serine has been researched along with Autosomal Dominant Juvenile Parkinson Disease in 24 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
Excerpt | Relevance | Reference |
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"For those greater than 60 years old, parkinsonism was present in 38." | 1.39 | Greater risk of parkinsonism associated with non-N370S GBA1 mutations. ( Alfonso, P; Barrett, MJ; Capablo, JL; Garcia-Rodriguez, B; Giraldo, P; Irun, P; Pastores, GM; Pocovi, M, 2013) |
"Parkinsonism is one of the phenotypic features associated also with the W748S mutation." | 1.35 | Parkinsonism associated with the homozygous W748S mutation in the POLG1 gene. ( Hinttala, R; Kärppä, M; Majamaa, K; Remes, AM; Soini, H; Takalo, R; Uusimaa, J, 2008) |
"The mean age at onset for parkinsonism was 60 years, range 30-79 years; fewer than 20% of the patients had symptoms before the age 50 years, while by 75 years >90% of them had developed symptoms." | 1.35 | Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease. ( Benecke, R; Berg, D; Bonifati, V; Brown, L; Cras, P; De Deyn, PP; Engelborghs, S; Farrer, MJ; Foroud, T; Gaig, C; Gasser, T; Gibson, JM; Goldwurm, S; Guidi, M; Hagenah, J; Haugarvoll, K; Kachergus, JM; Klein, C; Nichols, WC; Nuytemans, K; Pals, P; Pickut, B; Rademakers, R; Riboldazzi, G; Ross, OA; Samii, A; Tan, EK; Theuns, J; Tolosa, E; Uitti, RJ; Van Broeckhoven, C; Walter, U; Wszolek, ZK; Zabetian, CP, 2008) |
"Frontotemporal dementia with parkinsonism linked to chromosome 17q21-22 (FTDP-17) is an autosomal dominant tauopathy manifested by a variable combination of personality changes, cognitive decline and hypokinetic-rigid movement disorder." | 1.32 | Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family. ( Abramsky, O; Biran, I; Boher, M; Ekstein, D; Gal, A; Gomori, JM; Lossos, A; Meiner, Z; Newman, JP; Reches, A; Rosenmann, H; Soffer, D, 2003) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 14 (58.33) | 29.6817 |
2010's | 8 (33.33) | 24.3611 |
2020's | 2 (8.33) | 2.80 |
Authors | Studies |
---|---|
Nakahara, K | 3 |
Okuda, H | 3 |
Isonishi, A | 3 |
Kawabe, Y | 3 |
Tanaka, T | 3 |
Tatsumi, K | 3 |
Wanaka, A | 3 |
Vieweg, S | 1 |
Mulholland, K | 1 |
Bräuning, B | 1 |
Kachariya, N | 1 |
Lai, YC | 1 |
Toth, R | 1 |
Singh, PK | 1 |
Volpi, I | 1 |
Sattler, M | 1 |
Groll, M | 1 |
Itzen, A | 1 |
Muqit, MMK | 1 |
Salvatore, MF | 1 |
El Arfani, A | 1 |
Albertini, G | 1 |
Bentea, E | 1 |
Demuyser, T | 1 |
Van Eeckhaut, A | 1 |
Smolders, I | 1 |
Massie, A | 1 |
Morris, JK | 1 |
Zhang, H | 1 |
Gupte, AA | 1 |
Bomhoff, GL | 1 |
Stanford, JA | 1 |
Geiger, PC | 1 |
Munhoz, RP | 1 |
Teive, HA | 1 |
Francisco, AN | 1 |
Raskin, S | 1 |
Rogaeva, E | 1 |
Chalimoniuk, M | 1 |
Stolecka, A | 1 |
Ziemińska, E | 1 |
Stepień, A | 1 |
Langfort, J | 1 |
Strosznajder, JB | 1 |
Nguyen, XV | 1 |
Liu, M | 1 |
Kim, HC | 1 |
Bing, G | 1 |
Wider, C | 1 |
Dachsel, JC | 2 |
Farrer, MJ | 4 |
Dickson, DW | 2 |
Tsuboi, Y | 1 |
Wszolek, ZK | 2 |
Morissette, M | 1 |
Samadi, P | 1 |
Hadj Tahar, A | 1 |
Bélanger, N | 1 |
Di Paolo, T | 1 |
Malagelada, C | 1 |
Jin, ZH | 1 |
Jackson-Lewis, V | 1 |
Przedborski, S | 1 |
Greene, LA | 1 |
Valldeoriola, F | 2 |
Gaig, C | 3 |
Muxí, A | 1 |
Navales, I | 1 |
Paredes, P | 1 |
Lomeña, F | 1 |
De la Cerda, A | 1 |
Buongiorno, M | 1 |
Ezquerra, M | 2 |
Santacruz, P | 1 |
Martí, MJ | 2 |
Tolosa, E | 3 |
Barrett, MJ | 1 |
Giraldo, P | 1 |
Capablo, JL | 1 |
Alfonso, P | 1 |
Irun, P | 1 |
Garcia-Rodriguez, B | 1 |
Pocovi, M | 1 |
Pastores, GM | 1 |
van Nuenen, BF | 1 |
Helmich, RC | 1 |
Ferraye, M | 1 |
Thaler, A | 1 |
Hendler, T | 1 |
Orr-Urtreger, A | 1 |
Mirelman, A | 1 |
Bressman, S | 1 |
Marder, KS | 1 |
Giladi, N | 1 |
van de Warrenburg, BP | 1 |
Bloem, BR | 1 |
Toni, I | 1 |
Lossos, A | 1 |
Reches, A | 1 |
Gal, A | 1 |
Newman, JP | 1 |
Soffer, D | 1 |
Gomori, JM | 1 |
Boher, M | 1 |
Ekstein, D | 1 |
Biran, I | 1 |
Meiner, Z | 1 |
Abramsky, O | 1 |
Rosenmann, H | 1 |
Kobayashi, K | 2 |
Kidani, T | 2 |
Ujike, H | 2 |
Hayashi, M | 2 |
Ishihara, T | 2 |
Miyazu, K | 1 |
Kuroda, S | 2 |
Koshino, Y | 2 |
Iijima, M | 1 |
Nakano, H | 1 |
Sugimori, K | 1 |
Shimazaki, M | 1 |
Rajput, A | 1 |
Robinson, CA | 1 |
Ross, OA | 3 |
Lincoln, SJ | 1 |
Cobb, SA | 1 |
Rajput, ML | 1 |
Schüpbach, M | 1 |
Lohmann, E | 1 |
Anheim, M | 1 |
Lesage, S | 1 |
Czernecki, V | 1 |
Yaici, S | 1 |
Worbe, Y | 1 |
Charles, P | 1 |
Welter, ML | 1 |
Pollak, P | 1 |
Dürr, A | 1 |
Agid, Y | 1 |
Brice, A | 1 |
González-Fernández, MC | 1 |
Lezcano, E | 1 |
Gómez-Esteban, JC | 1 |
Gómez-Busto, F | 1 |
Velasco, F | 1 |
Alvarez-Alvarez, M | 1 |
Rodríguez-Martínez, MB | 1 |
Ciordia, R | 1 |
Zarranz, JJ | 1 |
Mata, IF | 1 |
de Pancorbo, MM | 1 |
Remes, AM | 1 |
Hinttala, R | 1 |
Kärppä, M | 1 |
Soini, H | 1 |
Takalo, R | 1 |
Uusimaa, J | 1 |
Majamaa, K | 1 |
Haugarvoll, K | 1 |
Rademakers, R | 1 |
Kachergus, JM | 1 |
Nuytemans, K | 1 |
Gibson, JM | 1 |
Tan, EK | 1 |
Goldwurm, S | 1 |
Guidi, M | 1 |
Riboldazzi, G | 1 |
Brown, L | 1 |
Walter, U | 1 |
Benecke, R | 1 |
Berg, D | 1 |
Gasser, T | 1 |
Theuns, J | 1 |
Pals, P | 1 |
Cras, P | 1 |
De Deyn, PP | 1 |
Engelborghs, S | 1 |
Pickut, B | 1 |
Uitti, RJ | 1 |
Foroud, T | 1 |
Nichols, WC | 1 |
Hagenah, J | 1 |
Klein, C | 1 |
Samii, A | 1 |
Zabetian, CP | 1 |
Bonifati, V | 1 |
Van Broeckhoven, C | 1 |
Muñoz, E | 1 |
Lladó, A | 1 |
Rey, MJ | 1 |
Cardozo, A | 1 |
Molinuevo, JL | 1 |
Lavedan, C | 1 |
Buchholtz, S | 1 |
Nussbaum, RL | 1 |
Albin, RL | 1 |
Polymeropoulos, MH | 1 |
1 trial available for serine and Autosomal Dominant Juvenile Parkinson Disease
Article | Year |
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Subthalamic nucleus stimulation is efficacious in patients with Parkinsonism and LRRK2 mutations.
Topics: Adult; Aged; Deep Brain Stimulation; Female; Glycine; Humans; Leucine-Rich Repeat Serine-Threonine P | 2007 |
23 other studies available for serine and Autosomal Dominant Juvenile Parkinson Disease
Article | Year |
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Amino acid transporter Asc-1 (SLC7A10) expression is altered in basal ganglia in experimental Parkinsonism and L-dopa-induced dyskinesia model mice.
Topics: Amino Acid Transport System ASC; Amino Acid Transport System y+; Animals; Basal Ganglia; Dopamine; D | 2023 |
Amino acid transporter Asc-1 (SLC7A10) expression is altered in basal ganglia in experimental Parkinsonism and L-dopa-induced dyskinesia model mice.
Topics: Amino Acid Transport System ASC; Amino Acid Transport System y+; Animals; Basal Ganglia; Dopamine; D | 2023 |
Amino acid transporter Asc-1 (SLC7A10) expression is altered in basal ganglia in experimental Parkinsonism and L-dopa-induced dyskinesia model mice.
Topics: Amino Acid Transport System ASC; Amino Acid Transport System y+; Animals; Basal Ganglia; Dopamine; D | 2023 |
Amino acid transporter Asc-1 (SLC7A10) expression is altered in basal ganglia in experimental Parkinsonism and L-dopa-induced dyskinesia model mice.
Topics: Amino Acid Transport System ASC; Amino Acid Transport System y+; Animals; Basal Ganglia; Dopamine; D | 2023 |
Amino acid transporter Asc-1 (SLC7A10) expression is altered in basal ganglia in experimental Parkinsonism and L-dopa-induced dyskinesia model mice.
Topics: Amino Acid Transport System ASC; Amino Acid Transport System y+; Animals; Basal Ganglia; Dopamine; D | 2023 |
Amino acid transporter Asc-1 (SLC7A10) expression is altered in basal ganglia in experimental Parkinsonism and L-dopa-induced dyskinesia model mice.
Topics: Amino Acid Transport System ASC; Amino Acid Transport System y+; Animals; Basal Ganglia; Dopamine; D | 2023 |
Amino acid transporter Asc-1 (SLC7A10) expression is altered in basal ganglia in experimental Parkinsonism and L-dopa-induced dyskinesia model mice.
Topics: Amino Acid Transport System ASC; Amino Acid Transport System y+; Animals; Basal Ganglia; Dopamine; D | 2023 |
Amino acid transporter Asc-1 (SLC7A10) expression is altered in basal ganglia in experimental Parkinsonism and L-dopa-induced dyskinesia model mice.
Topics: Amino Acid Transport System ASC; Amino Acid Transport System y+; Animals; Basal Ganglia; Dopamine; D | 2023 |
Amino acid transporter Asc-1 (SLC7A10) expression is altered in basal ganglia in experimental Parkinsonism and L-dopa-induced dyskinesia model mice.
Topics: Amino Acid Transport System ASC; Amino Acid Transport System y+; Animals; Basal Ganglia; Dopamine; D | 2023 |
PINK1-dependent phosphorylation of Serine111 within the SF3 motif of Rab GTPases impairs effector interactions and LRRK2-mediated phosphorylation at Threonine72.
Topics: HEK293 Cells; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Mitochondria; Parkinson | 2020 |
ser31 Tyrosine hydroxylase phosphorylation parallels differences in dopamine recovery in nigrostriatal pathway following 6-OHDA lesion.
Topics: Animals; Blotting, Western; Chromatography, High Pressure Liquid; Corpus Striatum; Dopamine; Male; O | 2014 |
Alterations in the motor cortical and striatal glutamatergic system and D-serine levels in the bilateral 6-hydroxydopamine rat model for Parkinson's disease.
Topics: Animals; Corpus Striatum; Disease Models, Animal; Glutamic Acid; Male; Motor Cortex; Oxidopamine; Pa | 2015 |
Measures of striatal insulin resistance in a 6-hydroxydopamine model of Parkinson's disease.
Topics: Adrenergic Agents; Animals; Basal Ganglia; Blotting, Western; Chromatography, High Pressure Liquid; | 2008 |
Unilateral pallidotomy in a patient with parkinsonism and G2019S LRRK2 mutation.
Topics: Female; Functional Laterality; Glycine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase- | 2009 |
Involvement of multiple protein kinases in cPLA2 phosphorylation, arachidonic acid release, and cell death in in vivo and in vitro models of 1-methyl-4-phenylpyridinium-induced parkinsonism--the possible key role of PKG.
Topics: Animals; Arachidonic Acid; Calcium; Catalytic Domain; Cell Death; Cyclic GMP; Cyclic GMP-Dependent P | 2009 |
Effects of prodynorphin deletion on striatal dopamine in mice during normal aging and in response to MPTP.
Topics: Aging; Amino Acid Sequence; Animals; Corpus Striatum; Disease Models, Animal; Dopamine; Enkephalins; | 2009 |
Elucidating the genetics and pathology of Perry syndrome.
Topics: Adult; Age of Onset; Aged; Animals; Brain; Chlorocebus aethiops; COS Cells; Depression; DNA-Binding | 2010 |
Striatal Akt/GSK3 signaling pathway in the development of L-Dopa-induced dyskinesias in MPTP monkeys.
Topics: Animals; Antiparkinson Agents; Benzoxazoles; Cabergoline; Corpus Striatum; Disease Models, Animal; D | 2010 |
Rapamycin protects against neuron death in in vitro and in vivo models of Parkinson's disease.
Topics: 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; Analysis of Variance; Animals; Cell Death; Cycloheximi | 2010 |
123I-MIBG cardiac uptake and smell identification in parkinsonian patients with LRRK2 mutations.
Topics: 3-Iodobenzylguanidine; Adult; Aged; Aged, 80 and over; Female; Glycine; Heart; Humans; Leucine-Rich | 2011 |
Greater risk of parkinsonism associated with non-N370S GBA1 mutations.
Topics: Adult; Aged; Amino Acid Substitution; beta-Glucosidase; Female; Genetic Association Studies; Genetic | 2013 |
Cerebral pathological and compensatory mechanisms in the premotor phase of leucine-rich repeat kinase 2 parkinsonism.
Topics: Adult; Analysis of Variance; Biomechanical Phenomena; Brain; Cerebral Cortex; DNA Mutational Analysi | 2012 |
Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family.
Topics: Adult; Algeria; Cerebral Cortex; Dementia; DNA Mutational Analysis; Family Health; Female; Humans; I | 2003 |
Another phenotype of frontotemporal dementia and parkinsonism linked to chromosome-17 (FTDP-17) with a missense mutation of S305N closely resembling Pick's disease.
Topics: Asparagine; Chromosomes, Human, Pair 17; Dementia; Dentate Gyrus; Genetic Linkage; Humans; Immunohis | 2003 |
Pick's disease pathology of a missense mutation of S305N of frontotemporal dementia and parkinsonism linked to chromosome 17: another phenotype of S305N.
Topics: Asparagine; Base Sequence; Brain; Dementia; DNA Mutational Analysis; Genetic Linkage; Heterozygote; | 2004 |
Parkinsonism, Lrrk2 G2019S, and tau neuropathology.
Topics: Aged; alpha-Synuclein; Brain; Cell Line; Disability Evaluation; Disease Progression; Female; Glycine | 2006 |
Lrrk2-associated parkinsonism is a major cause of disease in Northern Spain.
Topics: Adult; Aged; Arginine; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Dis | 2007 |
Parkinsonism associated with the homozygous W748S mutation in the POLG1 gene.
Topics: Aged; Cocaine; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Humans; Male; Mutation; Parkinsoni | 2008 |
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.
Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Arginine; Cysteine; DNA Mutational Analysis | 2008 |
Screening for the LRRK2 G2019S and codon-1441 mutations in a pathological series of parkinsonian syndromes and frontotemporal lobar degeneration.
Topics: Dementia; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Testing; Glyci | 2008 |
A mutation in the human neurofilament M gene in Parkinson's disease that suggests a role for the cytoskeleton in neuronal degeneration.
Topics: Adult; Age of Onset; Brain; Cytoskeleton; DNA Mutational Analysis; Female; Genetic Testing; Glycine; | 2002 |