treatment of Parkinson's disease with levodopa/carbidopa/entacapone (LCE) has been studied for a long time."( Li, K; Li, S; Liao, X; Liu, D; Shuai, B; Wu, N, 2020)
"Patients with Parkinson's disease and dementia were randomized to IRL752 or placebo treatment (3:1 ratio) for 28 days."( Bergquist, F; Dizdar, N; Grigoriou, S; Hansson, F; Johansson, A; Nyholm, D; Odin, P; Rinne, J; Sonesson, C; Svenningsson, P; Tedroff, J; Tsitsi, P; Wictorin, K, 2020)
"The 'poster child' for this scenario is Parkinson's disease (PD) medically managed by pharmacological treatments."( Kirby, A; Napier, TC; Persons, AL, 2020)
"Patients with Parkinson's disease and motor fluctuations were treated with opicapone 50 mg for 3 (Germany) or 6 (UK) months in addition to their current levodopa and other antiparkinsonian treatments."( Lees, A; Magalhães, D; Reichmann, H; Rocha, JF; Soares-da-Silva, P, 2020)
"Long-term treatment of Parkinson's disease (PD) by levodopa leads to motor complication "wearing-off"."( Ando-Kanagawa, Y; Cha, PC; Murata, M; Satake, W; Toda, T; Yamamoto, K, 2020)
"Furthermore, in patients with advanced Parkinson's disease receiving levodopa, concomitant rasagiline administration reduced the duration of "wearing-off"."( Hattori, N; Nagai, M, 2020)
"Chronic levodopa treatment in Parkinson's disease (PD) may promote undesirable motor and non-motor fluctuations."( Aracil-Bolaños, I; Bejr-Kasem, H; Calopa, M; Campolongo, A; Crespo-Cuevas, A; de Fàbregues, O; Horta-Barba, A; Izquierdo-Barrionuevo, C; Kulisevsky, J; Marín-Lahoz, J; Martinez-Horta, S; Pagonabarraga, J; Pascual-Sedano, B; Pérez-Pérez, J; Puente, V, 2020)
"Impulse control disorders in Parkinson's disease are common neuropsychiatric complications associated with dopamine replacement therapy."( Baig, F; Drew, DS; Hu, M; Husain, M; Kelly, M; Manohar, S; Muhammed, K; Okai, D; Saleh, Y; Sarangmat, N, 2020)
"Long-term treatment of Parkinson's disease (PD) with levodopa is hampered by motor complications related to the inability of residual nigrostriatal neurons to convert levodopa to dopamine (DA) and use it appropriately."( Blandini, F; Cerri, S, 2020)
"The natural pattern of progression of Parkinson's disease is largely unknown because patients are conventionally followed on treatment."( Akpalu, A; Bonvegna, S; Cereda, E; Cham, M; Cilia, R; Del Sorbo, F; Laryea, R; Obese, V; Oppon, K; Pezzoli, G; Sarfo, FS; Zecchinelli, AL, 2020)
"The treatment of Parkinson's disease (PD) is hampered by the blood-brain barrier (BBB)."( Chen, T; Chen, X; Li, Z; Liu, Y; Luo, J; Wang, Q; Xie, Z; Xiong, S; Zhang, H; Zhang, Y, 2020)
"Alzheimer's disease (AD), Parkinson's disease (PD), and depression are growing burdens for society globally, partly due to a lack of effective treatments."( Cho, J; Do, HTT, 2020)
"Current pharmacotherapy of Parkinson's disease (PD) is symptomatic and palliative, with levodopa/carbidopa therapy remaining the prime treatment, and nevertheless, being unable to modulate the progression of the neurodegeneration."( Behl, T; Brata, R; Bungau, S; Fratila, O; Hassan, SSU; Jhanji, R; Kaur, G; Kumar, A; Mehta, V; Zengin, G, 2020)
"Understanding Parkinson's disease (PD), in particular in its earliest phases, is important for diagnosis and treatment."( Ashrafi, A; Buttini, M; Garcia, P; Glaab, E; Hendrickx, DM; Kaoma, T; Kollmus, H; Nicot, N; Schmit, KJ; Sciortino, A; Vallar, L, 2021)
"The elevated risk of Parkinson's disease in patients with diabetes might be mitigated depending on the type of drugs prescribed to treat diabetes."( Athauda, D; Auld, G; Brauer, R; Foltynie, T; Girges, C; Ma, T; Vijiaratnam, N; Wei, L; Whittlesea, C; Wong, I, 2020)
"Levodopa (L-DOPA) treatment in Parkinson's disease is limited by the emergence of L-DOPA-induced dyskinesia."( Altwal, F; Moon, C; Steiner, H; West, AR, 2020)
"The exact pathogenesis of Parkinson's disease is quite complicated and the present anti-Parkinson's disease treatments appear to be clinically insufficient."( Agarwal, T; He, X; Shen, B; Singla, RK, 2021)
"Neuroinflammation is a hallmark of Parkinson's disease (PD), and we have previously shown that astrocytes in substantia nigra (SN) are enriched in AQP4 relative to cortical astrocytes, and that their complement of AQP4 is further increased following treatment with the parkinsonogenic toxin MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine)."( Amiry-Moghaddam, M; Ottersen, OP; Prydz, A; Skare, Ø; Skauli, N; Stahl, K; Zahl, S, 2020)
"Benserazide is used in the treatment of Parkinson's disease and was noticed to induce gamma globin in preclinical models."( Costa, FF; de Azevedo, PC; Fertrin, KY; Leonardo, DP; Olops, L; Piovesana, LG; Santos, MEHP; Tavares, AHJ; Vendrame, F, 2021)
"The clinical profile of patients with Parkinson's disease is paramount in deciding the most appropriate therapy for the treatment of motor fluctuations."( Alonso-Cánovas, A; Alonso-Frech, FA; Borrue-Fernández, C; Catalán, MJ; En Representación Del Grupo de Trastornos Del Movimiento de la Asociación Madrileña de Neurología, ERDGTDMAMN; Fanjul-Arbós, S; García Ruiz-Espiga, P; García-Cobos, E; García-Ramos, R; Herreros-Rodríguez, J; Kurtis-Urra, M; López-Lozano, JJ; López-Manzanares, L; Martínez-Castrillo, JC; Martínez-Fernández, R; Mata, M; Peña-Llamas, E; Pérez-Sánchez, JR; Posada, IJ; Rodríguez-Sanz, A; Rojo, A; Romero-Muñoz, JP; Ruiz-Huete, C; Sánchez-Alonso, MP; Vivancos-Matellano, F, 2020)
"The clinical diagnosis of Parkinson's disease (PD) requires the presence of parkinsonism and supportive criteria that include a clear and dramatic beneficial response to dopaminergic therapy."( Cairns, NJ; Criswell, S; Davis, AA; Hartlein, J; Kotzbauer, PT; Maiti, B; Martin, WRW; Miles, M; Norris, SA; Perlmutter, JS; Perrin, RJ; Racette, BA; Ushe, M; Zhong, Q, 2021)
"Current therapies for Parkinson's disease (PD) are palliative, of which the levodopa/carbidopa therapy remains the primary choice but is unable to modulate the progression of neurodegeneration."( Behl, T; Buhas, C; Bungau, S; Bustea, C; Fratila, O; Judea-Pusta, CT; Kaur, G; Negrut, N, 2021)
"Neurodegeneration in Parkinson's disease (PD) can be recapitulated in animals by administration of α-synuclein preformed fibrils (PFFs) into the brain."( Adlard, PA; Ayton, S; Bush, AI; Finkelstein, DI; Guiney, SJ; Lei, P; Mawal, CH, 2020)
"There is currently no cure for Parkinson's disease, and the most commonly used treatment, levodopa, only functions as a temporary relief of motor symptoms."( Adolfs, Y; Buijsman, RC; de Man, J; de Wit, J; Gerard Sterrenburg, J; Grobben, Y; Hartog, M; Kraneveld, AD; Muller, M; Pasterkamp, RJ; Perez-Pardo, P; Tutone, M; Uitdehaag, JCM; van Cauter, F; van Doornmalen, AM; Vu-Pham, D; Willemsen-Seegers, N; Zaman, GJR, 2021)
"Amantadine is commonly used to treat Parkinson's disease."( Lee, AJ; Poon, LH; Vuong, M; Zuzuarregui, JR, 2021)
"An 80-year-old man with Parkinson's disease diagnosed in 2015 was started on amantadine for treatment of progressive tremor and orofacial dyskinesias induced by levodopa."( Lee, AJ; Poon, LH; Vuong, M; Zuzuarregui, JR, 2021)
"Dopaminergic therapy is effective in Parkinson's disease (PD), but should be adjusted as neurodegeneration progresses."( Máñez-Miró, JU; Martínez-Martín, P; Vivancos-Matellano, F; Wetmore, J, 2021)
"STATEMENT OF SIGNIFICANCE: Parkinson's Disease remains a common neurodegenerative disease with palliative versus causal treatments."( Bindas, AJ; Koppes, AN; Koppes, RA; Kulkarni, S, 2021)
"Diabetic patients with Parkinson's disease being treated with DPP4 inhibitors had a higher baseline dopamine transporter availability in the anterior (2."( Baik, K; Chung, SJ; Hong, N; Jeong, SH; Jung, JH; Lee, PH; Lee, YH; Sohn, YH; Yoo, HS, 2021)
"Patients diagnosed with idiopathic Parkinson's disease had either daily 30-min treatment with bipolar (±50 V) transcranial pulsed electromagnetic stimulation (squared pulses, 3ms duration) for three eight-week periods separated by one-week pauses (T-PEMF group) (n = 16) or were included in a PD-control group (n = 8)."( Jensen, BR; Malling, ASB; Meyer, M; Morberg, BM; Schmidt, SI; Wermuth, L, 2021)
"Standard treatment of Parkinson's disease involves the dopaminergic medications."( Bonanno, L; Bramanti, P; Cartella, E; Corallo, F; Di Lorenzo, G; Lo Buono, V; Lucà Trombetta, M; Marino, S; Palmeri, R, 2021)
"Current therapeutic approaches for Parkinson's disease (PD) are based around treatments that alleviate symptoms but do not slow or prevent disease progression."( Azeggagh, S; Berwick, DC, 2022)
"The treatment of Parkinson's disease is adversely affected by several factors: the disease progresses relentlessly, the symptoms and rate of progression, other concomitant non-motor symptoms, and the appearance of complications caused by treatment show great heterogeneity."( Nagy, F, 2021)
"In 11 patients with Parkinson's disease (PD) who were using levodopa and had hallucinations and/or delusions considered to be attributed to use of dopamine agonists (DAs), we reduced or discontinued DAs and added zonisamide, and we then evaluated the effects of this treatment on psychiatric and motor symptoms."( Abe, T; Maruyama, H, 2021)
"Dyskinesia is a serious complication of Parkinson's disease during levodopa (L-DOPA) treatment."( Fan, HX; Li, JJ; Li, XX; Sheng, S; Zhang, F; Zheng, CQ, 2021)
"Important exclusion criteria were Parkinson's disease dementia, current delirium, and treatment with antipsychotics or drugs that have significant anti-cholinergic side effects."( Bloem, BR; de Bie, RMA; de Haan, RJ; Foncke, EMJ; Munts, AG; Post, B; Schmand, BA; Tissingh, G; van Harten, B; van Mierlo, TJM, 2021)
"Some patients with Parkinson's disease (PD) undergoing levodopa‒carbidopa intestinal gel (LCIG) treatment experience motor fluctuations in the afternoon."( Ando, R; Hosokawa, Y; Miyaue, N; Nagai, M; Tada, S; Yabe, H; Yamanishi, Y; Yoshida, A, 2021)
"Levodopa remains the gold-standard Parkinson's disease (PD) treatment, but the inevitable development of motor complications has led to intense activity in pursuit of its optimal delivery."( Ferreira, JJ; Jenner, P; Rascol, O; Rocha, JF; Soares-da-Silva, P, 2021)
"Current treatments for Parkinson's disease (PD) provide only symptomatic relief, with no disease-modifying therapies identified to date."( Brundin, P; Burbulla, LF; Jiang, W; Johnson, ME; Krainc, D; Song, P; Zheng, J, 2021)
"Most treatments for Parkinson's disease (PD) focus on improving the symptoms and the dopaminergic effects; nevertheless, they cannot delay the disease progression."( Habib, CN; Masoud, SI; Menze, ET; Mohamed, MR; Tadros, MG; Tolba, MF, 2022)
"A 57-year-old male with Parkinson's disease was experiencing worsening tremors and vivid hallucinations despite therapy optimization attempts."( Amin, N; Hanna, A; Matos, A; Michaud, V; Pizzolato, K; Thacker, D; Toro-Pagán, ND; Turgeon, J, 2021)
"The treatment of Parkinson's disease (PD), the second most common neurodegenerative human disorder, continues to be symptomatic."( Díaz-de-Villegas, MD; Gálvez, JA; José Galano-Frutos, J; Mahía, A; Navarro, S; Pallarés, I; Peña-Díaz, S; Pujols, J; Sancho, J; Ventura, S, 2021)
"A 59-year-old man with advanced Parkinson's disease treated using levodopa-carbidopa intestinal gel (LCIG) presented with leg edema, hypoalbuminemia, and proteinuria at 1 year after the treatment."( Ito, E; Sugiura, Y; Tokimura, R; Ugawa, Y, 2022)
"The treatment of Parkinson's disease (PD) has been hindered by the complex pathologies and multiple membrane barriers during drug delivery."( Hao, Q; Ji, W; Li, Y; Lu, Z; Peng, H; Shen, J; Wang, J; Wang, W; Wu, Y; Yang, J; Zhang, X; Zhao, R, 2022)
"Marketed drugs for Parkinson's disease (PD) treat disease motor symptoms but are ineffective in stopping or slowing disease progression."( Bernardini, R; Burgaletto, C; Cantarella, G; Carboni, E; Cardia, MC; Carta, AR; Casu, MA; Coroneo, V; De Simone, A; Ena, A; Etzi, M; Fusco, G; Greig, NH; Lai, F; Palmas, MF; Picci, L; Pisanu, A; Scerba, MT; Tweedie, D, 2022)
"Treatment of Parkinson's disease (PD), the second most prevalent neurodegenerative disorder, is currently considered a challenging issue since it causes substantial disability, poor quality of life, and mortality."( Azizi, G; Hossein-Khannazer, N; Mousavi, MA; Salahi, S; Vosough, M, 2022)
"The treatment of Parkinson's disease (PD) has not been consistently modified for more than 60 years."( Di Battista, V; Hey-Hawkins, E, 2022)
"Animal models of Parkinson's disease are useful to evaluate new treatments and to elucidate the etiology of the disease."( Avendaño-Estrada, A; Ávila-Rodríguez, MA; Verdugo-Díaz, L, 2022)
"Animal models of Parkinson's disease were built according to MPTP administration."( Ma, Y; Rong, Q, 2022)
"The drug indication is for Parkinson's disease as an adjunct therapy to levodopa/carbidopa."( Habet, S, 2022)
"Patients with Parkinson's disease (PD) often experience motor fluctuations (reduced and variable response to medication) following prolonged treatment with levodopa, which is currently the most effective treatment for the symptoms of PD."( Carroll, C; Chaudhuri, KR; Evans, J; Foltynie, T; Lees, A; Pavese, N; Reichmann, H; Schofield, C; Sharma, JC; Soares-da-Silva, P; Zurowska, L, 2022)
"This article selects Parkinson's disease patients from the provincial hospital to conduct investigations and group experiments on these people to test the effects of different levels of ropinirole hydrochloride in the treatment of Parkinson's disease."( Chen, Y; Gao, X; Kong, Q; Zhang, J, 2022)
"With the progression of Parkinson's disease (PD), pulsatile treatment with oral levodopa causes maladaptive changes within basal ganglia-thalamo-cortical circuits, which are clinically expressed as motor fluctuations and dyskinesias."( Flisar, D; Kojović, M; Kolmančič, K; Kramberger, MG; Pirtošek, Z; Trošt, M; Zupančič, NK, 2022)
"Dementia is a common feature in Parkinson's disease (PD); however, data on dementia treatment patterns in patients with PD are scarce."( Kim, HJ; Yoon, B, 2022)
"A 58-year-old man, diagnosed with Parkinson's disease, treated for six months with levodopa-carbidopa intestinal gel, administered through a percutaneous endoscopic gastrostomy (PEG) tube with jejunal extension, presented at the emergency department for abdominal pain."( García-Cano Lizcano, J; Gil Rojas, S; González Martínez, F; López Moreno, MB; Martínez Blanco, P; Olcina Domínguez, P, 2022)
"12 advanced Parkinson's disease patients on intrajejunal levodopa therapy who were additionally treated with overnight rotigotine transdermal patch (mean dose 5."( Ann Natividad, J; Chaudhuri, KR; Chung-Faye, G; Lau, YH; Leta, V; Metta, V; Parry, M; Rukavina, K, 2022)
"Levodopa is the standard treatment for Parkinson's disease, but its use is marred by the emergence of dyskinesia, for which treatment options remain limited."( Frouni, I; Huot, P, 2022)
"Long-term levodopa therapy for Parkinson's disease (PD) can cause levodopa induced dyskinesia (LID)."( Chaurasia, RN; Dwivedi, A; Dwivedi, N; Joshi, D; Kumar, A; Mishra, VN; Mohanty, S; Pathak, A; Singh, VK, 2023)
"Current treatment of Parkinson's disease (PD) ameliorates symptoms but fails to block disease progression."( Gao, Y; Hong, JS; Hou, L; Li, D; Li, N; Li, S; Liu, J; Tian, L; Tu, D; Wang, Q; Zhang, X; Zhao, J, 2022)
"Introduction: Parkinson's disease is a neurodegenerative disease, the symptoms of which can be treated reasonably well; however, therapeutic recommendations need to be refined based on the observations from everyday practice."( Baróti, B; Constantin, V; Forró, T; Frigy, A; Kelemen, K; Metz, J; Mihály, I; Orbán-Kis, K; Szász, JA; Szász, RM; Szatmári, S; Török, Á, 2022)
"Current treatments for Parkinson's Disease (PD) only provide symptomatic relief; however, they don't delay the disease progression, hence new treatment options should be considered."( Ahmed, HI; Albohy, A; Azab, SS; Kamal, RE; Menze, E, 2022)
"Quality of life (QoL) in patients with Parkinson's disease (PD) is increasingly used as an efficacy outcome in clinical studies of PD to evaluate the impact of treatment from the patient's perspective."( Li, T; Liang, Z; Liu, M; Zhang, Z; Zou, S, 2022)
"Pharmacotherapy in Parkinson's disease decreases the risk for cancers, including breast cancer."( An, X; Bhutia, YD; Chen, H; Chen, R; Chen, Z; Chu, M; Ganapathy, V; Huang, H; Kim, K; Kou, L; Sun, M; Xia, X; Yao, Q; Zhang, H, 2022)
"Advanced Parkinson's disease is characterized by motor and non-motor fluctuations to oral dopamine replacement therapy."( Arlt, C; Ebersbach, G; Eggert, K; Fritz, B; Möller, JC; Schwarz, J; Sensken, SC; Weiss, D, 2022)
"Two groups of patients with Parkinson's disease were included: 20 treated pharmacologically (PHT) and 20 newly qualified for STN-DBS (DBS) - with the first assessment prior to surgery, and the second 11 months after surgery on average."( Koziorowski, D; Marszalek, A; Migda, B; Samborska-Ćwik, J; Szlufik, S, 2022)
"Neurodegenerative diseases such as Parkinson's disease (PD) are known to be related to oxidative stress and neuroinflammation, and thus, modulating neuroinflammation offers a possible means of treating PD-associated pathologies."( Ahn, J; Chang, SC; Ha, NC; Hong, DG; Kim, J; Lee, H; Lee, J; Lee, M; Lee, S; Yang, S, 2022)
"The mainstay of Parkinson's disease treatment has centered around directly manipulating neural mechanisms to retain high dopamine levels, either by exogenous administration, increasing intrinsic production, or inhibiting the breakdown of dopamine."( Arshad, AR; Eqbal, F; Ijaz, F; Imran, L; Jawed, A; Khan, Z; Naeem, U, 2022)
"Early diagnosis of Parkinson's disease (PD) could significantly improve outcomes for patients and future disease-modifying treatments."( Feng, T; Gao, L; Liu, G; Yu, Z; Zheng, Y, 2022)
"Prior work on patients with Parkinson's disease (PD) has shown that the administration of dopaminergic medication in the early to intermediate stages of PD benefits (motor) functions associated with the dopamine-depleted dorsal striatal circuitry but may 'overdose' and interfere with (cognitive) functions associated with the relatively intact ventral striatal circuitry."( Abrahamse, EL; Notebaert, W; Ruitenberg, MFL; Santens, P, 2023)
"The treatment of Parkinson's disease (PD) is still symptomatic since disease-modifying treatments for PD are not available."( Ellmén, J; Kuoppamäki, M; Rouru, J; Sjöstedt, N; Tuunainen, J; Vahteristo, M; Yliperttula, M, 2023)
"The underlying causes of Parkinson's disease are complex, and besides recent advances in elucidating relevant disease mechanisms, no disease-modifying treatments are currently available."( Brüggemann, N; Kunert, L; Pizarro-Galleguillos, BM; Prasuhn, J, 2022)
"The underlying causes of Parkinson's disease are complex, and besides recent advances in elucidating relevant disease mechanisms, no disease-modifying treatments are currently available."( Brüggemann, N; Kunert, L; Pizarro-Galleguillos, BM; Prasuhn, J, 2022)
"The underlying causes of Parkinson's disease are complex, and besides recent advances in elucidating relevant disease mechanisms, no disease-modifying treatments are currently available."( Brüggemann, N; Kunert, L; Pizarro-Galleguillos, BM; Prasuhn, J, 2022)
"In participants with early Parkinson's disease who had never received levodopa and in whom treatment with dopaminergic medications was not planned, deferiprone was associated with worse scores in measures of parkinsonism than those with placebo over a period of 36 weeks."( Ayton, S; Behnke, S; Berg, D; Bloem, BR; Bordet, R; Bush, AI; Cabantchik, I; Carpentier, J; Chupin, M; Coelho, MVS; Compta, Y; Corvol, JC; de Bie, RMA; Defebvre, L; Deplanque, D; Devedjian, JC; Devos, D; Dexter, DT; Dodel, R; Duce, JA; Duhamel, A; Dušek, P; Eusebio, A; Ferreira, J; Fradette, C; Gago, M; Garçon, G; Guyon Delannoy, P; Habert, MO; Januario, C; Kuchcinski, G; Kulisevsky, J; Labreuche, J; Leclercq, C; Lehericy, S; Lopes, R; Maetzler, W; Mangin, JF; Marques, AR; Meissner, WG; Moreau, C; Nyholm, D; Ory-Magne, F; Otto, M; Ouk, T; Pavese, N; Pigny, P; Poewe, W; Post, B; Potey, C; Pruvo, JP; Rascol, O; Rolland, AS; Růžička, E; Scherfler, C; Seppi, K; Simonin, O; Spino, M; Thobois, S; Tranchant, C; Tricta, F; Viard, R; Vilas, D; Walter, U; Worth, P, 2022)
"In participants with early Parkinson's disease who had never received levodopa and in whom treatment with dopaminergic medications was not planned, deferiprone was associated with worse scores in measures of parkinsonism than those with placebo over a period of 36 weeks."( Ayton, S; Behnke, S; Berg, D; Bloem, BR; Bordet, R; Bush, AI; Cabantchik, I; Carpentier, J; Chupin, M; Coelho, MVS; Compta, Y; Corvol, JC; de Bie, RMA; Defebvre, L; Deplanque, D; Devedjian, JC; Devos, D; Dexter, DT; Dodel, R; Duce, JA; Duhamel, A; Dušek, P; Eusebio, A; Ferreira, J; Fradette, C; Gago, M; Garçon, G; Guyon Delannoy, P; Habert, MO; Januario, C; Kuchcinski, G; Kulisevsky, J; Labreuche, J; Leclercq, C; Lehericy, S; Lopes, R; Maetzler, W; Mangin, JF; Marques, AR; Meissner, WG; Moreau, C; Nyholm, D; Ory-Magne, F; Otto, M; Ouk, T; Pavese, N; Pigny, P; Poewe, W; Post, B; Potey, C; Pruvo, JP; Rascol, O; Rolland, AS; Růžička, E; Scherfler, C; Seppi, K; Simonin, O; Spino, M; Thobois, S; Tranchant, C; Tricta, F; Viard, R; Vilas, D; Walter, U; Worth, P, 2022)
"The most commonly used treatment for Parkinson's disease (PD) is levodopa, prescribed in conjunction with carbidopa."( Ko, HS; Kwatra, M; Kwon, DK; Wang, J, 2022)
"The most commonly used treatment for Parkinson's disease (PD) is levodopa, prescribed in conjunction with carbidopa."( Ko, HS; Kwatra, M; Kwon, DK; Wang, J, 2022)
"Immunotherapy in experimental Parkinson's disease (PD) has been shown to be consistently effective in preclinical models, yet the initial clinical trials with monoclonal antibodies (mAbs) yielded marginal results if any."( Benaim, C; Fassler, M; George, J, 2022)
"Immunotherapy in experimental Parkinson's disease (PD) has been shown to be consistently effective in preclinical models, yet the initial clinical trials with monoclonal antibodies (mAbs) yielded marginal results if any."( Benaim, C; Fassler, M; George, J, 2022)
"To compare the groups of Parkinson's Disease (PD) patients who were administered amantadine chronically and those who did not take this medication in the context of the incidence and severity of COVID-19 infection."( Dulski, J; Kasprzak, J; Koziorowski, D; Kwaśniak-Butowska, M; Przytuła, F; Roszmann, A; Schinwelski, M; Śmiłowska, K; Sołtan, W; Sławek, J, 2023)
"To compare the groups of Parkinson's Disease (PD) patients who were administered amantadine chronically and those who did not take this medication in the context of the incidence and severity of COVID-19 infection."( Dulski, J; Kasprzak, J; Koziorowski, D; Kwaśniak-Butowska, M; Przytuła, F; Roszmann, A; Schinwelski, M; Śmiłowska, K; Sołtan, W; Sławek, J, 2023)
"With Parkinson's disease, a total of 70 patients were included in the case-control research which indicates that the newly diagnosed patients are not receiving any treatment at the department of neurology."( Majdal, H; Natheer, M; Taher, Y, 2022)
"Patients with Parkinson's disease, restless legs syndrome and other conditions potentially treated with dopamine agonists, as well as patients treated for psychotic disorders, are vulnerable patient groups with theoretically increased risk of developing gambling disorder (GD), for example due to higher rates of mental ill-health in these groups."( Håkansson, A; Wolfschlag, M, 2023)
"The pathophysiology of Parkinson's disease (PD) tremor remains incompletely understood and there is a lack of clinical trials specifically addressing its pharmacological treatment."( Hallett, M; Katzenschlager, R; Pirker, W; Poewe, W, 2023)
"Levodopa treatment of Parkinson's disease tends to further elevate circulating homocysteine levels due to the metabolism of levodopa via catechol-O-methyltransferase (COMT)."( Ahlskog, JE, 2023)
"The early detection of Parkinson's disease (PD) can significantly improve treatment and quality of life in patients."( Badillo-Ramírez, I; Cialla-May, D; Landeros-Rivera, B; Popp, J; Saniger, JM, 2023)
"Timely referral of Parkinson's disease (PD) patients to specialized centers for treatment with device-aided therapies (DAT) is suboptimal."( Buskens, E; Lunter, G; Moes, HR; Mondria, T; Portman, AT; Ten Kate, JM; van Harten, B; van Kesteren, ME; van Laar, T, 2023)
"Multiplexed detection of Parkinson's disease (PD) biomarkers is of great significance for early diagnosis and personalized treatment."( Cao, X; Chen, M; Ge, S; Mao, H; Wang, Y, 2023)
"L-DOPA is the standard treatment for Parkinson's disease (PD), but chronic treatment typically leads to L-DOPA-induced dyskinesia (LID)."( Bishop, C; Centner, A; Conti Mazza, MM; Werner, DF, 2023)
"Methods: To create a cell model of Parkinson's disease, MPTP (2500 μmol/L) was administered to rat adrenal pheochromocytoma cells (PC-12) to produce an MPTP group."( Liang, L; Liao, C; Meng, F; Qiu, H; Wu, L; Yao, Y; Zheng, W, 2023)
"Rasagiline is indicated for treating idiopathic Parkinson's disease (PD) as monotherapy and adjunct therapy to levodopa in patients."( Cao, S; Chen, H; Hu, X; Liang, Z; Liu, Z; Mao, W; Shao, M; Song, Z; Su, W; Tang, B; Wei, W; Wu, Y; Zhang, K, 2023)
"Many patients with Parkinson's disease (PD) experiencing l-DOPA-induced dyskinesia (LID) receive adjunct treatment with dopamine agonists, whose functional impact on LID is unknown."( Cenci, MA; Espa, E; Grigoriou, S; Jakobsson, A; Odin, P; Timpka, J; von Grothusen, G, 2023)
"In rats with Parkinson's disease induced by rotenone, levels of malondialdehyde and TNF-α significantly increased and HVA levels decreased, whereas in mice treated with lacosamide, levels of malondialdehyde and TNF-α significantly decreased and HVA levels increased."( Bilal, B; Erbas, O; Erdogan, MA; Kirazlar, M; Yigitturk, G, 2023)
"Long-term use of levodopa for Parkinson's disease (PD) treatment is often hindered by development of motor complications, including levodopa-induced dyskinesia (LID)."( Alberico, SL; Ding, Y; Hu, Y; Jin, L; Kang, UJ; Ma, TC, 2023)
"In the advanced Parkinson's disease, motor and non-motor symptoms become more severe and more difficult to treat."( Bar, MR; Borovečki, F; Katzenschlager, R; Kovacs, N; LeWitt, PA; Perković, R, 2023)
"However, THA was difficult owing to Parkinson's disease and its treatment side effects, such as wearing-off, dyskinesia, and freezing of the gait, Thus, LCIG was initiated, and improvement in wearing-off and dyskinesia was observed."( Horiba, M; Imamura, A; Kuroyanagi, G; Matsukawa, N; Murakami, H; Sakai, H; Sato, T; Takahashi, A; Ueki, Y; Usami, T, 2023)
"Dopaminergic therapy for Parkinson's disease has revolutionised the treatment of the motor symptoms of the illness."( Jenner, P; Kanda, T; Mori, A, 2023)
"In patients with Parkinson's disease who are in the middle and late stages of the disease, the administration of Resagiline combined with levodopa and benserazide hydrochloride can significantly lower the body's serum Hcy level, significantly raise IGF-1 levels, and significantly improve motor function in patients with Parkinson's disease."( Gao, F; Gao, L; Miao, J; Yang, Y, 2023)
"Non-motor symptoms in Parkinson's disease (PD) are common, difficult to treat, and significantly impair quality of life."( Olsen, AL; Shen, M; Sodders, MJ, 2023)
"One of the treatment strategies for Parkinson's disease involves the use of drugs that aim to increase dopamine levels or simulate the action of dopamine in the brain."( Costa, EV; Costa, RA; Mary, YS; S Al-Otaibi, J; Tananta, VL, 2023)
"The gold-standard treatment for Parkinson's disease is levodopa (L-DOPA), which is taken orally and absorbed intestinally."( Appel-Cresswell, S; Cirstea, MS; Creus-Cuadros, A; Finlay, BB; Lo, C; Neilson, S; Serapio-Palacios, A; Yu, AC, 2023)

Research

Studies (32,738)

TimeframeStudies, This Condition (%)All Conditions %
pre-19905114 (15.62)23.3326
1990's4095 (12.51)12.5806
2000's7150 (21.84)18.1394
2010's10614 (32.42)28.8240
2020's5765 (17.61)9.53
DrugIndicatedRelationship StrengthStudiesTrials
acetylcarnitine0low80
dinitrochlorobenzene0low10
2,3-dihydroxybenzoic acid0medium42
2,3-diphosphoglycerate0low10
protocatechuic acid0low30
3-hydroxyanthranilic acid0low20
3-hydroxykynurenine0low70
acetoacetic acid0medium11
phosphoserine0low150
gamma-aminobutyric acid0medium27410
4-hydroxybenzyl alcohol0low20
4-hydroxybenzaldehyde0low20
4-hydroxybenzoic acid0low10
aminolevulinic acid0low10
5-hydroxytryptophan0medium448
acetic acid0low20
acetaldehyde0low30
acetamide0low10
adenine0low260
agmatine0low30
allantoin0low10
ammonium hydroxide0low30
anthranilic acid0low10
beta-alanine0low20
benzene0low10
benzoic acid0low10
betaine0low30
bromide0low10
1-butanol0low10
butyric acid0low60
carbamates0medium224
carbon monoxide0low110
formic acid0low40
aminooxyacetic acid0low10
carnitine0medium111
catechol0low150
methane0low150
chlordecone0low10
choline0medium617
citric acid, anhydrous0low40
chlorine0medium282
hydrochloric acid0medium62
coumarin0low40
cuminaldehyde0low10
salicylic acid0medium374
gallic acid0low30
octanoic acid0medium73
hydrogen sulfide0low250
nornicotine0low10
3-hydroxybutyric acid0medium131
bupropion0low110
n(1)-methylnicotinamide0low30
guaiacol0low30
methylmalonic acid0low70
n(1)-acetylspermidine0low10
n(g),n(g')-dimethyl-l-arginine0low10
malic acid0low10
3,4-dihydroxyphenylacetic acid0medium2274
dibenzofuran0low10
creatine0medium7914
cytosine0low100
lactic acid0low270
dihydroxyacetone phosphate0low10
dimethyl sulfoxide0low100
ethanolamine0low10
formaldehyde0low130
formamide0low10
hexachlorocyclohexane0low30
glycine0medium1141
glyceric acid0low10
glycerol0medium92
hydrogen carbonate0low60
histamine0low340
homogentisic acid0low10
hydrogen0medium196
hydroquinone0low10
hydroxylamine0low10
imidazole0low30
indoleacetic acid0low20
iodine0medium161
itaconic acid0low20
dihydroxyphenylalanine0medium1,629177
kynurenine0medium421
thioctic acid0medium181
malonic acid0low30
racemethionine0low10
methylmercaptan0low10
pyruvaldehyde0low130
methanol0low70
phytic acid0low40
inositol0low150
melatonin0medium12413
naphthalene0low10
nickel0low50
niacinamide0medium273
niacin0medium111
nitrates0low280
nitroxyl0low10
nitrites0low290
nitrous oxide0low30
1-octanol0low10
4-aminobenzoic acid0low10
palmitic acid0low20
phenanthrene0low10
phenol0low20
phenylacetic acid0low10
phenethylamine0low110
phosphorylcholine0low40
phosphorylethanolamine0low20
pqq cofactor0low40
1-propanol0medium155
propionic acid0low20
pteridines0low130
purine0low30
putrescine0medium61
pyrazinamide0low10
pyrazole0low20
pyridine0low40
pyridoxal phosphate0medium122
pyridoxine0medium804
pyrogallol0low10
pyruvic acid0low160
quinolinic acid0low210
dimethyl sulfide0low10
thiosulfates0low10
dithionite0low10
sarcosine0medium41
sulfites0low60
spermidine0medium81
spermine0medium41
succinic acid0low10
sulfur dioxide0low10
taurine0medium161
thiamine0low90
thymine0low100
toluene0low20
trimethyloxamine0low40
tryptamine0low10
tungstic(vi) acid0low10
uracil0low10
uric acid0medium16210
urea0medium838
vanillin0low20
xanthine0low80
isocitric acid0low10
2-amino-5-phosphonovalerate0low60
sk&f 812970low30
7-hydroxy-2-n,n-dipropylaminotetralin0low50
8-hydroxy-2-(di-n-propylamino)tetralin0low150
alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid0low100
sk&f 829580low50
3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid0low20
4-iodo-2,5-dimethoxyphenylisopropylamine0low30
1-hydroxy-3-amino-2-pyrrolidone0low20
ibotenic acid0low80
normetanephrine0medium61
sk&f 774340low10
sk&f-383930medium281
vanilmandelic acid0medium253
huperzine a0low10
(alpha-carboxycyclopropyl)glycine0low10
4-carboxy-3-hydroxyphenylglycine0low10
1,3-dipropyl-8-cyclopentylxanthine0low20
pk 111950medium91
1-anilino-8-naphthalenesulfonate0low80
1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine0medium9835
14,15-epoxy-5,8,11-eicosatrienoic acid0low10
n-(3-(aminomethyl)benzyl)acetamidine0low20
2,4-dichlorophenoxyacetic acid0low10
2,4-dinitrophenol0low30
mercaptoethanol0low10
monomethylpropion0low10
3,4-methylenedioxyamphetamine0low20
n-methyl-3,4-methylenedioxyamphetamine0low120
amitrole0low10
3-aminobenzamide0low20
tramiprosate0medium11
3-hydroxybenzylhydrazine0low10
3-methoxytyramine0low110
3-methoxytyrosine0medium6122
3-nitropropionic acid0low50
4-aminopyridine0medium61
homovanillic acid0medium33322
3-hydroxy-4-methoxyphenethylamine0low10
4-nonylphenol0low10
5,5-dimethyl-1-pyrroline-1-oxide0low20
phenytoin0low110
5,7-dichlorokynurenic acid0low10
hydroxyindoleacetic acid0medium19316
5-methoxytryptamine0low20
7-nitroindazole0low130
oxyquinoline0low10
tacrine0medium142
acetaminophen0medium162
acetazolamide0low30
acetohydroxamic acid0low10
acetyl-dl-leucine0low10
adrenic acid0low10
albendazole0medium21
albuterol0medium61
alfuzosin0low10
alpha-methyltyrosine methyl ester0low20
alprenolol0low20
am 2510low30
amantadine0medium641122
ambroxol0medium162
pimagedine0low10
theophylline0medium152
amiodarone0low30
amitriptyline0medium233
amlodipine0low20
amobarbital0low90
amodiaquine0low10
aniracetam0low10
antipyrine0low10
2-amino-4-phosphonobutyric acid0low30
acetovanillone0low70
aristolochic acid i0low20
aspirin0low240
astemizole0low10
atenolol0low20
atrazine0low30
azathioprine0medium51
azepexole0low10
baclofen0medium93
benextramine0low10
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c.i. direct blue 10low10
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nicergoline0low20
oxcarbazepine0low20
toloxatone0low50
2-aminotetralin0low10
s-adenosylmethionine0low50
zidovudine0low20
acetylgalactosamine0low20
5,7-dihydroxytryptamine0low60
paclitaxel0low90
etoposide0low20
substance p0low590
dobutamine0low20
norsalsolinol0low30
n,n'-bis(2-hydroxybenzyl)ethylenediamine-n,n'-diacetic acid0low10
2-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline0low60
amikacin0low10
phorbol 12,13-dibutyrate0low20
2,3,4,2',3',4'-hexachlorobiphenyl0low10
agent orange0low10
pendimethalin0low10
methyldopa0medium9715
sq-117250medium32
diltiazem0low10
1-methyl-4-phenylpyridinium0medium3241
n-acetyl-4-benzoquinoneimine0low10
vecuronium bromide0low10
ng-nitroarginine methyl ester0low70
permethrin0low50
exifone0medium11
chlorodiphenyl (54% chlorine)0low10
quisqualic acid0low10
decamethrin0low10
6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid0low60
nitazoxanide0low10
sufentanil0low10
eg 6260low10
desflurane0low30
enkephalin, methionine0low280
dihydroalprenolol0low20
propiconazole0medium42
paroxetine0medium248
captopril0low10
progabide0medium72
brofaromine0low10
salsoline0low200
pergolide0medium28054
colforsin0low140
agreal0low30
fluperlapine0medium21
alfentanil0low10
fomesafen0medium25113
fenoxycarb0low50
miglustat0low30
lovastatin0medium61
flupirtine0medium21
milacemide0medium21
simvastatin0medium164
idazoxan0medium112
remoxipride0medium51
quinpirole0low370
pravastatin0low10
cabergoline0medium13731
atomoxetine hydrochloride0medium158
alpidem0low10
raloxifene hydrochloride0low10
mifepristone0low40
itraconazole0medium31
spiradoline0medium11
ractopamine0low10
fluorodopa f 180medium20621
eticlopride0low10
finasteride0low20
mk 4580medium51
naxagolide0medium172
cy 208-2430medium52
n 0437, (-)-isomer0medium16151
remacemide0medium43
clopidogrel0low10
mibefradil0low10
eliprodil0low10
aripiprazole0low180
sipatrigine0low10
remifentanil0medium101
atorvastatin0low20
duloxetine hydrochloride0medium83
ziprasidone0medium91
zolmitriptan0low10
3-iodobenzylguanidine0medium20216
simendan0low10
capecitabine0low10
adenosine0medium711
safranal0low10
3-n-butylphthalide0low80
4-propionyloxy-4-phenyl-n-methylpiperidine0low10
vanadates0low10
trifluoromethanesulfonic acid0low10
isothiocyanic acid0low10
venlafaxine hydrochloride0medium72
trazodone hydrochloride0low10
hydrochlorothiazide-triamterene0low10
aluminum phosphate0low10
glucose, (beta-d)-isomer0low250
3,4-dihydro-2(1h)-quinolinone0low10
2-amino-3-phenylbutanoic acid0low10
ursolic acid0low30
n-methylnicotinamide0low20
norharman0low40
thiazolyl blue0low150
betulinic acid0low20
arctigenin0low20
baicalin0low30
oseltamivir0low10
5-methylcytosine0low40
epigallocatechin gallate0low320
n-acetylaspartic acid0medium506
5-dimethylaminonaphthalene-1-sulfonamide0low10
fluorexon0low40
gallocatechol0low10
aica ribonucleotide0low10
salvin0low30
metaperiodate0low10
xanthyletine0low10
lissamine rhodamine b sulfonyl chloride0low10
n,n-bis(trimethylsilyl)-2,2,2-trifluoroacetamide0low10
peroxynitric acid0low110
glutathione disulfide0low240
metamizil0low10
diethazine0low10
cephalosporin c0low10
tenilsetam0low10
tretoquinol0low10
prodipin0medium11
milnacipran0low10
eltoprazine0medium71
fce 238840medium11
repaglinide0low10
telmisartan0low10
xenon radioisotopes0low110
naphthalimides0low10
16-fluoroestradiol0medium11
1,7-phenanthroline0low20
triazoles0medium438
tangeretin0low50
isoimperatorin0low10
1-hexacosanol0low10
chloroethylaminouracil0low40
delphinidin0low20
n,n-carbonyldiimidazole0low10
hordenine0low20
1-octacosanol0medium11
setoperone0low10
fluorodeoxyglucose f180medium29414
sertraline0medium156
oxiperomide0medium21
rilmenidine0low10
ropinirole hydrochloride0low10
budipine0medium189
delta sleep-inducing peptide0low10
etisulergine0medium31
mesulergine0medium288
tianeptine0medium21
2,4-dihydroxyphenylacetic acid0low10
1-hydroxy-2(1h)-pyridinone0low10
2,2'-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride0low10
5-hydroxymethylcytosine0low30
bicinchoninic acid0low10
acamprosate0low10
n-methylscopolamine0low10
cromakalim0low10
lazabemide0medium123
atipamezole0low10
dexrazoxane0low10
masoprocol0low30
trichlorosucrose0low10
naftazone0medium22
bufuralol0low10
amezinium0low10
nipradilol0low10
bamipine0low10
terlipressin0medium11
hesperetin0low20
methotrimeprazine0low10
magnolol0low10
honokiol0low20
sesamin0low30
betulin0low10
nobiletin0low40
lycorine0low10
squalamine0low20
beta-amyrin0low10
alpha-amyrin0low10
Tormentic acid0low10
nicosulfuron0low10
isoalantolactone0low10
calpeptin0low10
gliclazide0low10
bilobalide0low10
maslinic acid0low10
oxazolidin-2-one0low30
ceric oxide0low30
methylimidazoleacetic acid0low10
2-aminoindan0low10
enpiperate0low20
rivastigmine0medium8224
rosiglitazone0low40
erucin0low20
propylsulfonic acid0low10
tricine0low10
3,7-dimethyl-7-octen-1-ol0low20
leucyl-alanine0low10
bexarotene0low10
s200980low30
8-(4-tolylsulfonylamino)quinoline0low10
4-phenyl-1,2,3,6-tetrahydropyridine0low90
3,4-dihydroxyphenylethanol0low130
biocytin0low20
clarithromycin0medium33
epidepride0medium42
sdds0low10
coenzyme a0low20
manganese sulfide0low10
2,3,6-trimethyl-1,4-naphthoquinone0low20
dihydroisotanshinone i0low10
nicotine0medium12511
fibrinogen0low130
tandospirone0medium11
aucubin0low10
2-tyrosine0low10
cadmium telluride0low30
3,4-dihydroxyphenylglycol0medium171
homocysteine0medium15121
salsolinol0medium373
5-(3-hydroxyphenyl)-5-phenylhydantoin0low10
pyridaben0low30
1-methyl-4-(2'-methylphenyl)-1,2,3,6-tetrahydropyridine0low40
1-methyl-1,2,3,4-tetrahydroisoquinoline0low80
7-amino-4-methylcoumarin0low10
melamine phosphate0low10
gamma-tocopherol0medium11
5-alpha-dihydroprogesterone0low10
21-deoxycortisol0low10
indole-3-lactic acid0low10
dextromoramide0low10
droxidopa0medium7011
glycidic acid0low10
5-Methoxyflavone0low10
glucuronic acid0low50
2-methyl-1,2,3,4-tetrahydroquinoline0low10
benzothiazoline0low10
atherospermine0low10
1,3,4-oxadiazole0low10
daq0low10
1,2,3,4-tetrahydro-1-(phenylmethyl)isoquinoline0low70
diosgenin0low40
1,2,3,4-tetrahydro-1-phenylisoquinoline0low20
fangchinoline0low10
n-acetyldopamine0low10
karanjin0low10
beta-(4-fluorobenzoyl)propionic acid0low10
berbine0low10
sesamolin0low10
n-methyladenosine0low40
phenglutarimide0low20
cobalt0low40
hydrogen sulfite0low20
1,2-bis(2-aminophenoxy)ethane-n,n,n',n'-tetraacetic acid0low10
1-amino-1,3-dicarboxycyclopentane0low10
carbidopa, levodopa drug combination0medium494113
tert-butylbicyclophosphorothionate0low10
arginyl-glycyl-aspartic acid0low10
vitamin b 60medium261
1,4-dihydropyridine0low20
sr1417160low50
s-nitrosoglutathione0low20
u 74006f0medium21
diacetyldichlorofluorescein0low20
u 74389f0low10
propidium iodide0low20
laurdan0low10
fructose 2,6-diphosphate0low10
cyanates0low20
3,4-methylenedioxyethamphetamine0low10
(3h)2-carbomethoxy-3-(4-fluorophenyl)tropane0medium374
deoxypyridinoline0medium11
epibatidine0low30
beta-n-methylamino-l-alanine0low140
s-ethyl glutathione0low20
u 78517f0low10
4-hydroxydebrisoquin0low20
3-((3-cholamidopropyl)dimethylammonium)-1-propanesulfonate0medium11
cgp 353480low10
1,1'-ethylidene bis(tryptophan)0low10
altertoxin ii0low10
saikosaponin d0low10
6-hydroxydopa0low70
perindopril0medium21
tryptoline0low20
geniposide0low40
procyanidin0low50
sr 955310low10
dityrosine0low60
epicatechin gallate0low20
4-desmethoxyverapamil0low10
ecopipam0medium11
deguelin0low10
fingolimod hydrochloride0low60
triptolide0low40
3-iodo-2-hydroxy-6-methoxy-n-((1-ethyl-2-pyrrolidinyl)methyl)benzamide0medium548
3,5-dihydroxyphenylglycine0low10
cobaltiprotoporphyrin0low10
n-acetylsulfamethazine0low10
alpha-(4-fluorophenyl)-4-(5-fluoro-2-pyrimidinyl)-1-piperazine butanol0low20
cafestol0low30
proanthocyanidin0low10
parthenolide0low10
tryptoquivaline0low10
dynorphin (1-8)0low10
senktide0low10
kt 58230low10
1-hexadecyl-2-acetyl-glycero-3-phosphocholine0low10
deoxyglucose0low510
tadalafil0low10
3-chloro-L-tyrosine0low10
anserine0low10
5,6-dihydroxyindole0low30
1-phenyl-2-decanoylamino-3-morpholino-1-propanol0low10
5-hydroxydopamine0low50
kahweol0low20
valerates0medium31
n-n-propyl-n-phenylethyl-4(3-hydroxyphenyl)ethylamine hydrochloride0low10
monochlorobimane0low10
tanshinone0low30
protoberberine0low10
gastrodin0low40
tyrosyl-prolyl-leucyl-glycinamide0low10
way 1001350low10
ponasterone a0low10
brassinolide0low10
3,5-dibromo-4-nitrosobenzenesulfonate0low10
ginkgolide a0low10
asiatic acid0low10
3-n-methylspiperone0low90
al-015670low10
efonidipine0low10
1-trichloromethyl-1,2,3,4-tetrahydro-beta-carboline0low50
1-o-hexyl-2,3,5-trimethylhydroquinone0low10
3,4-dihydroxyphenylacetaldehyde0low370
dioscin0low30
astilbin0low10
sch 239820low10
afdx 3840low10
gr 1138080low10
3-methyl-5-(1-methyl-2-pyrrolidinyl)isoxazole0low10
nitroflurbiprofen0low10
caprylates0medium124
5,6-dihydroxy-2-indolylcarboxylic acid0low10
pramipexole0medium38984
mosapride0medium22
pentosidine0low20
carboxypolymethylene0low10
yohimbane0low10
2-hydroxydesipramine0medium11
razadyne0low20
ezogabine0low20
2-methyltryptoline0low20
5-fluorodopa0low110
ly 1340460low10
sr 278970medium11
5-s-cysteinyldopamine0low110
soyasaponin bb0low10
dopamine 3-o-sulfate0low20
1-(4-methoxyphenyl)pyridinium0low10
2-(n,n-dipropyl)amino-5,6-dihydroxytetralin0low20
rti 1210low10
kallidin, des-arg(10)-0low10
2-formyl-5-(hydroxymethyl)pyrrole-1-norleucine0low10
5-fluorodopamine0low120
3-quinuclidinyl-4-iodobenzilate0low10
emoxypine succinate0low10
florox reagent0low10
a 689300low10
astragaloside a0low50
celastrol0low80
bruceine d0low10
gu 70low10
peroxynitrous acid0low230
1-aminoindan0low10
fullerene c600low20
imatinib mesylate0low20
dimyristoylphosphatidylserine0low10
cdp ethanolamine0low10
kf 17837s0low20
norketamine0low10
enkephalin-met, arg(6)-gly(7)-leu(8)-0low20
n(6)-carboxymethyllysine0low10
angiotensin ii, des-phe(8)-0low10
2-chloro-n(6)cyclopentyladenosine0low10
ro 8-05760medium12146
heliox0low10
angiotensin ii, des-asp(1)-des-arg(2)-ile(5)-0low20
n,n-dimethylarginine0low10
dihydrotetrabenazine0low440
3-(2,2,2-trimethylhydrazine)propionate0low10
4-iodoamphetamine0low20
1-((3,5-dichloro)-2,6-dihydroxy-4-methoxyphenyl)-1-hexanone0low50
head activator peptide0low10
4-(alpha-(4-allyl-2,5-dimethyl-1-piperazinyl)-3-methoxybenzyl)-n,n-diethylbenzamide0low10
dopamine 4-o-sulfate0low10
naadp0low30
27-hydroxycholesterol0low50
tyrosyl-isoleucyl-glycyl-seryl-arginine0low10
tetrahydrocurcumin0low20
1,2-dimethyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline0low10
skullcapflavone ii0low10
1,4,7-triazacyclononane-n,n',n''-triacetic acid0medium11
n(g)-aminoarginine0low10
n-methyl-1-(1,3-benzodioxol-5-yl)-2-butanamine0low10
glycerophosphoinositol 4,5-bisphosphate0low40
rti-coc 320medium11
cyclo(prolylglycyl)0low10
indatraline0low10
pre 0840low30
4-(2-amino-6-chloro-9h-purin-9-yl)-1,3-dioxolane-2-methanol0low10
methotrexate0low40
reboxetine0medium51
6-fluoro-3-tyrosine0low40
11-hydroxy-n-(n-propyl)noraporphine0low10
fpl 67047xx0low10
2'-iodospiperone0low10
delphinidin0low10
cyanidin0low10
3-n-(2-fluoroethyl)spiperone0low20
tamsulosin0low20
2-fluorodopa0low10
5,5'-dihydroxy-4,4'-bitryptamine0low10
n-isobutyrylcysteine0low10
nnc 1120low10
alpha-n-carboxy-beta-n-methylaminoalanine0low10
buthionine sulfoximine ethyl ester0low10
n-(3-phenyl-n-propyl)-1-phenyl-2-aminopropane0low10
safinamide0medium10423
4-amino-1-(6-chloro-2-pyridyl)piperidine hydrochloride0low30
n-nor-3-(4'-iodophenyl)tropane-2-carboxylic acid methyl ester0low10
odapipam0medium11
l 6903300low10
5-(2,3,5-trichlorophenyl)pyrimidine-2,4-diamine ethane sulfonate0low10
omega-n-methylarginine0low10
fim 10low10
l 7417420low10
sonepiprazole0low10
n-methylpiperidin-4-yl propionate0low10
ciladopa0medium83
sk&f 839590low10
febuxostat0medium11
lanthionine ketimine0low10
alpha-ergocryptine0low10
pomalidomide0low10
sk&f 100330-a0low10
xylose0low30
proline0low320
escitalopram0medium22
1-(1,3-benzodioxol-5-yl)-3-(1-piperidinyl)-1-propanone0low10
docetaxel0low10
bdp 120low10
1-methyl-4-phenyl-2,3-dihydropyridinium0low30
2,3-dihydro-1,4-benzothiazine0low10
threonic acid0low10
s-carbamylcysteine0low10
1-methyl-4-piperidyl acetate0medium11
3,4-dihydroxyphenylglycolaldehyde0low10
4-methylthioamphetamine0low10
phenyl di-n-pentylphosphinate0low10
moxifloxacin0medium22
mn(iii) 5,10,15,20-tetrakis(n-methylpyridinium-2-yl)porphyrin0low10
hyoscyamine0low10
tomentosin0low10
n-methyl-n-propargyl-(1-indanyl)-ammonium hydrochloride0low10
varespladib0low10
besonprodil0low10
ym 09151-20low40
naproxen0low10
hydroxyl radical0medium433
lubiprostone0medium31
rhodioloside0low30
adenosine 3'-phosphate-5'-phosphate0low10
tripchlorolide0low20
amotosalen0low10
resiquimod0low10
tetrahydroharmine0low10
singlet oxygen0low10
cryptotanshinone0low30
fenton's reagent0low20
8-(4-benzenesulfonylamino)quinoline0low10
chelirubine0low10
stephenanthrine0low10
ampelopsin0low70
2,9-dimethyl-beta-carbolinium0low20
dopamine quinone0low210
sclareol0low10
schizandrer a0low20
1-methyl-1,2-diphenylethylamine monohydrochloride0low10
cyclophellitol0low10
4-trifluoromethylsalicylic acid0low10
hydromethylthionine0low10
9-methyl-beta-carboline0low10
anacardic acid0low10
peiminine0low10
nardosinone0low10
boswellic acid0low10
6-aminodopamine0low20
aminochrome 10low170
etilevodopa0medium11
varenicline0low50
isopulegol0low10
biotin0low60
angiotensin ii0low160
5-hydroxy-2-n,n-dipropylaminotetralin0low20
methyl 4-azidophenylacetimidate0low10
4-chlorokynurenine0low10
a 690240low10
atropine0medium381
vasobral0low10
3-o-methyl-6-fluoro-dopa0low80
ml 230low20
sb 2035800low90
sb 2167630low10
zm 2413850low50
sch 582610low60
piboserod0low10
homocysteic acid0low10
limonin0low10
gvs 1110low10
iodoaminopotentidine0low10
psyllium0medium41
cyperin0low10
scutellarin0low10
aflatoxin b10low10
esculentin steroid0low10
isospaglumic acid0low20
bd 10470low20
ngd 94-10low10
carbocysteine0low30
2,6-difluoro-3,4-dihydroxyphenylalanine0low10
g(m1)-oligosaccharide0low10
1,3-dimethyl-2-((2-oxopropyl)thio)imidazolium0low10
latrepirdine0low20
tropatepine0low30
desmethylselegiline0medium52
anabasine0low10
ramelteon0medium41
tv33260low20
lapatinib0low10
fipamezole0medium11
eglumetad0low30
deferasirox0low10
dabigatran0low20
sorafenib0low10
lenalidomide0low10
solifenacin succinate0medium31
regadenoson0low10
roxindole0medium11
lacosamide0low10
cp 101,6060low10
demecolcine0low10
brazilin0low10
deoxycholic acid0low10
estradiol 3-benzoate0low20
cortisone0low10
2-aminoquinoxaline0low10
(R)-Roemerine0low10
3-nitrotyrosine0low240
propargylamine0low110
1',2'-dihydrorotenone0low10
benzofurans0medium252
calendula0low10
gardenin a0low10
withaferin a0low30
wortmannin0low10
withanolides0low40
trimethoprim, sulfamethoxazole drug combination0low20
taurochenodeoxycholic acid0low60
bortezomib0low10
calcein am0low10
acetogenins0low10
dihydropyridines0low110
nsc 1415370low10
leupeptins0low350
carboplatin0low30
lithium chloride0low40
schisanhenol0low10
s-adenosylhomocysteine0medium71
glycogen0low70
n-acetylneuraminic acid0low30
fibrin0low40
bradykinin0medium81
canavanine0low30
glucosamine0low10
carnosine0medium141
mevalonic acid0low30
naringenin0low80
oxytocin0low40
pantetheine0low10
theanine0low50
3,4-dihydroxyphenyllactic acid0low30
inositol 1,4,5-trisphosphate0low20
cysteinylglycine0medium51
ouabain0low10
monoiodotyrosine0medium21
nicotinamide-beta-riboside0medium32
nitroarginine0low40
cholesteryl glucoside0low10
inositol 3-phosphate0medium331
dehydroascorbic acid0low20
cortodoxone0low10
nivalenol0low10
arbutin0low10
psicose, (d)-isomer0low10
strychnine0low60
quinidine0medium31
meropenem0low10
pentazocine0low10
pancuronium0low10
rocuronium0low10
linezolid0low10
indican0low20
ginsenoside re0low20
ginsenoside rg10low40
farrerol0low10
genipin0low20
naringin0low20
swertiamarin0low10
dendrobine0low10
ochratoxin a0low20
Rhododendrin0low10
securinine0low10
lignans0low130
acetylleucyl-leucyl-norleucinal0low10
n-formylmethionine leucyl-phenylalanine0low10
diprenorphine0low20
sodium arsenite0low10
dironyl0medium154
vinpocetine0low40
betadex0low40
acetyl coenzyme a0low10
ergosterol0low10
trichostatin a0low10
tretinoin0medium231
arachidonic acid0medium201
phosphoramidon0low10
3-hydroxy-3-methylglutaryl-coenzyme a0low10
resveratrol0low260
retinol0low190
latrunculin a0low10
oleic acid0low80
tacrolimus0medium193
ferulic acid0low50
cocaine0medium18322
eicosapentaenoic acid0low30
alpha-methyl-4-carboxyphenylglycine0low10
thapsigargin0low20
mycophenolic acid0low10
clindamycin0low10
lycopene0low50
isofagomine0low40
stigmatellin0low10
t09013170low10
y 276320low50
adenosine-5'-(n-ethylcarboxamide)0low10
prostaglandin d20low40
diethylstilbestrol0low10
roflumilast0low20
h 890low10
afimoxifene0low10
imidazolidines0low10
decitabine0low20
pantethine0low10
iridoids0low80
wr-142,4900low10
dactinomycin0low20
aphidicolin0low10
enkephalin, leucine0medium601
benzyloxycarbonylleucyl-leucyl-leucine aldehyde0low350
schizandrin0low10
shikonin0low10
mg 2620low10
riboflavin0low60
sodium benzoate0low10
norlevorphanol0low30
bromochloroacetic acid0low10
11-mercaptoundecanoic acid0low10
amiridine0low10
carbenoxolone sodium0low10
alpha-asarone0low30
camalexin0low10
cinnamaldehyde0low10
trans-4-coumaric acid0low20
anethole0low30
geraniol0low50
dimethyl fumarate0low30
glycosides0low120
chalcone0low30
isomethyleugenol0medium582
piperine0low60
squalene0low10
stilbenes0low220
diethyl fumarate0low10
2'-hydroxychalcone0low10
isoliquiritigenin0low20
ilepcimide0low10
flavin-adenine dinucleotide0low10
cannabidiol0medium274
lypressin0medium11
arginine vasopressin0medium101
pyrophosphate0low20
gw96620low10
s 10330medium175
acetyl-aspartyl-glutamyl-valyl-aspartal0low30
polidocanol0low10
tropisetron0low10
sodium metabisulfite0low20
isopropyl thiogalactoside0low10
leuprolide0low10
propylthiouracil0low20
nsc 43470low10
sesquiterpenes0low70
chlorprothixene0low40
etomidate0low10
dexketoprofen0low10
3,3',4,5'-tetrahydroxystilbene0low20
phenylthiourea0low30
(e)-3-(4-t-butylphenyl)-n-(2,3-dihydrobenzo(b)(1,4)dioxin-6-yl)acrylamide0low10
levosulpiride0low10
caffeic acid0low90
rg1080low10
n-(1,3-benzodioxol-5-ylmethyl)-2,6-dichlorobenzamide0low10
n-(3-chlorophenyl)picolinamide0low20
cotinine0low10
vu 01550410low20
flunarizine0low60
eszopiclone0medium21
dieldrin0low140
curcumin0medium811
benztropine0medium307
nootkatone0low10
3-(1-azepanylsulfonyl)-n-(3-bromphenyl)benzamide0low20
methimazole0low10
urb 5970low40
cinnarizine0medium61
sulindac0low10
capsaicin0medium143
aurapten0low20
n-(4-(n-(3-methoxypyrazin-2-yl)sulfamoyl)phenyl)-3-(5-nitrothiophene-2-yl)acrylamide0low10
chlorogenic acid0low80
thiobarbituric acid0low10
thiourea0low30
D-fructopyranose0medium103
tempo0low10
ferric ferrocyanide0low10
digoxin0medium62
capsazepine0low20
tamoxifen0low130
3-pyridinylboronic acid0low10
nadp0low130
1,1-diphenyl-2-picrylhydrazyl0low10
3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2h-tetrazolium0low10
t 00709070low10
2-(4'-(methylamino)phenyl)-6-hydroxybenzothiazole0low230
sirtinol0low10
methyl-thiohydantoin-tryptophan0low10
1,1-bis(3'-indolyl)-1-(4-hydroxyphenyl)methane0low10
nabam0low10
rhyncophylline0low30
valinomycin0low30
thiopental0low30
ranitidine0low10
u 01260low40
6-methyl-2-(phenylethynyl)pyridine0low170
lithium0medium417
thiamylal0low10
zineb0low10
nitrogen dioxide0low70
maneb0low320
nizatidine0medium21
raclopride0medium8416
quinine0low10
md 2302540low10
(3-iodobenzyl)trozamicol0low10
5-iodo-n-((1-ethyl-2-pyrrolidinyl)methyl)-2,3-dihydrobenzofurancarboxamide0low30
5-o-methyldihydrotetrabenazine0low10
cystine0low80
ly3359790low10
sch 233900low40
bp 8970low10
freedom0low20
prucalopride0low10
azilect0low10
rasagiline0medium26354
dasatinib0low10
oxalylglycine0low10
glycyl-prolyl-glutamic acid0low20
sr 1445280low10
2-fluoro-2-deoxyglucose-6-phosphate0low10
cytellin0low20
silicon nitride0low10
ginsenosides0low80
quinagolide0medium21
2-(4-(2-carboxyethyl)phenethylamino)-5'-n-ethylcarboxamidoadenosine0low70
silybin0low10
phosphothreonine0low30
cambinol0low10
2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline0low30
ovalbumin0medium21
2-phenoxy-N-[5-(5,6,7,8-tetrahydronaphthalen-2-yl)-1,3,4-oxadiazol-2-yl]acetamide0low10
sodium dodecyl sulfate0low170
blister0low10
crocin0low50
dimethyldithiocarbamate0low10
2-chloro-5-hydroxyphenylglycine0low10
flavan-3-ol0low10
6-cyano-7-nitroquinoxaline-2,3-dione0low60
3-(2,4-dichloro-5-methoxyphenyl)-2-sulfanyl-4(3h)-quinazolinone0low10
fg 90410low30
(4-chlorophenyl)-[4-(8-nitro-5-quinolinyl)-1-piperazinyl]methanone0low10
cp 942530low20
alpha-chymotrypsin0low80
4-benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione0low10
17-ketosteroids0low40
naphthoquinones0medium72
4-(5-(4-bromophenyl)-3-(6-methyl-2-oxo-4-phenyl-1,2-dihydroquinolin-3-yl)-4,5-dihydro-1h-pyrazol-1-yl)-4-oxobutanoic acid0low10
am 6300low10
hydroxyethylcellulose0low10
alpha-carotene0low10
osteoprotegerin0medium11
3-(2-hydroxy-4-(1,1-dimethylheptyl)phenyl)-4-(3-hydroxypropyl)cyclohexanol0low20
rhodamine 1230low20
4-cresol sulfate0low10
tolcapone0medium13942
myelin basic protein0low110
tcn 2010low10
N-(1-benzylpiperidin-4-yl)-2-(pyridin-3-yl)quinazolin-4-amine0low10
jnj 77771200low20
ex 5270low10
ro 60-01750low10
ginkgetin0low10
ku 559330low10
sphingosine0low130
quercetin0low270
bilirubin0low210
dinoprostone0low80
dinoprost0low50
biochanin a0low20
sterigmatocystin0low10
vitexin0low10
acacetin0low20
apigenin0low50
luteolin0low20
7,3'-dihydroxy-4'-methoxyisoflavone0low10
linoleic acid0low30
calcitriol0low150
psychosine0low70
scopoletin0low10
vitamin k semiquinone radical0low60
beta carotene0low100
11-cis-retinal0low30
8,11,14-eicosatrienoic acid0low20
alprostadil0medium41
vitamin d 20medium22
stigmasterol0low10
cholecalciferol0medium122
rutin0low50
kaempferol0low50
prostaglandin a20low10
9-deoxy-delta-9-prostaglandin d20low20
alpha-linolenic acid0low20
harmine0medium111
genistein0low50
amphotericin b0low40
montelukast0low40
entacapone0medium24980
erucic acid0low10
nervonic acid0low40
astaxanthine0low90
fucoxanthin0low20
lutein0low50
isobavachalcone0low10
nsc 1063990low10
5,7-dihydroxychromone0low10
mezerein0low10
harman0low40
esculetin0low10
7-hydroxycoumarin0low10
humulene0medium222
oleuropein0low30
garcinol0low40
zearalenone0low20
agathisflavone0low10
amentoflavone0low10
baicalein0low150
chrysin0low40
diosmin0low10
fisetin0low70
galangin0low10
hyperoside0low20
mangiferin0low50
mangostin0low40
morin0low40
myricetin0low20
myricitrin0low40
scutellarein0low10
tricetin0low10
daidzein0low20
echinacoside0low20
caffeic acid phenethyl ester0low20
plantamajoside0low10
rosmarinic acid0low70
salvianolic acid a0low10
acteoside0low40
tectorigenin0low10
rottlerin0low20
ellagic acid0low100
ginkgolic acid0low10
coenzyme q100medium7511
anandamide0low70
arachidonyl dopamine0low10
geranylgeranylacetone0low10
domoic acid0low10
8-epi-prostaglandin f2alpha0low10
glyceryl 2-arachidonate0low40
1-palmitoyl-2-oleoylphosphatidylethanolamine0low10
1-palmitoyl-2-oleoylglycero-3-phosphoglycerol0low10
ro 61-80480low10
tocotrienol, delta0low10
menatetrenone0medium11
cinepazide0low10
4-hydroxy-2-nonenal0low250
n-oleoylethanolamine0low10
1-palmitoyl-2-oleoylglycero-3-phosphoserine0low10
menaquinone 60medium31
sphingosine 1-phosphate0low80
purmorphamine0low10
codeine0low30
phenylephrine hydrochloride0low110
beta-nitrostyrene0low10
diminazene aceturate0low20
levetiracetam0medium82
nabilone0medium43
nalorphine0low10
naloxone0medium296
oxycodone0medium61
proscillaridin0low10
sirolimus0low220
topiramate0medium94
trospium chloride0low20
6,7,4'-trihydroxyisoflavone0low10
brefeldin a0low30
alvocidib0low10
17-(dimethylaminoethylamino)-17-demethoxygeldanamycin0low10
lobeline0low10
morphine0medium201
a 853800low90
3-(2,4-dimethoxybenzylidene)anabaseine0low20
alpha-neoendorphin0low10
arachidonyl-2-chloroethylamide0low20
bibp 32260low10
istradefylline0medium8414
deamino arginine vasopressin0low10
dexmedetomidine0medium142
endomorphin 10low10
endomorphin 20low10
ly 3448640low10
herbimycin0low10
pd 1809700low10
kallidin0low10
goserelin0low10
preclamol0medium42
l 7458700low20
15-deoxy-delta(12,14)-prostaglandin j20low10
lysophosphatidylcholines0low30
mdl 1009070medium124
cytochalasin b0low10
nalbuphine0low10
neurokinin a0low30
neurokinin b0low10
pd 1233190low10
kn 930low20
1,2-oleoylphosphatidylcholine0low20
biliverdine0low10
bisdemethoxycurcumin0low10
Cudraflavone A0low10
7-demethylsuberosin0low10
syringin0low10
glycitein0low10
andrographolide0low40
isorhapontigenin0low10
icariin0low20
licochalcone a0low10
atractylenolide i0low10
sophoricoside0low10
squamosamide0low70
fluvoxamine0low40
nostocarboline0low10
casein kinase ii0low120
ag-4900low10
su 112480low10
palbociclib0low10
ergothioneine0low10
stellettin b0low10
lead0medium192
butylidenephthalide0low20
13-hydroperoxy-9,11-octadecadienoic acid0low10
6,7-dihydroxyflavone0low20
8-(3-chlorostyryl)caffeine0low40
5,5',6,6'-tetrachloro-1,1',3,3'-tetraethylbenzimidazolocarbocyanine0low30
diamide0low10
methyl-3-methoxy-4-hydroxystyryl ketone0low10
cinnamoyl chloride0low10
barium0low100
aluminum0low370
strontium0low10
bismuth0low30
thallium0low40
triethyltin0low10
arsenic0low70
indium0low10
naltrexone0medium113
dextromethorphan0medium154
dextrorphan0low20
alternariol monomethyl ether0low10
gallium0low20
indinavir sulfate0low10
sulfur0medium131
5-methyl-2-hepten-4-one0low10
methylazoxymethanol acetate0low10
geldanamycin0low60
musk0low10
monomethyl fumarate0low10
monocrotophos0low10
diphenylhexatriene0low10
puerarin0low90
3-acetyldeoxynivalenol0low10
sinomenine0low10
ecdysterone0low20
deoxyribose0low20
fumarates0low30
beryllium0low10
cysteine0medium1319
silicon0low70
phosphorus0medium191
boron0low20
2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid0low10
nitecapone0low40
2,3-dehydrosilybin0low10
demethoxycurcumin0low20
cinanserin0low10
enkephalin, ala(2)-mephe(4)-gly(5)-0low20
lespenefril0low10
6-(1h-imidazol-1-yl)-7-nitro-2,3(1h,4h)-quinoxalinedione0low10
troxerutin0low10
pregabalin0low10
3,8-dihydroxy-6h-dibenzo(b,d)pyran-6-one0low30
n-acetylsphingosine0low30
naltrindole0low10
gedunin0low10
guanabenz0low10
n-(2-aminoethyl)-4-chlorobenzamide hydrochloride0low10
bafilomycin a0low10
resiniferatoxin0low10
carbocyanines0low30
25-hydroxyvitamin d 20low30
salubrinal0low20
semapimod0low10
epimedin b0low30
1,2-dielaidoylphosphatidylethanolamine0low10
gw-50740low40
ajmaline0medium11
monorden0low10
coomassie brilliant blue0low30
tetrodotoxin0low30
selenium0low350
tellurium0low40
polonium0low10
1,1-diethyl-2-hydroxy-2-nitrosohydrazine0low10
octadecylsilane0low10
aluminum hydroxide, magnesium hydroxide, drug combination0low10
GSK3-XIII0low10
dihydroergotoxine0medium82
dizocilpine maleate0low320
antimycin a0low30
ubp 3100low10
methylazoxymethanol0low10
dolichols0medium11
bongkrekic acid0low10
1-palmitoyl-2-oleoylphosphatidylcholine0low30
bafilomycin a10low30
15-hydroperoxy-5,8,11,13-eicosatetraenoic acid0low10
3-(2-carboxypiperazine-4-yl)-1-propenyl-1-phosphonic acid0low10
dioleoyl phosphatidylethanolamine0low10
mofegiline0medium52
thermozymocidin0low10
1,2-dilinolenoyl-3-(4-aminobutyryl)propane-1,2,3-triol0low10
2,3,5,4'-tetrahydroxystilbene 2-o-glucopyranoside0low20
1,2-dioleoylphosphatidylserine0low10
n-(3-iodopropen-1-yl)-2-carbomethoxy-3-(4-chlorophenyl)tropane0medium115
eleganolone0low20
gbr 130690low10
pregna-4,17-diene-3,16-dione0low10
n-iodoallyl-2-carbomethoxy-3-(4-fluorophenyl)tropane0medium91
liga 200low20
sphingosyl beta-glucoside0low80
hydroxysafflor yellow a0low20
4,7,10,13,16,19-docosahexaenoic acid dopamine conjugate0low10
mkt 0770low10
trk 8200low10
4-oxo-2-nonenal0low40
globotriaosyl lysosphingolipid0low10
cdw17 antigen0low20
clopenthixol decanoate0medium11
trisialoganglioside gt10low20
ibutamoren mesylate0low10
salvianolic acid B0low20
i(3)so3-galactosylceramide0low10
cx 6140low10
oxepins0medium71
pros-methylimidazoleacetic acid0low10
alpha-cyperone0low10
(melle-4)cyclosporin0low10
cyclosporin h0low10
4-(2-chlorophenyl)butan-2-amine0low30
tanespimycin0low10
clovamide0low10
beta-escin0low130
a 776360low20
dihydrexidine0low20
7-hydroxy-2-n,n-dipropylaminotetralin, (r)-isomer0low20
l-1650410low10
s-nitroso-n-acetylpenicillamine0low20
sb 2222000low10
ro 25-69810low30
sb 334867-a0low10
iem 14600low20
lactacystin0low380
butylscopolammonium bromide0low10
gadolinium dtpa0low30
morphinans0medium51
ergoline0medium37079
adenosine-3',5'-cyclic phosphorothioate0low10
sq-233770low10
enkephalin, leucine-2-alanine0low40
tiapamil hydrochloride0medium91
stepholidine0low10
flibanserin0low20
rmp 70low10
dutasteride0low30
adrogolide hydrochloride0medium32
vilazodone hydrochloride0low20
sarizotan0medium42
lergotrile0low30
pardoprunox0medium64
fesoterodine0medium21
3-tyrosine0low10
isoborneol0low10
bromopyruvate0low10
epsilon-(gamma-glutamyl)-lysine0low10
staurosporine0low120
dioleoylphosphatidic acid0low10
hypericum0low20
phosphocreatine0medium92
cholanic acid0low10
sl 3270low10
mannich bases0low10
s 17430medium11
fenpyroximate0low10
n-(2-pyridone-6-yl)-n',n'-di-n-propylformamidine0low10
ferrihydrite0low10
3-((2-methyl-1,3-thiazol-4-yl)ethynyl)piperidine0low10
osu 61620low10
3-O-feruloyl-D-quinic acid0low10
gw 5015160low20
dp-b990low10
acth (4-7), pro-gly-pro-0low10
dinapsoline0low10
dihydrohonokiol0low10
cp 2930190low10
euk-1340low10
n-(4-(2-methoxyphenoxy)phenyl)-n-(2,2,2-trifluoroethylsulfonyl)pyrid-3-ylmethylamine0low20
pd 03259010low10
flash-edt20low10
tubuloside b0low10
jasplakinolide0low10
stalevo0medium2313
davunetide0low30
sincalide0medium31
gpi 14850medium43
hemantane0low20
nebicapone0medium21
2-propyl-4,5,5a,6,7,11b-hexahydro-3-thia-5-azacyclopent-1-ena(c)phenanthrene-9,10-diol0low10
ap 22380low10
ursodoxicoltaurine0low60
paliperidone palmitate0low10
conophylline0low10
st 15350low10
sm 3460low20
nrx 1942040low10
f 136400low10
mocetinostat0low170
mirabegron0medium72
alloin0low10
cgp 745880low10
ticagrelor0low10
rivaroxaban0low10
lipid a0low10
pi1030low10
3,5-bis(2-fluorobenzylidene)piperidin-4-one0low10
dapagliflozin0low10
mart-1 antigen0low10
g(m2) ganglioside0low10
flb 4570medium51
pnu 96415e0low10
dextromethorphan - quinidine combination0low10
3,9-bis((ethylthio)methyl)-k-252a0medium134
memoquin0low10
msi 14360low10
ginsenoside rg30low10
ammonium trichloro(dioxoethylene-o,o'-)tellurate0low10
perampanel0medium52
tofacitinib0low10
mavoglurant0medium53
diapocynin0low10
ly 3920980low10
tocotrienols0low60
glutinol0low10
l 7060000low10
elobixibat0medium11
bpc 1570low10
seletracetam0low10
pitolisant0low10
3,4-dihydro-5-(4-(1-piperidinyl)butoxy)-1(2h)-isoquinolinone0low10
tetramethylrhodamine0low10
cqa 206-2910medium42
1-(3,4-dimethoxyphenethyl)-4-(3-phenylpropyl)piperazine dihydrochloride0low10
chir 990210low10
benzyloxycarbonyl-isoleucyl-glutamyl(o-tert-butyl)-alanyl-leucinal0low30
ubiquinol0medium21
g(m1) ganglioside0medium408
aluminum oxide0low20
3,6'-dithiothalidomide0low10
n-((1-allyl-2-pyrrolidinyl)methyl)-5-(3-fluoropropyl)-2,3-dimethoxybenzamide0medium62
2-carbomethoxy-8-(3-fluoropropyl)-3-(4-iodophenyl)tropane0medium35224
caproctamine0low10
n-(1-methylethyl)-1,1,2-trimethylpropylamine0low10
methionine sulfoxide0low30
pimavanserin0medium758
masitinib0low10
corynoxine b0low10
linagliptin0low20
pazopanib0low20
2-(2-furanyl)-7-(2-(4-(4-(2-methoxyethoxy)phenyl)-1-piperazinyl)ethyl)-7h-pyrazolo(4,3-e)(1,2,4)triazolo(1,5-c)pyrimidine-5-amine0low30
tribulus0low10
coumaperine0low10
am 12410low10
a 4436540low10
noradrenochrome0low10
m 404030low20
homocarnosine0low10
ro 16-01540medium31
trans-sodium crocetinate0low10
saracatinib0low10
alpha-synuclein0medium5,57020
rocagloic acid0low10
11-hydroxy-n-(n-propyl)noraporphine hydrochloride, (r)-isomer0low10
fauc 2130low10
15-acetyldeoxynivalenol0low10
fauc 1130low10
desmethoxyfallypride0medium31
erinacine a0low20
msdc-01600low20
cosaldon0low10
3-amino-4-(2-dimethylaminomethylphenylsulfanyl)benzonitrile0low30
oxadiazoles0medium5810
sch 4424160low10
jaspamide b0low10
xanthostigmine0low10
hydroxymatairesinol0low10
ribose0low20
acebutolol0low10
lactulose0low30
schisandrol a0low20
hypoestoxide0low10
calpain inhibitor iii0low20
erastin0low10
epoxomicin0low50
amd 0700low10
5-hydroxy-2-n,n-dipropylaminotetralin, (s)-isomer0low20
tesofensine0medium32
lipocrine0low10
resolvin d20low10
inno-4060low10
mitoquinone0medium51
titanium boride0low10
mk-94700low10
ridaforolimus0low10
azd32410medium11
oleandrin0low10
hu 3080low10
sitagliptin phosphate0low20
cannabidivarin0low10
gw 25800low10
tozadenant0medium51
lorcaserin0low10
2-((2-((dimethylamino)methyl)phenyl)thio)-5-iodophenylamine0low10
losartan potassium0medium144
d-arg-dmt-lys-phe-nh20low10
tp 70low10
td-51080medium62
empagliflozin0low10
technetium tc 99m exametazime0medium311
altinicline maleate0medium21
peramivir0low10
calcimycin0low10
dextrothyroxine0low10
veliparib0low10
ferryl iron0low10
s-tetradecanoyl-coenzyme a0low10
sepharose0low20
scopolamine hydrobromide0medium263
pituitrin0low70
podophyllin0low10
virginiamycin0low10
lhrh, ala(6)-gly(10)-ethylamide-0low10
4'-diethylamino-3-hydroxyflavone0low10
monascin0low10
24-hydroxycholesterol0medium51
phytosterols0low20
dihydrotachysterol0low10
rifamycins0low10
tenuigenin0low40
clove0low10
dihydroergocryptine0medium62
acid phosphatase0low30
mefloquine0low20
neosolaniol0low10
2-(4,5-dihydro-1h-imidazol-2-yl)-1-methyl-1h-indole0low10
2',3'-dihydroxy-4',6'-dimethoxychalcone0low10
cysteinyldopa0low60
glaucocalyxin b0low10
id0low10
lyoniside0low20
cqp 201-4030low10
jaw0medium283
nad0medium534
n-(3-fluorophenyl)-1-((4-(((3s)-3-methyl-1-piperazinyl)methyl)phenyl)acetyl)-4-piperidinamine0medium11
imidazoleacetic acid ribotide0low10
nvp-tae6840low10
5-(alpha-methyl-4-bromobenzylamino)phosphonomethyl-1,4-dihydroquinoxaline-2,3-dione0low10
mf 4380low10
cytochrome c-t0low420
cosyntropin0low10
cholecystokinin0medium234
ceruletide0medium43
motilin0low10
dynorphins0medium171
atrial natriuretic factor0low30
tannins0low10
peptide i0low10
humanin0low20
nociceptin0low60
gastrins0low10
glucagon0low40
beta-endorphin0low90
neuropeptide y0low140
angiotensinogen0low10
tannins0low20
oligonucleotides0low130
liraglutide0low110
glucagon-like peptide 10low310
incretins0medium102
natriuretic peptide, c-type0low40
eriocalyxin b0low10
cellulose0low30
endothelin-10low30
phosphatidylcholines0medium221
azd 14800low10
vendex0medium487
aluminum lactate0low10
adenosine kinase0low20
hoe 333420low10
sodium salicylate0medium21
sphingosine kinase0low50
ubiquinone0medium10515
florbenazine f 180medium131
1-palmitoyl-2-(6-(n-(7-nitrobenz)-2-oxa-1,3-diazol-4-yl)aminocaproyl)phosphatidylcholine0low10
ethybenztropine0low10
calpain0low390
lucifer yellow0low10
sapogenins0low10
onjisaponin b0low10
xyloketal b0low10
v 20060low10
chitosan0low190
nnc 55-03960low10
technetium tc 99m sestamibi0low10
octyl galactopyranoside0low10
15-deoxyprostaglandin j20low10
s-nitro-n-acetylpenicillamine0low10
butaclamol0medium21
n(alpha)-acetylfusarinines0low10
sodium oxybate0medium74
bucladesine0medium41
sodium lactate0low20
sarkosyl0low10
sodium glutamate0low10
ro13-99040low40
sodium pertechnetate tc 99m0medium61
sodium ethylxanthate0medium71
chiniofon0low40
quinupristin-dalfopristin0low10
olaparib0low10
mogroside v0low10
s-adenosylmethionine0medium241
picrotoxin0low60
florbetapir f 180low10
ponatinib0low20
rg 16780low10
suvorexant0low10
jzl 1840low10
egg white0low20
quetiapine fumarate0medium7714
cardiovascular agents0low430
dcc-20360low10
rimorphin0low20
neurotensin0low250
apelin-13 peptide0low10
tolterodine tartrate0medium41
mannans0low10
kurarinone0low10
4'-geranyloxyferulic acid0low10
ganglioside, gd1a0low10
n,n-dimethyl-2-(2-amino-4-cyanophenylthio)benzylamine0low40
glycolipids0low230
piperidines0medium28858
resolvin d10low20
ly28113760low10
interleukin-80medium102
dabrafenib0low20
6-fluoro-2-(4-(pyridin-2-yl)but-3-yn-1-yl)imidazo(1,2-a)pyridine0medium21
punicalagin0low20
3-(1,3-benzodioxol-5-yl)-5-(3-bromophenyl)-1h-pyrazole0medium31
exenatide0medium256
gsk06600low10
5-methyl-n-(4-methylpyrimidin-2-yl)-4-(1h-pyrazol-4-yl)thiazol-2-amine0low10
lrrk2-in10low120
mannosylglycerate0low10
lgk9740low10
tubastatin a0low10
methylcellulose0medium71
isoquercitrin0low10
b3552520low10
1,2-dioleoyl-sn-glycero-3-phosphoglycerol0low30
vasoactive intestinal peptide0low170
natriuretic peptide, brain0low60
heme0low20
sr 82780low10
3,4-dihydroxybenzalacetone0low10
7-methyl-5-(1-((3-(trifluoromethyl)phenyl)acetyl)-2,3-dihydro-1h-indol-5-yl)-7h-pyrrolo(2,3-d)pyrimidin-4-amine0low20
heparitin sulfate0low60
ascorbic acid0medium784
novobiocin0low10
tetracycline0low80
minocycline0medium192
salicylates0low120
nedocromil0low20
dicumarol0low30
piroxicam0low10
mobic0low20
laquinimod0low10
warfarin0low260
metastat0low10
phenprocoumon0low10
l 7013240low10
almagate0low10
epidermal growth factor0medium201
gastrin-releasing peptide0low10
transforming growth factor beta0low190
phytoestrogens0low40
oleuropein aglycone0low20
semaglutide0low10
okadaic acid0low20
gkt1378310low10
gne-79150low10
HG-10-102-010low20
grn-5290low10
pyrethrins0low50
gsk2578215a0low30
bisphenol a glucuronide0low10
fti 2770low10
rome0low50
agar0low10
pf-064474750low20
cyclin d10low40
bms 2047560medium21
lysophosphatidylinositol0low10
caseins0low30
vce-0030low10
MLI-20low20
oligomycins0low10
phthalocyanine0low10
g(m3) ganglioside0low50
benzyloxycarbonylvalyl-alanyl-aspartyl fluoromethyl ketone0low80
azulenyl nitrone0low10
nitrophenols0medium13342
difopein0low30
glucagon-like peptide 20low20
calpastatin0low80
angiotensin i0low10
siagoside0low10
cobamamide0low10
hyaluronoglucosaminidase0low20
deltakephalin0low10
lipofectamine0low10
d-ala(2),mephe(4),met(0)-ol-enkephalin0low10
ginkgolide b0low20
neferine0low10
morroniside0low10
daptomycin0medium11
peoniflorin0low50
vitamin b 120medium7512
yuanhuacin0low10
ferric ammonium citrate0low20
s 89320low10
oxyntomodulin0low10
transforming growth factor alpha0medium31
moxidectin0low10
cyclosporine0medium243
silybin0low50
lactoferrin0low180
catalpol0low10
fusarenon-x0low10
n-(2-propynyl)-2-(5-benzyloxy-indolyl) methylamine0low20
ethylmethylhydroxypyridine succinate0low10
ngp 1-010low10
orabase0low30
muramidase0low100
amyloid beta-peptides0low140
liriodendrin, 1r-(1alpha,3abeta,4beta,6aalpha)-isomer0low10
chondroitin sulfates0low20
exudates0low220
angiogenin0low100
plicamycin0low10
euk-1890low40
11-dehydrosinulariolide0low20
acyclovir0medium41
levoleucovorin0medium11
cyclic gmp0medium182
sepiapterin0low30
deoxyguanosine0medium171
guanosine diphosphate0low30
guanosine triphosphate0low290
guanine0low120
guanosine0medium142
hypoxanthine0medium51
inosinic acid0low20
inosine0medium144
sapropterin0medium432
folic acid0medium6512
3-methyladenine0low60
queuine0low10
guanosine 5'-o-(3-thiotriphosphate)0low60
neopterin0medium111
rifampin0low60
clozapine0medium17824
dacarbazine0low30
didanosine0low10
ganciclovir0low10
olanzapine0medium356
pralidoxime0low10
zaprinast0low10
5,10-methylenetetrahydrofolic acid0low10
allopurinol0low100
2,2'-(hydroxynitrosohydrazono)bis-ethanamine0low10
azaguanine0low10
8-hydroxyguanosine0medium52
4-hydroxyquinazoline0low10
2,4-diaminohypoxanthine0low10
noc 180low10
tegaserod0medium11
norclozapine0medium11
sildenafil citrate0medium92
aprepitant0low10
vardenafil dihydrochloride0low10
azilsartan0low10
xav9390low20
8-hydroxyguanine0low40
trypan blue0low10
8-methylguanine0low10
8-hydroxy-2'-deoxyguanosine0medium181
clozapine n-oxide0low20
coelenterazine0low10
amg5310low10
8-thioguanosine0low10
8-bromoguanosine0low10
5-methyltetrahydrofolate0low10
5,7-dihydroxytryptamine creatinine0low10
cytidylyl-3'-5'-guanosine0low10
alpha-(4-pyridyl-1-oxide)-n-tert-butylnitrone0low10
neoechinulin0low10
opicapone0medium5211
fenobam0low10
eye0medium302
maltodextrin0low10
frondoside a0low10
carbidopa0medium1,269294
ego0low10
technetium tc 99m bicisate0medium235
technetium tc 99m-ethylenedicysteine0low20
chlorotoxin0low10
trypsinogen0low10
metallothionein0low210
preproenkephalin0low190
leptin0low200
hopeaphenol0low10
pyrimidinones0medium71
cyclo(7-aminoheptanoylphenylalanyl-tryptophyl-lysyl-benzylthreonyl)0low10
phenanthrenes0low120

Protein Targets (4,844)

ProteinPotency MeasurementsInhibition MeasurementsActivation MeasurementsDrugs
Sodium-dependent serotonin transporter014816165
Sodium-dependent dopamine transporter 01229132
thioredoxin reductase30200302
ATAD5 protein, partial21800218
GLS protein24200242
estrogen-related nuclear receptor alpha41300413
arylsulfatase A19400194
euchromatic histone-lysine N-methyltransferase 251600516
atrial natriuretic peptide receptor 1 precursor470047
atrial natriuretic peptide receptor 2 precursor490049
flap endonuclease 113700137
ras-related protein Rab-9A910091
serine/threonine-protein kinase mTOR isoform 110200102
M-phase phosphoprotein 810100101
NAD-dependent protein deacetylase sirtuin-20819
NAD-dependent protein deacetylase sirtuin-107112
NAD-dependent protein deacetylase sirtuin-3, mitochondrial0549
ATP-dependent phosphofructokinase22200222
Chain A, Ferritin light chain13300133
USP1 protein, partial24900249
Microtubule-associated protein tau27100272
thyroid stimulating hormone receptor24800248
glucocerebrosidase830083
chromobox protein homolog 130400304
mitogen-activated protein kinase 116900169
nuclear receptor ROR-gamma isoform 121400214
DNA polymerase kappa isoform 115300153
survival motor neuron protein isoform d17900179
lethal factor (plasmid)16600166
Transient receptor potential cation channel subfamily V member 10729
Alpha-synuclein5222377
Transient receptor potential cation channel subfamily V member 1091125
Ataxin-220800208
Peptidyl-prolyl cis-trans isomerase B0011
Peptidyl-prolyl cis-trans isomerase F, mitochondrial0011
Peptidyl-prolyl cis-trans isomerase A 0213
Chain A, Putative fructose-1,6-bisphosphate aldolase10500105
Chain A, JmjC domain-containing histone demethylation protein 3A11800118
Niemann-Pick C1 disease protein, partial1001
Caspase 6, apoptosis-related cysteine peptidase0006
Methyl-CpG binding domain protein 20101
Apoptotic peptidase activating factor 10202
Smad310800108
67.9K protein13100131
bromodomain adjacent to zinc finger domain 2B10200102
heat shock protein 900066
lysosomal alpha-glucosidase preproprotein550055
NPC intracellular cholesterol transporter 1 precursor720072
E3 ubiquitin-protein ligase UHRF1 isoform 10101
parathyroid hormone/parathyroid hormone-related peptide receptor precursor710071
caspase-9 isoform alpha precursor0202
importin subunit beta-1 isoform 1620062
DNA polymerase beta680068
caspase-3 isoform a preproprotein0202
snurportin-1620062
peptidyl-prolyl cis-trans isomerase NIMA-interacting 1970097
DNA polymerase iota isoform a (long)17600176
dual specificity tyrosine-phosphorylation-regulated kinase 1A00011
geminin41100411
muscleblind-like protein 1 isoform 1690069
replicative DNA helicase0004
recombinase A0044
POsterior Segregation001010
D068379
Sodium-dependent noradrenaline transporter 014618164
Caspase-7231027
Caspase-90305
D(2) dopamine receptor013519166
Zinc finger protein mex-50099
Nrf2250025
WRN140014
phosphopantetheinyl transferase21800218
TDP1 protein52500525
thioredoxin glutathione reductase610061
aldehyde dehydrogenase 1 family, member A134500345
corticotropin-releasing hormone receptor 20224
regulator of G-protein signaling 420300203
corticotropin releasing factor-binding protein0224
heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa)590059
15-hydroxyprostaglandin dehydrogenase [NAD(+)] isoform 115100151
vitamin D3 receptor isoform VDRA19200192
serine/threonine-protein kinase PLK1430043
Vpr230023
Glycoprotein hormones alpha chain170017
Amine oxidase [flavin-containing] A080186
Amine oxidase [flavin-containing] B081689
Chain A, MAJOR APURINIC/APYRIMIDINIC ENDONUCLEASE29800298
Parkin570057
IDH112900129
nuclear factor erythroid 2-related factor 2 isoform 211400115
huntingtin isoform 2560056
urokinase-type plasminogen activator precursor810081
plasminogen precursor810081
urokinase plasminogen activator surface receptor precursor810081
D(1A) dopamine receptor579066
Bloom syndrome protein isoform 116300163
lamin isoform A-delta1034800348
Metabotropic glutamate receptor 80619
Metabotropic glutamate receptor 606615
Glutamate receptor 11623654
Glutamate receptor 2204206239
Glutamate receptor 31620651
Glutamate receptor 41620651
Glutamate receptor ionotropic, kainate 1117425
Metabotropic glutamate receptor 108412
Metabotropic glutamate receptor 20246
Metabotropic glutamate receptor 30246
Metabotropic glutamate receptor 40279
Metabotropic glutamate receptor 5010414
Metabotropic glutamate receptor 60134
Metabotropic glutamate receptor 70145
Glutamate receptor ionotropic, NMDA 1 0611184
Metabotropic glutamate receptor 5015927
Glutamate receptor ionotropic, kainate 2116323
Glutamate receptor ionotropic, kainate 3122026
Metabotropic glutamate receptor 80033
Glutamate receptor ionotropic, NMDA 2A 058878
Glutamate receptor ionotropic, NMDA 2B060981
Glutamate receptor ionotropic, NMDA 2C058879
Glutamate receptor ionotropic, kainate 4114018
Metabotropic glutamate receptor 1013521
Metabotropic glutamate receptor 2012723
Metabotropic glutamate receptor 704411
Metabotropic glutamate receptor 305311
Metabotropic glutamate receptor 409921
Glutamate receptor ionotropic, NMDA 2D054874
Glutamate receptor ionotropic, kainate 5114119
Glutamate receptor ionotropic, NMDA 3B054874
Glutamate receptor ionotropic, NMDA 3A054874
Chain B, pheromone binding protein0011
Chain A, pheromone binding protein0011
Chain A, RNA-directed RNA polymerase NS50404
acid sphingomyelinase270027
GTP-binding nuclear protein Ran isoform 1360036
DNA polymerase eta isoform 1510051
fibroblast growth factor 22 isoform 1 precursor0004
Mitogen-activated protein kinase 130121628
Beta-lactamase010010
Transthyretin091327
Fatty acid-binding protein, intestinal07411
Fatty acid-binding protein, adipocyte08412
Cyclin-A2013014
Cannabinoid receptor 1021627
Cyclin-dependent kinase 20272958
Choline O-acetyltransferase0505
Mitogen-activated protein kinase 120121830
Guanine nucleotide-binding protein G600060
Fatty acid-binding protein 50527
Fatty acid-binding protein 50033
Mitogen-activated protein kinase 110122840
Mitogen-activated protein kinase 140413172
glucocorticoid receptor [Homo sapiens]35600356
farnesoid X nuclear receptor22700227
estrogen nuclear receptor alpha53700537
Voltage-dependent calcium channel gamma-2 subunit19000190
Cellular tumor antigen p5331900319
Choline O-acetyltransferase 0608
Alpha-mannosidase0404
alpha-galactosidase440044
Trehalase 0202
Trehalase0101
Maltase-glucoamylase, intestinal0808
Trehalase 0202
Lysosomal acid glucosylceramidase08110
Alpha-galactosidase A0101
Alpha-glucosidase MAL620303
Lactase-phlorizin hydrolase0202
Lysosomal alpha-glucosidase0909
Beta-glucosidase A0101
Sucrase-isomaltase, intestinal0707
Alpha-1B adrenergic receptor012216139
Sucrase-isomaltase, intestinal0909
Alpha-1D adrenergic receptor08916108
Beta-glucosidase0202
Protein-lysine 6-oxidase0606
Alpha-mannosidase 20202
Glycogen debranching enzyme0202
Glycogen debranching enzyme0202
Alpha-glucosidase MAL320303
Alpha-1A adrenergic receptor013718156
Oligo-1,6-glucosidase IMA10404
Alpha-glucosidase MAL120909
Oxysterols receptor LXR-beta05713
Spike glycoprotein186723216
Alpha-amylase 0101
Trehalose synthase/amylase TreS0202
Lactase-phlorizin hydrolase 0303
Oxysterols receptor LXR-alpha05814
Neutral alpha-glucosidase AB0303
Ceramide glucosyltransferase0202
Lysosomal acid glucosylceramidase0202
Probable maltase-glucoamylase 20505
Beta-glucosidase 0101
Lysosomal alpha-glucosidase0505
Cytosolic beta-glucosidase0101
Non-lysosomal glucosylceramidase0303
Putative alpha-glucosidase0202
Chain A, Cruzipain920092
Platelet-activating factor receptor4207
Inositol monophosphatase 110000100
Polyphenol oxidase 2047061
Tyrosinase020020
Lethal factor0505
Glutaminyl-peptide cyclotransferase0808
dopamine D1 receptor510051
Phenylethanolamine N-methyltransferase014016
Chain A, High-affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A0101
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4D0101
Chain A, Phosphodiesterase 9A0101
Chain A, Class I phosphodiesterase PDEB10101
Chain A, High affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8A0101
Chain A, cGMP-dependent 3',5'-cyclic phosphodiesterase0101
Chain A, cGMP-specific 3',5'-cyclic phosphodiesterase catalytic domain, Cone cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha chimera0101
Chain A, cGMP-specific 3',5'-cyclic phosphodiesterase catalytic domain, Cone cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha chimera0101
Chain A, High affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A0101
Chain A, High affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A0101
glp-1 receptor, partial11600116
Phosphodiesterase 0707
cytochrome P450 3A4 isoform 129100291
histone acetyltransferase KAT2A isoform 116200162
cGMP-dependent 3',5'-cyclic phosphodiesterase011011
Gamma-aminobutyric acid receptor subunit pi2915310354
Monocarboxylate transporter 40205
High affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8A0707
cGMP-specific 3',5'-cyclic phosphodiesterase022124
High affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A0404
Renin09111
Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1A 0808
cAMP-specific 3',5'-cyclic phosphodiesterase 4D 0506
cAMP-specific 3',5'-cyclic phosphodiesterase 4C0506
cAMP-specific 3',5'-cyclic phosphodiesterase 4B0507
Gamma-aminobutyric acid receptor subunit beta-12915310354
Gamma-aminobutyric acid receptor subunit delta2915310354
Gamma-aminobutyric acid receptor subunit gamma-22915412357
Gamma-aminobutyric acid receptor subunit alpha-52915410355
Gamma-aminobutyric acid receptor subunit alpha-32915310354
Gamma-aminobutyric acid receptor subunit gamma-12915410355
Gamma-aminobutyric acid receptor subunit alpha-22915310354
Adenosine receptor A1149766
Gamma-aminobutyric acid receptor subunit alpha-42915310354
Gamma-aminobutyric acid receptor subunit gamma-32915310354
Adenosine receptor A3015016
Adenosine receptor A2a0482081
Adenosine receptor A2b021738
Adenosine receptor A2b019329
Gamma-aminobutyric acid receptor subunit alpha-62915310354
Adenosine receptor A10431469
Adenosine receptor A2a049974
Sodium-dependent serotonin transporter060668
Adenosine receptor A2a0303
Cone cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha'0404
cAMP-specific 3',5'-cyclic phosphodiesterase 4A0506
Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1A012013
Gamma-aminobutyric acid receptor subunit alpha-12915512358
Gamma-aminobutyric acid receptor subunit beta-32915410355
Gamma-aminobutyric acid receptor subunit beta-22915312356
Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1B0808
Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1B013014
Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1B0505
cAMP-specific 3',5'-cyclic phosphodiesterase 4B018120
cAMP-specific 3',5'-cyclic phosphodiesterase 4D023125
cGMP-inhibited 3',5'-cyclic phosphodiesterase B017018
Voltage-dependent L-type calcium channel subunit alpha-1C050152
High affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A0606
Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1C015016
cGMP-inhibited 3',5'-cyclic phosphodiesterase A019020
Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1C0505
Phosphodiesterase 0101
GABA theta subunit2915310354
Phosphodiesterase 0505
Gamma-aminobutyric acid receptor subunit epsilon2915310354
cAMP-specific 3',5'-cyclic phosphodiesterase 7B0505
Dihydropteridine reductase0303
Amine oxidase [flavin-containing] B018022
Solute carrier family 22 member 10507
Solute carrier family 22 member 2033045
Solute carrier family 22 member 1 072091
Solute carrier family 22 member 20506
Solute carrier family 22 member 3018021
Solute carrier family 22 member 30507
POU domain, class 2, transcription factor 20104
Solute carrier family 22 member 1029039
Solute carrier family 22 member 2026033
Chain A, HADH2 protein18800188
Chain B, HADH2 protein18800188
RAR-related orphan receptor gamma33900339
GLI family zinc finger 336500365
AR protein46300463
estrogen receptor 2 (ER beta)21800218
nuclear receptor subfamily 1, group I, member 331100311
progesterone receptor23400234
retinoic acid nuclear receptor alpha variant 134800348
pregnane X nuclear receptor32500325
aryl hydrocarbon receptor20100201
thyroid stimulating hormone receptor17200172
activating transcription factor 615500155
nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 (p105), isoform CRA_a15600156
v-jun sarcoma virus 17 oncogene homolog (avian)19700197
thyroid hormone receptor beta isoform 236600366
nuclear factor erythroid 2-related factor 2 isoform 135200352
Kelch-like ECH-associated protein 10145
Histone acetyltransferase KAT80305
hypoxia-inducible factor 1 alpha subunit13300133
SMAD family member 212800128
SMAD family member 312800128
caspase 7, apoptosis-related cysteine protease830083
retinoid X nuclear receptor alpha29900299
peroxisome proliferator activated receptor gamma25400254
caspase-3830083
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_a23000230
Histone H2A.x15400154
heat shock protein beta-114700147
thyroid hormone receptor beta isoform a14700147
G-protein coupled receptor 840347
Chain A, ATP-DEPENDENT DNA HELICASE Q1870087
Chain A, TYROSYL-DNA PHOSPHODIESTERASE18200182
Lysosomal Pro-X carboxypeptidase0505
Sigma non-opioid intracellular receptor 1029535
Phenylethanolamine N-methyltransferase0416
CD44 antigen0011
CD44 antigen0112
Alpha-2B adrenergic receptor0721588
Alpha-2C adrenergic receptor0711587
Alpha-2A adrenergic receptor0741590
Nicotinamide N-methyltransferase0505
hypoxia-inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)12200122
peripheral myelin protein 22 isoform 1990099
muscarinic acetylcholine receptor M116000160
5-hydroxytryptamine receptor 1A07129101
Adenosine receptor A3068677
Adenosine receptor A10909
Vasopressin V2 receptor0003
Mu-type opioid receptor07523110
Adenosine receptor A10437
Adenylate cyclase type 50618
Adenylate cyclase type 10216
Sigma non-opioid intracellular receptor 1029433
relaxin receptor 1 isoform 17007
Rap guanine nucleotide exchange factor 3470047
Beta-lactamase 0202
endonuclease IV760076
Chain A, Beta-lactamase14000140
Chain A, 2-oxoglutarate Oxygenase20300203
galanin receptor type 30303
eyes absent homolog 2 isoform a170017
Chain A, Retinaldehyde-binding protein 10011
Chain A, Retinaldehyde-binding protein 10011
D(2) dopamine receptor017827217
Tyrosine 3-monooxygenase0202
D(3) dopamine receptor054361
5-hydroxytryptamine receptor 1A014719170
D(1A) dopamine receptor010816132
D(1B) dopamine receptor032032
5-hydroxytryptamine receptor 2A016914190
D(4) dopamine receptor037138
Histamine H1 receptor014523
D(3) dopamine receptor016315187
prostaglandin E2 receptor EP2 subtype2006
Transient receptor potential cation channel subfamily A member 1021721
Peroxisome proliferator-activated receptor gamma0152744
Lysine-specific demethylase 6B0404
Lysine-specific demethylase 4B0202
Heat shock protein HSP 90-alpha0121427
Heat shock protein HSP 90-beta010924
Cholesteryl ester transfer protein0325
Lysine-specific demethylase 5A0606
Endoplasmin0246
Hypoxia-inducible factor 1-alpha0819
Endothelial PAS domain-containing protein 10606
Lysine-specific demethylase 4C0505
Sodium-dependent dopamine transporter064771
Transporter040445
Cytochrome P450 1A2065476
Cytochrome P450 2D601014113
Cytochrome P450 2C19054260
Mu-type opioid receptor0411257
Chain A, Proto-oncogene serine/threonine-protein kinase Pim-10101
Chain A, Proto-oncogene serine/threonine-protein kinase Pim-10101
Chain A, Methyltransferase Wbdd0101
15-lipoxygenase, partial12800128
NFKB1 protein, partial10200102
Thrombopoietin810081
EWS/FLI fusion protein24500246
cytochrome P450 2D6 isoform 116700167
cellular tumor antigen p53 isoform a12700127
cytochrome P450 2C19 precursor14700147
cytochrome P450 2C9 precursor13200132
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform071523
Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha0202
Serine/threonine-protein kinase PLK4072734
Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta021416
Polyunsaturated fatty acid lipoxygenase ALOX15B12480132
Bromodomain-containing protein 40336
5-hydroxytryptamine receptor 401285133
Integrin beta-39481103
Integrin alpha-IIb9471102
Neuronal acetylcholine receptor subunit alpha-419321063
Serine/threonine-protein kinase pim-10132744
Neuronal acetylcholine receptor subunit beta-219301061
Casein kinase II subunit alpha'0202646
Proteinase-activated receptor 10214
Bromodomain-containing protein 20303
Phosphatidylinositol 3-kinase regulatory subunit alpha0405
5-hydroxytryptamine receptor 2C01628173
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform0101
Type-1 angiotensin II receptor0527
5-hydroxytryptamine receptor 2B01566163
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform0111628
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform 0101
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform071524
Serine/threonine-protein kinase mTOR0121628
Serine/threonine-protein kinase mTOR0101
Histamine H2 receptor212125245
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform 0111527
Glycogen synthase kinase-3 beta0302959
Serine/threonine-protein kinase PLK10192443
Casein kinase II subunit beta020020
Casein kinase II subunit alpha0241539
DNA-dependent protein kinase catalytic subunit013013
Serine-protein kinase ATM0505
Serine/threonine-protein kinase ATR04913
Bromodomain-containing protein 30101
Serine/threonine-protein kinase pim-3021517
Phosphoinositide 3-kinase regulatory subunit 50202
Serine/threonine-protein kinase PLK3091524
Serine/threonine-protein kinase PLK2071421
Amyloid-beta precursor protein647660
D(1A) dopamine receptor13300133
nonstructural protein 1770077
neuropeptide S receptor isoform A710071
Cytosol aminopeptidase0101
Urokinase-type plasminogen activator0606
5-hydroxytryptamine receptor 2C0781594
Leukotriene A-4 hydrolase0718
5-hydroxytryptamine receptor 2A09819119
Aminopeptidase N0303
5-hydroxytryptamine receptor 1B09911111
5-hydroxytryptamine receptor 1D0341247
5-hydroxytryptamine receptor 1F0331145
5-hydroxytryptamine receptor 2B0691584
5-hydroxytryptamine receptor 60161026
5-hydroxytryptamine receptor 7 0321143
5-hydroxytryptamine receptor 5A0151025
5-hydroxytryptamine receptor 5B0151025
5-hydroxytryptamine receptor 3A0311142
Bacterial leucyl aminopeptidase0101
5-hydroxytryptamine receptor 4 0191233
5-hydroxytryptamine receptor 3B0311142
interferon gamma precursor00016
Delta-type opioid receptor050664
Delta-type opioid receptor036950
Adenosine receptor A10202
Adenosine receptor A10213
Adenosine receptor A2a0101
Adenosine receptor A30213
Cannabinoid receptor 20437
Peptidyl-prolyl cis-trans isomerase FKBP50235
Luciferase18600186
vitamin D (1,25- dihydroxyvitamin D3) receptor24200242
TAR DNA-binding protein 4310010101
Prostaglandin D2 receptor0202
Prostaglandin D2 receptor 20314
peroxisome proliferator-activated receptor delta22800228
Cytochrome P450 2A6021325
Neutrophil cytosol factor 10505
Cytochrome P450 2A50809
Proteasome subunit beta type-5024026
DNA repair and recombination protein RadA0022
Sulfotransferase 1A1 0005
Sulfotransferase 1E10001
Sulfotransferase 1A10102
Sulfotransferase 2A10102
ClpP150015
pregnane X receptor670067
apical membrane antigen 1, AMA1620062
Nuclear receptor ROR-gamma796388
BRCA1190019
neutrophil cytosol factor 10505
voltage-dependent T-type calcium channel subunit alpha-1H isoform a0011
Voltage-dependent T-type calcium channel subunit alpha-1G0426
Voltage-dependent T-type calcium channel subunit alpha-1H0516
Voltage-dependent T-type calcium channel subunit alpha-1I0516
Alcohol dehydrogenase E chain0516
Alcohol dehydrogenase S chain0516
D(1) dopamine receptor0134
interleukin 8670067
acetylcholinesterase16600166
cytochrome P450 family 3 subfamily A polypeptide 432500325
G21600216
cytochrome P450 2D626900269
potassium voltage-gated channel subfamily H member 2 isoform d18300183
peripheral myelin protein 2218100181
Nuclear receptor subfamily 1 group I member 2031922
Interferon beta29100291
HLA class I histocompatibility antigen, B alpha chain 21600216
Nuclear factor erythroid 2-related factor 201713
Inositol hexakisphosphate kinase 121600216
cytochrome P450 2C9, partial21600216
ATP-dependent translocase ABCB1024631
Xanthine dehydrogenase/oxidase [Includes: Xanthine dehydrogenase 0404
Multidrug resistance-associated protein 1 015122
Chain A, Neutrophil gelatinase-associated lipocalin0011
72 kDa type IV collagenase019019
Matrilysin0808
Prolyl 4-hydroxylase subunit alpha-1012012
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT60606
Alpha-(1,3)-fucosyltransferase 70606
CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 10606
Glutamate receptor ionotropic, kainate 107210
Glutamate receptor 1014419
Glutamate receptor 2014318
Glutamate receptor 3011314
Glutamate receptor 4013418
Glutamate receptor ionotropic, kainate 208210
Glutamate receptor ionotropic, kainate 30606
Peroxisome proliferator-activated receptor alpha981633
ATPase family AAA domain-containing protein 511800118
Pyruvate dehydrogenase E1 component subunit alpha, mitochondrial0101
Pyruvate dehydrogenase E1 component subunit beta, mitochondrial0101
histone deacetylase 9 isoform 3420042
Glycogen synthase kinase-3 alpha0172643
Carbonic anhydrase 12057175
Carbonic anhydrase 101101141
Carbonic anhydrase 201227160
Polyunsaturated fatty acid 5-lipoxygenase034035
Tyrosine-protein phosphatase non-receptor type 1043247
Carbonic anhydrase 7051167
Carbonic anhydrase 9065286
Carbonic anhydrase 14036152
ORF730045
pyruvate kinase260026
serine-protein kinase ATM isoform a230023
DNA dC->dU-editing enzyme APOBEC-3G isoform 1288036
Acetylcholinesterase014014
Cholinesterase064165
Endothelin receptor type B66012
Endothelin-1 receptor6107
Substance-P receptor022027
Quinone oxidoreductase00011
Xanthine dehydrogenase/oxidase024130
electroneutral potassium-chloride cotransporter KCC20033
Synaptic vesicular amine transporter0718
Synaptic vesicular amine transporter09211
Cytochrome P450 3A4012912154
Glutamate receptor ionotropic, NMDA 2B032336
Amine oxidase [flavin-containing] A0506
Fumarate hydratase12000120
polyprotein12000120
Gamma-butyrobetaine dioxygenase0314
polyunsaturated fatty acid lipoxygenase ALOX12380038
Chain A, SOLUBLE ACETYLCHOLINE RECEPTOR0011
Chain E, SOLUBLE ACETYLCHOLINE RECEPTOR0011
Chain A, Soluble acetylcholine receptor0011
Chain E, Soluble acetylcholine receptor0011
Chain A, SOLUBLE ACETYLCHOLINE RECEPTOR0011
Chain E, SOLUBLE ACETYLCHOLINE RECEPTOR0011
Chain F, SOLUBLE ACETYLCHOLINE RECEPTOR0011
Chain J, SOLUBLE ACETYLCHOLINE RECEPTOR0011
Acetylcholine receptor subunit alpha09413
Acetylcholine receptor subunit gamma09413
Acetylcholine receptor subunit beta09413
Neuronal acetylcholine receptor subunit beta-2019628
Neuronal acetylcholine receptor subunit beta-4011619
Neuronal acetylcholine receptor subunit alpha-3012619
Neuronal acetylcholine receptor subunit alpha-70141125
Neuronal acetylcholine receptor subunit alpha-4018626
Acetylcholine-binding protein0123
Neuronal acetylcholine receptor subunit alpha-70191030
Acetylcholine receptor subunit delta09413
Nicotinamidase0202
Poly [ADP-ribose] polymerase 20404
Poly [ADP-ribose] polymerase 1016521
Poly [ADP-ribose] polymerase 1 0101
Chain A, Phenazine biosynthesis protein phzF0011
isocitrate dehydrogenase 1, partial110011
glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase0505
glucose-6-phosphate 1-dehydrogenase isoform b0505
large T antigen017118
pyruvate kinase PKM isoform b230023
Ornithine decarboxylase231025
4-aminobutyrate aminotransferase, mitochondrial0214
Protein skinhead-10202
Monocarboxylate transporter 20505
Solute carrier family 22 member 20013013
Solute carrier family 22 member 6013013
ATP-dependent translocase ABCB108916138
Calmodulin-1010212
Androgen receptor125544
Pyruvate kinase PKM09211
Polyunsaturated fatty acid lipoxygenase ALOX15012012
Polyunsaturated fatty acid lipoxygenase ALOX120808
Xanthine dehydrogenase/oxidase032033
Fatty acid synthase010010
Cytochrome P450 1B1037139
Aurora kinase B0252651
Dipeptidyl peptidase 3011011
HSP40, subfamily A [Plasmodium falciparum 3D7]0006
Kynureninase0001
D(4) dopamine receptor0771297
POU domain, class 2, transcription factor 10109
Trace amine-associated receptor 10189
Acetylcholine receptor subunit alpha0729
Acetylcholine receptor subunit beta0628
Acetylcholine receptor subunit gamma0628
Acetylcholine receptor subunit delta0639
Neuronal acetylcholine receptor subunit alpha-3014723
Muscarinic acetylcholine receptor M1045960
Muscarinic acetylcholine receptor M30411156
Muscarinic acetylcholine receptor M4039750
Muscarinic acetylcholine receptor M5039750
Muscarinic acetylcholine receptor M2044858
Neuronal acetylcholine receptor subunit alpha-208514
Neuronal acetylcholine receptor subunit beta-307614
Neuronal acetylcholine receptor subunit beta-4014723
Neuronal acetylcholine receptor subunit alpha-507513
Neuronal acetylcholine receptor subunit alpha-609616
Neuronal acetylcholine receptor subunit alpha-907513
Neuronal acetylcholine receptor subunit alpha-1007513
Chain A, DNA-3-methyladenine glycosylase I0011
Chain A, DNA-3-METHYLADENINE GLYCOSYLASE I0011
Chain A, Dna-3-methyladenine Glycosylase I0011
thyrotropin-releasing hormone receptor320032
hemoglobin subunit beta160016
Delta-aminolevulinic acid dehydratase0202
Isocitrate lyase 10202
Isocitrate lyase0303
Isocitrate lyase0101
pyruvate kinase PKM isoform a9009
Tubulin--tyrosine ligase0202
Regulatory protein E20011
Aldo-keto reductase family 1 member C3011011
Large neutral amino acids transporter small subunit 1011012
Calcium dependent protein kinase0101
hypothetical protein, conserved290029
luciferase8008
P53120012
Replicase polyprotein 1ab0202545
FAD-linked sulfhydryl oxidase ALR0004
lethal(3)malignant brain tumor-like protein 1 isoform I300030
glycogen synthase kinase-3 alpha00010
serine/threonine-protein kinase 33 isoform a0057
endoribonuclease toxin MazF0044
Arginase-10101
Tyrosine-protein kinase Lck0332963
Dipeptidyl peptidase 40606
ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 10808
Tyrosine-protein kinase SYK0143347
Lactoylglutathione lyase017017
Myosin light chain kinase, smooth muscle072633
Arginase-10404
Rap guanine nucleotide exchange factor 4400040
phosphoglycerate kinase150015
Transient receptor potential cation channel subfamily M member 20213
Chain A, Penicillin Amidohydrolase0303
Chain B, Penicillin Amidohydrolase0303
Chain A, Penicillin Amidohydrolase0303
Chain B, Penicillin Amidohydrolase0303
Chain A, Penicillin Amidohydrolase0303
Chain B, Penicillin Amidohydrolase0303
Chain A, Penicillin Amidohydrolase0303
Chain B, Penicillin Amidohydrolase0303
Chain A, Penicillin Amidohydrolase0303
Chain B, Penicillin Amidohydrolase0303
Chain A, Penicillin Amidohydrolase0303
Chain B, Penicillin Amidohydrolase0303
Chain A, Penicillin Amidohydrolase0303
Chain B, Penicillin Amidohydrolase0303
Chain A, Protocatechuate 3,4-dioxygenase0011
Chain M, Protocatechuate 3,4-dioxygenase0011
Olfactory receptor class A-like protein 10022
RGS12110011
alkaline phosphatase, intestinal0134
alkaline phosphatase, tissue-nonspecific isozyme isoform 1 preproprotein0314
intestinal alkaline phosphatase precursor0314
guanine nucleotide-binding protein G(i) subunit alpha-1 isoform 19009
alkaline phosphatase, germ cell type preproprotein0134
Inhibitor of nuclear factor kappa-B kinase subunit beta041419
RAF proto-oncogene serine/threonine-protein kinase0121528
Ribosomal protein S6 kinase beta-1032528
Mitogen-activated protein kinase 10122840
RAC-alpha serine/threonine-protein kinase0142640
RAC-beta serine/threonine-protein kinase042630
Vascular endothelial growth factor receptor 20261745
MAP kinase-activated protein kinase 2052631
5'-AMP-activated protein kinase subunit gamma-1012325
Dual specificity mitogen-activated protein kinase kinase 10122638
5'-AMP-activated protein kinase catalytic subunit alpha-1022831
Serine/threonine-protein kinase Nek1012627
5'-AMP-activated protein kinase subunit beta-10124
High affinity nerve growth factor receptor082735
Vascular endothelial growth factor receptor 1 0111627
Vascular endothelial growth factor receptor 3091524
Mitogen-activated protein kinase kinase kinase 9041519
Protein delta homolog 10224
Mitogen-activated protein kinase kinase kinase 10031518
Mitogen-activated protein kinase kinase kinase 11032629
Glutamate receptor ionotropic, NMDA 2D022224
Glutamate receptor ionotropic, NMDA 2C022224
histone-lysine N-methyltransferase 2A isoform 2 precursor550055
Kappa-type opioid receptor013420
Mu-type opioid receptor0451059
Kappa-type opioid receptor018827
Delta-type opioid receptor0541986
Kappa-type opioid receptor032644
Kappa-type opioid receptor0581889
Mu-type opioid receptor017426
Genome polyprotein 0213
transcriptional regulator ERG isoform 3330033
Thiopurine S-methyltransferase0303
Succinate-semialdehyde dehydrogenase, mitochondrial0707
4-aminobutyrate aminotransferase, mitochondrial09010
Dihydropteroate synthase 0011
Chain A, Toluene-4-monooxygenase system protein A0101
Potassium channel subfamily K member 20111425
Potassium voltage-gated channel subfamily A member 30213
Acetylcholinesterase015015
Pteridine reductase 10505
Potassium voltage-gated channel subfamily A member 10516
Potassium voltage-gated channel subfamily H member 201631168
[tau protein] kinase 0101
G2/mitotic-specific cyclin-B2013015
cAMP-dependent protein kinase catalytic subunit alpha0909
Beta-casein0101
Protein kinase C alpha type0808
Cyclin-dependent kinase 10242147
Protein kinase C delta type0808
Protein kinase C epsilon type0808
Protein kinase C zeta type0808
Replicase polyprotein 1ab0442670
Replicase polyprotein 1ab0693099
G2/mitotic-specific cyclin-B1021023
Protein kinase C gamma type0808
Protein kinase C beta type0808
Protein kinase C eta type0808
G2/mitotic-specific cyclin-B3013015
Protein kinase C theta type0808
Tissue alpha-L-fucosidase0404
Transient receptor potential cation channel subfamily A member 105712
Chain A, Nadph Dehydrogenase 10011
Chain A, PROTOCATECHUATE 3,4-DIOXYGENASE0101
Chain M, PROTOCATECHUATE 3,4-DIOXYGENASE0101
Chain A, PROTOCATECHUATE 3,4-DIOXYGENASE0101
Chain M, PROTOCATECHUATE 3,4-DIOXYGENASE0101
Chain A, PROTOCATECHUATE 3,4-DIOXYGENASE0101
Chain M, PROTOCATECHUATE 3,4-DIOXYGENASE0101
Chain A, PROTOCATECHUATE 3,4-DIOXYGENASE0101
Chain M, PROTOCATECHUATE 3,4-DIOXYGENASE0101
Chain A, PROTOCATECHUATE 3,4-DIOXYGENASE0101
Chain M, PROTOCATECHUATE 3,4-DIOXYGENASE0101
Chain A, Protocatechuate 3,4-dioxygenase0101
Chain M, Protocatechuate 3,4-dioxygenase0101
Carbonic anhydrase 3035148
Carbonic anhydrase 4071187
Carbonic anhydrase 6045160
Carbonic anhydrase 5A, mitochondrial046366
Carbonic anhydrase010010
Carbonic anhydrase 15034041
Carbonic anhydrase 13026040
Toll-like receptor 2 0202
Carbonic anhydrase 5B, mitochondrial038155
Tyrosinase014014
Hepatocyte growth factor receptor0112637
Carbonic anhydrase 0707
Beta-carbonic anhydrase 1013013
Carbonic anhydrase 08015
Carbonic anhydrase011019
3-phosphoinositide-dependent protein kinase 1041620
Purine nucleoside phosphorylase0044
cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A0809
5-hydroxytryptamine receptor 2C 0809
5-hydroxytryptamine receptor 2A0506
5-hydroxytryptamine receptor 5A016016
Liver carboxylesterase 1010017
Caspase-7380038
caspase-3380038
nuclear factor NF-kappa-B p105 subunit isoform 1230225
Estrogen receptor1391052
Sarcoplasmic/endoplasmic reticulum calcium ATPase 1015116
Sex hormone-binding globulin001515
Aldo-keto reductase family 1 member B101150115
Alpha-2A adrenergic receptor014611163
60 kDa chaperonin017017
60 kDa heat shock protein, mitochondrial020020
Beta-3 adrenergic receptor0321446
Androgen receptor053054
Substance-K receptor038039
10 kDa heat shock protein, mitochondrial020020
Thiosulfate sulfurtransferase020020
60 kDa chaperonin 020020
10 kDa chaperonin 020020
D(2) dopamine receptor022022
5-hydroxytryptamine receptor 4 0101
Chain A, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain B, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain A, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain B, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain A, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain B, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain A, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain B, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain A, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain B, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain A, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain B, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain A, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain B, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain A, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain B, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain A, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Chain B, AROMATIC AMINO ACID AMINOTRANSFERASE0011
Histone deacetylase 3026129
Histone deacetylase 4026231
Histone deacetylase 1035340
Histone deacetylase 7024127
Histone deacetylase 2031235
Polyamine deacetylase HDAC10021124
Histone deacetylase 11 022125
Histone deacetylase 8029233
NAD-dependent protein deacylase sirtuin-5, mitochondrial0808
Histone deacetylase 6032338
Histone deacetylase 9023126
Histone deacetylase 5025128
nuclear receptor subfamily 1, group I, member 2350035
Stromelysin-107411
Peregrin0011
Beta-lactamase 0237
Prostaglandin G/H synthase 1035238
Melatonin receptor type 1A07310
G-protein coupled bile acid receptor 1031417
Chain A, Carbonic Anhydrase Ii0011
Beta-1 adrenergic receptor016425
Beta-2 adrenergic receptor0314
5-hydroxytryptamine receptor 7045148
Beta-2 adrenergic receptor0421861
Glucocorticoid receptor127855
5-hydroxytryptamine receptor 1D020127
5-hydroxytryptamine receptor 1B018422
Cholecystokinin receptor type A07310
Gastrin/cholecystokinin type B receptor0426
5-hydroxytryptamine receptor 601021107
Fatty-acid amide hydrolase 1320024
5-hydroxytryptamine receptor 4012518
Transient receptor potential cation channel subfamily M member 80315
Cytochrome P450 2C9 01086118
Metabotropic glutamate receptor 80224
D-amino-acid oxidase0314
D-amino-acid oxidase0628
D-aspartate oxidase 0101
Reverse transcriptase/RNaseH 014423
Hydroxycarboxylic acid receptor 20527
PPM1D protein980098
Thymidylate synthase0103
Canalicular multispecific organic anion transporter 10608
Integrase 028028
G-protein coupled receptor 350131225
Catechol O-methyltransferase011113
Chain A, N-methyl-D-aspartate Receptor Subunit 10202
Chain A, N-methyl-D-aspartate Receptor Subunit 10202
Chain A, N-methyl-D-aspartate Receptor Subunit 10202
Pancreatic triacylglycerol lipase015016
Guanylate cyclase soluble subunit beta-20101
Guanylate cyclase soluble subunit alpha-20101
Translation factor GUF1, mitochondrial0101
Guanylate cyclase soluble subunit alpha-10101
Guanylate cyclase soluble subunit beta-10101
Acetylcholinesterase01073112
Prostaglandin G/H synthase 1048049
Prostaglandin G/H synthase 20551777
Dehydrogenase/reductase SDR family member 90202
DNA polymerase III, partial190019
hexokinase-4 isoform 1180018
runt-related transcription factor 1 isoform AML1b140014
glucokinase regulatory protein180018
core-binding factor subunit beta isoform 2140014
ubiquitin carboxyl-terminal hydrolase 2 isoform a590059
DNA-(apurinic or apyrimidinic site) endonuclease0202
DNA repair protein RAD52 homolog0505
C-terminal-binding protein 16006
Bile acid receptor07613
beta-2 adrenergic receptor9009
Luciferin 4-monooxygenase0415
2,3-bisphosphoglycerate-independent phosphoglycerate mutase120012
caspase-1 isoform alpha precursor260026
Aromatase036037
Aldo-keto reductase family 1 member B1010010
Hsf1 protein001012
Beta-secretase 1026230
Histamine H3 receptor07210
ERAP1 protein0003
Acetylcholinesterase054157
Glyceraldehyde-3-phosphate dehydrogenase0707
Seed linoleate 13S-lipoxygenase-1016024
Aldo-keto reductase family 1 member B1040041
Glyceraldehyde-3-phosphate dehydrogenase, glycosomal0404
Genome polyprotein0101
Small conductance calcium-activated potassium channel protein 30505
Cholinesterase041144
Sorbitol dehydrogenase0505
Induced myeloid leukemia cell differentiation protein Mcl-10909
Zn finger protein 0202
Dihydroorotate dehydrogenase 010010
Tyrosine-protein kinase Yes0102636
Proto-oncogene tyrosine-protein kinase receptor Ret092736
Mast/stem cell growth factor receptor Kit0172037
Interferon-induced, double-stranded RNA-activated protein kinase041519
Tyrosine-protein kinase receptor UFO031518
Serine/threonine-protein kinase Nek4011415
Tyrosine-protein kinase Mer032124
Receptor-interacting serine/threonine-protein kinase 1061622
Protein-tyrosine kinase 6022628
Inhibitor of nuclear factor kappa-B kinase subunit epsilon012627
NT-3 growth factor receptor011617
BDNF/NT-3 growth factors receptor021517
Discoidin domain-containing receptor 20102636
Eukaryotic translation initiation factor 2-alpha kinase 1012526
Myosin light chain kinase 2, skeletal/cardiac muscle011516
Eukaryotic translation initiation factor 2-alpha kinase 30101
Serine/threonine-protein kinase WNK20101
Mitogen-activated protein kinase kinase kinase kinase 5012627
Amine oxidase [flavin-containing] A 030133
Nitric oxide synthase, endothelial0608
Nitric oxide synthase, endothelial09010
Nitric oxide synthase, brain015118
Nitric oxide synthase, brain 09011
Nitric oxide synthase, inducible017018
Nitric oxide synthase, inducible011116
Nitric oxide synthase, endothelial 0101
aryl hydrocarbon receptor0011
nuclear receptor subfamily 1 group I member 2 isoform 10011
Amine oxidase [flavin-containing] B041044
Amine oxidase [flavin-containing] B0607
Beta-glucuronidase 0101
PAX800010
LacZ protein (plasmid)0044
tumor necrosis factor6208
type-1 angiotensin II receptor0404
apelin receptor0505
nucleotide-binding oligomerization domain-containing protein 1 isoform 10112
nucleotide-binding oligomerization domain-containing protein 2 isoform 10112
streptokinase A precursor002020
Estrogen receptor011012
NF-kappa-B inhibitor alpha0022
Methionine aminopeptidase 20202
Methionine aminopeptidase 10202
Transcription factor p65013015
Estrogen receptor beta011012
Solute carrier family 40 member 10202
mu opioid receptor, partial0022
Sphingosine-1-phosphate receptor 40101
Microphthalmia-associated transcription factor0002
delta-type opioid receptor0224
kappa-type opioid receptor isoform 10202
sphingosine 1-phosphate receptor 10101
DNA dC->dU-editing enzyme APOBEC-3F isoform a190019
Cyclin-dependent kinases regulatory subunit 10101
S-phase kinase-associated protein 20101
Beta-galactosidase0022
cAMP-specific 3',5'-cyclic phosphodiesterase 4A018221
cAMP-specific 3',5'-cyclic phosphodiesterase 4C012012
Purine nucleoside phosphorylase0407
mu-type opioid receptor isoform MOR-1001111
5-hydroxytryptamine receptor 2A001111
Translocator protein017523
Alpha-1D adrenergic receptor01169133
Alpha-1A adrenergic receptor0431467
Alpha-1B adrenergic receptor0361256
5-hydroxytryptamine receptor 7033033
D0707
5-hydroxytryptamine receptor 2A0505
Sigma non-opioid intracellular receptor 101152117
Lysosomal alpha-glucosidase0303
Chain A, Avidin0022
Chain A, Avidin0022
Chain B, Avidin0022
Olfactory receptor 51E20077
2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase0022
Trypsin0708
Coagulation factor VII012012
Tissue factor016016
Oxoeicosanoid receptor 10202
Ubiquitin carboxyl-terminal hydrolase isozyme L30202
RAC-gamma serine/threonine-protein kinase032629
cystic fibrosis transmembrane conductance regulator ATP-binding cassette sub-family C member 70003
Cytochrome P450 1A1029232
Polyunsaturated fatty acid 5-lipoxygenase013018
Potassium voltage-gated channel subfamily E member 1010010
Potassium voltage-gated channel subfamily A member 50505
Receptor-type tyrosine-protein kinase FLT30242752
Potassium voltage-gated channel subfamily KQT member 1011011
Mitogen-activated protein kinase 100182846
Disintegrin and metalloproteinase domain-containing protein 17453048
Inositol polyphosphate multikinase0707
Inositol hexakisphosphate kinase 20707
Potassium voltage-gated channel subfamily D member 30707
Sialidase-2014014
ATP-binding cassette sub-family C member 302380238
Multidrug resistance-associated protein 402410247
Solute carrier family 22 member 6021024
UDP-glucuronosyltransferase 1A902114
Bile salt export pump052054
Bile salt export pump03740376
Cytochrome P450 2B10305
Cytochrome P450 1A10125
Myoglobin0101
Polyunsaturated fatty acid lipoxygenase ALOX15029029
UDP-glucuronosyltransferase 1-6011116
Arachidonate 5-lipoxygenase-activating protein0404
UDP-glucuronosyltransferase 1A1 020130
Cytochrome P450 2J2052054
Canalicular multispecific organic anion transporter 102290231
toxin B0001
Chain A, CARBONIC ANHYDRASE II0011
Chain A, CARBONIC ANHYDRASE II0011
Chain A, CARBONIC ANHYDRASE II0011
Chain A, Carbonic Anhydrase Ii0011
Chain A, Carbonic Anhydrase Ii0011
Chain A, Endochitinase0202
Chain A, Endochitinase0202
Chain A, Endochitinase0202
Chain A, Class Iii Chitinase Chia10101
Chain A, Carbonic anhydrase 130101
Chain A, Carbonic anhydrase II0101
Chain A, Carbonic anhydrase 20101
Chain A, Carbonic anhydrase 20101
Chain A, Carbonic anhydrase 20101
Chain A, Carbonic anhydrase 20101
Chain A, Carbonic anhydrase 20101
Chain A, Carbonic anhydrase 20101
Chain A, Carbonic anhydrase 20101
Chain A, Carbonic anhydrase 20101
Chain A, Carbonic anhydrase 20101
Chain A, Carbonic anhydrase0101
Chain B, Carbonic anhydrase0101
Chain A, Carbonic anhydrase 20101
Carbonic anhydrase 0006
Carbonic anhydrase 011011
GALC protein380038
Carbonic anhydrase 0808
Carbonic anhydrase 0909
Carbonic anhydrase0909
Carbonic anhydrase0505
Prolyl endopeptidase0404
Carbonic anhydrase-related protein 110103
Glycogen phosphorylase, muscle form013013
Carbonic anhydrase 20303
Cathepsin B0202
Steryl-sulfatase0203
Cytochrome P450 2C8019123
Cytochrome P450 2B6012216
Carbonic anhydrase 5A, mitochondrial0303
Serum paraoxonase/arylesterase 10505
Dipeptidyl peptidase 4018222
Endochitinase0202
Carbonic anhydrase021027
Carbonic anhydrase0202
Corticosteroid 11-beta-dehydrogenase isozyme 10314
Carbonic anhydrase07014
Carbonic anhydrase 2010010
Squalene synthase0404
Carbonic anhydrase, alpha family 010010
Carbonic anhydrase 3011011
Carbonic anhydrase06014
Carbonic anhydrase 0808
Sigma intracellular receptor 2017017
Delta carbonic anhydrase0808
Renin0101
Carbonic anhydrase 06013
Endochitinase A10202
Multidrug resistance-associated protein 10303
Carbonic anhydrase 13018123
Carbonic anhydrase 409014
Acidic mammalian chitinase0202
Carbonic anhydrase 70101
Carbonic anhydrase 0303
Carbonic anhydrase 0101
Carbonic anhydrase 2, isoform A 0101
Free fatty acid receptor 30033
Free fatty acid receptor 20224
Tyrosine-protein kinase Fyn0312758
Fibrinogen C domain-containing protein 10202
Urease0607
Urease subunit alpha013013
Succinyl-diaminopimelate desuccinylase0505
Collagenase 309010
Peptide deformylase0101
Urease subunit beta013013
Urease subunit gamma0101
Urease subunit beta0101
Urease subunit alpha0101
Urease subunit beta 0202
N-alpha-acetyltransferase 500022
Chain A, caspase-3, p17 subunit0101
Chain B, caspase-3, p12 subunit0101
Chain A, caspase-3, p17 subunit0101
Chain B, caspase-3, p12 subunit0101
Chain A, caspase-3, p17 subunit0101
Chain B, caspase-3, p12 subunit0101
Caspase-1012114
Caspase-30606
Caspase-20123
Caspase-60101
Caspase-80101
Putative glycosyltransferase WbgO0001
Killer cell lectin-like receptor subfamily B member 1A0101
Early activation antigen CD690101
Calpain small subunit 10101
Calpain-1 catalytic subunit0505
Cathepsin B0909
Calpain-1 catalytic subunit0303
DNA topoisomerase 2-alpha0122044
Fibroblast growth factor receptor 4031519
integrase, partial0606
lens epithelium-derived growth factor p750606
Arginase 0707
Protein kinase C alpha type0192445
Prostaglandin G/H synthase 2021022
Chain E, Purine nucleoside phosphorylase0101
Thymidine kinase 0304
Thymidine kinase, cytosolic07012
Solute carrier family 22 member 6017025
Thymidine kinase 0101
Solute carrier family 22 member 8014022
Thymidine kinase0203
Chain A, MTA/SAH nucleosidase0101
Chain A, Ribosome-inactivating protein alpha-trichosanthin0011
Chain A, Ricin A chain0011
Chain A, Ribosome-inactivating protein 30011
Chain A, Phenylethanolamine N-methyltransferase0011
Chain A, Phenylethanolamine N-methyltransferase0011
Chain A, Phenylethanolamine N-methyltransferase0011
Chain A, Phenylethanolamine N-methyltransferase0011
Chain A, Phenylethanolamine N-methyltransferase0011
Chain A, Phenylethanolamine N-methyltransferase0011
Chain A, Phenylethanolamine N-methyltransferase0011
Chain A, Phenylethanolamine N-methyltransferase0011
Chain A, Phenylethanolamine N-methyltransferase0011
Chain A, Phenylethanolamine N-methyltransferase0011
Chain A, Phenylethanolamine N-methyltransferase0011
Chain A, Phenylethanolamine N-methyltransferase0011
Chain A, Phenylethanolamine N-methyltransferase0011
tumor susceptibility gene 101 protein120012
Protein mono-ADP-ribosyltransferase PARP150505
Leucine-rich repeat serine/threonine-protein kinase 20171532
Chain A, Membrane lipoprotein tmpC0033
Chain A, Membrane lipoprotein tmpC0033
Chain A, Membrane lipoprotein tmpC0033
Chain A, Structure of PAE2307 in complex with adenosine0011
Chain B, Structure of PAE2307 in complex with adenosine0011
Chain A, ADENOSINE RECEPTOR A2A0202
Chain A, ADENOSINE RECEPTOR A2A0202
Chain A, tRNA (guanine-N(1)-)-methyltransferase0011
Chain A, Uncharacterized protein MJ08830011
signal transducer and activator of transcription 6, interleukin-4 induced6006
NPYLR7B0099
glycogen synthase kinase-3 beta isoform 1001112
high affinity choline transporter 1 isoform a0404
Sodium/nucleoside cotransporter 10404
Calcium dependent protein kinase0101
Mitogen-activated protein kinase kinase kinase 7001717
Sodium/nucleoside cotransporter 20505
Epidermal growth factor receptor0532780
Phosphoglycerate kinase 1 0101
Adenosine deaminase0001
Avidin0011
Adenosine deaminase0001
Receptor tyrosine-protein kinase erbB-20201535
Insulin receptor0102738
Phosphoglycerate kinase 20101
Platelet-derived growth factor receptor beta0182746
Heat shock 70 kDa protein 1A 0213
Heat shock cognate 71 kDa protein0044
Fibroblast growth factor receptor 10122741
Inosine-5'-monophosphate dehydrogenase 2051824
Endoplasmin0337
Inosine-5'-monophosphate dehydrogenase 1 0405
Fibroblast growth factor receptor 2021518
Fibroblast growth factor receptor 3021619
Streptavidin0022
Adenosylhomocysteinase0205
Adenylate kinase 2, mitochondrial0203
Adenylate kinase isoenzyme 1 0203
Phosphatidylinositol 4-kinase alpha0607
Adenosine kinase022124
Adenosine deaminase 0102
Equilibrative nucleoside transporter 20404
Phosphatidylinositol 4-kinase type 2-beta0506
Histone-lysine N-methyltransferase, H3 lysine-79 specific0516
Equilibrative nucleoside transporter 10707
Phosphatidylinositol 4-kinase type 2-alpha0607
Solute carrier family 28 member 30505
Adenosine kinase0102
Phosphatidylinositol 4-kinase beta061421
5-methylthioadenosine/S-adenosylhomocysteine deaminase0002
Adenosine transporter 10102
Chain A, EOSINOPHIL-DERIVED NEUROTOXIN0202
Chain A, EOSINOPHIL-DERIVED NEUROTOXIN0202
Chain A, EOSINOPHIL-DERIVED NEUROTOXIN0202
Chain A, Ribonuclease pancreatic0202
Chain A, Ribonuclease pancreatic0202
Chain A, Ribonuclease pancreatic0202
Chain A, Ribonuclease pancreatic0202
Chain A, Ribonuclease pancreatic0202
Chain A, heparan sulfate (glucosamine) 3-O-sulfotransferase 10011
P2Y purinoceptor 10235
Chain A, Heat Shock Protein 900011
Chain A, GLUTAMINE PHOSPHORIBOSYLPYROPHOSPHATE AMIDOTRANSFERASE0011
Chain B, GLUTAMINE PHOSPHORIBOSYLPYROPHOSPHATE AMIDOTRANSFERASE0011
Chain A, Myosin Ie Heavy Chain0011
Chain A, Preprotein translocase secA0011
Chain A, Phosphoribosylformylglycinamidine synthase0101
Chain A, nucleoside diphosphate kinase A0011
Chain B, nucleoside diphosphate kinase A0011
Chain D, DNA polymerase III subunit gamma0011
Chain D, DNA polymerase III subunit gamma0011
Chain A [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 30011
Chain A [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 30011
Chain A, Kinesin-like protein KIF110101
HPr kinase/phosphorylase0011
ATP-dependent molecular chaperone HSP820214
2-dehydropantoate 2-reductase0246
Endoplasmic reticulum chaperone BiP0011
Pyruvate kinase PKM 0001
Pyruvate kinase PKLR 0001
Heat shock cognate 71 kDa protein0011
5'-nucleotidase0303
P2Y purinoceptor 20066
P2X purinoceptor 10134
P2Y purinoceptor 10156
P2X purinoceptor 10112
P2X purinoceptor 40235
P2X purinoceptor 50022
P2X purinoceptor 60123
P2X purinoceptor 30224
Heat shock protein 75 kDa, mitochondrial0202
P2Y purinoceptor 60066
P2Y purinoceptor 110033
P2Y purinoceptor 120325
Sensor protein kinase WalK0101
P2X purinoceptor 20123
Chain A, Glycogen Phosphorylase B0011
Chain B, Glycogen Phosphorylase B0011
Chain A, ADP-dependent glucokinase0101
Chain A, Ribonuclease pancreatic0202
Chain A, Ribonuclease pancreatic0202
Chain A, phosphodiesterase-nucleotide pyrophosphatase0101
Chain A, GLYCOGEN PHOSPHORYLASE B0011
Chain B, GLYCOGEN PHOSPHORYLASE B0011
Chain A, GLYCOGEN PHOSPHORYLASE B0011
2'-deoxynucleoside 5'-phosphate N-hydrolase 10101
2'-deoxynucleoside 5'-phosphate N-hydrolase 10101
5'-AMP-activated protein kinase subunit beta-20012
L-lactate dehydrogenase A chain0426
Adenylate kinase isoenzyme 10001
Fructose-1,6-bisphosphatase 10101
Alkaline phosphatase, tissue-nonspecific isozyme0506
Fructose-1,6-bisphosphatase 10708
Inosine-5'-monophosphate dehydrogenase0102
Proto-oncogene tyrosine-protein kinase Src0302758
5'-nucleotidase0304
GTP:AMP phosphotransferase AK3, mitochondrial0001
5'-AMP-activated protein kinase catalytic subunit alpha-2011618
Adenylate kinase 2, mitochondrial002122
Glycine--tRNA ligase0101
Adenosine deaminase-like protein0001
Protease 011417
5'-AMP-activated protein kinase subunit gamma-30012
5'-AMP-activated protein kinase subunit gamma-2002223
Chain A, Endoplasmin0011
vasopressin V1b receptor4004
thyrotropin-releasing hormone receptor1001
relaxin receptor 2 isoform 14004
Transmembrane domain-containing protein TMIGD30101
Thyroid hormone receptor beta0404
Aflatoxin B1 aldehyde reductase member 30101
Adenosine receptor A10202
Endoplasmin0011
2-oxoglutarate receptor 10101
ubiquitin-conjugating enzyme E2 N0909
Phospholipase D20101
Estrogen-related receptor gamma0325
Phospholipase D10202
Estrogen receptor beta1251036
Acetylcholinesterase021223
chaperonin-containing TCP-1 beta subunit homolog8008
Tyrosine-protein kinase JAK20102436
Tyrosine-protein kinase JAK1062735
Tyrosine-protein kinase JAK30111630
Tyrosyl-DNA phosphodiesterase 10303
Cystathionine gamma-lyase0606
Cystathionine beta-synthase0303
Polyamine oxidase 10101
Nischarin0606
Deoxyhypusine synthase0101
Bifunctional purine biosynthesis protein ATIC0405
Histidine triad nucleotide-binding protein 10011
Aldo-keto reductase family 1 member A10202
Alanine racemase, biosynthetic0001
Proton-coupled amino acid transporter 1018019
Adenosine deaminase0001
Vif0607
Methionine aminopeptidase0202
Beta-1 adrenergic receptor0381654
Beta-2 adrenergic receptor 0147
Beta-2 adrenergic receptor0121125
Corticosteroid-binding globulin010011
Mineralocorticoid receptor 110619
Mineralocorticoid receptor0112
Solute carrier organic anion transporter family member 1A107014
Alpha-1A adrenergic receptor0549
Alpha-1A adrenergic receptor010414
Sodium channel protein type 5 subunit alpha033033
Thioredoxin reductase 1, cytoplasmic0202
Bifunctional epoxide hydrolase 2014014
5-lipoxygenase 0303
P2Y purinoceptor 120808
Thioredoxin reductase 2, mitochondrial0101
Hypoxanthine-guanine phosphoribosyltransferase0105
Nuclear receptor ROR-gamma0202
Shiga toxin subunit A0202
Histamine H3 receptor06112
Chain A, Xcogt0011
Chain A, Xcogt0011
Chain A, Xcogt0011
Sigma non-opioid intracellular receptor 10202
Tryptophan 5-hydroxylase 1011011
D(2) dopamine receptor0909
5-hydroxytryptamine receptor 2B0505
Glutamate receptor ionotropic, NMDA 3B019221
Glutamate receptor 10213
Glutamate receptor 20202
Excitatory amino acid transporter 10405
Excitatory amino acid transporter 20405
Excitatory amino acid transporter 30405
Glutamate receptor ionotropic, NMDA 1028230
Glutamate receptor ionotropic, NMDA 2A026228
Glutamate receptor ionotropic, kainate 40202
Glutamate receptor ionotropic, kainate 50404
Glutamate receptor ionotropic, NMDA 3A019221
Glutamate receptor 40202
Glutamate receptor 30202
Botulinum neurotoxin type A 0606
Tyrosine-protein kinase 0011
DNA topoisomerase 1010014
3-hydroxy-3-methylglutaryl-coenzyme A reductase0909
3-hydroxy-3-methylglutaryl-coenzyme A reductase0202
D(3) dopamine receptor isoform e3003
ATP-dependent translocase ABCB1023023
Alpha-2B adrenergic receptor01345145
Alpha-2C adrenergic receptor012010136
phospholipase A2 precursor0101
cysteine protease ATG4B isoform a0101
Free fatty acid receptor 10055
Prostaglandin G/H synthase 1 016018
Free fatty acid receptor 40033
Mas-related G-protein coupled receptor member X20077
Albumin0152545
Translocator protein010112
Gamma-aminobutyric acid receptor subunit alpha-10401959
Gamma-aminobutyric acid receptor subunit gamma-20381654
Cholecystokinin receptor type A110011
Gamma-aminobutyric acid receptor subunit alpha-50341246
Gamma-aminobutyric acid receptor subunit alpha-3034943
Gamma-aminobutyric acid receptor subunit alpha-20341044
Gamma-aminobutyric acid receptor subunit beta-20351550
Cholecystokinin receptor type A0707
Beta-2 adrenergic receptor012117
Thromboxane-A synthase 019019
Prostaglandin E2 receptor EP3 subtype0303
Prostaglandin E2 receptor EP4 subtype0314
Prostaglandin E2 receptor EP1 subtype0303
Prostacyclin receptor0426
Nuclear receptor subfamily 4 group A member 20088
Solute carrier organic anion transporter family member 2A10307
Nuclear receptor subfamily 4 group A member 20011
Nuclear receptor subfamily 4 group A member 20011
Prostaglandin E2 receptor EP2 subtype0314
Solute carrier organic anion transporter family member 2A10307
Solute carrier organic anion transporter family member 2B10203
Solute carrier organic anion transporter family member 3A10001
Chain A, Protein (glycogen Phosphorylase)0101
Leukotriene C4 synthase001414
Glycogen synthase kinase-3 beta 0404
[Tau protein] kinase 0404
Bone morphogenetic protein receptor type-1B002525
Serine/threonine-protein kinase 25001515
ATP-dependent RNA helicase DDX3X002121
Pyridoxal kinase002122
Citron Rho-interacting kinase012627
Serine/threonine-protein kinase RIO3001515
Dual specificity mitogen-activated protein kinase kinase 7011415
Serine/threonine-protein kinase Chk1032629
Peripheral plasma membrane protein CASK001414
Aurora kinase A092736
Cyclin-G-associated kinase012728
Serine/threonine-protein kinase DCLK1001515
Inhibitor of nuclear factor kappa-B kinase subunit alpha021416
Muscle, skeletal receptor tyrosine-protein kinase001515
Ephrin type-B receptor 6002525
Peroxisomal acyl-coenzyme A oxidase 3002121
Mitogen-activated protein kinase kinase kinase 13001414
Death-associated protein kinase 3001616
Receptor-interacting serine/threonine-protein kinase 2062632
Mitotic checkpoint serine/threonine-protein kinase BUB1002121
NUAK family SNF1-like kinase 1041519
Dynamin-like 120 kDa protein, mitochondrial002121
Phosphatidylinositol 4-phosphate 5-kinase type-1 gamma001414
Cyclin-T10808
Eukaryotic translation initiation factor 5B001212
Rho-associated protein kinase 2062632
Serine/threonine-protein kinase ULK1002525
Serine/threonine-protein kinase/endoribonuclease IRE1022527
Ribosomal protein S6 kinase alpha-5042731
U5 small nuclear ribonucleoprotein 200 kDa helicase002121
Ribosomal protein S6 kinase alpha-4002626
Serine/threonine-protein kinase 16002727
Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma001414
Cyclin-K0202
Serine/threonine-protein kinase PAK 3001515
Cyclin-dependent kinase-like 5002020
Serine/threonine-protein kinase 17B011516
Serine/threonine-protein kinase 10002626
Serine/threonine-protein kinase D3082735
Cyclin-dependent kinase 14001515
Structural maintenance of chromosomes protein 2002020
Mitogen-activated protein kinase kinase kinase 6002424
Serine/threonine-protein kinase OSR1001414
Mitogen-activated protein kinase kinase kinase kinase 4002626
Serine/threonine-protein kinase LATS1002626
Serine/threonine-protein kinase PAK 4022628
Serine/threonine-protein kinase Chk2011415
G1/S-specific cyclin-E20202
Tyrosine-protein kinase ABL10303367
Vitamin K-dependent protein C0202
Guanine nucleotide-binding protein G(i) subunit alpha-2001414
Protein kinase C gamma type010212
ADP/ATP translocase 2002121
Protein kinase C beta type0142337
Glycogen phosphorylase, liver form022123
Tyrosine-protein kinase Fes/Fps012728
Macrophage colony-stimulating factor 1 receptor0121527
Adenine phosphoribosyltransferase001515
Tyrosine-protein kinase Lyn072633
Insulin-like growth factor 1 receptor082634
Signal recognition particle receptor subunit alpha002020
Cytochrome c1, heme protein, mitochondrial002121
Tyrosine-protein kinase HCK072633
Proto-oncogene tyrosine-protein kinase ROS011516
Tyrosine-protein kinase Fgr002222
Wee1-like protein kinase 2001414
Uncharacterized serine/threonine-protein kinase SBK3001414
Serine/threonine-protein kinase A-Raf032124
Glycogen phosphorylase, brain form022123
Breakpoint cluster region protein0132643
Myosin light chain kinase, smooth muscle031215
Cyclin-dependent kinase 40142540
ADP/ATP translocase 3002121
cAMP-dependent protein kinase type II-alpha regulatory subunit002020
Insulin receptor-related protein001515
Serine/threonine-protein kinase B-raf0132842
G2/mitotic-specific cyclin-B0808
Phosphorylase b kinase gamma catalytic chain, liver/testis isoform002727
Ribosyldihydronicotinamide dehydrogenase [quinone]0122335
Platelet-derived growth factor receptor alpha0141832
Tyrosine-protein kinase Fer002626
cAMP-dependent protein kinase catalytic subunit alpha0142640
General transcription and DNA repair factor IIH helicase subunit XPD002121
Glycogen synthase kinase-3 beta0909
Ras-related protein Rab-6A001919
Serine/threonine-protein kinase MAK001414
Cyclin-dependent kinase 11B001515
Ephrin type-A receptor 1012526
Receptor tyrosine-protein kinase erbB-3001414
Multifunctional protein ADE2002121
Nucleoside diphosphate kinase B0022
Dual specificity protein kinase CLK10202
cAMP-dependent protein kinase catalytic subunit gamma0112031
cAMP-dependent protein kinase catalytic subunit beta0112637
Ferrochelatase, mitochondrial002121
G1/S-specific cyclin-D1012013
Protein kinase C eta type091726
G1/S-specific cyclin-E10707
Beta-adrenergic receptor kinase 1022325
Probable ATP-dependent RNA helicase DDX6002121
Activin receptor type-2A001515
Mitogen-activated protein kinase 3 082736
MAP/microtubule affinity-regulating kinase 3002626
Deoxycytidine kinase012125
Ephrin type-A receptor 2032629
Ephrin type-A receptor 3001717
Ephrin type-A receptor 8001515
Ephrin type-B receptor 2022628
Leukocyte tyrosine kinase receptor011516
Non-receptor tyrosine-protein kinase TYK2042733
UMP-CMP kinase 001212
Phosphatidylethanolamine-binding protein 1001515
G1/S-specific cyclin-D20203
G1/S-specific cyclin-D30304
Wee1-like protein kinase002626
Heme oxygenase 2002121
Mitogen-activated protein kinase 4001515
S-adenosylmethionine synthase isoform type-2011718
DnaJ homolog subfamily A member 1002121
G protein-coupled receptor kinase 4001414
Dual specificity protein kinase TTK022527
DNA replication licensing factor MCM4001919
Myosin-10011819
Tyrosine-protein kinase receptor Tie-1001515
Dual specificity mitogen-activated protein kinase kinase 2082634
Bone morphogenetic protein receptor type-1A002626
Activin receptor type-1B002626
TGF-beta receptor type-1022628
Serine/threonine-protein kinase receptor R3001919
TGF-beta receptor type-2002626
Electron transfer flavoprotein subunit beta001515
Tyrosine-protein kinase CSK052631
Glycine--tRNA ligase002121
Protein kinase C iota type082634
Exosome RNA helicase MTR4002121
Megakaryocyte-associated tyrosine-protein kinase001414
Tyrosine-protein kinase Tec022628
Tyrosine-protein kinase TXK021517
Tyrosine-protein kinase ABL2032629
Tyrosine-protein kinase FRK012627
Tyrosine-protein kinase ZAP-70021517
26S proteasome regulatory subunit 6B012122
Mitogen-activated protein kinase 8042832
Mitogen-activated protein kinase 9042832
Dual specificity mitogen-activated protein kinase kinase 4022224
Dual specificity mitogen-activated protein kinase kinase 3002626
Casein kinase I isoform alpha062531
Casein kinase I isoform delta062632
Cyclin-dependent kinase 8011516
Elongation factor Tu, mitochondrial002121
Choline-phosphate cytidylyltransferase A001313
Cysteine--tRNA ligase, cytoplasmic001717
Casein kinase I isoform epsilon052732
Very long-chain specific acyl-CoA dehydrogenase, mitochondrial002121
Dual specificity protein kinase CLK1022628
Dual specificity protein kinase CLK2012728
Dual specificity protein kinase CLK3002525
Cyclin-dependent kinase 7052631
Cyclin-dependent kinase 9082634
Ras-related protein Rab-27A002020
Tyrosine-protein kinase Blk041519
Interleukin-1 receptor-associated kinase 1002525
Ribosomal protein S6 kinase alpha-3032629
Cytoplasmic tyrosine-protein kinase BMX031619
cAMP-dependent protein kinase catalytic subunit PRKX001515
Cyclin-H0505
CDK-activating kinase assembly factor MAT10303
Serine/threonine-protein kinase Nek2022628
Serine/threonine-protein kinase Nek3002525
Dual specificity mitogen-activated protein kinase kinase 6002626
Death-associated protein kinase 10121527
LIM domain kinase 1012627
LIM domain kinase 2012627
Tyrosine--tRNA ligase, cytoplasmic002121
Ephrin type-B receptor 3002626
Ephrin type-A receptor 5002626
Ephrin type-B receptor 4052732
Ephrin type-B receptor 1001515
Ephrin type-A receptor 4002626
Hormonally up-regulated neu tumor-associated kinase001414
Serine/threonine-protein kinase SIK1021517
Receptor-interacting serine/threonine-protein kinase 4001414
Ras-related protein Rab-10002121
Cell division control protein 2 homolog001414
Actin-related protein 3002121
Actin-related protein 2002020
Calcium-dependent protein kinase 1001414
GTP-binding nuclear protein Ran002121
Tubulin alpha-1A chain001212
Phosphatidylinositol 5-phosphate 4-kinase type-2 beta001515
SRSF protein kinase 2001515
Casein kinase I isoform gamma-2012526
Cyclin-A1010011
Serine/threonine-protein kinase PknB001414
Cyclin-dependent kinase 3002525
Cyclin-dependent kinase-like 1001414
Cyclin-dependent kinase 60102131
Cyclin-dependent-like kinase 5 0152641
Cyclin-dependent kinase 16002727
Cyclin-dependent kinase 17002626
Cyclin homolog0707
ATP-dependent 6-phosphofructokinase, platelet type001919
Protein kinase C epsilon type0141731
Angiopoietin-1 receptor071825
DNA topoisomerase 2-beta032232
Protein kinase C theta type092736
Activin receptor type-1012627
Macrophage-stimulating protein receptor012526
Focal adhesion kinase 1042630
Protein kinase C zeta type0111728
Protein kinase C delta type0122840
Tyrosine-protein kinase BTK032629
Tyrosine-protein kinase receptor TYRO3001515
Cyclin-dependent kinase 18001717
Activated CDC42 kinase 1012627
Epithelial discoidin domain-containing receptor 1082634
Tyrosine-protein kinase ITK/TSK041519
Myotonin-protein kinase021517
Mitogen-activated protein kinase kinase kinase kinase 2002525
Mitogen-activated protein kinase kinase kinase 12001414
Serine/threonine-protein kinase 4012728
Serine/threonine-protein kinase PAK 1031518
Dual specificity mitogen-activated protein kinase kinase 5002525
Mitogen-activated protein kinase 7002626
Serine/threonine-protein kinase PAK 2002424
Serine/threonine-protein kinase 3012627
Mitogen-activated protein kinase kinase kinase 1002525
cGMP-dependent protein kinase 2001515
Integrin-linked protein kinase002121
Rho-associated protein kinase 1042529
Non-receptor tyrosine-protein kinase TNK1002626
Serine/threonine-protein kinase PRP4 homolog001414
Calcium/calmodulin-dependent protein kinase type II subunit beta041519
Calcium/calmodulin-dependent protein kinase type II subunit gamma022628
Calcium/calmodulin-dependent protein kinase type II subunit delta022628
Dual specificity tyrosine-phosphorylation-regulated kinase 1A062531
Activin receptor type-2B002626
Bone morphogenetic protein receptor type-2002626
cGMP-dependent protein kinase 1 012627
Cyclin-dependent kinase 13002525
Calcium/calmodulin-dependent protein kinase type 1001616
Protein-tyrosine kinase 2-beta002626
Maternal embryonic leucine zipper kinase002626
Structural maintenance of chromosomes protein 1A001818
Chromodomain-helicase-DNA-binding protein 4002020
Peroxisomal acyl-coenzyme A oxidase 1001717
Cyclin-dependent kinase 5 activator 1014014
Cyclin-dependent kinase 10001010
Serine/threonine-protein kinase D1081624
Serine/threonine-protein kinase 38001515
Receptor tyrosine-protein kinase erbB-4031417
Ribosomal protein S6 kinase alpha-2001616
Ephrin type-A receptor 7002121
Delta(24)-sterol reductase002020
Ribosomal protein S6 kinase alpha-1032629
Dual specificity testis-specific protein kinase 1002626
Serine/threonine-protein kinase STK11002626
Rhodopsin kinase GRK1021416
Serine/threonine-protein kinase N1022628
Serine/threonine-protein kinase N2022628
Calcium/calmodulin-dependent protein kinase type IV002626
Mitogen-activated protein kinase 6001515
Phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform001515
AP2-associated protein kinase 1012728
Myosin light chain kinase 3012425
La-related protein 70101
Serine/threonine-protein kinase SBK1001414
Mitogen-activated protein kinase kinase kinase 19001414
Putative heat shock protein HSP 90-beta 2001919
Serine/threonine-protein kinase TNNI3K011516
Rab-like protein 3001616
Serine/threonine-protein kinase MRCK alpha002626
Dual specificity tyrosine-phosphorylation-regulated kinase 1A0404
Serine/threonine-protein kinase MRCK gamma002626
Acyl-CoA dehydrogenase family member 10001919
Serine/threonine-protein kinase Nek5001515
Serine/threonine-protein kinase N3001818
Serine/threonine-protein kinase ULK3002525
Dual serine/threonine and tyrosine protein kinase011415
Mitogen-activated protein kinase kinase kinase 15001414
Uncharacterized protein FLJ45252002121
Acyl-CoA dehydrogenase family member 11002020
Serine/threonine-protein kinase/endoribonuclease IRE2002020
Serine/threonine-protein kinase MARK2002727
ATP-dependent RNA helicase DHX30001616
Serine/threonine-protein kinase TAO1002525
STE20-related kinase adapter protein alpha002121
Myosin-14002121
AarF domain-containing protein kinase 1002121
Serine/threonine-protein kinase tousled-like 2001515
Serine/threonine-protein kinase 32C001515
ATP-dependent RNA helicase DDX42001414
Serine/threonine-protein kinase VRK2001414
Myosin light chain kinase family member 4001515
Homeodomain-interacting protein kinase 1011415
Calcium/calmodulin-dependent protein kinase type 1D001616
Mitogen-activated protein kinase kinase kinase kinase 3002626
Cyclin-dependent kinase-like 3001414
MAP kinase-activated protein kinase 5042630
Serine/threonine-protein kinase BRSK2001515
Serine/threonine-protein kinase NIM1001414
Serine/threonine-protein kinase ULK2001414
Misshapen-like kinase 1002020
Serine/threonine-protein kinase DCLK2001515
Calcium/calmodulin-dependent protein kinase kinase 1001515
Casein kinase I isoform alpha-like001515
Homeodomain-interacting protein kinase 4011415
Myosin-IIIa001515
Ankyrin repeat and protein kinase domain-containing protein 1001515
Serine/threonine-protein kinase Nek11001414
Atypical kinase COQ8A, mitochondrial002626
Phosphatidylinositol 5-phosphate 4-kinase type-2 gamma002525
Mitogen-activated protein kinase 15002626
Serine/threonine-protein kinase Nek9002626
Serine/threonine-protein kinase BRSK1001515
Serine/threonine-protein kinase 35001414
Serine/threonine-protein kinase Nek7002222
Rhodopsin kinase GRK7001414
Serine/threonine-protein kinase 32A001414
Myosin-IIIb001515
ATP-dependent RNA helicase DDX1002121
Dual specificity tyrosine-phosphorylation-regulated kinase 2011415
Cyclin-dependent kinase-like 2001414
Mitogen-activated protein kinase kinase kinase kinase 1002626
Serine/threonine-protein kinase Sgk3001414
Atypical kinase COQ8B, mitochondrial001515
MAP/microtubule affinity-regulating kinase 4012627
Calcium/calmodulin-dependent protein kinase type 1G001818
Cyclin-dependent kinase 15001414
PAS domain-containing serine/threonine-protein kinase001919
Calcium/calmodulin-dependent protein kinase kinase 2012728
EKC/KEOPS complex subunit TP53RK002121
Dual specificity testis-specific protein kinase 2001515
SRSF protein kinase 1001515
Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase062632
Mitogen-activated protein kinase kinase kinase 5012627
Phosphatidylinositol 4-phosphate 5-kinase type-1 alpha001515
Mitogen-activated protein kinase kinase kinase 3002525
Serine/threonine-protein kinase RIO1001515
MAP kinase-interacting serine/threonine-protein kinase 1011516
Serine/threonine-protein kinase RIO2001414
Cyclin-dependent kinase 19011516
Transient receptor potential cation channel subfamily M member 6001414
Testis-specific serine/threonine-protein kinase 1001515
Serine/threonine-protein kinase 33001515
Nucleolar GTP-binding protein 1001919
Serine/threonine-protein kinase D2002626
Serine/threonine-protein kinase DCLK3001515
Cyclin-dependent kinase 10808
NUAK family SNF1-like kinase 2002525
RNA cytidine acetyltransferase002121
Serine/threonine-protein kinase SIK2012627
STE20-like serine/threonine-protein kinase 002727
Serine/threonine-protein kinase TAO3002525
Homeodomain-interacting protein kinase 2011415
Tyrosine-protein kinase Srms001515
Homeodomain-interacting protein kinase 3011415
dCTP pyrophosphatase 1022123
Dual specificity protein kinase CLK4012526
MAP kinase-interacting serine/threonine-protein kinase 2041620
Serine/threonine-protein kinase Nek6011516
Casein kinase I isoform gamma-1012728
Serine/threonine-protein kinase PAK 6012122
SNF-related serine/threonine-protein kinase001414
Serine/threonine-protein kinase LATS2001515
Serine/threonine-protein kinase 36011516
Phenylalanine--tRNA ligase beta subunit002121
Isoleucine--tRNA ligase, mitochondrial001212
BMP-2-inducible protein kinase002727
Obg-like ATPase 1001717
Midasin002020
Interleukin-1 receptor-associated kinase 4002525
Serine/threonine-protein kinase 32B001515
Mitogen-activated protein kinase kinase kinase 20012627
Cyclin-dependent kinase 12012122
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 13012021
Serine/threonine-protein kinase MARK1001515
Serine/threonine-protein kinase pim-2002525
Serine/threonine-protein kinase PAK 5011516
Serine/threonine-protein kinase 26012627
eIF-2-alpha kinase GCN2001515
Serine/threonine-protein kinase NLK012627
Serine/threonine-protein kinase 17A001616
STE20/SPS1-related proline-alanine-rich protein kinase001414
Ephrin type-A receptor 6001515
Serine/threonine-protein kinase TBK1032528
Septin-9002121
Death-associated protein kinase 2001616
Ribosomal protein S6 kinase alpha-6002626
TRAF2 and NCK-interacting protein kinase012728
Serine/threonine-protein kinase tousled-like 1001515
Serine/threonine-protein kinase TAO2002525
Long-chain-fatty-acid--CoA ligase 5001515
ALK tyrosine kinase receptor051722
SRSF protein kinase 3001414
Serine/threonine-protein kinase ICK002424
Cyclin-dependent kinase 11A001515
Aurora kinase C021618
Calcium/calmodulin-dependent protein kinase type II subunit alpha041519
Serine/threonine-protein kinase 38-like001919
Microtubule-associated serine/threonine-protein kinase 1001414
Serine/threonine-protein kinase SIK3012526
Mitogen-activated protein kinase kinase kinase 2002525
Thyroid hormone receptor-associated protein 3001818
Dual specificity tyrosine-phosphorylation-regulated kinase 1B022022
Receptor-interacting serine/threonine-protein kinase 3042125
Serine/threonine-protein kinase MRCK beta002626
Interleukin-1 receptor-associated kinase 3002626
Serine/threonine-protein kinase 24002323
Casein kinase I isoform gamma-3002626
Mitogen-activated protein kinase kinase kinase 4002626
Cannabinoid receptor 1032949
Cannabinoid receptor 2 0271044
Cannabinoid receptor 204610
putative alpha-glucosidase2002
Matrix protein 20123
Matrix protein 20235
Multidrug and toxin extrusion protein 1042042
Muscarinic acetylcholine receptor M209712117
Muscarinic acetylcholine receptor M40937105
Muscarinic acetylcholine receptor M50936103
Muscarinic acetylcholine receptor M1010614128
Muscarinic acetylcholine receptor M301018113
C-X-C chemokine receptor type 10303
C-X-C chemokine receptor type 20404
C-C chemokine receptor type 10101
C-C chemokine receptor type 20909
C-C chemokine receptor type 40606
C-C chemokine receptor type 50303
C-X-C chemokine receptor type 40112
Mcl-10808
Valosin-containing protein0101
Spike glycoprotein072330
hypothetical protein SA14220202
Gamma-aminobutyric acid receptor subunit pi027027
Gamma-aminobutyric acid receptor subunit delta027027
Transmembrane protease serine 2072330
Group 10 secretory phospholipase A20203
Phospholipase A20101
Procathepsin L0122335
Neutrophil elastase017017
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-10202
Replicase polyprotein 1a0152338
Replicase polyprotein 1ab0102333
Phospholipase A2, membrane associated0305
Matrix metalloproteinase-9012113
Vascular endothelial growth factor A0011
Gamma-aminobutyric acid receptor subunit beta-1029433
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-10101
Gamma-aminobutyric acid receptor subunit beta-3035742
Cytosolic phospholipase A20101
Gamma-aminobutyric acid receptor subunit alpha-4030434
Placenta growth factor0011
Gamma-aminobutyric acid receptor subunit epsilon027027
Delta-type opioid receptor0101
5-hydroxytryptamine receptor 1D0202
Gamma-aminobutyric acid receptor subunit alpha-6032436
Gamma-aminobutyric acid receptor subunit gamma-1027027
Gamma-aminobutyric acid receptor subunit gamma-3027027
Angiotensin-converting enzyme 2 092433
Poly [ADP-ribose] polymerase 20549
Gamma-aminobutyric acid receptor subunit theta027027
M1-family alanyl aminopeptidase0303
Solute carrier organic anion transporter family member 2B1 010015
Thrombopoietin receptor0011
Solute carrier organic anion transporter family member 1B3040049
Broad substrate specificity ATP-binding cassette transporter ABCG2050558
Solute carrier organic anion transporter family member 1B1046054
Aminoglycoside 3'-phosphotransferase 0002
Gamma-aminobutyric acid receptor subunit rho-10159
Solute carrier family 15 member 1011011
Solute carrier family 15 member 10606
Solute carrier family 15 member 20707
Voltage-dependent L-type calcium channel subunit alpha-1C015015
Solute carrier organic anion transporter family member 1A408016
Voltage-dependent L-type calcium channel subunit alpha-1F037138
Lysine-specific demethylase PHF20101
Thyroid hormone receptor alpha0101
Thyroid hormone receptor alpha0549
Thyroid hormone receptor beta0549
Carnitine O-palmitoyltransferase 2, mitochondrial0404
Histamine H2 receptor062466
Endothelin-1 receptor0617
B2 bradykinin receptor07110
Melanocortin receptor 40808
C-8 sterol isomerase0707
Melanocortin receptor 5014014
Sodium channel protein type 1 subunit alpha013013
Sodium channel protein type 4 subunit alpha015018
Squalene synthase0101
Melanocortin receptor 30808
Carnitine O-palmitoyltransferase 1, liver isoform0404
Sodium channel protein type 7 subunit alpha010010
Voltage-dependent L-type calcium channel subunit alpha-1D 037138
Voltage-dependent L-type calcium channel subunit alpha-1S037138
Squalene monooxygenase0101
3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase0819
Sodium channel protein type 9 subunit alpha018018
Lysine-specific demethylase 7A0202
Carnitine O-palmitoyltransferase 1, muscle isoform0303
Sodium channel protein type 2 subunit alpha014014
Sodium channel protein type 3 subunit alpha015015
Sodium channel protein type 11 subunit alpha010010
Histone lysine demethylase PHF80202
Sodium channel protein type 8 subunit alpha010010
Sodium channel protein type 10 subunit alpha011011
Albumin001515
Angiotensin-converting enzyme058059
D(1B) dopamine receptor021227
UDP-glucuronosyltransferase 1A4010126
Histamine H1 receptor017219
Histamine H1 receptor0918104
UDP-glucuronosyltransferase 1A30018
Voltage-dependent N-type calcium channel subunit alpha-1B013114
Nuclear receptor subfamily 3 group C member 3 053053
Histamine H3 receptor023430
NEDD8-activating enzyme E1 regulatory subunit isoform a0101
NEDD8-conjugating enzyme Ubc120101
Voltage-dependent L-type calcium channel subunit alpha-1C010010
Potassium channel subfamily K member 2 0404
Chain A, Histamine N-methyltransferase0202
Chain A, Histamine N-methyltransferase0202
Chain A, Histamine N-methyltransferase0202
Chain A, Histamine N-methyltransferase0202
transient receptor potential cation channel subfamily V member 17007
Histamine H4 receptor018929
Beta-lactamase 0001
Beta-lactamase 0001
Beta-lactamase 0002
Beta-lactamase 0002
Beta-lactamase 0002
Beta-lactamase SHV-10001
Beta-lactamase SHV-10003
Beta-lactamase0003
B2 metallo-beta-lactamase 0003
Solute carrier family 15 member 20505
Beta-lactamase 0001
Beta-lactamase 0001
Beta-lactamase 0001
Beta-lactamase 0001
Synaptojanin-20303
Synaptojanin-10303
Substance-P receptor0404
Chain A, Mutant Al2 6e7p9g0011
Beta-lactamase 0001
Beta-lactamase 0002
Beta-lactamase 0002
Metallo-beta-lactamase type 20125
Metallo-beta-lactamase VIM-11 0002
Metallo-beta-lactamase VIM-20002
Beta-lactamase 0002
Metallo-beta-lactamase0002
Beta-lactamase 0002
Beta-lactamase OXA-70002
Beta-lactamase 0001
Beta-lactamase 0001
Beta-lactamase 0001
Metallo-beta-lactamase VIM-130103
Efflux transporter 0002
Beta-lactamase 0002
Beta-lactamase Toho-10002
Beta-lactamase 0002
Class D beta-lactamase0001
Metallo-beta-lactamase0002
Beta-lactamase 0002
Metallo-b-lactamase 0003
Carbapenem-hydrolyzing beta-lactamase KPC0003
Beta-lactamase class B VIM-2 0126
Beta-lactamase VIM-1 0103
Plasma kallikrein02111
Peroxisome proliferator-activated receptor delta010922
Histone acetyltransferase p3000506
Probable linoleate 9S-lipoxygenase 50101
Histone acetyltransferase KAT2B0303
Histone acetyltransferase KAT50303
SUMO-activating enzyme subunit 10202
Fatty-acid amide hydrolase 1013013
Fatty-acid amide hydrolase 10203
Potassium channel subfamily K member 30404
Fatty acid-binding protein, liver0606
Cannabinoid receptor 10628
Corticotropin-releasing factor receptor 20404
Lanosterol 14-alpha demethylase017219
Transient receptor potential cation channel subfamily V member 2010313
Nuclear factor NF-kappa-B p105 subunit0909
Signal transducer and activator of transcription 30617
Hexokinase-20202
Atrial natriuretic peptide receptor 30202
Type-1A angiotensin II receptor 07310
Type-1 angiotensin II receptor0011
Type-1B angiotensin II receptor0909
Type-1 angiotensin II receptor014423
Type-2 angiotensin II receptor010010
Type-2 angiotensin II receptor0729
Aminopeptidase N0202
Interleukin-1 receptor antagonist protein0101
Endoplasmic reticulum aminopeptidase 20101
Endoplasmic reticulum aminopeptidase 10101
Leucyl-cystinyl aminopeptidase0101
M17 leucyl aminopeptidase0202
Steroid C26-monooxygenase0044
Cytochrome P450 1300022
Cytochrome P450 1300022
Nicotinate phosphoribosyltransferase0808
Apelin receptor0112
DNA polymerase catalytic subunit0101
DNA polymerase catalytic subunit0101
DNA polymerase beta0606
DNA polymerase beta0404
DNA polymerase catalytic subunit0101
DNA polymerase catalytic subunit0101
DNA polymerase alpha catalytic subunit0213
DNA polymerase delta catalytic subunit0101
DNA polymerase catalytic subunit0101
DNA polymerase subunit gamma-10101
DNA polymerase lambda0101
Chain A, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0202
Chain B, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0202
Chain A, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0202
Chain B, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0202
Chain A, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0202
Chain B, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0202
Chain A, Transthyretin0055
Chain A, Transthyretin0055
Chain A, Transthyretin0055
Chain A, Transthyretin0055
Chain B, Transthyretin0055
Chain A, Transthyretin0055
Chain B, Transthyretin0055
Chain A, Casein kinase II subunit alpha0202
Chain A, Casein kinase II subunit alpha0202
Chain A, Casein Kinase Ii Subunit Alpha0202
Neuraminidase 022022
Aldo-keto reductase family 1 member B10019019
Poly [ADP-ribose] polymerase tankyrase-10628
Lysozyme C-10202
Cationic trypsin0808
Myeloperoxidase016016
Beta-glucuronidase0303
Sialidase010010
Cystic fibrosis transmembrane conductance regulator0268
17-beta-hydroxysteroid dehydrogenase type 10505
Mucin-10101
Testosterone 17-beta-dehydrogenase 30606
17-beta-hydroxysteroid dehydrogenase type 20909
Peroxisome proliferator-activated receptor gamma011213
Homeobox protein Nkx-2.5 0202
Estrogen receptor0033
Lactoperoxidase0408
MO15-related protein kinase Pfmrk 0808
Transcription factor GATA-4 0202
Substance-K receptor016016
Casein kinase II subunit alpha 3013013
Enoyl-acyl-carrier protein reductase 014014
NACHT, LRR and PYD domains-containing protein 3 0404
Myocilin0022
Prenyltransferase homolog0005
Poly [ADP-ribose] polymerase tankyrase-207411
Carboxylic ester hydrolase 010012
NADPH oxidase 40404
Estrogen receptor beta0033
Short transient receptor potential channel 50606
E3 ubiquitin-protein ligase Mdm20404
D019019
Substance-P receptor015217
Neuromedin-K receptor09413
Substance-P receptor0101
Chain A, ADIPOCYTE LIPID-BINDING PROTEIN0011
Chain A, SERUM ALBUMIN0022
Chain A, SERUM ALBUMIN0022
Calmodulin 0146
Cytosolic phospholipase A2 gamma0202
Polyphenol oxidase 10202
Taste receptor type 2 member 160023
Chain E, LYSINE, ARGININE, ORNITHINE-BINDING PROTEIN0033
Chain E, LYSINE, ARGININE, ORNITHINE-BINDING PROTEIN0033
Chain E, LYSINE, ARGININE, ORNITHINE-BINDING PROTEIN0033
Cationic amino acid transporter 30202
Vasopressin V2 receptor0539
Oxytocin receptor0347
Vasopressin V1a receptor0135
Vasopressin V1a receptor07411
Vasopressin V1b receptor0336
Vasopressin V2 receptor0011
Vasopressin V1b receptor0215
Translocator protein0203
Oxytocin receptor0213
Vasopressin V2 receptor 0326
Integrin beta-10303
Integrin alpha-V 0202
Integrin alpha-50202
Integrin beta-50101
5-hydroxytryptamine receptor 3E014319
5-hydroxytryptamine receptor 3A0325
5-hydroxytryptamine receptor 3B014319
5-hydroxytryptamine receptor 3A026533
3-hydroxy-3-methylglutaryl-coenzyme A reductase 0909
5-hydroxytryptamine receptor 3D014319
Multidrug and toxin extrusion protein 2021021
5-hydroxytryptamine receptor 3C014319
Chain A, Hyaluronidase, phage associated0101
Pancreatic alpha-amylase0202
Albumin0315
Prolyl 4-hydroxylase subunit alpha-10001
Hyaluronate lyase0101
Prolyl hydroxylase EGLN20146
Egl nine homolog 104611
Prolyl hydroxylase EGLN30045
Hypoxia-inducible factor 1-alpha inhibitor0304
Solute carrier family 23 member 10101
Pancreatic alpha-amylase0709
Tyrosine-protein phosphatase non-receptor type 2011011
Neutral amino acid transporter A0505
Neutral amino acid transporter B(0)0505
Carbonic anhydrase-like protein, putative00010
Amino acid transporter0505
Excitatory amino acid transporter 40202
Glutamate transporter homolog0011
N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase0202
Chain A, Phospholipase A2 isoform 30011
GTP-binding protein (rab7)0033
ras protein, partial0033
Rac1 protein0033
cell division cycle 42 (GTP binding protein, 25kDa), partial0033
Prostaglandin-H2 D-isomerase0202
Prostaglandin G/H synthase 2 0708
Fatty acid-binding protein, liver012214
Glutathione hydrolase 1 proenzyme0101
Urotensin-2 receptor0202
4-aminobutyrate aminotransferase, mitochondrial0303
Ras-related protein Rab-2A0033
Rho-associated protein kinase 20505
Polycomb protein EED0314
HLA class I histocompatibility antigen, A alpha chain 0156
Glycine receptor subunit alpha-102911
Somatostatin receptor type 20101
Somatostatin receptor type 40101
Somatostatin receptor type 30101
Somatostatin receptor type 50101
Sigma intracellular receptor 20909
Heparanase0044
Beta-1 adrenergic receptor 04814
Insulin receptor 0707
Dipeptidyl peptidase 40101
Atrial natriuretic peptide receptor 10112
Atrial natriuretic peptide receptor 1 0011
cystic fibrosis transmembrane conductance regulator0101
short transient receptor potential channel 6 isoform 10033
Muscarinic acetylcholine receptor M10349
Muscarinic acetylcholine receptor M40517
Muscarinic acetylcholine receptor08312
PINK1110011
NADH dehydrogenase [ubiquinone] iron-sulfur protein 8, mitochondrial0101
Cytochrome c oxidase subunit NDUFA40101
Acyl carrier protein, mitochondrial0101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10101
NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial0101
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 5, mitochondrial0101
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 30101
NADH dehydrogenase [ubiquinone] 1 subunit C1, mitochondrial0101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2 0101
NADH dehydrogenase [ubiquinone] iron-sulfur protein 50101
NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial0101
NADH dehydrogenase [ubiquinone] iron-sulfur protein 2, mitochondrial0101
NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial0101
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 10101
NADH dehydrogenase [ubiquinone] iron-sulfur protein 3, mitochondrial0101
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 60101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 30101
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 4 0101
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 8, mitochondrial0101
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 2, mitochondrial0101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 70101
NADH dehydrogenase [ubiquinone] 1 subunit C20101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10, mitochondrial0101
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 100101
NADH-ubiquinone oxidoreductase chain 10101
NADH-ubiquinone oxidoreductase chain 20101
NADH-ubiquinone oxidoreductase chain 30101
NADH-ubiquinone oxidoreductase chain 4L0101
NADH-ubiquinone oxidoreductase chain 40102
NADH-ubiquinone oxidoreductase chain 50101
NADH-ubiquinone oxidoreductase chain 60101
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 70101
NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial0101
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial0101
NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial0101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 80101
NADH dehydrogenase [ubiquinone] flavoprotein 3, mitochondrial0101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 60101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 50101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9, mitochondrial0101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 110101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 20101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 30101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 4-like 20101
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial0101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 40101
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 120101
Complex I intermediate-associated protein 30, mitochondrial0101
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 90101
Thromboxane A2 receptor 0227
Sodium/bile acid cotransporter010111
Leukotriene B4 receptor 21125
DNA (cytosine-5)-methyltransferase 10707
Histone-lysine N-methyltransferase EHMT20808
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2, isoform CRA_a0022
Transcriptional activator protein LasR0101
Protein-arginine deiminase type-40909
tyrosine-protein kinase Yes260026
Membrane-associated progesterone receptor component 1001515
Cell division cycle 7-related protein kinase001111
Signal transducer and activator of transcription 5A0101
G protein-coupled receptor kinase 6031518
Phosphatidylinositol 5-phosphate 4-kinase type-2 alpha101718
MAP kinase-activated protein kinase 30066
Eukaryotic peptide chain release factor GTP-binding subunit ERF3B0088
Beta-glucuronidase0404
Gamma-aminobutyric acid type B receptor subunit 20325
Gamma-aminobutyric acid type B receptor subunit 20606
Gamma-aminobutyric acid type B receptor subunit 10325
Gamma-aminobutyric acid type B receptor subunit 10505
V-type proton ATPase subunit S10101
Vacuolar proton pump subunit B 0101
Lysine-specific demethylase 4E0808
Lysine-specific histone demethylase 1A021022
Progesterone receptor013420
Trypsin-10808
Trypsin-20606
Cytochrome P450 11B1, mitochondrial0202
Cyclic AMP-responsive element-binding protein 10001
Sodium- and chloride-dependent GABA transporter 10808
Sodium- and chloride-dependent GABA transporter 20808
Sodium- and chloride-dependent GABA transporter 30808
Trypsin-30606
Prostaglandin G/H synthase 2 09011
Linoleate 9S-lipoxygenase-40303
1-deoxy-D-xylulose 5-phosphate reductoisomerase0505
Sodium- and chloride-dependent betaine transporter0808
Prolyl endopeptidase0909
Receptor-type tyrosine-protein phosphatase S0404
Prostaglandin G/H synthase 1 010012
Polyunsaturated fatty acid lipoxygenase ALOX15B0101
15-hydroxyprostaglandin dehydrogenase [NAD(+)]0101
Neuropeptide Y receptor type 10517
Neuropeptide Y receptor type 50202
Zinc finger protein mex-50011
Genome polyprotein0101
Poly(ADP-ribose) glycohydrolase0101
Chain A, Integrase0101
Chain A, Integrase0101
Chain A, T4 LYSOZYME0011
Chain A, GCN4P10011
Chain B, GCN4P10011
Chain C, GCN4P10011
Chain A, T4 LYSOZYME0011
Chain A, T4 LYSOZYME0011
Chain A, Replicase polyprotein 1ab0101
Chain A, 3C-like proteinase0101
Endolysin0044
Chain A, GTPase KRas, isoform 2B0011
Chain A, GTPase KRas, isoform 2B0011
Membrane primary amine oxidase 0303
GTPase KRas0123
Membrane primary amine oxidase0406
Glutaminyl-peptide cyclotransferase0505
Chain A, Oxygen-insensitive Nad(p)h Nitroreductase0101
Chain B, Oxygen-insensitive Nad(p)h Nitroreductase0101
Monocarboxylate transporter 10205
D-aspartate oxidase0404
Serine racemase0404
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit0202
Chain A, PROTEIN (TRYPSIN)0101
Chain A, PROTEIN (TRYPSIN)0101
Membrane primary amine oxidase0103
Amiloride-sensitive amine oxidase [copper-containing]0102
Lysyl oxidase homolog 20404
5-hydroxytryptamine receptor 3B0606
Proteasome subunit beta type-108010
Proteasome subunit beta type-208010
Proteasome subunit beta type-110304
Calpain-90303
Proteasome subunit alpha type-70304
Indoleamine 2,3-dioxygenase 1014116
Calpain-2 catalytic subunit0303
Proteasome subunit alpha type-10304
Proteasome subunit alpha type-20304
Proteasome subunit alpha type-30304
Proteasome subunit alpha type-40304
Proteasome subunit beta type-80304
Proteasome subunit beta type-90304
Proteasome subunit alpha type-50304
Proteasome subunit beta type-40304
Proteasome subunit beta type-60304
Proteasome subunit beta type-100304
Cathepsin K0303
Proteasome subunit beta type-30304
Proteasome subunit alpha type-60359
Proteasome subunit alpha-type 80304
Proteasome subunit beta type-70304
Gamma-secretase subunit PEN-20213
Telomerase reverse transcriptase0404
Neuraminidase0404
Neuraminidase0505
Aldo-keto reductase family 1 member C2 0707
Prolyl endopeptidase0303
core protein, partial0101
Sodium- and chloride-dependent GABA transporter 10303
Sodium- and chloride-dependent GABA transporter 20404
Sodium- and chloride-dependent GABA transporter 30404
Sodium- and chloride-dependent betaine transporter0202
Sodium- and chloride-dependent GABA transporter 30202
Sodium- and chloride-dependent GABA transporter 20202
LMP1 [Human herpesvirus 4]0004
NAD0106
Aryl hydrocarbon receptor0135
NAD(P)H dehydrogenase [quinone] 10005
E3 ubiquitin-protein ligase Mdm2 isoform a0112
protein Mdm4 isoform 10101
Carboxypeptidase A10202
Thermolysin0607
Breast cancer type 1 susceptibility protein0101
BRCA1-associated RING domain protein 10101
Collagenase ColG0202
Chain A, D-MALTODEXTRIN BINDING PROTEIN0011
Chain A, Limit Dextrinase0011
Chain A, Solute-binding protein0011
Chain A, Solute-binding protein0011
Chain B, SusD0011
Chain A, SusD0011
Chain A, SusD0011
Chain A, Alpha-hemolysin0011
Chain B, Alpha-hemolysin0011
Chain C, Alpha-hemolysin0011
Chain D, Alpha-hemolysin0011
Chain E, Alpha-hemolysin0011
Chain F, Alpha-hemolysin0011
Chain G, Alpha-hemolysin0011
Chain A, Betaine ABC transporter permease and substrate binding protein0011
Chain A, Osmoprotection protein (ProX)0011
Chain A, Glycine betaine/carnitine/choline-binding protein0022
Chain A, Glycine betaine/carnitine/choline-binding protein0022
Chain A, Glycine betaine/carnitine/choline-binding protein0022
Chain A, Glycine betaine/carnitine/choline-binding protein0022
Ectonucleoside triphosphate diphosphohydrolase 10202
5'-nucleotidase0303
Ubiquitin-like modifier activating enzyme 20303
SUMO1 activating enzyme subunit 10303
SUMO-conjugating enzyme UBC90303
Zinc finger protein GLI10202
Env polyprotein 0033
Phosphodiesterase isozyme 4 0101
Transmembrane prolyl 4-hydroxylase0145
Non-structural protein 1 0202
Cytochrome P450 26A10202
Retinoic acid receptor alpha04614
Retinoic acid receptor beta04613
Retinoic acid receptor gamma 04613
Retinoic acid receptor RXR-alpha091325
Retinoic acid receptor RXR-alpha0145
Retinoic acid receptor RXR-beta0358
Retinoic acid receptor RXR-beta0145
Retinoic acid receptor RXR-gamma0145
Retinoic acid receptor RXR-gamma0358
Retinoic acid receptor RXR-alpha0011
Cytochrome P450 26B10101
Neuropeptide Y receptor type 20303
Neuropeptide Y receptor type 40101
NPY-Y2 receptor 0101
Neuropeptide FF receptor 10112
Neuropeptide FF receptor 20112
STAT3, partial0213
signal transducer and activator of transcription 1-alpha/beta isoform alpha0213
transcription factor p65 isoform 10022
Estrogen receptor beta0225
Triosephosphate isomerase0303
Carbonyl reductase [NADPH] 108010
Estrogen receptor0225
Beta-hydroxyacyl-ACP dehydratase precursor (Fatty acid synthesis protein)011011
Chain A, Avidin0011
Chain A, Protein (streptavidin)0011
Chain B, Protein (streptavidin)0011
Chain A, Streptavidin0011
Chain D, Streptavidin0011
Chain A, Streptavidin0011
Chain D, Streptavidin0011
Chain A, Streptavidin0011
Chain D, Streptavidin0011
Chain A, Streptavidin Complex With Biotin0011
Chain D, Circularly Permuted Core-streptavidin E51/a460011
Chain A, Core-streptavidin0011
Chain D, Core-streptavidin0011
Chain A, Core-streptavidin0011
Chain D, Core-streptavidin0011
Chain A, Core-streptavidin0011
Chain D, Core-streptavidin0011
Chain A, Core-streptavidin0011
Chain D, Core-streptavidin0011
Chain A, Avidin0011
Chain A, Streptavidin0011
Chain B, Streptavidin0011
Chain A, Streptavidin0011
Chain B, Streptavidin0011
nonstructural protein 10202
green fluorescent protein, partial0101
insulin-degrading enzyme isoform 10033
Receptor-type tyrosine-protein phosphatase beta0003
CPG DNA methylase0303
Multidrug resistance protein CDR10101
Chain A, Estrogen-related receptor gamma0011
Chain A, Estrogen-related receptor gamma0011
Chain A, Estrogen-related receptor gamma0011
Chain A, Estrogen-related receptor gamma0011
GTP-binding protein Rheb0011
Myosin-2 heavy chain, non muscle0101
Myosin-2 heavy chain0101
Myosin IC heavy chain0101
Myosin-90101
Unconventional myosin-X0101
Myosin-70101
Unconventional myosin-Ib0101
Myosin-40101
Myosin-140101
Nonmuscle myosin heavy chain0101
Unconventional myosin-Va0101
Myosin heavy chain, non-muscle0101
Unconventional myosin-XV0101
Beta-lactamase0102
Chain H, Proteasome component PUP10101
Chain I, Proteasome component PUP30101
Chain K, Proteasome component PRE20101
Chain L, Proteasome component C50101
Chain K, Proteasome component PRE20101
Chain L, Proteasome component C50101
26S proteasome non-ATPase regulatory subunit 110101
26S proteasome non-ATPase regulatory subunit 120101
26S proteasome non-ATPase regulatory subunit 140202
26S proteasome non-ATPase regulatory subunit 30101
Prothrombin010617
Chymotrypsinogen A09010
Cathepsin G0303
Lysosomal protective protein0101
Chymotrypsinogen B0505
26S proteasome regulatory subunit 6A0101
Chymase0101
Proteasome subunit beta type-80101
26S proteasome regulatory subunit 70101
Lon protease homolog, mitochondrial0101
26S proteasome non-ATPase regulatory subunit 80101
26S proteasome non-ATPase regulatory subunit 70101
26S proteasome non-ATPase regulatory subunit 40101
26S proteasome complex subunit SEM10101
26S proteasome regulatory subunit 40101
26S proteasome regulatory subunit 80101
26S proteasome regulatory subunit 10B0101
Nuclear factor NF-kappa-B p100 subunit 0707
26S proteasome non-ATPase regulatory subunit 20101
26S proteasome non-ATPase regulatory subunit 60101
Proteasomal ubiquitin receptor ADRM10101
ATP-dependent Clp protease proteolytic subunit0112
NACHT, LRR and PYD domains-containing protein 3 0303
26S proteasome non-ATPase regulatory subunit 10101
26S proteasome non-ATPase regulatory subunit 130101
Prostaglandin E synthase0707
D(3) dopamine receptor0314
Angiotensin-converting enzyme 015117
B2 bradykinin receptor0101
B1 bradykinin receptor0404
kelch-like ECH-associated protein 10004
major prion protein preproprotein Prp precursor0202
nuclear receptor subfamily 0 group B member 10707
steroidogenic factor 10707
Genome polyprotein 010313
Nuclear hormone receptor family member daf-120011
oxysterols receptor LXR-beta isoform 10011
Thymidine phosphorylase0014
Thymidylate kinase0202
Thymidine kinase0003
Thymidylate kinase0303
N-acetyltransferase Eis0505
cAMP-dependent protein kinase type I-alpha regulatory subunit0011
cAMP-dependent protein kinase type II-beta regulatory subunit0011
cAMP-dependent protein kinase catalytic subunit beta isoform 10011
cAMP-dependent protein kinase catalytic subunit beta isoform 30011
Solute carrier family 12 member 20101
Potassium channel subfamily K member 30101
Potassium channel subfamily K member 90101
UDP-glucuronosyltransferase 2B7012125
UDP-glucuronosyltransferase 2B10 010111
Beta-3 adrenergic receptor09110
Alpha-2A adrenergic receptor0303
Chain A, Nitrile Hydratase alpha subunit0101
Chain B, Nitrile Hydratase beta subunit0101
Methyl-accepting chemotaxis protein NahY0044
Vesicular glutamate transporter 30202
RNA polymerase beta subunit (EC 2.7.7.6), partial0101
90-kda heat shock protein beta HSP90 beta, partial0606
heat shock protein HSP 90-alpha isoform 206016
Lipoxygenase 0101
Neuraminidase0202
Interstitial collagenase013114
Tyrosine-protein phosphatase non-receptor type 70404
Dual specificity protein phosphatase 30404
Anthrax toxin receptor 20707
Hyaluronidase-10303
BiP isoform A0101
Aldo-keto reductase family 1 member A10202
Aldo-keto reductase family 1 member C40404
Aldo-keto reductase family 1 member C10606
Chain A, Glycogen Phosphorylase0101
Chain A, Glycogen phosphorylase, liver form0022
Chain A, glycogen phosphorylase, liver form0022
Chain A, Glycogen phosphorylase, liver form0022
Chain A, Glycogen phosphorylase, liver form0022
Chain A, Chitinase0101
Glycogen phosphorylase, liver form0303
Glycogen phosphorylase, muscle form0101
Chitotriosidase-10415
Adenosine receptor A2b0103
Palmitoleoyl-protein carboxylesterase NOTUM0235
Endochitinase B10415
Guanine deaminase0304
TSHR protein2002
XBP10202
DNA damage-inducible transcript 3 protein0202
heat shock protein 90, putative00010
Chain A, Vitamin D Nuclear Receptor0011
Vitamin D3 receptor0011
Vitamin D-binding protein0011
Vitamin D3 receptor07718
Vitamin D3 receptor0113
Vitamin D3 receptor0022
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial0213
Vitamin D3 receptor0112
Transporter011011
Vitamin D3 receptor A0022
Calpain-1 catalytic subunit0101
Cathepsin D0405
Pro-cathepsin H0101
Falcipain 2B 0101
Cysteine proteinase falcipain 2a 0202
NAD-dependent protein deacetylase HST20303
Sphingomyelin phosphodiesterase 30101
Cytochrome P450 2C11 0303
Steroid 17-alpha-hydroxylase/17,20 lyase 0303
Cytochrome P450 3A50619
Cytochrome P450 3A70202
N-acylethanolamine-hydrolyzing acid amidase0202
Heat sensitive channel TRPV30123
Transient receptor potential cation channel subfamily M member 80516
Transient receptor potential cation channel subfamily V member 40336
G-protein coupled receptor 550145
Diacylglycerol lipase-alpha0202
G-protein coupled receptor 60011
Transient receptor potential cation channel subfamily V member 30112
Transient receptor potential cation channel subfamily V member 40112
Transient receptor potential cation channel subfamily V member 20112
Chain A, Beta-lactoglobulin0011
Chain A, Beta-lactoglobulin0011
UDP-3-O-acyl-N-acetylglucosamine deacetylase0011
NADH-ubiquinone oxidoreductase chain 10303
Transient receptor potential cation channel subfamily M member 80101
Chain A, angiotensin converting enzyme0101
Chain A, angiotensin converting enzyme0101
Neprilysin0202
Neprilysin0303
EEF1AKMT4-ECE2 readthrough transcript protein0202
Leukotriene A-4 hydrolase0101
Endothelin-converting enzyme 10202
Angiotensin-converting enzyme0606
Beta-lactamase TEM0103
Beta-lactamase 0304
Beta-lactamase 0303
Muscarinic acetylcholine receptor M30227
Muscarinic acetylcholine receptor M20217
Major prion protein0077
Sodium channel protein type 1 subunit alpha010010
Sodium channel protein type 2 subunit alpha014115
Sodium channel protein type 3 subunit alpha0909
Frizzled-80011
P2X purinoceptor 40415
Lactoperoxidase0202
Kinesin-like protein KIF110202
Cytochrome P450 2E10303
Chain A, PAPAIN2002
CDGSH iron-sulfur domain-containing protein 1016016
Chain A, serum paraoxonase0101
Glutathione reductase, mitochondrial012014
Glutathione reductase0202
Solute carrier family 22 member 50001
Solute carrier family 22 member 50102
Solute carrier family 22 member 160001
Solute carrier family 22 member 210001
Solute carrier family 22 member 50001
Secreted chorismate mutase0404
Toll-like receptor 40202
Potassium channel subfamily K member 100101
Chain A, Protein kinase CK2, alpha Subunit0101
Chain A, PROTEIN KINASE CK2, alpha SUBUNIT0101
Chain A, Protein Kinase Ck2, Alpha Subunit0101
Serine/threonine-protein kinase Sgk10303
Casein kinase II subunit alpha 0202
Casein kinase II subunit beta0202
Single-stranded DNA cytosine deaminase120012
Melatonin receptor type 1B0538
Chain A, Neutrophil gelatinase-associated lipocalin0011
3-dehydroquinate synthase0203
Potassium-transporting ATPase subunit beta0102
Potassium-transporting ATPase alpha chain 10102
Autoinducer 2-binding periplasmic protein LuxP0303
L-ornithine N(5)-monooxygenase0112
Ubiquitin carboxyl-terminal hydrolase 20202
Ubiquitin carboxyl-terminal hydrolase isozyme L10101
Nuclear receptor subfamily 4 group A member 10011
Receptor-type tyrosine-protein phosphatase epsilon0303
Tyrosine-protein phosphatase non-receptor type 60707
Tryptophan 2,3-dioxygenase0506
Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN0101
Heat shock factor protein 10213
Tyrosine-protein phosphatase non-receptor type 1108010
Receptor-type tyrosine-protein phosphatase eta0303
Regulator of G-protein signaling 170213
Ubiquitin carboxyl-terminal hydrolase 150101
Ubiquitin carboxyl-terminal hydrolase isozyme L50101
Chain A, Carbonic anhydrase II0101
Cytochrome c oxidase subunit 10101
Cytochrome c oxidase subunit 20101
Catechol O-methyltransferase0202
Cytochrome c oxidase subunit 20202
Quinolone resistance protein NorA0405
Prostaglandin G/H synthase 10404
Cruzipain012012
Sodium/hydrogen exchanger 10101
Indoleamine 2,3-dioxygenase 10505
Prostaglandin G/H synthase 20607
Prostaglandin G/H synthase 10101
Cyclooxygenase-2 0202
Beta-lactamase 0001
Beta-lactamase 0001
Beta-lactamase0001
Beta-lactamase0407
Beta-lactamase OXA-100001
Beta-lactamase0001
Beta-lactamase0001
Beta-lactamase 0001
Beta-lactamase 0001
Beta-lactamase 0002
Solute carrier family 22 member 704010
Beta-lactamase 0002
Beta-lactamase IMP-1 0002
Beta-lactamase 0001
Beta-lactamase 0002
Beta-lactamase 0002
Solute carrier family 22 member 1107014
Solute carrier family 22 member 80609
Solute carrier family 22 member 70408
Mitochondrial sodium/calcium exchanger protein0101
perilipin-50707
perilipin-10707
1-acylglycerol-3-phosphate O-acyltransferase ABHD5 isoform a0707
Dihydrofolate reductase013017
Tubulin beta-4A chain09618
Tubulin beta chain09618
Tubulin alpha-3C chain09618
Tumor necrosis factor receptor superfamily member 1A0101
Stromal cell-derived factor 10101
Polyunsaturated fatty acid 5-lipoxygenase0101
Tubulin alpha-1B chain09618
Tubulin alpha-4A chain09618
Tubulin beta-4B chain09618
Tubulin beta-3 chain010619
Tubulin beta-2A chain09618
Tubulin beta-8 chain09618
Tubulin alpha-3E chain09618
Tubulin alpha-1A chain09618
Sortase A0303
Tubulin alpha-1C chain09618
Tubulin beta-6 chain09618
Tubulin beta-2B chain09618
Tubulin beta-1 chain09618
Sarcoplasmic/endoplasmic reticulum calcium ATPase 1 0202
Sarcoplasmic/endoplasmic reticulum calcium ATPase 2 0101
Aromatic-L-amino-acid decarboxylase0101
Bcl-2-like protein 10505
Ileal sodium/bile acid cotransporter0505
Bile acid receptor0123
Dihydroxyacetone phosphate acyltransferase0002
30S ribosomal protein S60516
30S ribosomal protein S70516
50S ribosomal protein L150516
50S ribosomal protein L100516
50S ribosomal protein L110516
50S ribosomal protein L7/L120516
50S ribosomal protein L190516
50S ribosomal protein L10516
50S ribosomal protein L200516
50S ribosomal protein L270516
50S ribosomal protein L280516
50S ribosomal protein L290516
50S ribosomal protein L310516
50S ribosomal protein L31 type B0516
50S ribosomal protein L320516
50S ribosomal protein L330516
50S ribosomal protein L340516
50S ribosomal protein L350516
50S ribosomal protein L360516
30S ribosomal protein S100516
30S ribosomal protein S110516
30S ribosomal protein S120516
30S ribosomal protein S130516
30S ribosomal protein S160516
30S ribosomal protein S180516
30S ribosomal protein S190516
30S ribosomal protein S200516
30S ribosomal protein S20516
30S ribosomal protein S30516
30S ribosomal protein S40516
30S ribosomal protein S50516
30S ribosomal protein S80516
30S ribosomal protein S90516
50S ribosomal protein L130516
50S ribosomal protein L140516
50S ribosomal protein L160516
50S ribosomal protein L230516
30S ribosomal protein S150516
50S ribosomal protein L170516
50S ribosomal protein L210516
50S ribosomal protein L300516
50S ribosomal protein L60516
30S ribosomal protein S140516
30S ribosomal protein S170516
30S ribosomal protein S10516
50S ribosomal protein L180516
50S ribosomal protein L20516
50S ribosomal protein L30516
50S ribosomal protein L240516
50S ribosomal protein L40516
50S ribosomal protein L220516
50S ribosomal protein L50516
30S ribosomal protein S210516
50S ribosomal protein L250516
50S ribosomal protein L36 20516
Methionine--tRNA ligase, mitochondrial0011
Gamma-aminobutyric acid receptor subunit alpha-107010
Gamma-aminobutyric acid receptor subunit beta-107010
Gamma-aminobutyric acid receptor subunit alpha-20609
Gamma-aminobutyric acid receptor subunit alpha-30609
Gamma-aminobutyric acid receptor subunit alpha-40609
Gamma-aminobutyric acid receptor subunit gamma-20609
Gastrin/cholecystokinin type B receptor1719
Chain A, BCL-2-RELATED PROTEIN A10055
calcineurin A1, putative0033
hepatocyte nuclear factor 4-alpha isoform 20303
protein AF-9 isoform a0003
melanocortin receptor 40213
CAAX prenyl protease0002
bcl-2-related protein A10606
hexokinase HKDC10101
DNA repair protein RAD52 homolog isoform a0005
bcl-2-like protein 11 isoform 10055
Trypanothione reductase018018
Peroxisomal N(1)-acetyl-spermine/spermidine oxidase0202
Spermine oxidase0101
1,3-beta-D-glucan synthase catalytic subunit 0101
Dihydrofolate reductase 0404
DNA ligase0101
Riboflavin-binding protein0123
Histidine-rich protein PFHRP-II0405
Spike glycoprotein0314
DNA ligase 10101
Calcium-dependent protein kinase 10011
DNA ligase A0101
Phosphoethanolamine N-methyltransferase0101
Cysteine proteinase falcipain 2a 0101
MBT domain-containing protein 10303
Lethal(3)malignant brain tumor-like protein 40303
Lethal(3)malignant brain tumor-like protein 30303
Chloroquine resistance transporter0303
Lethal(3)malignant brain tumor-like protein 10303
NADPH oxidase 10505
Snq2p00014
Adenylate cyclase type 1 0404
Major prion protein0011
Cys-loop ligand-gated ion channel0101
Sphingomyelin phosphodiesterase0303
Adenylate cyclase type 30404
Adenylate cyclase type 20415
Adenylate cyclase type 40404
Pleiotropic ABC efflux transporter of multiple drugs014028
Adenylate cyclase type 80404
Gastrin/cholecystokinin type B receptor0606
Aldehyde oxidase 10101
Adenylate cyclase type 60404
Aldehyde oxidase08010
Adenylyl cyclase 7 0404
Acetylcholinesterase 0101
Carboxylic ester hydrolase 0101
Chain A, Acetylcholinesterase0022
Chain A, Acetylcholinesterase0022
Chain A, Acetylcholinesterase0022
Chain A, Acetylcholinesterase0022
Chain A, Acetylcholinesterase0022
Chain A, Acetylcholinesterase0022
Chain A, Acetylcholinesterase0022
Chain A, Putative Glycine Betaine-binding Abc Transporter Protein0011
Chain A, PUTATIVE GLYCINE BETAINE-BINDING ABC TRANSPORTER PROTEIN0011
Chain A, Choline-binding protein0011
Sodium- and chloride-dependent creatine transporter 10101
High affinity choline transporter 10101
Chain A, Glycogen phosphorylase, muscle form0101
Chain A, Glycogen phosphorylase, muscle form0101
3-oxoacyl-acyl-carrier protein reductase 011011
Potassium-transporting ATPase alpha chain 10202
Potassium-transporting ATPase subunit beta0202
Solute carrier family 22 member 40303
Platelet glycoprotein VI0236
shiga toxin 1 variant A subunit1001
shiga toxin 1 B subunit1001
Cell division protein FtsZ0115
Transient receptor potential cation channel subfamily A member 10055
Estrogen receptor 10213
estrogen receptor beta isoform 10505
DNA gyrase subunit B0101
DNA gyrase subunit A0101
DNA gyrase subunit B0406
DNA gyrase subunit A07012
DNA gyrase subunit B07112
DNA topoisomerase 4 subunit A0202
DNA topoisomerase 4 subunit B0203
DNA topoisomerase 4 subunit A0304
DNA gyrase subunit A0406
Multidrug resistance protein MdtK0011
DNA gyrase subunit B0608
DNA gyrase subunit A0709
Enoyl-[acyl-carrier-protein] reductase [NADH]0205
DNA topoisomerase 4 subunit A0101
DNA topoisomerase 4 subunit B0101
Sodium-dependent noradrenaline transporter0505
Aromatase0101
Sodium-dependent serotonin transporter0505
Sodium-dependent dopamine transporter0808
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0202
Chain A, N5-carboxyaminoimidazole ribonucleotide mutase0011
Chain B, N5-carboxyaminoimidazole ribonucleotide mutase0011
Chain A, N5-carboxyaminoimidazole ribonucleotide mutase0011
Chain B, N5-carboxyaminoimidazole ribonucleotide mutase0011
Beta-lactamase0202
3-dehydroquinate dehydratase0011
ATP-citrate synthase 0304
Ribonuclease T0001
Cell death-related nuclease 40001
3-dehydroquinate dehydratase0011
Prolyl 4-hydroxylase0606
Alpha-ketoglutarate-dependent dioxygenase FTO0606
N(G),N(G)-dimethylarginine dimethylaminohydrolase 10709
General amino-acid permease GAP10001
LAP40011
MEP20011
Histamine H3 receptor0415
Histamine H4 receptor0448
Peroxisome proliferator-activated receptor alpha0268
Trypanothione reductase0101
Envelope glycoprotein0044
Translocator protein0202
Alpha-1B adrenergic receptor 0044
Alpha-2B adrenergic receptor0406
Alpha-2C adrenergic receptor0406
Alpha-2A adrenergic receptor0406
Nischarin010010
Amine oxidase [flavin-containing] A 012013
Sigma intracellular receptor 20101
5-hydroxytryptamine receptor 3A0707
Endothelin receptor type B0606
D(2) dopamine receptor0303
5-hydroxytryptamine receptor 1A0707
Chain A, CHIMERA OF IG KAPPA CHAIN: HUMAN CONSTANT REGION AND MOUSE VARIABLE REGION0011
Chain B, CHIMERA OF IG GAMMA-1 CHAIN: HUMAN CONSTANT REGION AND MOUSE VARIABLE REGION0011
Chain H, Fab M82G2, Heavy chain0011
Chain L, Fab M82G2, Light chain0011
Chain H, Fab M82g2, Heavy Chain0011
Chain L, Fab M82g2, Light Chain0011
Fatty acid-binding protein, heart0303
Muscarinic acetylcholine receptor M20123
Leukotriene B4 receptor 11103
Cytochrome P450 2D10606
Cytochrome P450 2D260707
Cytochrome P450 2D30707
Cytochrome P450 2D40707
Tubulin alpha-1A chain0428
Tubulin beta chain0426
Vesicular acetylcholine transporter0202
Tubulin polymerization-promoting protein0011
Tubulin beta-2B chain08114
Similar to alpha-tubulin isoform 1 05111
Similar to alpha-tubulin isoform 1 05010
CREB-binding protein4307
Solute carrier family 2, facilitated glucose transporter member 10516
Adenylate cyclase type 80112
Relaxin receptor 10011
Nuclear receptor subfamily 1 group I member 20044
B2 bradykinin receptor0404
Dihydrofolate reductase0404
Beta-galactosidase0304
Ectonucleotide pyrophosphatase/phosphodiesterase family member 20303
PH domain leucine-rich repeat-containing protein phosphatase 20101
Chymotrypsin-C0202
TPA: protein transporter TIM230303
Sterol 14-alpha demethylase0213
RNA-directed RNA polymerase 0113
Glycine receptor subunit alpha-1025025
Glycine receptor subunit beta024024
Glycine receptor subunit alpha-2024024
Glycine receptor subunit alpha-3024024
Exportin-10101
NAD-dependent histone deacetylase SIR20305
Sodium- and chloride-dependent creatine transporter 10101
ATP-binding cassette sub-family C member 90123
ATP-binding cassette sub-family C member 80437
ATP-sensitive inward rectifier potassium channel 110325
ATP-sensitive inward rectifier potassium channel 80011
Cocaine esterase0505
Papain0101
Receptor-type tyrosine-protein phosphatase C0202
Receptor-type tyrosine-protein phosphatase F0505
Tyrosine-protein phosphatase non-receptor type 90101
Protease 0819
Chain A, Breast cancer type 1 susceptibility protein8008
toll-like receptor 90101
TPA: protein transporter TIM100505
Phospholipase A20416
Neuronal proto-oncogene tyrosine-protein kinase Src 0102
Heme oxygenase 1 0404
Glutathione S-transferase P0303
Microtubule-associated protein tau0719
Sarcoplasmic/endoplasmic reticulum calcium ATPase 2 0101
Sarcoplasmic/endoplasmic reticulum calcium ATPase 20202
Heme oxygenase 20303
Voltage-dependent L-type calcium channel subunit alpha-1D0707
Voltage-dependent L-type calcium channel subunit alpha-1S0606
Thioredoxin reductase 1, cytoplasmic0405
Thioredoxin reductase 30303
Sarcoplasmic/endoplasmic reticulum calcium ATPase 30202
Cysteine protease 0101
Thioredoxin reductase 2, mitochondrial0303
Lymphocyte antigen 960011
Beta lactamase (plasmid)0202
Multidrug resistance-associated protein 50203
RPL19A0011
transactivating tegument protein VP16 [Human herpesvirus 1]0707
COUP transcription factor 2 isoform a0202
Glucose transporter0101
Hexose transporter 1 0101
Eukaryotic initiation factor 4A-I0101
Peptidyl-prolyl cis-trans isomerase FKBP1A0628
Peptidyl-prolyl cis-trans isomerase FKBP30101
Peptidyl-prolyl cis-trans isomerase FKBP40101
Peptidyl-prolyl cis-trans isomerase NIMA-interacting 10516
Peptidyl-prolyl cis-trans isomerase FKBP140101
Peptidyl-prolyl cis-trans isomerase NIMA-interacting 40101
Chain A, Glutamate [NMDA] receptor subunit zeta 10101
Chain A, Glutamate [NMDA] receptor subunit zeta 10101
Chain A, Glutamate [NMDA] receptor subunit zeta 10101
S-adenosylmethionine synthase isoform type-10102
D-alanine--D-alanine ligase0101
UDP-N-acetylmuramoyl-tripeptide--D-alanyl-D-alanine ligase 0101
chaperonin GroEL1001
Glycogen phosphorylase, muscle form0202
Histone-lysine N-methyltransferase SETD70909
Histone-lysine N-methyltransferase EHMT10505
nuclear receptor coactivator 1 isoform 1 [Homo sapiens]0404
nuclear receptor coactivator 3 isoform a0404
Thymidine kinase 2, mitochondrial0101
Thymidine kinase0203
Thymidylate synthase0507
Thymidine kinase0101
Probable deoxycytidylate deaminase0002
Cytidine deaminase0204
Enoyl-[acyl-carrier-protein] reductase [NADH] 0303
Deoxynucleoside kinase0101
Ribonucleoside-diphosphate reductase large subunit0103
Ribonucleoside-diphosphate reductase subunit M20002
2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase0101
2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase0022
Ribonucleoside-diphosphate reductase subunit M2 B0002
Solute carrier family 2, facilitated glucose transporter member 30101
Solute carrier family 2, facilitated glucose transporter member 40101
Deoxycytidine kinase0001
Alpha-tocopherol transfer protein0011
Coagulation factor X0505
Plasminogen0505
Coagulation factor XII0707
Tissue-type plasminogen activator0404
Serine protease hepsin0404
Pirin0101
Uncharacterized aarF domain-containing protein kinase 5001515
RAD510202
Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 10101
Growth factor receptor-bound protein 20102
Pantothenate synthetase0202
Growth factor receptor-bound protein 2 0101
Peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase0011
rac GTPase-activating protein 1 isoform a0303
Aldehyde dehydrogenase, mitochondrial0325
Sodium/glucose cotransporter 10325
Sodium/glucose cotransporter 20325
Sodium/glucose cotransporter 20011
Sodium/myo-inositol cotransporter 20202
Solute carrier family 5 member 40101
Prothrombin 0202
Glandular kallikrein0101
6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase 0101
Dihydrofolate reductase0607
Tyrosine-protein kinase ABL10303
Proto-oncogene tyrosine-protein kinase Src0459
Proto-oncogene tyrosine-protein kinase LCK 0303
Tyrosine-protein kinase Blk0101
Myelin transcription factor 10101
Breakpoint cluster region protein0101
Protein cereblon016527
Succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial001515
NF-kappa-B essential modulator0101
Chain A, Tyrosine-protein kinase ABL10101
Chain A, Tyrosine-protein kinase ABL10101
Chain A, Tyrosine-protein kinase ABL10101
Acetylcholinesterase0101
exodeoxyribonuclease V subunit RecD0202
exodeoxyribonuclease V subunit RecB0202
exodeoxyribonuclease V subunit RecC0202
Lysine-specific demethylase 4A0415
Flavin reductase (NADPH)0044
Lysine-specific demethylase 6A0101
Lysine-specific demethylase 5C0202
Lysine-specific demethylase 2B0101
Deoxyhypusine hydroxylase0202
Lysine-specific demethylase 2A0202
Methylcytosine dioxygenase TET20202
Beta-glucuronidase0202
Glucose-6-phosphate 1-dehydrogenase0808
Glucose-6-phosphate 1-dehydrogenase 0101
NPC1-like intracellular cholesterol transporter 10011
Solute carrier organic anion transporter family member 1A50007
Solute carrier organic anion transporter family member 1A20106
Solute carrier organic anion transporter family member 1A30208
ATP-binding cassette sub-family C member 110002
Solute carrier organic anion transporter family member 1A10001
Solute carrier organic anion transporter family member 1B20104
Chain A, STEROID DELTA-ISOMERASE0011
Steroid Delta-isomerase0011
Thymidine kinase 2 0101
AAA family ATPase 0001
AAA family ATPase 0001
Sterol O-acyltransferase 10202
Muscarinic acetylcholine receptor M50214
Trace amine-associated receptor 10022
Trace amine-associated receptor 10044
Trace amine-associated receptor 10077
Taste receptor type 2 member 460033
metallo beta-lactamase0101
metallo-beta-lactamase IMP-10101
LANA0002
glutathione S-transferase, partial0011
BZLF20101
Fatty acid synthase0606
Gamma-aminobutyric acid 0235
Alpha-1-acid glycoprotein 10001
Gamma-aminobutyric acid receptor subunit alpha-60235
Gamma-aminobutyric acid receptor subunit gamma-20235
Gamma-aminobutyric acid receptor subunit delta0235
Gamma-aminobutyric acid receptor subunit alpha-20235
Gamma-aminobutyric acid receptor subunit alpha-30235
Gamma-aminobutyric acid receptor subunit gamma-30235
Gamma-aminobutyric acid receptor subunit beta-10235
Gamma-aminobutyric acid receptor subunit alpha-10336
Gamma-aminobutyric acid receptor subunit beta-30235
Gamma-aminobutyric acid receptor subunit alpha-50235
Gamma-aminobutyric acid receptor subunit pi0235
Sphingosine-1-phosphate lyase 10202
Gamma-aminobutyric acid receptor subunit alpha-40235
Gamma-aminobutyric acid receptor subunit theta0235
Gamma-aminobutyric acid receptor subunit gamma-10235
Nicotinamide phosphoribosyltransferase0011
NAD0101
ATP phosphoribosyltransferase0101
Proprotein convertase subtilisin/kexin type 70202
UDP-glucose 4-epimerase0101
Cysteinyl leukotriene receptor 10415
High mobility group protein B10044
2-amino-3-carboxymuconate-6-semialdehyde decarboxylase0202
Chain A, DigA160011
Chain A, DigA160011
Sodium/potassium-transporting ATPase subunit alpha-1 0708
Sodium/potassium-transporting ATPase subunit beta-10708
Sodium/potassium-transporting ATPase subunit alpha-20708
Solute carrier organic anion transporter family member 4C10205
Sodium/potassium-transporting ATPase subunit alpha-20202
Sodium/potassium-transporting ATPase subunit alpha-3 0202
Sodium/potassium-transporting ATPase subunit beta-1 0202
Sodium/potassium-transporting ATPase subunit alpha-30405
Sodium/potassium-transporting ATPase subunit beta-20405
Sodium/potassium-transporting ATPase subunit alpha-10101
Sodium/potassium-transporting ATPase subunit beta-30405
Sodium/potassium-transporting ATPase subunit gamma0405
Sodium/potassium-transporting ATPase subunit alpha-40405
Sodium/potassium-transporting ATPase subunit alpha-40202
Solute carrier organic anion transporter family member 4C10002
Solute carrier organic anion transporter family member 1A40001
Neuronal acetylcholine receptor subunit alpha-50123
Neuronal acetylcholine receptor subunit beta-40303
Neuronal acetylcholine receptor subunit beta-20314
Chain A, HTH-type transcriptional regulator qacR0011
Chain B, HTH-type transcriptional regulator qacR0011
Chain A, HTH-type transcriptional regulator qacR0011
Chain B, HTH-type transcriptional regulator qacR0011
Chain A, HTH-type transcriptional regulator qacR0011
Chain A, HTH-type transcriptional regulator qacR0011
Chain B, HTH-type transcriptional regulator qacR0011
Chain A, HTH-type transcriptional regulator qacR0011
Chain B, HTH-type transcriptional regulator qacR0011
fatty acid synthase0202
Chain A, ALDOLASE0011
Cereblon isoform 40606
Insulin-like growth factor-binding protein 50011
Furin0101
Diamine acetyltransferase 10101
Acid-sensing ion channel 10101
Acid-sensing ion channel 20101
Glutathione S-transferase omega-10404
Prostaglandin E2 receptor EP1 subtype0325
Prostaglandin E2 receptor EP4 subtype0314
Prostaglandin F2-alpha receptor0202
Prostaglandin F2-alpha receptor0224
Prostaglandin E2 receptor EP3 subtype0325
Prostaglandin E2 receptor EP2 subtype0314
Prostaglandin F2-alpha receptor0011
Solute carrier organic anion transporter family member 2A10202
Prostaglandin E2 receptor EP4 subtype0112
Prostaglandin E2 receptor EP2 subtype0112
Solute carrier family 22 member 70001
Histamine N-methyltransferase0103
Calcium release-activated calcium channel protein 10202
Protein orai-20101
Protein orai-30101
Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit delta0303
3',5'-cyclic-AMP phosphodiesterase 0606
Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha0303
Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma0303
Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta0303
Retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma0303
Exopolyphosphatase PRUNE10101
Dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11A0505
Phosphodiesterase 0404
polypyrimidine tract-binding protein 1 isoform a1001
bifunctional UDP-N-acetylglucosamine pyrophosphorylase/glucosamine-1-phosphate N-acetyltransferase0404
Carbamate kinase0101
Retinal dehydrogenase 10303
Gasdermin-D0202
Lysyl oxidase homolog 30202
Lysyl oxidase homolog 40202
Monoglyceride lipase0404
Gasdermin-D0202
hypothetical protein CAALFM_CR05890CA0003
H3 histone acetyltransferase0003
Growth hormone-releasing hormone receptor0101
Acetylcholinesterase 015015
Cholinesterase0505
Acetylcholine receptor subunit epsilon0325
Acyl-CoA:cholesterol acyltransferase 0404
Carboxylic ester hydrolase 016016
N-arachidonyl glycine receptor0112
Lysophosphatidylserine lipase ABHD120101
Monoacylglycerol lipase ABHD60101
3-oxo-5-alpha-steroid 4-dehydrogenase 10303
3-oxo-5-alpha-steroid 4-dehydrogenase 20404
3 beta-hydroxysteroid dehydrogenase/Delta 5-->4-isomerase0202
Ultraspiracle0606
20-hydroxy-ecdysone receptor 0606
Ecdysone receptor0303
Ecdysone receptor0202
Protein ultraspiracle0101
Ultraspiracle 0101
20-hydroxy-ecdysone receptor 0101
Ultraspiracle protein 0101
20-hydroxy-ecdysone receptor 0101
UDP-glucuronosyltransferase 2B170012
UDP-glucuronosyltransferase 1A70115
Eyes absent homolog 20101
Chain A, Protein (peroxisome Proliferator Activated Receptor (ppar-delta))0101
N-methyl-D-aspartate receptor 0101
Chain A, Casein kinase II subunit alpha0101
acetyl-CoA acetyltransferase/HMG-CoA reductase0101
unnamed protein product0202
heat shock 70kDa protein 1A0101
Aldehyde oxidase 10101
fructose-bisphosphate aldolase A3003
glyceraldehyde-3-phosphate dehydrogenase isoform 13003
dual specificity protein phosphatase 30101
eukaryotic translation initiation factor 4 gamma 1 isoform 40202
mothers against decapentaplegic homolog 3 isoform 10101
heat shock cognate 71 kDa protein isoform 10101
eukaryotic translation initiation factor 4E isoform 10202
Tat0404
dual specificity protein phosphatase 60101
heat shock cognate 71 kDa protein isoform 20101
Nucleophosmin0202
Glutathione S-transferase Mu 10101
Macrophage migration inhibitory factor010111
Mitogen-activated protein kinase kinase kinase 80202
Squalene monooxygenase 0304
DNA primase0202
Tyrosine-protein kinase Lyn 0101
Polypeptide N-acetylgalactosaminyltransferase 20325
ELAV-like protein 30404
Tyrosine-protein kinase Fgr0101
Glutathione S-transferase0101
Translin-associated protein X0101
DNA polymerase iota0101
DNA polymerase eta0101
Cysteine protease ATG4B0101
likely tRNA 2'-phosphotransferase0202
Chain A, PROTEIN KINASE CK2, ALPHA SUBUNIT0101
Chain A, Casein kinase II, alpha chain0101
Chain A, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0011
Chain B, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0011
3-hydroxyacyl-[acyl-carrier-protein] dehydratase FabZ0303
Protein tyrosine phosphatase type IVA 30202
Accessory gene regulator protein A0101
Genome polyprotein0101
Casein kinase II subunit alpha0101
Genome polyprotein 0404
Opioid receptor, delta 1b 0202
Opioid receptor homologue0202
Proenkephalin-B0011
Mu-type opioid receptor0202
Catechol O-methyltransferase0505
UDP-glucuronosyltransferase 2B150013
Enoyl-[acyl-carrier-protein] reductase [NADH] FabI0505
Apoptosis regulator Bcl-20404
Glucose-6-phosphate 1-dehydrogenase0202
6-phosphogluconate dehydrogenase, decarboxylating0606
Chain A, Troponin C, slow skeletal and cardiac muscles0011
Chain A, Peptidyl-prolyl cis-trans isomerase NIMA-interacting 10011
Chain A, POLYMERASE PA0101
Chain A, Polymerase Pa0101
Chain A, Polymerase Pa0101
Chain A, Polymerase Pa0101
Chain A, Polymerase Pa0101
galactokinase4004
NAD kinase0213
Polymerase acidic protein0213
Plasminogen activator inhibitor 10202
Urokinase-type plasminogen activator0202
Alpha-amylase 1A 0606
Phosphoglycerate mutase 10202
Signal transducer and activator of transcription 1-alpha/beta0011
Matrix metalloproteinase-140101
BH3-interacting domain death agonist0101
Bcl-2-related protein A10101
3-oxoacyl-[acyl-carrier-protein] reductase 0101
Bcl-2-like protein 20101
Bcl2-associated agonist of cell death 0202
Bcl-2-like protein 100101
Cathepsin S0101
HRAS, partial0001
Voltage-dependent anion-selective channel protein 20011
Cystine/glutamate transporter0505
Adenylate cyclase 0101
Solute carrier family 22 member 40101
Motilin receptor0011
low molecular weight phosphotyrosine protein phosphatase isoform c0101
Motilin receptor0123
Chitinase B0101
Low molecular weight phosphotyrosine protein phosphatase0404
MPI protein0303
ERAP2 protein0002
M17 leucyl aminopeptidase0101
M18 aspartyl aminopeptidase0303
M1-family alanyl aminopeptidase0101
leucyl-cystinyl aminopeptidase [Mus musculus]0002
Lanosterol 14-alpha demethylase0022
UDP-glucuronosyltransferase 1A100217
Voltage-dependent calcium channel subunit alpha-2/delta-10303
Type IV secretion-like conjugative transfer relaxase protein TraI 0101
Acetylcholine receptor subunit delta0101
Acetylcholine receptor subunit alpha0101
Acetylcholine receptor subunit gamma0101
Acetylcholine receptor subunit beta0101
Cytochrome P450 11B1, mitochondrial0303
Cytochrome P450 11B2, mitochondrial0303
Regulatory protein E20011
DNA topoisomerase 20001
DNA topoisomerase 2-alpha 0001
Ubiquitin carboxyl-terminal hydrolase isozyme L30101
Ubiquitin carboxyl-terminal hydrolase isozyme L10101
Potassium voltage-gated channel subfamily KQT member 30025
Potassium voltage-gated channel subfamily KQT member 20025
UDP-glucuronosyltransferase 2B110011
Potassium voltage-gated channel subfamily KQT member 20011
Potassium voltage-gated channel subfamily KQT member 3 0011
UDP-glucuronosyltransferase 2B40011
UDP-glucuronosyltransferase 2A10011
UDP-glucuronosyltransferase 2A20011
UDP-glucuronosyltransferase 1A50011
Potassium voltage-gated channel subfamily KQT member 40012
UDP-glucuronosyltransferase 2A30011
UDP-glucuronosyltransferase 2B280011
UDP-glucuronosyltransferase 1A80017
Potassium voltage-gated channel subfamily KQT member 50013
Potassium voltage-gated channel subfamily KQT member 2 0011
5-hydroxytryptamine receptor 2A0516
Trypanothione reductase0101
Chain E, cAMP-dependent protein kinase, alpha-catalytic subunit0202
Chain I, cAMP-dependent protein kinase inhibitor, alpha form0202
Chain B, Rho-associated protein kinase 10202
Chain A, Rho-associated protein kinase 10202
Chain A, Rho-associated protein kinase 10202
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit0202
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit0202
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit0202
Chain I, cAMP-dependent protein kinase inhibitor alpha0202
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit0202
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit0202
Chain I, cAMP-dependent protein kinase inhibitor alpha0202
Chain A, Rho-associated protein kinase 10202
cAMP-dependent protein kinase catalytic subunit alpha isoform Calpha10001
cAMP-dependent protein kinase catalytic subunit alpha 0314
C-C motif chemokine 20202
Cell division control protein 42 homolog0202
Ras-related C3 botulinum toxin substrate 10123
Rho-associated protein kinase 20202
Fatty acid-binding protein, liver0123
Peroxisome proliferator-activated receptor alpha0011
Chain A, GLUTAMATE RECEPTOR SUBUNIT 20202
Chain A, Glutamate Receptor Subunit 20202
Chain B, Glutamate Receptor Subunit 20202
3 beta-hydroxysteroid dehydrogenase/Delta 5-->4-isomerase type 10101
3-oxo-5-alpha-steroid 4-dehydrogenase 1 0404
3-oxo-5-alpha-steroid 4-dehydrogenase 20404
Sphingosine 1-phosphate receptor 10123
RCG53912, isoform CRA_a 0001
Sphingosine kinase 1 0001
Sphingosine kinase 20304
Sphingosine kinase 10203
Chain B, Cell division protein kinase 60101
Dihydroorotate dehydrogenase (fumarate)0202
Dihydroorotate dehydrogenase 0202
Potassium voltage-gated channel subfamily D member 20303
Steroid 17-alpha-hydroxylase/17,20 lyase0404
Lanosterol 14-alpha demethylase0112
Malate dehydrogenase, cytoplasmic0303
Cytochrome P450 1440022
Steroid C26-monooxygenase0022
Mycocyclosin synthase0011
Lanosterol 14-alpha demethylase0011
Sterol 14-alpha demethylase0011
14-alpha sterol demethylase 0011
Skn7p0002
Voltage-dependent L-type calcium channel subunit beta-10101
Voltage-dependent calcium channel subunit alpha-2/delta-10101
Voltage-dependent N-type calcium channel subunit alpha-1B0202
Chain A, Uracil Phosphoribosyltransferase0101
Solute carrier family 22 member 80203
Potassium voltage-gated channel subfamily C member 10202
Gastrin/cholecystokinin type B receptor 0101
Serine hydroxymethyltransferase, mitochondrial0202
Acid-sensing ion channel 30202
Acid-sensing ion channel 10202
Cytochrome P450 1A2 0204
Chain A, Dihydrofolate reductase0011
Thymidylate synthase0505
Dihydrofolate reductase08311
Folylpolyglutamate synthase, mitochondrial0104
Folylpolyglutamate synthase, mitochondrial0104
Multidrug resistance associated protein0103
Chain A, Human Phospholipase A20101
1-alkyl-2-acetylglycerophosphocholine esterase 0101
Menin0011
Lecithin retinol acyltransferase0101
Protein Rev 0011
Corticosteroid 11-beta-dehydrogenase isozyme 10314
Holo-[acyl-carrier-protein] synthase0101
Dopamine beta-hydroxylase 0405
Dopamine beta-hydroxylase0101
Gamma-aminobutyric acid receptor subunit rho-30014
Gamma-aminobutyric acid receptor subunit rho-20025
Sterol O-acyltransferase 10022
Lipopolysaccharide heptosyltransferase 10101
PA-I galactophilic lectin0011
Jacalin0011
Protein disulfide-isomerase0202
Chain A, ACETYLCHOLINESTERASE0101
Chain A, Acetylcholinesterase0101
L-selectin0101
P-selectin0101
E-selectin0101
Sodium- and chloride-dependent GABA transporter 10202
Sodium- and chloride-dependent taurine transporter0202
Sodium- and chloride-dependent betaine transporter0101
Transitional endoplasmic reticulum ATPase0101
Small conductance calcium-activated potassium channel protein 20202
Small conductance calcium-activated potassium channel protein 10202
Chain A, Estrogen receptor 1 (alpha)0101
Chain A, Transthyretin0011
Chain A, Transthyretin0011
Steroid hormone receptor ERR20101
Steroid hormone receptor ERR10303
Ornithine decarboxylase0202
Solute carrier family 2, facilitated glucose transporter member 40303
Cystic fibrosis transmembrane conductance regulator0011
DNA (cytosine-5)-methyltransferase 3-like0303
DNA (cytosine-5)-methyltransferase 3A0404
beta-amyloid peptide, A beta {N-terminal} [human, cerebrospinal fluid, conditioned medium of mixed-brain cell cultures, Peptide Partial, 33 aa]1001
alpha synuclein, partial1001
Phosphatidylcholine:ceramide cholinephosphotransferase 1 0101
Phosphatidylcholine:ceramide cholinephosphotransferase 20101
Glucagon-like peptide 1 receptor0011
Glucagon-like peptide 1 receptor0336
Glucagon receptor0011
Glucagon receptor0011
Asialoglycoprotein receptor 10112
Chain A, Slr1257 protein0011
Chain A, Glucosamine--fructose-6-phosphate aminotransferase [isomerizing]0101
Bifunctional aspartokinase/homoserine dehydrogenase 10101
Excitatory amino acid transporter 3 0001
Glutamate racemase0001
Glutamate carboxypeptidase 20203
Glutamate racemase0001
Chain A, Glutamine Binding Protein0011
Asc-type amino acid transporter 10202
Glutathione reductase0102
ATP synthase subunit beta, mitochondrial0101
ATP synthase subunit delta, mitochondrial0101
ATP synthase subunit gamma, mitochondrial0101
ATP synthase subunit epsilon, mitochondrial0101
Cholesteryl ester transfer protein0101
Chain B, EUKARYOTIC TRANSLATION INITIATION FACTOR 4E0011
Sodium- and chloride-dependent glycine transporter 10303
Sodium- and chloride-dependent glycine transporter 20101
High mobility group protein B10001
Corticosteroid 11-beta-dehydrogenase isozyme 20112
Chain A, 3-phosphoshikimate 1-carboxyvinyltransferase0101
Chain A, 3-phosphoshikimate 1-carboxyvinyltransferase0101
Glutamine synthetase 0101
Cytochrome P450 71B10102
Glutamine synthetase 0101
2-dehydro-3-deoxyphosphooctonate aldolase0101
Peroxisome proliferator-activated receptor delta0134
guanine nucleotide-binding protein subunit alpha-150224
trace amine-associated receptor 10224
Ricin0202
Purine nucleoside phosphorylase 0125
Chain A, Probable hydrogenase nickel incorporation protein hypB0011
Chain B, Probable hydrogenase nickel incorporation protein hypB0011
Chain A, ELONGATION FACTOR TU (EF-TU)0011
Chain A, Elongation Factor G0011
Chain A, ADP-RIBOSYLATION FACTOR-LIKE PROTEIN 30011
Chain A, Eukaryotic peptide chain release factor GTP-binding subunit0011
Chain A, ras-related C3 botulinum toxin substrate 1 isoform Rac1b0011
Chain A, ras-related C3 botulinum toxin substrate 1 isoform Rac1b0011
Chain A, interferon-inducible GTPase0011
Chain A, interferon-inducible GTPase0011
Chain A, Elongation factor 20011
Chain A, Guanine nucleotide-binding protein G(i), alpha-1 subunit0011
Ras-related protein Rab-7a0022
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT50101
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase 90404
Chain A, Uracil Phosphoribosyltransferase0011
Chain B, Uracil Phosphoribosyltransferase0011
Chain C, Uracil Phosphoribosyltransferase0011
Chain A, BDNF/NT-3 GROWTH FACTORS RECEPTOR0101
Chain A, BDNF/NT-3 GROWTH FACTORS RECEPTOR0101
Chain A, BDNF/NT-3 GROWTH FACTORS RECEPTOR0101
Macrophage colony-stimulating factor 1 receptor0202
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 4, mitochondrial0202
Protein-glutamine gamma-glutamyltransferase 20303
M-phase inducer phosphatase 10404
Receptor protein-tyrosine kinase 0303
Dual specificity tyrosine-phosphorylation-regulated kinase 40202
Kinesin-like protein KIF150101
Cyclin-dependent kinase 5, regulatory subunit 1 (p35)0002
CDK50002
Chain E, C-amp-dependent Protein Kinase0101
Chain I, Protein Kinase Inhibitor Peptide0101
Chain E, C-amp-dependent Protein Kinase0101
Chain E, C-amp-dependent Protein Kinase0101
Chain I, Protein Kinase Inhibitor Peptide0101
cAMP-dependent protein kinase type II-alpha regulatory subunit0202
cAMP-dependent protein kinase catalytic subunit beta 0202
cAMP-dependent protein kinase type II-beta regulatory subunit0202
Vitamin D-binding protein0101
Integrin alpha-40202
AP-2 complex subunit sigma0101
Calcitonin gene-related peptide type 1 receptor0101
Zinc finger protein 6640101
Vesicular acetylcholine transporter0505
STE240002
DNA repair and recombination protein RAD54-like isoform 10001
Chain A, Dual specificity tyrosine-phosphorylation-regulated kinase 1A0101
CDC-like kinase 1, isoform CRA_c0001
dual specificity protein kinase CLK41001
Dual specificity protein kinase CLK20101
Dual specificity protein kinase CLK30101
Dual specificity protein kinase CLK40101
Dual specificity tyrosine-phosphorylation-regulated kinase 30101
Sodium-dependent dopamine transporter0101
Neuromedin-B receptor0101
Mitogen-activated protein kinase 10202
Serine/threonine-protein kinase haspin0101
Chain E, Fibrin beta chain0303
Vesicular acetylcholine transporter0202
Chain A, TYROSINE PHOSPHATASE0101
Chain A, Tyrosine Phosphatase0101
carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 isoform 10202
Chain A, CARBONIC ANHYDRASE II0011
Chain A, Protein (female-specific Histamine Binding Protein 2)0011
aryl hydrocarbon receptor nuclear translocator0001
transforming acidic coiled-coil-containing protein 30001
Histamine N-methyltransferase 0202
Equilibrative nucleoside transporter 40001
Histamine H4 receptor0235
Histamine H4 receptor 0202
Chain A, HISTIDINE-BINDING PROTEIN0011
Histidine-binding periplasmic protein0011
Phosphatidylcholine-sterol acyltransferase0011
G-protein coupled receptor 10011
N-glycosylase/DNA lyase0404
Aspartate aminotransferase, cytoplasmic0202
Chain A, Acetylcholinesterase0101
Chain A, Carbonic anhydrase 20101
Chain A, Carbonic anhydrase 20101
Chain A, Carbonic anhydrase 20101
Cyclic GMP-AMP synthase0202
Toll-like receptor 90101
Toll-like receptor 70114
Uracil nucleotide/cysteinyl leukotriene receptor0404
Chain A, Phospholipase A20011
Chain A, Phospholipase A2 VRV-PL-VIIIa0011
2-5A-dependent ribonuclease0304
Chain A, Purine-nucleoside Phosphorylase0101
Chain C, Xanthine dehydrogenase/oxidase0011
Caspase-40303
Caspase-50303
Dehydrogenase/reductase SDR family member 90101
3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase0101
Chain A, PROTO-ONCOGENE TYROSINE-PROTEIN KINASE ABL0101
Chain A, Tyrosine-protein kinase SYK0101
BCR/ABL p210 fusion protein 0101
L-lactate dehydrogenase A chain0101
Mast/stem cell growth factor receptor Kit0202
Platelet-derived growth factor receptor beta0303
Platelet-derived growth factor receptor alpha 0202
Platelet-derived growth factor receptor beta0101
Lysine--tRNA ligase0123
Epoxide hydrolase 10002
Chain A, Cell Division Protein Kinase 20101
Chain A, CELL DIVISION PROTEIN KINASE 20101
Chain A, Cell Division Protein Kinase 20101
Chain A, CELL DIVISION PROTEIN KINASE 20101
Chain A, CELL DIVISION PROTEIN KINASE 20101
Chain A, CELL DIVISION PROTEIN KINASE 20101
Chain A, CELL DIVISION PROTEIN KINASE 20101
Chain A, CELL DIVISION PROTEIN KINASE 20101
Chain A, CELL DIVISION PROTEIN KINASE 20101
Chain A, CELL DIVISION PROTEIN KINASE 20101
Chain A, CELL DIVISION PROTEIN KINASE 20101
Chain A, CELL DIVISION PROTEIN KINASE 20101
Chain A, CELL DIVISION PROTEIN KINASE 20101
Chain A, Cell Division Protein Kinase 20101
Chain A, PROTEIN (PROTEASE)0101
Chain B, PROTEIN (PROTEASE)0101
Chain A, PROTEIN (PROTEASE)0101
Chain B, PROTEIN (PROTEASE)0101
Chain A, HIV-1 PROTEASE0101
Chain B, HIV-1 PROTEASE0101
Chain A, HIV-II PROTEASE0101
Chain B, HIV-II PROTEASE0101
Chain A, POL polyprotein0011
Chain B, POL polyprotein0011
Chain A, POL polyprotein0011
Chain B, POL polyprotein0011
Chain A, POL polyprotein0011
Chain B, POL polyprotein0011
Chain A, POL polyprotein0011
Chain B, POL polyprotein0011
Chain A, protease RETROPEPSIN0101
Chain B, protease RETROPEPSIN0101
Chain A, protease RETROPEPSIN0101
Chain B, protease RETROPEPSIN0101
Chain A, protease RETROPEPSIN0101
Chain B, protease RETROPEPSIN0101
Chain A, POL polyprotein0101
Chain B, POL polyprotein0101
Chain A, POL polyprotein0101
Chain B, POL polyprotein0101
Chain A, HIV-1 protease0101
Chain B, HIV-1 protease0101
Chain A, Pol polyprotein0101
Chain B, Pol polyprotein0101
Chain A, Pol polyprotein0101
Chain B, Pol polyprotein0101
Chain A, Pol polyprotein0101
Chain B, Pol polyprotein0101
Chain A, Pol polyprotein0101
Chain B, Pol polyprotein0101
Chain A, Hiv-1 Protease0101
Chain B, Hiv-1 Protease0101
Chain A, Hiv-1 Protease0101
Chain B, Hiv-1 Protease0101
Chain A, Hiv-1 Protease0101
Chain B, Hiv-1 Protease0101
Gag-Pol polyprotein0202
Gag-Pol polyprotein0202
Gag-Pol polyprotein0202
Gag polyprotein0101
Gag-Pol polyprotein0101
Gag-Pol polyprotein0303
Gag-Pol polyprotein0101
Thromboxane-A synthase0001
Protease 0101
Chain A, Glycogen Synthase Kinase-3 Beta0101
Chain B, Glycogen Synthase Kinase-3 Beta0101
Chain A, Glycogen Synthase Kinase-3 Beta0101
Kynurenine--oxoglutarate transaminase 10101
Peptide deformylase 1A, chloroplastic/mitochondrial0101
Peptide deformylase 0101
Chain A, membrane-associated prostaglandin E synthase-20101
Phospholipase A2, major isoenzyme0303
Interleukin-80101
C-X-C chemokine receptor type 30404
Prostaglandin D2 receptor 0202
Chain A, ADENOSINE DEAMINASE0101
Chain A, ADENOSINE DEAMINASE0101
Chain A, Hypoxanthine Phosphoribosyltransferase0101
Chain A, HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE0101
Chain A, hypoxanthine phosphoribosyltransferase0011
Chain A, hypoxanthine phosphoribosyltransferase0011
Chain A, HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE0011
Chain B, HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE0011
Chain A, HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE0011
Chain A, Hypoxanthine-guanine phosphoribosyltransferase0101
Chain B, Pulmonary surfactant-associated protein D0101
Chain A, Pulmonary surfactant-associated protein D0101
Chain A, BETA-SPECTRIN0011
Chain A, Phospholipase C Delta-10011
Chain A, Inositol 1,4,5-trisphosphate receptor type 10011
Inositol-trisphosphate 3-kinase A0101
Inositol 1,4,5-trisphosphate receptor type 1 0022
Inositol 1,4,5-trisphosphate receptor type 20101
Inositol 1,4,5-trisphosphate receptor type 30112
Inositol polyphosphate-5-phosphatase A0101
Inositol 1,4,5-trisphosphate receptor type 10112
Liver carboxylesterase 10202
Transcriptional activator Myb0202
Dihydroorotate dehydrogenase (quinone), mitochondrial0404
Beta-galactosidase0101
3-oxoacyl-[acyl-carrier-protein] synthase 3 0101
Formamidopyrimidine-DNA glycosylase0101
Endonuclease III-like protein 10101
Putative FAD-containing monooxygenase MymA0101
Dihydrofolate reductase0303
Endonuclease 8-like 10101
Chain A, beta-galactosidase0101
Chain A, Beta-galactosidase0101
Chain A, Beta-galactosidase0101
Chain A, Beta-galactosidase0101
Chain A, Beta-galactosidase0101
Chain A, Beta-galactosidase0101
Chain A, Beta-galactosidase0101
Chain A, Beta-galactosidase0101
Chain A, Beta-galactosidase0101
Chain A, Beta-galactosidase0101
Chain A, Beta-galactosidase0101
Chain A, Beta-galactosidase0101
Chain A, Beta-galactosidase0101
Chain A, Beta-galactosidase0101
Chain A, Beta-galactosidase0101
Beta-galactosidase0101
Beta-2 adrenergic receptor0112
Beta-3 adrenergic receptor0011
Beta-1 adrenergic receptor0415
Taste receptor type 2 member 380036
Taste receptor type 2 member 390011
Taste receptor type 2 member 400011
Taste receptor type 2 member 410011
Taste receptor type 2 member 430011
Taste receptor type 2 member 310044
Taste receptor type 2 member 450011
Taste receptor type 2 member 300011
Taste receptor type 2 member 190011
Taste receptor type 2 member 200011
Taste receptor type 2 member 500011
Taste receptor type 2 member 600022
Taste receptor type 2 member 420011
Taste receptor type 2 member 140023
Taste receptor type 2 member 130022
Taste receptor type 2 member 100023
Taste receptor type 2 member 90022
Taste receptor type 2 member 80011
Taste receptor type 2 member 70011
Taste receptor type 2 member 50011
Taste receptor type 2 member 40022
Taste receptor type 2 member 30011
Taste receptor type 2 member 10022
Voltage-dependent L-type calcium channel subunit alpha-1C0101
Histamine H1 receptor 0101
Chain A, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0101
Chain B, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0101
Dual specificity protein phosphatase 10202
M-phase inducer phosphatase 20404
Dual specificity protein phosphatase 60202
Monoglyceride lipase0101
Monoglyceride lipase0101
Protein E60404
E3 ubiquitin-protein ligase XIAP0202
Chain A, Glutamate receptor 20022
Chain A, Glutamate receptor 20022
Chain C, Glutamate receptor 20022
3-oxoacyl-[acyl-carrier-protein] synthase 30101
Gap junction alpha-1 protein0101
Gap junction beta-2 protein0101
Acyl-protein thioesterase 10101
25-hydroxyvitamin D-1 alpha hydroxylase, mitochondrial0101
25-hydroxyvitamin D-1 alpha hydroxylase, mitochondrial0202
Camphor 5-monooxygenase0001
Steroid 21-hydroxylase0101
Cholesterol side-chain cleavage enzyme, mitochondrial 0101
Cytochrome P450 2A20101
Cytochrome P450 11B1, mitochondrial 0202
Cytochrome P450 7A1 0101
Gonadotropin-releasing hormone receptor0314
Cytochrome P450 4F20202
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial0101
Cytochrome P450 7A10101
Lanosterol 14-alpha demethylase 0202
7,8-dihydro-8-oxoguanine triphosphatase0303
Calcium/calmodulin-dependent protein kinase type II subunit beta0101
Calcium/calmodulin-dependent protein kinase type II subunit alpha0101
Calcium/calmodulin-dependent protein kinase type II subunit gamma0101
Calcium/calmodulin-dependent protein kinase type II subunit delta0101
G protein-coupled receptor GPR350022
microphthalmia-associated transcription factor isoform 90404
5-hydroxytryptamine receptor 1E0606
bioA0001
Sodium channel protein type 10 subunit alpha0101
Splicing factor 3B subunit 30303
Chain A, Lectin0011
Chain A, Lectin0011
Chain A, Lectin0011
Chain A, Lectin0011
Chain A, ERYTHRINA CRISTA-GALLI LECTIN0011
Chain A, ERYTHRINA CRISTA-GALLI LECTIN0011
Chain A, cellulase0011
Chain A, cellulase0011
Chain A, Galectin-30011
Chain A, Anti-tumor lectin0101
Galectin-30101
Galectin-90011
Galectin-80011
Beta-galactoside-binding lectin0101
Galectin-10113
Galectin-30112
Galectin-30113
Galectin-70011
Alpha 1,4 galactosyltransferase0001
phosphoethanolamine/phosphocholine phosphatase isoform 10101
WD repeat-containing protein 50303
Histone-lysine N-methyltransferase 2A0404
Cytosolic endo-beta-N-acetylglucosaminidase0202
Indoleamine 2,3-dioxygenase 20303
Chain A, Epidermal growth factor receptor0101
Alpha-1A adrenergic receptor 0101
Voltage-dependent L-type calcium channel subunit alpha-1C0202
Voltage-dependent L-type calcium channel subunit alpha-1S0202
Voltage-dependent L-type calcium channel subunit alpha-1D0202
Voltage-dependent L-type calcium channel subunit alpha-1F0202
Actin0101
DNA-binding protein Ikaros0027
DNA damage-binding protein 10325
Zinc finger protein Aiolos0022
Chain A, AMINOPEPTIDASE0202
Chain A, AMINOPEPTIDASE0202
Chain A, Leucine Aminopeptidase0101
Intestinal-type alkaline phosphatase0404
Phospholipase A-2-activating protein0404
Gonadotropin-releasing hormone receptor0101
Synaptic vesicle glycoprotein 2A0202
SLC16A10 protein0004
Monocarboxylate transporter 100004
CAAX prenyl protease 2 isoform 20001
Protein-serine O-palmitoleoyltransferase porcupine0101
Protein-serine O-palmitoleoyltransferase porcupine0101
Isocitrate dehydrogenase [NADP] cytoplasmic0213
Potassium channel subfamily K member 180101
Dipeptidyl peptidase 90101
Dipeptidyl peptidase IV0101
Prolyl endopeptidase FAP0101
Prolyl endopeptidase FAP0101
Dipeptidyl peptidase 80101
Dipeptidyl peptidase 90101
Dipeptidyl peptidase 20101
Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial0101
Dual specificity tyrosine-phosphorylation-regulated kinase 1A0101
Renin0303
Sterol O-acyltransferase 10303
Sterol O-acyltransferase 10404
inositol monophosphatase 11001
5-hydroxytryptamine receptor 2C0011
Type-1 angiotensin II receptor0213
Chain A, Antigen Cd11a (p180)0101
Integrin beta-20101
Intercellular adhesion molecule 10101
Integrin alpha-L0213
Bromodomain testis-specific protein0112
retinoic acid receptor alpha isoform 10101
retinoic acid receptor RXR-alpha isoform a0101
histidine kinase 0101
Chemotaxis protein CheA0101
Cytosol aminopeptidase0202
Macrophage metalloelastase0202
Protein polybromo-10011
DNA topoisomerase 10101
Chain A, Phenylethanolamine N-methyltransferase0101
Chain A, Phenylethanolamine N-methyltransferase0101
5-hydroxytryptamine receptor 1F0314
Beta-secretase 10101
3-hydroxy-3-methylglutaryl-coenzyme A reductase0101
Beta-secretase 20102
Transcription factor HES-10101
Sodium-dependent dopamine transporter0101
Chain A, Ribulose-1,5 bisphosphate carboxylase/oxygenase large subunit N-methyltransferase, chloroplast0101
Chain A, Ribulose-1,5 bisphosphate carboxylase/oxygenase large subunit N-methyltransferase, chloroplast0101
Chain A, Retinoic acid receptor RXR-alpha0011
Chain A, Peroxisome proliferator-activated receptor gamma0011
Carboxylic ester hydrolase 0101
Chain A, Phosphoenolpyruvate carboxykinase0101
D-aspartate oxidase 0101
D-aspartate oxidase0101
Serine racemase0303
Sphingomyelin phosphodiesterase0101
Stimulator of interferon genes protein0011
Stimulator of interferon genes protein0112
Alpha-mannosidase 2C10112
Fucose-binding lectin PA-IIL0101
CD209 antigen0101
histone-lysine N-methyltransferase NSD2 isoform 10001
Cysteinyl leukotriene receptor 10202
Calmodulin-domain protein kinase 10101
Neuronal acetylcholine receptor subunit alpha-20202
Androgen receptor0022
Nociceptin receptor0112
Melatonin receptor type 1C0011
Melatonin receptor type 1A0224
Melatonin receptor type 1C0224
Melatonin receptor type 1B0224
Quinone oxidoreductase0001
Vitamin K-dependent gamma-carboxylase 0001
Mucosa-associated lymphoid tissue lymphoma translocation protein 10202
Metallo-beta-lactamase VIM-19 0001
Metallo-beta-lactamase VIM-20001
BlaVIM-1 0001
Tumor necrosis factor0314
Hydroxyacid oxidase 10101
Aldehyde oxidase 1 0404
Chain A, Methionyl-tRNA synthetase0011
Chain A, Methionyl-tRNA synthetase0011
Chain A, Aminopeptidase0101
Chain A, Methionine aminopeptidase0101
S-ribosylhomocysteine lyase0101
Adenylate cyclase type 50102
S-adenosylmethionine synthase isoform type-20001
Chain B, DIHYDROFOLATE REDUCTASE0011
Chain B, DIHYDROFOLATE REDUCTASE0011
Chain B, DIHYDROFOLATE REDUCTASE0011
Thymidylate synthase 0101
Thymidylate synthase 0101
ATP-binding cassette sub-family C member 30102
Dihydrofolate reductase0304
Dihydrofolate reductase0101
Dihydrofolate reductase0405
Bifunctional dihydrofolate reductase-thymidylate synthase0303
Dihydrofolate reductase0303
Thymidylate synthase0202
Bifunctional dihydrofolate reductase-thymidylate synthase0303
Folate receptor beta0101
Folate receptor alpha0101
Histidine decarboxylase0145
Trifunctional purine biosynthetic protein adenosine-30101
Reduced folate transporter0202
Bifunctional dihydrofolate reductase-thymidylate synthase0203
Bifunctional dihydrofolate reductase-thymidylate synthase0101
Trifunctional purine biosynthetic protein adenosine-30101
Dihydrofolate reductase 0303
Dihydrofolate reductase0203
Proton-coupled folate transporter0101
T cell receptor, partial1001
luteinizing hormone receptor1001
Dihydrolipoyl dehydrogenase, mitochondrial0102
Dihydrolipoyl dehydrogenase 0102
Thioredoxin reductase 0101
Flavodoxin0002
Stearoyl-CoA desaturase0101
Acyl-CoA (8-3)-desaturase0101
Acyl-CoA 6-desaturase0101
Acyl-CoA desaturase 10404
Acyl-CoA 0101
Acyl-CoA 6-desaturase 0101
G-protein coupled receptor 0101
Sodium channel protein type 4 subunit alpha0101
Voltage-dependent L-type calcium channel subunit beta-30101
Chain A, PROGESTERONE RECEPTOR0101
Glucocorticoid receptor 0101
Tegument protein VP160011
Glucocorticoid receptor0225
Glucocorticoid receptor0112
Progesterone receptor0011
Glucocorticoid receptor0101
Sucrase-isomaltase 0101
Ceramide glucosyltransferase0101
Beta-galactosidase0101
Lysosomal alpha-glucosidase0101
Non-lysosomal glucosylceramidase0102
Multidrug transporter MdfA0202
Leucine-rich repeat serine/threonine-protein kinase 20011
Mitogen-activated protein kinase kinase kinase 140101
Nuclear receptor corepressor 10101
Nuclear receptor corepressor 20404
Retina-specific copper amine oxidase0303
Iodotyrosine deiodinase0011
fMet-Leu-Phe receptor0303
Tyrosine 3-monooxygenase0101
Iodotyrosine deiodinase 10011
Chain A, HEAT SHOCK PROTEIN 900011
Chain A [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 10101
Chain A [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 30101
Chain A, Atp-dependent Molecular Chaperone Hsp820011
Chain A, Atp-dependent Molecular Chaperone Hsp820011
Chain B, Type 2 DNA topoisomerase 6 subunit B0011
Chain A, Virulence sensor histidine kinase phoQ0011
Virulence sensor histidine kinase PhoQ0011
ATP-dependent molecular chaperone HSC820202
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial0202
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 2, mitochondrial0112
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 3, mitochondrial0101
Proto-oncogene tyrosine-protein kinase Src 0101
Histidine kinase 0101
Leukotriene C4 synthase0101
Cysteinyl leukotriene receptor 20101
Islet amyloid polypeptide0101
Low molecular weight phosphotyrosine protein phosphatase0101
DNA-3-methyladenine glycosylase0101
Solute carrier family 22 member 120101
Solute carrier family 22 member 120404
Class A sortase SrtA 0202
Nociceptin receptor0101
Mu-type opioid receptor0101
DNA gyrase subunit B0202
Mitochondrial pyruvate carrier 20101
5-hydroxytryptamine receptor 1B0202
Chain A, Inosine-5'-Monophosphate Dehydrogenase 20101
Inosine-5'-monophosphate dehydrogenase0102
Chain A, Proto-oncogene serine/threonine-protein kinase Pim-10202
Chain A, Proto-oncogene serine/threonine-protein kinase Pim-10202
Chain A, Proto-oncogene serine/threonine-protein kinase Pim-10202
Chain A, Proto-oncogene serine/threonine-protein kinase Pim-10202
Chain A, Pancreatic alpha-amylase0101
Chain A, Pancreatic alpha-amylase0101
DNA dC->dU-editing enzyme APOBEC-3A isoform a0101
Tyrosine-protein kinase transforming protein Fps0101
Solute carrier family 2, facilitated glucose transporter member 20202
Insulin-degrading enzyme0101
Solute carrier family 2, facilitated glucose transporter member 4 0202
DNA primase TraC0101
Aldo-keto reductase family 1 member C210303
Prolyl 4-hydroxylase, beta polypeptide0002
RNA-editing ligase 1, mitochondrial0101
Toll-like receptor 20202
Dynamin-10101
Glutamate receptor, metabotropic 41012
metabotropic glutamate receptor0011
metabotropic glutamate receptor 6 precursor0011
metabotropic glutamate receptor 2 precursor0011
metabotropic glutamate receptor 3 precursor0011
metabotropic glutamate receptor 1 isoform alpha precursor0011
metabotropic glutamate receptor 5 precursor0011
metabotropic glutamate receptor 8 precursor0011
metabotropic glutamate receptor 4 precursor1012
Growth hormone secretagogue receptor type 10022
Sialidase-40202
Sialidase-10202
Sialidase-30202
Formyl peptide receptor-related sequence 10011
fMet-Leu-Phe receptor0325
N-formyl peptide receptor 20022
FML2_HUMAN 0011
Muscarinic acetylcholine receptor 0011
Muscarinic acetylcholine receptor 0101
FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE) (FATTY-ACID-CoA SYNTHASE)0001
Acid ceramidase0202
Glucose-dependent insulinotropic receptor0011
Glucose-dependent insulinotropic receptor0011
Chain A, PROTEIN (5-AMINOLAEVULINIC ACID DEHYDRATASE)0101
N(G),N(G)-dimethylarginine dimethylaminohydrolase 10002
N(G),N(G)-dimethylarginine dimethylaminohydrolase 10001
Chain B, Exotoxin A0011
Chain B, Exotoxin A0011
Chain B, Exotoxin A0011
ubiquitin-like modifier-activating enzyme 10101
ubiquitin-conjugating enzyme E2 variant 1 isoform a0101
Complement C1r subcomponent0101
Complement C1s subcomponent0202
Neutrophil collagenase0202
Hepatocyte growth factor activator0213
Suppressor of tumorigenicity 14 protein0202
Nociceptin receptor0337
Chain A, Cholix toxin0101
Beta-hexosaminidase subunit alpha0101
Hormone-sensitive lipase0101
Chain A, Hth-type Transcriptional Regulator Ttgr0022
Chain A, Hth-type Transcriptional Regulator Ttgr0022
Chain A, Mitogen-activated protein kinase 140101
Chain A, Mitogen-activated protein kinase 140101
Chain A, Mitogen-activated protein kinase 140101
Chain A, Mitogen-activated protein kinase 140101
Chain A, Mitogen-activated protein kinase 140101
Chain A, Mitogen-activated protein kinase 140101
Chain A, Mitogen-activated protein kinase 140101
Chain A, Mitogen-activated protein kinase 140101
Chain A, Mitogen-activated protein kinase 140101
G protein-activated inward rectifier potassium channel 20011
G protein-activated inward rectifier potassium channel 40011
G protein-activated inward rectifier potassium channel 10011
Chain A, PROTOCATECHUATE 3,4-DIOXYGENASE ALPHA CHAIN0011
Chain B, PROTOCATECHUATE 3,4-DIOXYGENASE BETA CHAIN0011
Neuromedin-K receptor0145
Substance-K receptor0156
Substance-K receptor0303
Substance-K receptor0303
Neuromedin-K receptor0213
Neurotensin receptor type 10011
Neurotensin receptor type 20214
Myelin basic protein0011
Neurotensin receptor type 10315
Neurotensin receptor type 10349
Neurotensin receptor type 20325
Sortilin0202
Hydroxycarboxylic acid receptor 30011
Hydroxycarboxylic acid receptor 20011
Hydroxycarboxylic acid receptor 20112
Chain A, NAD-dependent deacetylase0101
NAD(+) hydrolase SARM10101
NAD-dependent protein deacetylase sirtuin-60314
NAD-dependent protein deacetylase 0101
Neuronal acetylcholine receptor subunit alpha-40213
Neuronal acetylcholine receptor subunit alpha-40101
Acetylcholine receptor subunit beta-like 20202
Neuronal acetylcholine receptor subunit alpha-70404
Neuronal acetylcholine receptor subunit beta-30112
Neuronal acetylcholine receptor subunit alpha-60112
Cytochrome P450 2A130437
Neuronal acetylcholine receptor subunit alpha-50202
Liver carboxylesterase B-10101
Neuronal acetylcholine receptor subunit beta-30202
Neuronal acetylcholine receptor subunit alpha-30202
Soluble acetylcholine receptor0101
Neuronal acetylcholine receptor subunit alpha-20202
Neuronal acetylcholine receptor subunit alpha-60202
Integrin beta0011
Glycoprotein IIb0011
Voltage-dependent L-type calcium channel subunit beta-40202
Voltage-dependent P/Q-type calcium channel subunit alpha-1A0202
Voltage-dependent calcium channel gamma-3 subunit0202
Voltage-dependent L-type calcium channel subunit beta-30202
Voltage-dependent calcium channel subunit alpha-2/delta-10405
Voltage-dependent calcium channel gamma-7 subunit0202
Voltage-dependent L-type calcium channel subunit beta-10202
Voltage-dependent calcium channel gamma-1 subunit0202
Voltage-dependent L-type calcium channel subunit beta-20202
Voltage-dependent R-type calcium channel subunit alpha-1E0202
Voltage-dependent calcium channel subunit alpha-2/delta-40202
Voltage-dependent calcium channel subunit alpha-2/delta-30202
Voltage-dependent calcium channel gamma-8 subunit0202
Voltage-dependent calcium channel gamma-6 subunit0202
Voltage-dependent calcium channel subunit alpha-2/delta-20404
Voltage-dependent calcium channel gamma-4 subunit0202
Voltage-dependent calcium channel gamma-5 subunit0202
Voltage-dependent calcium channel gamma-2 subunit0202
Pyruvate-flavodoxin oxidoreductase0101
Anoctamin-10101
Sodium/iodide cotransporter0101
G-protein coupled receptor 550101
Platelet-activating factor receptor0101
Nitric oxide synthase, inducible0202
Nitric oxide synthase, brain0202
Nociceptin receptor0134
Chain A, Glutathione-requiring prostaglandin D synthase0101
Chain A, Gyrase0011
DNA gyrase subunit B0101
DNA gyrase subunit B0101
Cell division inhibitor SulA0001
Heat shock protein HSP 900101
DNA topoisomerase 4 subunit B0101
DNA topoisomerase 0101
Microtubule-associated proteins 1A/1B light chain 3B0213
Microtubule-associated proteins 1A/1B light chain 3A0213
Chain A, G protein-coupled receptor kinase 60011
Adenosine kinase0101
Casein kinase I isoform alpha0101
Glycogen synthase kinase 3 0101
ALK tyrosine kinase receptor0101
Echinoderm microtubule-associated protein-like 40101
L-cysteine:1D-myo-inositol 2-amino-2-deoxy-alpha-D-glucopyranoside ligase0101
Solute carrier family 22 member 190001
Protein mono-ADP-ribosyltransferase PARP60202
Protein mono-ADP-ribosyltransferase PARP100224
Protein mono-ADP-ribosyltransferase PARP80011
Protein mono-ADP-ribosyltransferase PARP160224
Protein mono-ADP-ribosyltransferase PARP120202
Protein mono-ADP-ribosyltransferase PARP40325
Protein mono-ADP-ribosyltransferase PARP30347
Neurogenic locus notch homolog protein 10101
Phosphotyrosine protein phosphatase 0101
Hemagglutinin [Cleaved into: Hemagglutinin HA1 chain; Hemagglutinin HA2 chain]0011
Receptor-type tyrosine-protein phosphatase alpha0202
Chain A, Adipocyte Lipid-binding Protein0011
Chain A, MUSCLE FATTY ACID BINDING PROTEIN0022
Chain A, MUSCLE FATTY ACID BINDING PROTEIN0022
Chain A, MUSCLE FATTY ACID BINDING PROTEIN0022
putative potassium channel subunit0011
Bifunctional cytochrome P450/NADPH--P450 reductase0011
Bombesin receptor subtype-30011
Potassium-transporting ATPase alpha chain 20001
Interleukin-6 receptor subunit alpha0101
Thyrotropin-releasing hormone receptor0101
Glycine receptor subunit alpha-40101
Leukotriene B4 receptor 10101
Chain A, ARGINASE 10101
Chain A, Arginase 10101
Chain A, ARGINASE 10101
Chain A, L-ARGININE\\:GLYCINE AMIDINOTRANSFERASE0101
Neuraminidase 0202
Neuraminidase 0202
Neuraminidase0202
Acyl-CoA desaturase 10101
Neuraminidase 0202
Neuraminidase 0202
Neuraminidase0101
Neuraminidase0101
Chain H, Igg2b-kappa 40-50 Fab (heavy Chain)0101
Chain L, Igg2b-kappa 40-50 Fab (light Chain)0101
Chain A, Na, K-ATPase alpha subunit0011
Kruppel-like factor 50101
Sodium/potassium-transporting ATPase subunit alpha-1 0101
Sodium/potassium-transporting ATPase subunit beta-30101
Kynurenine 3-monooxygenase0202
Prolyl 4-hydroxylase subunit alpha-10202
Kynurenine/alpha-aminoadipate aminotransferase, mitochondrial0101
Lysine-specific demethylase 5D0101
Lysine-specific demethylase 5B0101
Lysine-specific demethylase 3A0101
polyadenylate-binding protein 10303
MCOLN3 protein0011
transient receptor potential cation channel, subfamily N, member 10011
Muscarinic acetylcholine receptor DM10303
Chain A, Bacterial leucyl aminopeptidase0101
Oxytocin receptor0011
Beta-tubulin 0202
Nucleotide-binding oligomerization domain-containing protein 20101
Chain B, Cell division protein kinase 60101
Chain B, Cell division protein kinase 60101
Chain A, Fatty acid-binding protein, adipocyte0101
Chain A, cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A0101
cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A 0202
Photosystem I iron-sulfur center 0001
Pyrroline-5-carboxylate reductase 1, mitochondrial0101
Beta-adrenergic receptor kinase 10202
Rhodopsin kinase GRK10101
G protein-coupled receptor kinase 50202
G protein-coupled receptor kinase 50101
Beta-adrenergic receptor kinase 10001
UDP-N-acetylglucosamine 1-carboxyvinyltransferase0101
UDP-N-acetylglucosamine 1-carboxyvinyltransferase0101
Dual specificity mitogen-activated protein kinase kinase 10101
Chain A, Proto-oncogene tyrosine-protein kinase ABL10101
Chain A, Proto-oncogene tyrosine-protein kinase ABL10101
Chain A, Proto-oncogene tyrosine-protein kinase ABL10101
Chain A, Proto-oncogene tyrosine-protein kinase ABL10101
Chain A, Proto-oncogene tyrosine-protein kinase ABL10101
Dual specificity mitogen-activated protein kinase kinase 2 0101
Dual specificity mitogen-activated protein kinase kinase 1 0101
Aldehyde oxidase 10101
Aldehyde oxidase 10101
Arylacetamide deacetylase0103
Arylacetamide deacetylase0001
Arylacetamide deacetylase0001
Chain A, Immunoglobulin0011
Chain B, Immunoglobulin0011
Chain A, TRYPSIN0101
Chain A, TRYPSIN0101
Chain A, TRYPSIN0101
Chain A, TRYPSIN0101
Chain A, TRYPSIN0101
Chain A, TRYPSIN0101
Chain A, Lysozyme0011
Chain A, Lysozyme0011
Chain A, Lysozyme0011
Chain A, Lysozyme0011
Chain A, Ferritin light chain0022
Chain A, Ferritin light chain0022
Chain A, Ferritin light chain0022
Chain A, Ferritin light chain0022
Chain A, Ferritin light chain0022
Chain A, Ferritin light chain0022
Chain A, Ferritin light chain0022
Alpha-1B adrenergic receptor0606
Alkaline phosphatase, tissue-nonspecific isozyme 0101
Intestinal-type alkaline phosphatase0101
Large neutral amino acids transporter small subunit 1 0101
Myeloblastin0101
Chain A, PROTEIN (CATECHOL OXIDASE)0101
Sodium/hydrogen exchanger 9B20101
Protein kinase C alpha type0101
Proto-oncogene vav0011
Protein kinase C delta type0112
Transient receptor potential cation channel subfamily V member 4 0011
Chain E, THERMOLYSIN0101
Chain E, Thermolysin0101
Neprilysin0202
Acetylcholinesterase0101
Chain D, PROTEIN (PHOSPHOGLYCERATE MUTASE 1)0101
Chain A, PROTEIN (PHOSPHOGLYCERATE MUTASE 1)0101
Chain A, Beta-arrestin 10011
Chain A, PHOSPHOTIDYLINOSITOL 3 KINASE 59F0101
Chain A, PHOSPHOTIDYLINOSITOL 3 KINASE 59F0101
Chain A, PHOSPHOTIDYLINOSITOL 3 KINASE 59F0101
Chain A, PHOSPHOTIDYLINOSITOL 3 KINASE 59F0101
Rapamycin-insensitive companion of mTOR0101
Regulatory-associated protein of mTOR0202
Target of rapamycin complex 2 subunit MAPKAP10101
Target of rapamycin complex subunit LST80202
Ubiquitin carboxyl-terminal hydrolase 10303
WD repeat-containing protein 480303
CDGSH iron-sulfur domain-containing protein 10202
Peroxisome proliferator-activated receptor gamma0101
Carnitine O-palmitoyltransferase 2, mitochondrial0202
CDGSH iron-sulfur domain-containing protein 20202
Nuclear receptor subfamily 1 group I member 3 0101
Programmed cell death protein 10202
E3 ubiquitin-protein ligase ZFP910001
Programmed cell death 1 ligand 10202
Coiled-coil domain-containing protein 60101
Sodium/potassium/calcium exchanger 40112
Sodium/potassium/calcium exchanger 20112
Renin 0101
Beta-casein0202
Alpha-2A adrenergic receptor0202
luciferase0001
Glutamine synthetase0011
Pannexin-10101
Solute carrier organic anion transporter family member 1C10202
Pannexin-10101
Vascular cell adhesion protein 10101
Histamine H2 receptor0101
Glutamate 5-kinase0001
Free fatty acid receptor 20011
Nuclear receptor subfamily 2 group E member 10044
NADH-cytochrome b5 reductase 3 0101
Thyroid peroxidase0101
tyrosine-protein phosphatase non-receptor type 7 isoform 20202
Chain A, Protocatechuate 3,4-dioxygenase alpha chain0011
Chain B, Protocatechuate 3,4-dioxygenase beta chain0011
cathepsin L10202
Smoothened homolog0011
Sonic hedgehog protein0011
Smoothened homolog0101
Chain A, PUTRESCINE-BINDING PROTEIN0011
Chain A, S-ADENOSYLMETHIONINE DECARBOXYLASE ALPHA CHAIN0101
Chain B, S-ADENOSYLMETHIONINE DECARBOXYLASE BETA CHAIN0101
Chain A, S-ADENOSYLMETHIONINE DECARBOXYLASE ALPHA CHAIN0101
Chain B, S-ADENOSYLMETHIONINE DECARBOXYLASE BETA CHAIN0101
S-adenosylmethionine decarboxylase proenzyme0001
Chain A, Mitogen-activated protein kinase 100101
Chain A, Mitogen-activated protein kinase 100101
Chain A, Mitogen-activated protein kinase 100101
Serine/threonine-protein kinase ULK30022
Serine/threonine-protein kinase 30022
Trans-sialidase0101
Trans-sialidase0101
P2X purinoceptor 20112
P2X purinoceptor 30101
P2X purinoceptor 10101
P2Y purinoceptor 40033
P2X purinoceptor 70112
Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 0101
P2X purinoceptor 50101
P2X purinoceptor 70202
P2X purinoceptor 40101
Chain A, dATP pyrophosphohydrolase0101
Chain A, Adenylate cyclase type 50101
Chain B, Adenylate cyclase type 20101
Monocarboxylate transporter 20002
C-terminal-binding protein 20101
Chain A, APH(2')-Id0101
glucose-6-phosphate dehydrogenase0101
hexokinase0202
Chymotrypsin-like elastase family member 10101
Epoxide hydrolase 1 0101
Heterogeneous nuclear ribonucleoprotein A10011
Malate dehydrogenase0404
Aldo-keto reductase family 1 member A10202
Aldo-keto reductase family 1 member B10101
cGMP-dependent 3',5'-cyclic phosphodiesterase0303
ELAV-like protein 10101
Multidrug resistance protein 1a0001
Advanced glycosylation end product-specific receptor0011
Beta-lactamase 0101
Advanced glycosylation end product-specific receptor0011
Dihydroorotate dehydrogenase 0101
Carbon monoxide dehydrogenase small chain0011
Dipeptidyl peptidase 40011
Chain A, Glutamate Receptor 20101
Chain A, Glutamate Receptor 20101
Gastric inhibitory polypeptide receptor0101
Chromaffin granule amine transporter0101
Synaptic vesicular amine transporter0202
Toll-like receptor 80013
Chain A, Troponin C, slow skeletal and cardiac muscles0011
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Aryl hydrocarbon receptor0101
Myc proto-oncogene protein0102
N1L 0101
Chain A, PLASMA RETINOL-BINDING PROTEIN PRECURSOR0011
Retinol-binding protein 40011
Beta-lactoglobulin0011
Sodium- and chloride-dependent glycine transporter 10001
DNA (cytosine-5)-methyltransferase 3B0202
Ribonuclease HI0202
Chain A, 6,7-Dimethyl-8-ribityllumazine Synthase0011
Chain B, 6,7-Dimethyl-8-ribityllumazine Synthase0011
Chain H, Immunoglobulin Igg1 Heavy chain0011
Chain L, Immunoglobulin Igg1 Lambda Light Chain0011
Chain A, DODECIN0011
Chain A, DODECIN0011
Chain C, DODECIN0011
Chain E, DODECIN0011
DNA-directed RNA polymerase subunit beta0101
NH(3)-dependent NAD(+) synthetase0202
DNA-directed RNA polymerase subunit beta0101
Butyrophilin subfamily 3 member A10011
4-hydroxy-3-methylbut-2-enyl diphosphate reductase0101
Geranylgeranyl pyrophosphate synthase0202
Farnesyl pyrophosphate synthase0303
Farnesyl pyrophosphate synthase 0202
Farnesyl diphosphate synthase0101
Farnesyl pyrophosphate synthase 0101
H0101
Phosphotransferase 0101
Farnesyl diphosphate synthase0101
Diacylglycerol kinase alpha0101
Chain A, Activated Factor Xa Heavy Chain0101
Acetylcholine receptor subunit epsilon0101
Cholinesterase0101
Kynurenine 3-monooxygenase0202
Kynurenine 3-monooxygenase0101
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4B0202
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4B0202
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4B0202
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4B0202
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4B0202
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4B0202
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4D0202
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4D0202
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4D0202
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4D0202
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4B0202
Chain B, cAMP-specific 3',5'-cyclic phosphodiesterase 4B0202
Chain A, cGMP-specific 3',5'-cyclic phosphodiesterase0202
Chain A, cGMP-specific 3',5'-cyclic phosphodiesterase0202
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4B0101
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4D0101
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4D0101
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4D0101
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4D0101
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4D0101
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4D0101
Phosphodiesterase 0202
High affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8B0202
cGMP-specific 3',5'-cyclic phosphodiesterase0404
Endothelin-1 receptor0101
Thrombin 0011
Transcription factor AP-10202
UDP-galactopyranose mutase0022
UDP-galactopyranose mutase0022
NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial0101
Acyl carrier protein, mitochondrial0101
Eukaryotic elongation factor 2 kinase0101
RuvB-like 10202
Neuromedin-U receptor 20022
Low-density lipoprotein receptor0101
Fibronectin0101
Proprotein convertase subtilisin/kexin type 90101
NS5 0101
Chain A, ADENINE-N6-DNA-METHYLTRANSFERASE TAQI0011
Chain A, Adenine-n6-dna-methyltransferase Taqi0011
Chain A, Histamine N-Methyltransferase0101
Chain A, Histamine N-Methyltransferase0101
Chain A, Modification Methylase Rsri0011
Chain A, Modification Methylase Rsri0011
Chain A, Ermc' Methyltransferase0101
Chain A, Ermc' Rrna Methyltransferase0101
Chain A, Uroporphyrin-III C-methyltransferase0101
Chain B, ADENINE-N6-DNA-METHYLTRANSFERASE TAQI0011
Chain A, Ribulose-1,5 bisphosphate carboxylase/oxygenase0011
Chain A, Ribulose-1,5 bisphosphate carboxylase/oxygenase large subunit N-methyltransferase0011
Chain A, Ribulose-1,5 bisphosphate carboxylase/oxygenase large subunit N-methyltransferase0011
Chain A, Ribulose-1,5 bisphosphate carboxylase/oxygenase large subunit N-methyltransferase0011
tRNA (cytosine(38)-C(5))-methyltransferase0112
Protein arginine N-methyltransferase 50112
Histone-lysine N-methyltransferase SUV39H10202
Adenosylhomocysteinase0001
Protein arginine N-methyltransferase 30101
Indolethylamine N-methyltransferase0101
Histone-lysine N-methyltransferase NSD20202
Adenosylhomocysteinase0001
rRNA adenine N-6-methyltransferase0101
tRNA (guanine-N(1)-)-methyltransferase0011
Histone-lysine N-methyltransferase SETDB10101
Retinoblastoma-binding protein 50101
Histone-lysine N-methyltransferase EZH20202
tRNA (guanine-N(1)-)-methyltransferase0011
N6-adenosine-methyltransferase catalytic subunit0101
Histone-arginine methyltransferase CARM10101
Histone-lysine N-methyltransferase KMT5C0101
Histone-lysine N-methyltransferase EZH10202
Protein arginine N-methyltransferase 10404
Methylosome protein 500112
Protein dpy-30 homolog0101
Histamine N-methyltransferase0001
Histone-lysine N-methyltransferase SUV39H20101
tRNA (guanine-N(1)-)-methyltransferase0011
N-lysine methyltransferase SMYD20101
Protein arginine N-methyltransferase 70101
Set1/Ash2 histone methyltransferase complex subunit ASH20101
Met repressor 0022
Histone H3K27 methylase0001
S-adenosylmethionine decarboxylase proenzyme0102
Protein-L-isoaspartate(D-aspartate) O-methyltransferase0101
Catechol O-methyltransferase0001
RmtA0101
Chain A, Lysr-type Regulatory Protein0011
Chain A, Lysr-type Regulatory Protein0011
Chain A, Lysr-type Regulatory Protein0011
Chain A, 146aa long hypothetical transcriptional regulator0011
Chain A, Anthranilate phosphoribosyltransferase0101
Chain A, Anthranilate phosphoribosyltransferase0101
Chain A, Anthranilate phosphoribosyltransferase0101
Chain B, Anthranilate phosphoribosyltransferase0101
Chain C, Anthranilate phosphoribosyltransferase0101
Chain A, Anthranilate phosphoribosyltransferase0101
Anthranilate phosphoribosyltransferase0101
Tyrosine-protein phosphatase YopH0101
Ubiquitin-like domain-containing CTD phosphatase 10101
B-cell CLL/lymphoma 9 protein0202
Cadherin-10101
Pancreatic triacylglycerol lipase0101
Catenin beta-10213
Transcription factor 7-like 20101
phospholipase A2, group III0101
Alanine aminotransferase 10002
Chain A, Proto-oncogene tyrosine-protein kinase Src0101
Tau-tubulin kinase 10101
Tau-tubulin kinase 20101
Chain A, Erk20101
Mitogen-activated protein kinase 20101
Mitogen-activated protein kinase 14 0112
5-hydroxytryptamine receptor 1D0101
Orexin receptor type 10406
Orexin receptor type 20405
Adenylate cyclase type 60101
Adenylate cyclase type 3 0101
Adenylate cyclase type 90101
Adenylate cyclase type 70101
Adenylate cyclase type 20101
Adenylate cyclase type 40101
Adenosine receptor A30101
Histone-lysine N-methyltransferase SMYD30101
Type-1 angiotensin II receptor0101
Transcriptional activator protein LuxR0202
Sterol O-acyltransferase 20101
Tyrosine-protein phosphatase 10101
Pyruvate kinase PKLR0101
Neuraminidase0101
photoreceptor-specific nuclear receptor0101
Cholecystokinin receptor type A0101
Eukaryotic translation initiation factor 4E0011
Peptidyl-prolyl cis-trans isomerase FKBP1A0101
Peptidyl-prolyl cis-trans isomerase FKBP1B0022
Programmed cell death protein 40011
Serine/threonine-protein kinase mTOR 0101
epidermal growth factor receptor isoform a precursor0101
Laccase 0101
Free fatty acid receptor 30011
Interleukin-50101
Interleukin-5 receptor subunit alpha0101
Chain A, Mitogen-activated protein kinase 140011
Chain A, Mitogen-activated protein kinase 140011
Chain A, Mitogen-activated protein kinase 140011
Chain A, Mitogen-activated protein kinase 140011
Chain A, Mitogen-activated protein kinase 140011
Chain A, Mitogen-activated protein kinase 140011
Chain A, Mitogen-activated protein kinase 140011
Chain A, VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR 20101
Chain A, VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR 20101
Chain A, VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR 20101
Chain A, VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR 20101
Chain A, VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR 20101
Cyclin-C0112
Serine/threonine-protein kinase B-raf 0101
Vascular endothelial growth factor receptor 30101
Vascular endothelial growth factor receptor 20101
Vascular endothelial growth factor receptor 20101
RuvB-like 20112
Sulfate anion transporter 10001
C-X-C chemokine receptor type 5 isoform 10101
C-C chemokine receptor type 60101
Endoglycoceramidase II 0001
cAMP-dependent protein kinase catalytic subunit alpha 0101
Sphingosine 1-phosphate receptor 20112
Sphingosine 1-phosphate receptor 40112
Sphingosine 1-phosphate receptor 30112
Sphingosine 1-phosphate receptor 50112
alternatively spliced Trp40011
5-hydroxytryptamine receptor 1E0101
sphingosine 1-phosphate receptor 30101
D(3) dopamine receptor0101
5-hydroxytryptamine receptor 7 0101
D(4) dopamine receptor0101
D(1B) dopamine receptor0101
Chain A, Mineralocorticoid receptor0101
Chain A, Mineralocorticoid receptor0101
neurotensin receptor type 10011
Nuclear receptor subfamily 1 group D member 10011
Cathepsin B0101
Chain A, Ribosomal protein S6 kinase alpha-10101
Chain X, Tyrosine-protein kinase Lyn0101
Chain A, Dual specificity protein kinase TTK0011
Chain A, Dual specificity protein kinase TTK0011
Zinc finger protein GLI20101
Chain A, Cytochrome B0101
Chain F, Ubiquinol-cytochrome C Reductase Iron-sulfur Subunit0101
Glycine receptor subunit beta0101
Bromodomain-containing protein 90011
Bromodomain-containing protein 70011
Chain A, Protein (aspartate Aminotransferase)0011
Chain A, Aspartate Aminotransferase0011
NADP-dependent malic enzyme, mitochondrial0001
Solute carrier family 13 member 30101
Chain A, MALTOPORIN0011
Chain B, MALTOPORIN0011
ATP-dependent 6-phosphofructokinase0101
Dihydropteroate synthase0101
Cytochrome P450 2C180202
Chain A, Glutathione S-transferase0101
Fibroblast growth factor 10011
Transcription regulator protein BACH10101
Transcription factor MafK 0101
Nuclear factor erythroid 2-related factor 20001
Kelch-like ECH-associated protein 10001
Complement C50011
D(2) dopamine receptor0101
Carboxypeptidase M0101
5-hydroxytryptamine receptor 1B0101
Orexin receptor type 10101
Orexin receptor type 20101
Chain A, Oxysterols receptor LXR-beta0101
Chain A, Oxysterols receptor LXR-beta0101
Nuclear receptor ROR-alpha0314
Presenilin-10112
Presenilin-20112
Oxysterols receptor LXR-beta0011
Oxysterols receptor LXR-beta0011
Gamma-secretase subunit APH-1B0112
Nicastrin0112
Nuclear receptor ROR-beta0213
Gamma-secretase subunit APH-1A0112
Chain A, ACETYLCHOLINESTERASE0101
Chain A, liver Carboxylesterase I0101
Gastrotropin0011
Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform0202
cGMP-specific 3',5'-cyclic phosphodiesterase0123
Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma0101
Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha0101
Cone cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha'0101
Retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma0101
Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta0101
Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit delta0101
Chain A, CES1 protein0101
Phospholipase D1 0101
Platelet-activating factor acetylhydrolase0101
Emopamil-binding protein-like0202
7-dehydrocholesterol reductase0112
Alpha-1D adrenergic receptor0101
Alpha-1B adrenergic receptor0101
Alpha-1A adrenergic receptor0101
Corticotropin releasing hormone receptor 20101
Heat-shock protein0101
Putative heat shock protein HSP 90-alpha A40101
menin isoform 11001
Genome polyprotein0213
Polycomb protein SUZ120101
Sodium/bile acid cotransporter0002
Bile salt export pump0002
Neuropeptide FF receptor 20001
Tetracycline resistance protein, class B0001
Ras guanyl-releasing protein 30011
PSMD14 protein0101
TPA: prothrombin0101
72 kDa type IV collagenase isoform 1 preproprotein0101
Chain A, Pyridoxal kinase0101
Chain A, Pyridoxal Kinase0101
Serine palmitoyltransferase 10011
Serine palmitoyltransferase 20101
Chain A, ykoF0011
Chain B, ykoF0011
Chain A, ThiT0011
Thiamine transporter ThiT0011
Transketolase0011
Thiamine-binding periplasmic protein0011
1-deoxy-D-xylulose-5-phosphate synthase0011
1-deoxy-D-xylulose-5-phosphate synthase0011
Cathepsin D 0101
Urease subunit alpha0101
Janus kinase 2 (a protein tyrosine kinase)0202
Thymidine phosphorylase0001
Thymidine kinase, cytosolic 0003
Thymidine kinase 0204
Thymidine kinase0103
Thymidine phosphorylase0101
Chain A, ODORANT-BINDING PROTEIN0101
Chain A, ODORANT-BINDING PROTEIN0101
Chain B, Odorant-binding Protein0101
Chain A, ODORANT-BINDING PROTEIN0101
Chain A, ODORANT-BINDING PROTEIN0101
Chain A, ODORANT-BINDING PROTEIN0101
Chain X, Thyroid hormone receptor beta-10022
Chain X, Thyroid hormone receptor beta-10022
Proliferating cell nuclear antigen0202
Malate dehydrogenase, mitochondrial0101
Monocarboxylate transporter 80001
Solute carrier organic anion transporter family member 1C10001
P2Y purinoceptor 130101
Chain A, Tyrosine-protein kinase0101
Chain A, Tyrosine-protein kinase0101
Chain A, Tyrosine-protein kinase JAK20101
Tyrosine-protein kinase JAK30101
Tyrosine-protein kinase JAK20101
Tyrosine-protein kinase JAK30101
Krueppel-like factor 100101
Chain A, Carbonic anhydrase 10101
Carbonic anhydrase 20101
Sentrin-specific protease 10202
Chain A, RIO-type serine/threonine-protein kinase Rio10011
Cytochrome P450 4B10101
Cytochrome P450 2A70101
Cytochrome P450 2F10101
Cytochrome P450 4F80101
Cytochrome P450 4A110101
Cytochrome P450 4F30101
Cytochrome P450 4A220101
Vitamin D 25-hydroxylase0101
Cytochrome P450 2U10101
Cytochrome P450 2W10101
Cytochrome P450 2S10101
Cytochrome P450 3A43 0101
REST corepressor 30101
Chain A, X-ray structure of the sucrose-phosphatase (SPP) from Synechocystis sp.PCC6803 in complex with trehalose0101
Chain A, X-ray structure of the sucrose-phosphatase (SPP) from Synechocystis sp.PCC6803 in complex with cellobiose0101
Chain A, X-ray structure of the sucrose-phosphatase (SPP) from Synechocystis sp.PCC6803 in complex with maltose0101
Trehalose-phosphatase0101
Chain A, Nuclear Receptor ROR-beta0101
Ornithine decarboxylase0001
Retinoic acid receptor alpha0123
Retinoic acid receptor gamma0123
Retinoic acid receptor beta0123
Cellular retinoic acid-binding protein 20011
Cellular retinoic acid-binding protein 10102
Cellular retinoic acid-binding protein 10011
Chain A, HDLP (HISTONE DEACETYLASE-LIKE PROTEIN)0101
Chain B, HDLP (HISTONE DEACETYLASE-LIKE PROTEIN)0101
Chain A, Histone deacetylase 7a0101
Chain A, Histone deacetylase 7a0101
Histone deacetylase 80202
Histone deacetylase 0101
unnamed protein product0001
Histone deacetylase 10303
Histone deacetylase 30101
Histone deacetylase 20101
Histone deacetylase 10101
Histone deacetylase 0101
Histone deacetylase 40101
Polyamine deacetylase HDAC100101
Histone deacetylase 30101
Histone deacetylase-like amidohydrolase0202
Histone deacetylase 70101
Histone deacetylase 80101
Histone deacetylase 110101
HD2 type histone deacetylase HDA106 0202
Histone deacetylase 90101
Histone deacetylase 70101
Histone deacetylase 6 0101
Histone deacetylase 40101
Histone deacetylase 0101
Histone deacetylase 60213
Histone deacetylase 50101
Histone deacetylase 0101
Calcium-dependent protein kinase 40101
Solute carrier organic anion transporter family member 4A10001
Chain A, Dihydrofolate Reductase0011
Chain A, Dihydrofolate reductase0101
Chain A, dihydrofolate reductase (DHFR)0101
Chain A, Dihydrofolate reductase0101
Chain A, Dihydrofolate reductase0101
Dihydrofolate reductase 0102
Dihydrofolate reductase type 10102
Dihydrofolate reductase0101
Dihydrofolate reductase0101
Dihydrofolate reductase type 1 from Tn40030101
Dihydrofolate reductase0101
Bifunctional dihydrofolate reductase-thymidylate synthase0101
Bifunctional dihydrofolate reductase-thymidylate synthase0101
Dihydrofolate reductase0101
Dihydrofolate reductase0101
Trace amine-associated receptor 50011
Dihydrofolate reductase 0101
Dihydrofolate reductase 0101
Proteinase-activated receptor 20101
Chain A, CARBONIC ANHYDRASE II0101
5-hydroxytryptamine receptor 4 0001
Dopamine beta-hydroxylase0202
Strictosidine synthase0001
5-hydroxytryptamine receptor 5A0101
Chain A, Trp Rna-binding Attenuation Protein0011
Chain K, Trp Rna-binding Attenuation Protein0011
Chain B, tryptophanyl-tRNA synthetase0011
Chain C, Tryptophanyl-tRNA synthetase II0011
Tryprostatin B synthase0001
Polyamine deacetylase HDAC100101
Chain A, CHORISMATE MUTASE0101
Chain A, TYROSYL-tRNA SYNTHETASE0011
Tyrosine 3-monooxygenase0101
Aromatic-L-amino-acid decarboxylase0101
Chain A, Glutamate Receptor, Ionotropic Kainate 10011
Chain A, Glutamate Receptor, Ionotropic Kainate 10011
Chain A, Uracil-DNA Glycosylase0101
Coagulation factor XIII A chain0101
Fatty-acid amide hydrolase 20101
Solute carrier family 2, facilitated glucose transporter member 90112
Chain A, Cytidine Deaminase0101
Uridine-cytidine kinase 1 0001
Seminal ribonuclease0101
Ribonuclease pancreatic0101
P2Y purinoceptor 140022
P2Y purinoceptor 60011
P2Y purinoceptor 40011
N-acetyllactosaminide alpha-1,3-galactosyltransferase0101
P2Y purinoceptor 2 0112
P2Y purinoceptor 20011
Basic phospholipase A2 10101
Hemagglutinin0011
Basic phospholipase A2 PLA-A0101
Acidic phospholipase A2 EC-I0101
Ubiquitin carboxyl-terminal hydrolase 70101
Ubiquitin carboxyl-terminal hydrolase 470101
Ghrelin O-acyltransferase0101
Chain A, Arginase 10101
Aldo-keto reductase family 1 member A10101
Aldo-keto reductase family 1 member B70101
D-alanyl-D-alanine dipeptidase0101
Transcription intermediary factor 1-alpha0101
E3 ubiquitin-protein ligase TRIM330101
85/88 kDa calcium-independent phospholipase A20102
Phospholipase A2, membrane associated0101
Phospholipase A2 group V0102
Phospholipase A2 group V0101
Putative inactive group IIC secretory phospholipase A20102
Group XIIB secretory phospholipase A2-like protein0102
Group XIIA secretory phospholipase A20102
Group IIF secretory phospholipase A20102
Group 3 secretory phospholipase A20102
Group IIE secretory phospholipase A20102
Group IIE secretory phospholipase A20101
Group 10 secretory phospholipase A20101
Group IIF secretory phospholipase A20101
Group IID secretory phospholipase A20102
Group IID secretory phospholipase A20101
Phospholipase A20101
Coenzyme A biosynthesis bifunctional protein CoaBC0101
Protein mono-ADP-ribosyltransferase PARP140202
Glycoprotein0101
Vitamin K epoxide reductase complex subunit 1-like protein 10101
Vitamin K epoxide reductase complex subunit 10101
Vitamin K epoxide reductase complex subunit 1-like protein 10101
Vitamin K epoxide reductase complex subunit 1 0202
fructose-bisphosphate aldolase0101
Chain A, Tankyrase-20011
Chain A, Tankyrase-10101
Chain A, Tankyrase-10101
Protein Wnt-3a0101
Protein Wnt-3a0101
Protein mono-ADP-ribosyltransferase PARP110101
Axin-20011
cGMP-specific 3',5'-cyclic phosphodiesterase0101
Alkaline phosphatase, tissue-nonspecific isozyme 0101
Alkaline phosphatase, germ cell type0101
G-protein coupled receptor 350011
PTK2B protein tyrosine kinase 2 beta0101
Ectonucleoside triphosphate diphosphohydrolase 10001
Chain A, Human Adenosine A2A receptor/T4 lysozyme chimera0011
Chain A, Adenosine receptor A2a0011
Chain A, Adenosine receptor A2a0011
Hexokinase-40101
Amine oxidase [flavin-containing]0101
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]