glycine has been researched along with Genetic Predisposition in 189 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "However, treatment of hyperlipidemia with statins reduces the probability of a CV event." | 5.34 | Receptor for advanced glycation end products Glycine 82 Serine polymorphism and risk of cardiovascular events in rheumatoid arthritis. ( Carroll, L; Frazer, IH; Marwick, TH; Thomas, R; Turner, M, 2007) |
| "Circulating levels of glycine have previously been associated with lower incidence of coronary heart disease (CHD) and type 2 diabetes (T2D) but it remains uncertain if glycine plays an aetiological role." | 5.01 | Assessing the causal association of glycine with risk of cardio-metabolic diseases. ( Burgess, S; Butterworth, AS; Danesh, J; Day, FR; Erdmann, J; Forouhi, NG; Griffin, JL; Howson, JMM; Imamura, F; Karthikeyan, S; Khaw, KT; Koulman, A; Langenberg, C; Lotta, LA; Oliver-Williams, C; Schunkert, H; Scott, RA; Stewart, ID; Surendran, P; Wareham, NJ; Wittemans, LBL; Wood, AM; Zeng, L, 2019) |
| "GLYT1 encephalopathy is a form of glycine encephalopathy caused by disturbance of glycine transport." | 4.02 | GLYT1 encephalopathy: Further delineation of disease phenotype and discussion of pathophysiological mechanisms. ( Casellas-Vidal, D; Diego-Álvarez, D; Espuña-Capote, N; García-González, MDM; Mademont-Soler, I; Maroto, A; Obón, M; Perapoch, J; Queralt, X; Ruiz, MD; Trujillo, A, 2021) |
| "We conducted a genome-wide association study (GWAS) in Singaporean Chinese participants and investigated if genetically determined serum glycine were associated with incident coronary artery disease (CAD) (711 cases and 1,246 controls), cardiovascular death (1,886 cases and 21,707 controls) and angiographic CAD severity (as determined by the Modified Gensini score, N = 1,138)." | 4.02 | The association of genetically determined serum glycine with cardiovascular risk in East Asians. ( Chan, MY; Chang, X; Dorajoo, R; Friedlander, Y; Guan, SP; Heng, CK; Kennedy, BK; Khor, CC; Koh, WP; Liu, J; Low, AF; Wang, L; Yuan, JM, 2021) |
| "The composite endpoint of screened deep vein thrombosis (DVT) and symptomatic pulmonary embolism (PE) during prophylaxis did not differ significantly between patients with or without these mutations." | 2.70 | Factor V Leiden (G1691A) and prothrombin gene G20210A mutations as potential risk factors for venous thromboembolism after total hip or total knee replacement surgery. ( Andersson, C; Bylock, A; Eriksson, BI; Frison, L; Gustafsson, D; Larson, G; Lindahl, TL; Wåhlander, K, 2002) |
| "The genetic factors that underlie idiopathic dilated cardiomyopathy (IDCM) have not yet been elucidated." | 2.69 | Characterization of a unique genetic variant in the beta1-adrenoceptor gene and evaluation of its role in idiopathic dilated cardiomyopathy. CARDIGENE Group. ( Amouyel, P; Cambien, F; Charron, P; Desnos, M; Dorent, R; Jullières, Y; Komajda, M; Nicaud, V; Peuchmaurd, M; Poirier, O; Roizès, G; Schwartz, K; Tesson, F; Tiret, L, 1999) |
| "Seven studies comprising 744 chronic periodontitis cases and 855 controls and four studies consisting of a total of 295 aggressive periodontitis cases and 456 controls were included in the meta-analysis." | 2.45 | TLR4 as a risk factor for periodontal disease: a reappraisal. ( Ozturk, A; Vieira, AR, 2009) |
| "As in all other forms of dystrophic epidermolysis bullosa, the molecular pathology involves mutations in the gene encoding the anchoring fibril protein, type VII collagen (COL7A1), but there is no clear genotype-phenotype correlation in EBP." | 2.44 | Clinical and molecular dilemmas in the diagnosis of familial epidermolysis bullosa pruriginosa. ( Ee, HL; Goh, CL; Liu, L; McGrath, JA, 2007) |
| "CAGexp of subjects with and without parkinsonism were different (medians of 42 and 39 repeats) as well as of subjects with and without dystonia (44 and 40 repeats)." | 1.46 | Neurological phenotypes in spinocerebellar ataxia type 2: Role of mitochondrial polymorphism A10398G and other risk factors. ( Augustin, MC; Barsottini, O; Jardim, LB; Locks-Coelho, LD; Monte, TL; Pedroso, JL; Pereira, FS; Reckziegel, EDR; Santos, ASP; Saraiva-Pereira, ML; Vargas, FR, 2017) |
| "This glycine was located in strand 5B and was well conserved in other serpins." | 1.46 | Mutation in a highly conserved glycine residue in strand 5B of plasminogen activator inhibitor 1 causes polymerisation. ( Iwaki, T; Kanayama, N; Nagahashi, K; Suzuki-Inoue, K; Takano, K; Umemura, K; Urano, T, 2017) |
| "About 5% of PTC is hereditary familial nonmedullary thyroid cancer (FNMTC)." | 1.43 | HABP2 G534E Mutation in Familial Nonmedullary Thyroid Cancer. ( Xing, M; Zhang, T, 2016) |
| "Stroke is a multi-factorial disease influenced by both genetic and environmental factors." | 1.43 | Association between Endothelial nitric oxide synthase G894T gene polymorphism and risk of ischemic stroke in North Indian population: a case-control study. ( Chakravarty, K; Kathuria, P; Kumar, A; Kumar, P; Misra, S; Pandit, AK; Prasad, K; Sagar, R; Yadav, AK, 2016) |
| "All cancers combined, nonskin cancers, smoking-related cancers, hormone-related cancers, and other types of cancer." | 1.42 | Higher frequency of certain cancers in LRRK2 G2019S mutation carriers with Parkinson disease: a pooled analysis. ( Aasly, J; Agalliu, I; Bressman, S; Friedman, E; Giladi, N; Hassin-Baer, S; Inzelberg, R; Marti-Masso, JF; Mirelman, A; Orr-Urtreger, A; Ruiz-Martinez, J; San Luciano, M; Saunders-Pullman, R; Waro, B, 2015) |
| "Ameloblastoma is a common benign odontogenic tumour with inherently aggressive behaviour." | 1.39 | XRCC1 gene polymorphisms and risk of ameloblastoma. ( Boonsuwan, T; Kitkumthorn, N; Mutirangura, A; Yanatatsaneejit, P, 2013) |
| "A total of 130 patients with type 2 diabetes and 133 healthy subjects as control were randomly selected from January 2008 to January 2011 in endocrine wards of Zhengzhou People's Hospital." | 1.39 | Association of the G-250A promoter polymorphism in the hepatic lipase gene with the risk of type 2 diabetes mellitus. ( Fan, S; Guo, Y; Ou, L; Yao, L, 2013) |
| "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." | 1.38 | Dyskinesias in patients with Parkinson's disease: effect of the leucine-rich repeat kinase 2 (LRRK2) G2019S mutation. ( Cohen, OS; Friedman, E; Hassin-Baer, S; Inzelberg, R; Kaplan, N; Korczyn, AD; Kozlova, E; Rosset, S; Vituri, A; Yahalom, G, 2012) |
| "Parkinson's disease is a promising target of applying personalized medicine." | 1.38 | [The absence of the common LRRK2 G2019S mutation in 120 young onset Hungarian Parkinon's disease patients]. ( Balicza, P; Balogh, I; Bereznai, B; Dibó, G; Hidasi, E; Klivényi, P; Molnár, MJ; Takáts, A, 2012) |
| "Schizophrenia is a heritable, complex mental disorder." | 1.37 | Association study of DRD3 gene in schizophrenia in Mexican sib-pairs. ( Aguilar, A; Apiquián, R; Camarena, B; Carnevale, A; Fresán, A; Nicolini, H; Orozco, L; Urraca, N, 2011) |
| "Hypertension is a major risk factor for cardiovascular disease." | 1.36 | Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals. ( Aoyagi, Y; Kato, K; Metoki, N; Nozawa, Y; Oguri, M; Satoh, K; Watanabe, S; Yamada, Y; Yokoi, K; Yoshida, H; Yoshida, T, 2010) |
| "UK Medical Research Council; UK Parkinson's Disease Society; UK Brain Research Trust; Internationaal Parkinson Fonds; Volkswagen Foundation; National Institutes of Health: National Institute of Neurological Disorders and Stroke and National Institute of Aging; Udall Parkinson's Disease Centre of Excellence; Pacific Alzheimer Research Foundation Centre; Italian Telethon Foundation; Fondazione Grigioni per il Morbo di Parkinson; Michael J Fox Foundation for Parkinson's Research; Safra Global Genetics Consortium; US Department of Veterans Affairs; French Agence Nationale de la Recherche." | 1.35 | Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. ( Aasly, J; Berciano, J; Bhatia, KP; Bonifati, V; Bressman, S; Brice, A; Durr, A; Falchi, M; Ferreira, JJ; Gasser, T; Goldwurm, S; Healy, DG; Kay, DM; Klein, C; Lang, AE; Lees, AJ; Lynch, T; Marras, C; O'Sullivan, SS; Schapira, AH; Tolosa, E; Williams, DR; Wood, NW; Wszolek, ZK; Zabetian, CP, 2008) |
| "In the present study seizure threshold doses of TZG were tested in the wild type and mutant mice." | 1.35 | Seizure responses and induction of Fos by the NMDA agonist (tetrazol-5-yl)glycine in a genetic model of NMDA receptor hypofunction. ( Duncan, GE; Farrington, JS; Inada, K; Koller, BH, 2008) |
| "For the purpose, 195 subjects with type 2 diabetes with PDR were compared with 143 subjects with type 2 diabetes of duration of more than 10 years who had no clinical signs of diabetic retinopathy." | 1.35 | K469E polymorphism of the intracellular adhesion molecule 1 gene is associated with proliferative diabetic retinopathy in Caucasians with type 2 diabetes. ( Osredkar, J; Petrovic, D; Petrovic, MG; Saraga-Babić, M, 2008) |
| "However, treatment of hyperlipidemia with statins reduces the probability of a CV event." | 1.34 | Receptor for advanced glycation end products Glycine 82 Serine polymorphism and risk of cardiovascular events in rheumatoid arthritis. ( Carroll, L; Frazer, IH; Marwick, TH; Thomas, R; Turner, M, 2007) |
| "Two patients with Crohn's disease were heterozygous for the interleukin-10 Gly15Arg mutation." | 1.33 | A functional interleukin-10 mutation in Dutch patients with Crohn's disease. ( Boor, PP; Crusius, JB; de Jong, DJ; de Rooij, FW; Kuipers, EJ; Naber, TH; van Bodegraven, AA; van der Linde, K; Wilson, JH, 2005) |
| "Autism is a spectrum of neurodevelopmental disorders with a primarily genetic etiology exhibiting deficits in (1) development of language and (2) social relationships and (3) patterns of repetitive, restricted behaviors or interests and resistance to change." | 1.33 | Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors. ( Blakely, RD; Delahanty, RJ; Folstein, SE; Han, Q; Jiang, L; Li, C; McCauley, JL; Prasad, HC; Sutcliffe, JS, 2005) |
| "Parkinson disease related to LRRK2 is characterized by typical clinical features, and the similarities between patients with homozygous and heterozygous mutations do not support a gene dosage effect." | 1.33 | Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations. ( Amouri, R; Brice, A; Dürr, A; Farrer, MJ; Foroud, TM; Gibson, R; Griffith, A; Hattori, N; Hentati, F; Ishihara, L; Leppert, D; Lesage, S; Middleton, L; Nichols, WC; Tazir, M; Uitti, RJ; Warren, L; Watts, R; Wszolek, ZK; Zabetian, CP, 2006) |
| "A sexually dimorphic pattern of genetic susceptibility to OCD may be present." | 1.32 | Gender in obsessive-compulsive disorder: clinical and genetic findings. ( Corfield, VA; Hemmings, SM; Kinnear, CJ; Knowles, JA; Lochner, C; Moolman-Smook, JC; Niehaus, DJ; Stein, DJ, 2004) |
| "Primary sclerosing cholangitis (PSC) is an immune-mediated chronic cholestatic liver disease associated with IBD." | 1.32 | Susceptibility to primary sclerosing cholangitis is associated with polymorphisms of intercellular adhesion molecule-1. ( Chapman, RW; Cullen, SN; Jewell, DP; Li, JH; Yang, X, 2004) |
| "There is substantial evidence for genetic susceptibility to diabetic nephropathy." | 1.32 | Role of alpha-adducin DNA polymorphisms in the genetic predisposition to diabetic nephropathy. ( Brady, HR; Conway, BR; Martin, R; Maxwell, AP; McKnight, AJ; Savage, DA, 2004) |
| "The increased risk of colorectal cancer in biallelic and monoallelic MYH gene mutation carriers was not consistently associated with the development of multiple adenomatous polyps." | 1.32 | Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk. ( Aronson, M; Cleary, SP; Cotterchio, M; Croitoru, ME; Di Nicola, N; Gallinger, S; Gryfe, R; Knight, J; Manno, M; Redston, M; Selander, T, 2004) |
| "PTZ-induced seizures were inhibited by three standard anticonvulsant drugs, but not by the group III selective mGluR agonist (R,S)-4-phosphonophenylglycine (PPG)." | 1.31 | Increased seizure susceptibility in mice lacking metabotropic glutamate receptor 7. ( Burnashev, N; Bushell, TJ; Clarke, VR; Collett, VJ; Collingridge, GL; Duvoisin, RM; Flor, PJ; Gasparini, F; Hampson, DR; Klebs, K; Knoepfel, T; Kuhn, R; Portet, C; Rozov, A; Sansig, G; Schmutz, M; Schroeder, M; Shigemoto, R; van Der Putten, H; Zhang, C, 2001) |
| "This leukoencephalopathy has an autosomal-recessive mode of inheritance." | 1.30 | Increased cerebrospinal fluid glycine: a biochemical marker for a leukoencephalopathy with vanishing white matter. ( Gabreëls, FJ; Jaeken, J; Kure, S; van der Knaap, MS; van Raaij-Selten, B; Verhoeven, NM; Wevers, RA, 1999) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 7 (3.70) | 18.2507 |
| 2000's | 114 (60.32) | 29.6817 |
| 2010's | 63 (33.33) | 24.3611 |
| 2020's | 5 (2.65) | 2.80 |
| Authors | Studies |
|---|---|
| Yang, Q | 2 |
| Wang, J | 1 |
| Tian, X | 1 |
| Shen, F | 1 |
| Lan, J | 1 |
| Zhang, Q | 2 |
| Fan, X | 1 |
| Yi, S | 1 |
| Li, M | 2 |
| Shen, Y | 1 |
| Wei, J | 1 |
| Shi, Z | 1 |
| Na, R | 2 |
| Wang, CH | 1 |
| Resurreccion, WK | 1 |
| Zheng, SL | 2 |
| Hulick, PJ | 1 |
| Cooney, KA | 1 |
| Helfand, BT | 1 |
| Isaacs, WB | 1 |
| Xu, J | 2 |
| Mademont-Soler, I | 1 |
| Casellas-Vidal, D | 1 |
| Trujillo, A | 1 |
| Espuña-Capote, N | 1 |
| Maroto, A | 1 |
| García-González, MDM | 1 |
| Ruiz, MD | 1 |
| Diego-Álvarez, D | 1 |
| Queralt, X | 1 |
| Perapoch, J | 1 |
| Obón, M | 1 |
| Jäger, S | 1 |
| Cuadrat, R | 1 |
| Wittenbecher, C | 1 |
| Floegel, A | 1 |
| Hoffmann, P | 1 |
| Prehn, C | 1 |
| Adamski, J | 1 |
| Pischon, T | 1 |
| Schulze, MB | 1 |
| Chang, X | 1 |
| Wang, L | 1 |
| Guan, SP | 1 |
| Kennedy, BK | 1 |
| Liu, J | 2 |
| Khor, CC | 1 |
| Low, AF | 1 |
| Chan, MY | 1 |
| Yuan, JM | 1 |
| Koh, WP | 1 |
| Friedlander, Y | 1 |
| Dorajoo, R | 1 |
| Heng, CK | 1 |
| Lee, AJ | 1 |
| Wang, Y | 2 |
| Alcalay, RN | 1 |
| Mejia-Santana, H | 1 |
| Saunders-Pullman, R | 4 |
| Bressman, S | 5 |
| Corvol, JC | 1 |
| Brice, A | 5 |
| Lesage, S | 4 |
| Mangone, G | 1 |
| Tolosa, E | 4 |
| Pont-Sunyer, C | 1 |
| Vilas, D | 1 |
| Schüle, B | 1 |
| Kausar, F | 1 |
| Foroud, T | 1 |
| Berg, D | 1 |
| Brockmann, K | 1 |
| Goldwurm, S | 3 |
| Siri, C | 1 |
| Asselta, R | 1 |
| Ruiz-Martinez, J | 2 |
| Mondragón, E | 1 |
| Marras, C | 2 |
| Ghate, T | 1 |
| Giladi, N | 2 |
| Mirelman, A | 2 |
| Marder, K | 1 |
| Monte, TL | 1 |
| Pereira, FS | 1 |
| Reckziegel, EDR | 1 |
| Augustin, MC | 1 |
| Locks-Coelho, LD | 1 |
| Santos, ASP | 1 |
| Pedroso, JL | 1 |
| Barsottini, O | 1 |
| Vargas, FR | 1 |
| Saraiva-Pereira, ML | 1 |
| Jardim, LB | 1 |
| Vandenbeek, R | 1 |
| Khan, NP | 1 |
| Estall, JL | 1 |
| Wittemans, LBL | 1 |
| Lotta, LA | 1 |
| Oliver-Williams, C | 1 |
| Stewart, ID | 1 |
| Surendran, P | 1 |
| Karthikeyan, S | 1 |
| Day, FR | 1 |
| Koulman, A | 1 |
| Imamura, F | 1 |
| Zeng, L | 1 |
| Erdmann, J | 1 |
| Schunkert, H | 1 |
| Khaw, KT | 2 |
| Griffin, JL | 1 |
| Forouhi, NG | 1 |
| Scott, RA | 1 |
| Wood, AM | 1 |
| Burgess, S | 1 |
| Howson, JMM | 1 |
| Danesh, J | 1 |
| Wareham, NJ | 1 |
| Butterworth, AS | 1 |
| Langenberg, C | 1 |
| Jia, Q | 1 |
| Han, Y | 1 |
| Huang, P | 1 |
| Woodward, NC | 1 |
| Gukasyan, J | 1 |
| Kettunen, J | 1 |
| Ala-Korpela, M | 1 |
| Anufrieva, O | 1 |
| Wang, Q | 2 |
| Perola, M | 1 |
| Raitakari, O | 1 |
| Lehtimäki, T | 1 |
| Viikari, J | 1 |
| Järvelin, MR | 1 |
| Boehnke, M | 1 |
| Laakso, M | 1 |
| Mohlke, KL | 1 |
| Fiehn, O | 1 |
| Wang, Z | 4 |
| Tang, WHW | 1 |
| Hazen, SL | 1 |
| Hartiala, JA | 1 |
| Allayee, H | 1 |
| Ng, R | 1 |
| Manring, H | 1 |
| Papoutsidakis, N | 1 |
| Albertelli, T | 1 |
| Tsai, N | 1 |
| See, CJ | 1 |
| Li, X | 1 |
| Park, J | 1 |
| Stevens, TL | 1 |
| Bobbili, PJ | 1 |
| Riaz, M | 1 |
| Ren, Y | 1 |
| Stoddard, CE | 1 |
| Janssen, PM | 1 |
| Bunch, TJ | 1 |
| Hall, SP | 1 |
| Lo, YC | 1 |
| Jacoby, DL | 1 |
| Qyang, Y | 1 |
| Wright, N | 1 |
| Ackermann, MA | 1 |
| Campbell, SG | 1 |
| Simpson, M | 1 |
| Johanssen, V | 1 |
| Boyd, A | 1 |
| Klug, G | 1 |
| Masters, CL | 1 |
| Li, QX | 1 |
| Pamphlett, R | 1 |
| McLean, C | 1 |
| Lewis, V | 1 |
| Collins, SJ | 1 |
| Schaefer, N | 1 |
| Langlhofer, G | 1 |
| Kluck, CJ | 1 |
| Villmann, C | 1 |
| Yamamoto, H | 1 |
| Higasa, K | 1 |
| Sakaguchi, M | 1 |
| Shien, K | 1 |
| Soh, J | 1 |
| Ichimura, K | 1 |
| Furukawa, M | 1 |
| Hashida, S | 1 |
| Tsukuda, K | 1 |
| Takigawa, N | 1 |
| Matsuo, K | 1 |
| Kiura, K | 1 |
| Miyoshi, S | 1 |
| Matsuda, F | 1 |
| Toyooka, S | 1 |
| Cao, D | 1 |
| Ouyang, S | 1 |
| Liu, Z | 1 |
| Ma, F | 1 |
| Wu, J | 1 |
| Nishie, W | 1 |
| Natsuga, K | 1 |
| Nakamura, H | 1 |
| Ito, T | 1 |
| Toyonaga, E | 1 |
| Sato, H | 1 |
| Shimizu, H | 1 |
| Yilmaz, BS | 1 |
| Kor, D | 1 |
| Ceylaner, S | 1 |
| Mert, GG | 1 |
| Incecik, F | 1 |
| Kartal, E | 1 |
| Mungan, NO | 1 |
| Yahalom, G | 2 |
| Orlev, Y | 1 |
| Cohen, OS | 2 |
| Kozlova, E | 2 |
| Friedman, E | 3 |
| Inzelberg, R | 3 |
| Hassin-Baer, S | 3 |
| Hartney, JM | 1 |
| Stidham, T | 1 |
| Goldstrohm, DA | 1 |
| Oberley-Deegan, RE | 1 |
| Weaver, MR | 1 |
| Valnickova-Hansen, Z | 1 |
| Scavenius, C | 1 |
| Benninger, RK | 1 |
| Leahy, KF | 1 |
| Johnson, R | 1 |
| Gally, F | 1 |
| Kosmider, B | 1 |
| Zimmermann, AK | 1 |
| Enghild, JJ | 1 |
| Nozik-Grayck, E | 1 |
| Bowler, RP | 1 |
| Kumar, CV | 1 |
| Swetha, RG | 1 |
| Ramaiah, S | 1 |
| Anbarasu, A | 1 |
| Panagiotou, OA | 1 |
| Travis, RC | 1 |
| Campa, D | 1 |
| Berndt, SI | 1 |
| Lindstrom, S | 1 |
| Kraft, P | 1 |
| Schumacher, FR | 1 |
| Siddiq, A | 1 |
| Papatheodorou, SI | 1 |
| Stanford, JL | 1 |
| Albanes, D | 1 |
| Virtamo, J | 1 |
| Weinstein, SJ | 1 |
| Diver, WR | 1 |
| Gapstur, SM | 1 |
| Stevens, VL | 1 |
| Boeing, H | 1 |
| Bueno-de-Mesquita, HB | 1 |
| Barricarte Gurrea, A | 1 |
| Kaaks, R | 1 |
| Krogh, V | 1 |
| Overvad, K | 1 |
| Riboli, E | 1 |
| Trichopoulos, D | 1 |
| Giovannucci, E | 1 |
| Stampfer, M | 1 |
| Haiman, C | 1 |
| Henderson, B | 1 |
| Le Marchand, L | 1 |
| Gaziano, JM | 1 |
| Hunter, DJ | 1 |
| Koutros, S | 1 |
| Yeager, M | 1 |
| Hoover, RN | 1 |
| Chanock, SJ | 1 |
| Wacholder, S | 1 |
| Key, TJ | 1 |
| Tsilidis, KK | 1 |
| Agalliu, I | 1 |
| San Luciano, M | 1 |
| Waro, B | 1 |
| Aasly, J | 2 |
| Marti-Masso, JF | 1 |
| Orr-Urtreger, A | 1 |
| Demirkan, A | 1 |
| Henneman, P | 1 |
| Verhoeven, A | 1 |
| Dharuri, H | 1 |
| Amin, N | 1 |
| van Klinken, JB | 1 |
| Karssen, LC | 1 |
| de Vries, B | 1 |
| Meissner, A | 1 |
| Göraler, S | 1 |
| van den Maagdenberg, AM | 1 |
| Deelder, AM | 1 |
| C 't Hoen, PA | 1 |
| van Duijn, CM | 2 |
| van Dijk, KW | 1 |
| Su, S | 1 |
| Chien, M | 1 |
| Lin, C | 1 |
| Chen, M | 2 |
| Yang, S | 1 |
| Yin, YW | 1 |
| Sun, QQ | 1 |
| Hu, AM | 1 |
| Liu, HL | 1 |
| Wu, H | 1 |
| Yang, L | 1 |
| Jerbi, S | 1 |
| Jolles, B | 1 |
| Bouceba, T | 1 |
| Jean-Jean, O | 1 |
| Zhang, T | 1 |
| Xing, M | 1 |
| Nosworthy, MG | 1 |
| Brunton, JA | 1 |
| Kumar, A | 1 |
| Misra, S | 1 |
| Kumar, P | 1 |
| Sagar, R | 1 |
| Prasad, K | 1 |
| Pandit, AK | 1 |
| Chakravarty, K | 1 |
| Kathuria, P | 1 |
| Yadav, AK | 1 |
| Cao, M | 1 |
| Gu, ZQ | 1 |
| Li, Y | 3 |
| Zhang, H | 1 |
| Dan, XJ | 1 |
| Cen, SS | 1 |
| Li, DW | 1 |
| Chan, P | 1 |
| Ding, Y | 1 |
| Pedersen, ER | 1 |
| Svingen, GF | 1 |
| Helgeland, Ø | 1 |
| Gregory, JF | 1 |
| Løland, KH | 1 |
| Meyer, K | 1 |
| Tell, GS | 1 |
| Ueland, PM | 1 |
| Nygård, OK | 1 |
| Iwaki, T | 1 |
| Nagahashi, K | 1 |
| Takano, K | 1 |
| Suzuki-Inoue, K | 1 |
| Kanayama, N | 1 |
| Umemura, K | 1 |
| Urano, T | 1 |
| McMahon, GM | 1 |
| Hwang, SJ | 1 |
| Clish, CB | 1 |
| Tin, A | 1 |
| Larson, MG | 1 |
| Rhee, EP | 1 |
| Levy, D | 1 |
| O'Donnell, CJ | 1 |
| Coresh, J | 1 |
| Young, JH | 1 |
| Gerszten, RE | 1 |
| Fox, CS | 1 |
| Hulihan, MM | 2 |
| Ishihara-Paul, L | 1 |
| Kachergus, J | 1 |
| Warren, L | 2 |
| Amouri, R | 3 |
| Elango, R | 1 |
| Prinjha, RK | 1 |
| Upmanyu, R | 1 |
| Kefi, M | 1 |
| Zouari, M | 1 |
| Sassi, SB | 1 |
| Yahmed, SB | 1 |
| El Euch-Fayeche, G | 1 |
| Matthews, PM | 1 |
| Middleton, LT | 1 |
| Gibson, RA | 1 |
| Hentati, F | 3 |
| Farrer, MJ | 6 |
| Healy, DG | 1 |
| Falchi, M | 1 |
| O'Sullivan, SS | 1 |
| Bonifati, V | 2 |
| Durr, A | 4 |
| Zabetian, CP | 4 |
| Ferreira, JJ | 1 |
| Kay, DM | 2 |
| Klein, C | 3 |
| Williams, DR | 1 |
| Lang, AE | 1 |
| Wszolek, ZK | 2 |
| Berciano, J | 2 |
| Schapira, AH | 1 |
| Lynch, T | 1 |
| Bhatia, KP | 1 |
| Gasser, T | 1 |
| Lees, AJ | 1 |
| Wood, NW | 1 |
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| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| A Randomised Double Blind Study of the Effects of Homocysteine Lowering Therapy on Mortality and Cardiac Events in Patients Undergoing Coronary Angiography[NCT00354081] | Phase 3 | 3,096 participants (Actual) | Interventional | 1999-04-30 | Completed | ||
| Use of Metformin in Prevention and Treatment of Cardiac Fibrosis in PAI-1 Deficient Population[NCT05317806] | Phase 4 | 15 participants (Anticipated) | Interventional | 2022-10-10 | Active, not recruiting | ||
| Genetically Determined Response to Atenolol in Patients With Persistent Atrial Fibrillation[NCT01719367] | 38 participants (Actual) | Interventional | 2013-01-31 | Completed | |||
| A Randomised Non-pharmacological Intervention Study for Prevention of Ischaemic Heart Disease Inter99[NCT00289237] | 61,301 participants (Actual) | Interventional | 1999-03-31 | Completed | |||
| Hypertension in High School Students: Genetic and Environmental Factors[NCT06049641] | 2,638 participants (Actual) | Observational | 2014-10-31 | Completed | |||
| The DNA and Cell Bank of IFR of Neurosciences: Clinical and Genetic Study of Parkinson's Disease and Epilepsies[NCT00142363] | 1,700 participants | Observational | 2004-05-31 | Terminated | |||
| GenHAT - Genetics of Hypertension Associated Treatments - Ancillary to ALLHAT[NCT00563901] | 37,939 participants (Actual) | Observational | 2000-09-30 | Completed | |||
| Parkin Mutations and Their Functional Consequences[NCT00136721] | 2,500 participants | Observational | 2002-06-30 | Active, not recruiting | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
After baseline vital signs and ECG are recorded, patients will be asked to perform a baseline standardized (modified Bruce) exercise protocol. Heart rate will be recorded during each stage of the exercise protocol. Patients will be asked to exercise to sub-maximal exertion. After the baseline exercise protocol, patients will be given a single dose of oral atenolol. After a two hour waiting period to allow for peak effect of atenolol, patients will repeat the exercise protocol. The primary study outcome measure will be the difference in pre- and post-atenolol ventricular rate response to exercise. The primary outcome measure will be compared in patients with various polymorphisms in genes that might play a role in the inter-individual response to atenolol. (NCT01719367)
Timeframe: after 5minutes of exercise
| Intervention | beats per minute (Mean) |
|---|---|
| Atenolol: Ancestral Alleles | -10 |
| Atenolol: Variant Carriers | -13 |
After baseline vital signs and ECG are recorded, patients will be asked to perform a baseline standardized (modified Bruce) exercise protocol. Heart rate will be recorded during each stage of the exercise protocol. Patients will be asked to exercise to sub-maximal exertion. After the baseline exercise protocol, patients will be given a single dose of oral atenolol. After a two hour waiting period to allow for peak effect of atenolol, patients will repeat the exercise protocol. The primary study outcome measure will be the difference in pre- and post-atenolol ventricular rate response to exercise. The primary outcome measure will be compared in patients with various polymorphisms in genes that might play a role in the inter-individual response to atenolol. (NCT01719367)
Timeframe: after 10 amd 15 minutes of exercise
| Intervention | beats per minute (Mean) | |
|---|---|---|
| After 10 minutes | After 15 minutes | |
| Atenolol: Ancestral Alleles | -11 | -25.5 |
| Atenolol: Variant Carriers | -19.7 | -35.2 |
19 reviews available for glycine and Genetic Predisposition
| Article | Year |
|---|---|
Linking Metabolic Disease With the PGC-1α Gly482Ser Polymorphism.
Topics: Amino Acid Substitution; Diabetes Mellitus, Type 2; Genetic Linkage; Genetic Predisposition to Disea | 2018 |
Assessing the causal association of glycine with risk of cardio-metabolic diseases.
Topics: Coronary Disease; Diabetes Mellitus, Type 2; Genetic Loci; Genetic Predisposition to Disease; Genome | 2019 |
Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease.
Topics: Biomarkers; Coronary Artery Disease; Female; Genetic Loci; Genetic Predisposition to Disease; Genome | 2019 |
Glycine receptor mouse mutants: model systems for human hyperekplexia.
Topics: Animals; Disease Models, Animal; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glycine | 2013 |
Association of the ADIPOQ T45G polymorphism with insulin resistance and blood glucose: a meta-analysis.
Topics: Adiponectin; Amino Acid Substitution; Blood Glucose; Case-Control Studies; Cross-Sectional Studies; | 2014 |
A genome-wide pleiotropy scan for prostate cancer risk.
Topics: Disease Progression; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Gly | 2015 |
Toll-like receptor 4 gene Asp299Gly and Thr399Ile polymorphisms in type 2 diabetes mellitus: a meta-analysis of 15,059 subjects.
Topics: Amino Acid Substitution; Aspartic Acid; Case-Control Studies; Diabetes Mellitus, Type 2; Genetic Pre | 2015 |
Arg753Gln Polymorphisms in Toll-Like Receptor 2 Gene are Associated with Tuberculosis Risk: A Meta-Analysis.
Topics: Arginine; Genetic Predisposition to Disease; Glycine; Humans; Polymorphism, Genetic; Toll-Like Recep | 2015 |
TLR4 as a risk factor for periodontal disease: a reappraisal.
Topics: Aggressive Periodontitis; Alleles; Aspartic Acid; Chronic Periodontitis; Gene Frequency; Genetic Mar | 2009 |
IGFBP3 polymorphisms and risk of cancer: a meta-analysis.
Topics: Alanine; Alleles; Amino Acid Substitution; Case-Control Studies; Confidence Intervals; Genetic Predi | 2010 |
Dopamine receptor D3 (DRD3) genotype and allelic variants and risk for essential tremor.
Topics: Adult; Age of Onset; Aged; Aged, 80 and over; Case-Control Studies; DNA Mutational Analysis; Essenti | 2009 |
LRRK2 G2019S in the North African population: a review.
Topics: Africa, Northern; Genetic Predisposition to Disease; Glycine; Humans; Leucine-Rich Repeat Serine-Thr | 2010 |
α-adducin Gly460Trp polymorphism and essential hypertension risk in Chinese: a meta-analysis.
Topics: Adult; Aged; Asian People; Calmodulin-Binding Proteins; China; Female; Genetic Association Studies; | 2011 |
[S20G mutation of amylin gene--amyloid diabetes due to S20G amylin gene mutation].
Topics: Amino Acid Sequence; Amino Acid Substitution; Amyloid; Animals; Diabetes Mellitus, Type 2; Genetic P | 2005 |
[HNF-1alpha G319S mutation in Oji-Cree type 2 diabetes].
Topics: Amino Acid Substitution; Canada; Diabetes Mellitus, Type 2; DNA-Binding Proteins; Genetic Predisposi | 2005 |
Clinical and molecular dilemmas in the diagnosis of familial epidermolysis bullosa pruriginosa.
Topics: Adolescent; Adult; Amino Acid Substitution; Asian People; Child; Collagen Type VII; Diagnosis, Diffe | 2007 |
AGAT, GAMT and SLC6A8 distribution in the central nervous system, in relation to creatine deficiency syndromes: a review.
Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Animals; Brain; Creatine; Developmental D | 2008 |
HLA genetics for diagnosis of susceptibility to early-onset periodontitis.
Topics: Aggressive Periodontitis; Alleles; Antigen-Antibody Reactions; Aspartic Acid; Bacterial Outer Membra | 1999 |
Pharmacogenetics of tardive dyskinesia: combined analysis of 780 patients supports association with dopamine D3 receptor gene Ser9Gly polymorphism.
Topics: Adult; Aged; Analysis of Variance; Chi-Square Distribution; Confidence Intervals; Dyskinesia, Drug-I | 2002 |
5 trials available for glycine and Genetic Predisposition
| Article | Year |
|---|---|
Methylenetetrahydrofolate Dehydrogenase 1 Polymorphisms Modify the Associations of Plasma Glycine and Serine With Risk of Acute Myocardial Infarction in Patients With Stable Angina Pectoris in WENBIT (Western Norway B Vitamin Intervention Trial).
Topics: Aged; Angina, Stable; Coronary Angiography; Female; Gene Frequency; Genetic Predisposition to Diseas | 2016 |
A novel germline mutation in HOXB13 is associated with prostate cancer risk in Chinese men.
Topics: Aged; Aged, 80 and over; Amino Acid Substitution; Asian People; China; Genetic Predisposition to Dis | 2013 |
Antihypertensive therapy, the alpha-adducin polymorphism, and cardiovascular disease in high-risk hypertensive persons: the Genetics of Hypertension-Associated Treatment Study.
Topics: Aged; Amlodipine; Antihypertensive Agents; Blood Pressure; Calmodulin-Binding Proteins; Chlorthalido | 2007 |
Characterization of a unique genetic variant in the beta1-adrenoceptor gene and evaluation of its role in idiopathic dilated cardiomyopathy. CARDIGENE Group.
Topics: Adult; Alleles; Arginine; Cardiomyopathy, Dilated; Evaluation Studies as Topic; Female; Genetic Code | 1999 |
Factor V Leiden (G1691A) and prothrombin gene G20210A mutations as potential risk factors for venous thromboembolism after total hip or total knee replacement surgery.
Topics: Activated Protein C Resistance; Adolescent; Adult; Aged; Aged, 80 and over; Anticoagulants; Arthropl | 2002 |
165 other studies available for glycine and Genetic Predisposition
| Article | Year |
|---|---|
A novel variant of IHH in a Chinese family with brachydactyly type 1.
Topics: Adult; Amino Acid Substitution; Aspartic Acid; Brachydactyly; China; DNA Mutational Analysis; Exome | 2020 |
Germline HOXB13 G84E mutation carriers and risk to twenty common types of cancer: results from the UK Biobank.
Topics: Adult; Aged; Amino Acid Substitution; Biological Specimen Banks; Case-Control Studies; Female; Gene | 2020 |
GLYT1 encephalopathy: Further delineation of disease phenotype and discussion of pathophysiological mechanisms.
Topics: Abortion, Spontaneous; Arthrogryposis; Female; Genetic Predisposition to Disease; Glycine; Glycine P | 2021 |
Mendelian Randomization Study on Amino Acid Metabolism Suggests Tyrosine as Causal Trait for Type 2 Diabetes.
Topics: Adult; Amino Acids, Aromatic; Amino Acids, Branched-Chain; Case-Control Studies; Diabetes Mellitus, | 2020 |
The association of genetically determined serum glycine with cardiovascular risk in East Asians.
Topics: Asian People; Biomarkers; Carbamoyl-Phosphate Synthase (Ammonia); Case-Control Studies; China; Coron | 2021 |
Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry.
Topics: Adult; Aged; Aged, 80 and over; Cohort Studies; Family Health; Female; Gene Frequency; Genetic Predi | 2017 |
Neurological phenotypes in spinocerebellar ataxia type 2: Role of mitochondrial polymorphism A10398G and other risk factors.
Topics: Adult; Aged; Alanine; Ataxin-2; Dementia; Dystonia; Female; Genetic Predisposition to Disease; Glyci | 2017 |
Patient mutations linked to arrhythmogenic cardiomyopathy enhance calpain-mediated desmoplakin degradation.
Topics: Adult; Arrhythmias, Cardiac; Calpain; Cardiomyopathies; Desmoplakins; Female; Genetic Predisposition | 2019 |
Unusual clinical and molecular-pathological profile of gerstmann-Sträussler-Scheinker disease associated with a novel PRNP mutation (V176G).
Topics: Creutzfeldt-Jakob Syndrome; Female; Genetic Predisposition to Disease; Gerstmann-Straussler-Scheinke | 2013 |
Novel germline mutation in the transmembrane domain of HER2 in familial lung adenocarcinomas.
Topics: Adenocarcinoma; Adenocarcinoma of Lung; Adult; Asian People; Aspartic Acid; Female; Genetic Predispo | 2014 |
A recurrent 'hot spot' glycine substitution mutation, G2043R in COL7A1, induces dominant dystrophic epidermolysis bullosa associated with intracytoplasmic accumulation of pro-collagen VII.
Topics: Amino Acid Substitution; Cells, Cultured; Collagen Type VII; Cytoplasm; DNA Mutational Analysis; Epi | 2014 |
Two novel missense mutations in nonketotic hyperglycinemia.
Topics: Aminomethyltransferase; Epilepsies, Myoclonic; Female; Genetic Predisposition to Disease; Glycine; G | 2015 |
Motor progression of Parkinson's disease with the leucine-rich repeat kinase 2 G2019S mutation.
Topics: Aged; Disease Progression; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glyc | 2014 |
A common polymorphism in extracellular superoxide dismutase affects cardiopulmonary disease risk by altering protein distribution.
Topics: Animals; Antioxidants; Arginine; Bronchoalveolar Lavage Fluid; Genetic Predisposition to Disease; Ge | 2014 |
Tryptophan to Glycine mutation in the position 116 leads to protein aggregation and decreases the stability of the LITAF protein.
Topics: Codon; Genetic Predisposition to Disease; Glycine; Humans; Hydrogen Bonding; Models, Molecular; Mole | 2015 |
Higher frequency of certain cancers in LRRK2 G2019S mutation carriers with Parkinson disease: a pooled analysis.
Topics: Aged; Aged, 80 and over; Europe; Female; Genetic Association Studies; Genetic Predisposition to Dise | 2015 |
Insight in genome-wide association of metabolite quantitative traits by exome sequence analyses.
Topics: Exome; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Glycine; Humans; Me | 2015 |
RAGE gene polymorphism and environmental factor in the risk of oral cancer.
Topics: Adenine; Areca; Base Pairing; Base Sequence; Carcinogenesis; Case-Control Studies; Cytosine; Female; | 2015 |
Studies on human eRF3-PABP interaction reveal the influence of eRF3a N-terminal glycin repeat on eRF3-PABP binding affinity and the lower affinity of eRF3a 12-GGC allele involved in cancer susceptibility.
Topics: Alleles; Binding Sites; Genetic Predisposition to Disease; Genetic Variation; Glycine; Humans; Model | 2016 |
HABP2 G534E Mutation in Familial Nonmedullary Thyroid Cancer.
Topics: Adult; Aged; Carcinoma; Carcinoma, Papillary; Female; Genetic Predisposition to Disease; Germ-Line M | 2016 |
Cysteinyl-glycine reduces mucosal proinflammatory cytokine response to fMLP in a parenterally-fed piglet model.
Topics: Animals; Cysteine; Cytokines; Dipeptides; Disease Models, Animal; Genetic Predisposition to Disease; | 2016 |
Association between Endothelial nitric oxide synthase G894T gene polymorphism and risk of ischemic stroke in North Indian population: a case-control study.
Topics: Adult; Aged; Brain Ischemia; Case-Control Studies; Female; Genetic Association Studies; Genetic Pred | 2016 |
Olfactory Dysfunction in Parkinson's Disease Patients with the LRRK2 G2385R Variant.
Topics: Aged; Aged, 80 and over; Arginine; Female; Genetic Predisposition to Disease; Genotype; Glycine; Hum | 2016 |
Mutation in a highly conserved glycine residue in strand 5B of plasminogen activator inhibitor 1 causes polymerisation.
Topics: Aged; Amino Acid Substitution; Animals; Arginine; Chlorocebus aethiops; Conserved Sequence; COS Cell | 2017 |
Urinary metabolites along with common and rare genetic variations are associated with incident chronic kidney disease.
Topics: Aged; Amino Acid Transport Systems, Basic; Amino Acids; Biomarkers; Case-Control Studies; Chi-Square | 2017 |
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study.
Topics: Age Factors; Case-Control Studies; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glyc | 2008 |
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study.
Topics: Age Factors; Age of Onset; Case-Control Studies; DNA Mutational Analysis; Family Health; Female; Gen | 2008 |
Seizure responses and induction of Fos by the NMDA agonist (tetrazol-5-yl)glycine in a genetic model of NMDA receptor hypofunction.
Topics: Animals; Brain; Disease Models, Animal; Dose-Response Relationship, Drug; Drug Resistance; Excitator | 2008 |
Genetic screening for LRRK2 gene G2019S mutation in Parkinson's disease patients from Southern Italy.
Topics: Adult; Age of Onset; Aged; DNA Mutational Analysis; Female; Fluorodeoxyglucose F18; Gene Frequency; | 2009 |
Differential coupling of Arg- and Gly389 polymorphic forms of the beta1-adrenergic receptor leads to pathogenic cardiac gene regulatory programs.
Topics: Animals; Arginine; Gene Regulatory Networks; Genetic Predisposition to Disease; Glycine; Humans; Mic | 2008 |
A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations.
Topics: Aged; DNA Mutational Analysis; Family Health; Female; France; Genetic Predisposition to Disease; Gly | 2009 |
LRRK2 gene G2019S mutation and SNPs [haplotypes] in subtypes of Parkinson's disease.
Topics: Age of Onset; Aged; Aged, 80 and over; DNA Mutational Analysis; Female; Gene Frequency; Genetic Pred | 2009 |
Constraints on the evolution of tolerance to herbicide in the common morning glory: resistance and tolerance are mutually exclusive.
Topics: Drug Resistance; Drug Tolerance; Genetic Predisposition to Disease; Genetic Variation; Glycine; Glyp | 2008 |
Genetic analysis for five LRRK2 mutations in a Sardinian parkinsonian population: importance of G2019S and R1441C mutations in sporadic Parkinson's disease patients.
Topics: Adult; Age Factors; Aged; Aged, 80 and over; Arginine; Cysteine; DNA Mutational Analysis; Female; Ge | 2009 |
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity.
Topics: Amino Acid Sequence; Cells, Cultured; Collagen Diseases; Collagen Type VI; Connective Tissue; Diseas | 2008 |
K469E polymorphism of the intracellular adhesion molecule 1 gene is associated with proliferative diabetic retinopathy in Caucasians with type 2 diabetes.
Topics: Aged; Alanine; Case-Control Studies; Cross-Sectional Studies; Diabetes Mellitus, Type 2; Diabetic Re | 2008 |
Association of the dopamine D3 receptor Ser9Gly and of the serotonin 2C receptor gene polymorphisms with tardive dyskinesia in Greeks with chronic schizophrenic disorder.
Topics: Amino Acid Substitution; Chronic Disease; Dyskinesias; Female; Genetic Predisposition to Disease; Gl | 2009 |
Genetic study of BDNF, DRD3, and their interaction in tardive dyskinesia.
Topics: Adult; Akathisia, Drug-Induced; Analysis of Variance; Brain-Derived Neurotrophic Factor; Chi-Square | 2009 |
Association analysis of glycine- and serine-related genes in a Japanese population of patients with schizophrenia.
Topics: Adult; Case-Control Studies; Chi-Square Distribution; D-Amino-Acid Oxidase; DNA Mutational Analysis; | 2009 |
Genetic variants of D2 but not D3 or D4 dopamine receptor gene are associated with rapid onset and poor prognosis of methamphetamine psychosis.
Topics: Adult; Case-Control Studies; Central Nervous System Stimulants; DNA Mutational Analysis; Female; Gen | 2009 |
The increased incidence of the RET p.Gly691Ser variant in French-Canadian vesicoureteric reflux patients is not replicated by a larger study in Ireland.
Topics: Alleles; Amino Acid Substitution; Canada; Case-Control Studies; Female; France; Gene Frequency; Gene | 2009 |
The G1057D polymorphism of IRS-2 gene is not associated with type 2 diabetes and obese patients among ethnic groups in Tunisian population.
Topics: Aspartic Acid; Black People; Diabetes Mellitus, Type 2; Ethnicity; Female; Genetic Predisposition to | 2009 |
3-Methylcrotonyl-CoA carboxylase deficiency: phenotypic variability in a family.
Topics: Adult; Brain; Carbon-Carbon Ligases; Carnitine; Cells, Cultured; Child, Preschool; DNA Mutational An | 2009 |
LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease.
Topics: Aged; Arginine; DNA Mutational Analysis; Exons; Family Health; Female; Gene Frequency; Genetic Predi | 2009 |
Motor complications in patients form the German Competence Network on Parkinson's disease and the DRD3 Ser9Gly polymorphism.
Topics: Aged; Aged, 80 and over; Antipsychotic Agents; Community Networks; Dyskinesia, Drug-Induced; Female; | 2009 |
Association of LT-alpha Ala252Gly gene polymorphism and the genetic predisposition of coronary heart disease in Chinese.
Topics: Alanine; Asian People; Case-Control Studies; China; Coronary Disease; Female; Genetic Predisposition | 2010 |
Prepulse inhibition and genetic mouse models of schizophrenia.
Topics: Animals; Brain; Disease Models, Animal; Environment; Genetic Predisposition to Disease; Glutamic Aci | 2009 |
DRD3 Ser9Gly polymorphism is related to thermal pain perception and modulation in chronic widespread pain patients and healthy controls.
Topics: Adult; Amino Acid Sequence; Chronic Disease; DNA Mutational Analysis; Dopamine; Female; Fibromyalgia | 2009 |
[Analysis of TGFBI gene mutation in a Chinese family with atypical Reis-Buckler corneal dystrophy].
Topics: Asian People; Aspartic Acid; Corneal Dystrophies, Hereditary; Corneal Stroma; Exons; Extracellular M | 2009 |
[The genotype-phenotype correlation of the MYH7 gene c.1273G > a mutation in familial hypertrophic cardiomyopathy].
Topics: Adult; Amino Acid Sequence; Animals; Arginine; Cardiac Myosins; Cardiomyopathy, Hypertrophic, Famili | 2009 |
Analysis of the LRRK2 Gly2385Arg variant in Alzheimer's disease in Taiwan.
Topics: Aged; Aged, 80 and over; Alzheimer Disease; Arginine; DNA Mutational Analysis; Female; Gene Frequenc | 2010 |
Association of Gly972Arg polymorphism of IRS1 gene with type 2 diabetes mellitus in lean participants of a national health survey in Mexico: a candidate gene study.
Topics: Aged; Arginine; Body Mass Index; Diabetes Mellitus, Type 2; Gene Frequency; Genetic Predisposition t | 2010 |
Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals.
Topics: Aged; Alanine; Asian People; Cell Adhesion Molecules; Cysteine; Female; Genetic Predisposition to Di | 2010 |
The LRRK2 G2385R variant is a risk factor for sporadic Parkinson's disease in the Korean population.
Topics: Adult; Aged; Aged, 80 and over; Arginine; Chi-Square Distribution; Female; Gene Frequency; Genetic P | 2010 |
Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations.
Topics: Arginine; Choline O-Acetyltransferase; Electric Stimulation; Electroencephalography; Enzyme Inhibito | 2010 |
Study of association of IRS-1 and IRS-2 genes polymorphisms with clinical and metabolic features in women with polycystic ovary syndrome. Is there an impact?
Topics: Adult; Amino Acid Substitution; Arginine; Aspartic Acid; Case-Control Studies; Female; Genetic Predi | 2010 |
Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients.
Topics: Amino Acid Substitution; Arginine; Female; Gene Frequency; Genetic Predisposition to Disease; Genoty | 2011 |
LRRK2 Gly2385Arg polymorphism, cigarette smoking, and risk of sporadic Parkinson's disease: a case-control study in Japan.
Topics: Aged; Arginine; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Gen | 2010 |
Substantia nigra hyperechogenicity with LRRK2 G2019S mutations.
Topics: Adult; Age Factors; Aged; Female; Genetic Predisposition to Disease; Glycine; Humans; Leucine-Rich R | 2011 |
Identical glycine substitution mutations in type VII collagen may underlie both dominant and recessive forms of dystrophic epidermolysis bullosa.
Topics: Adolescent; Adult; Amino Acid Substitution; Biopsy; Child; Child, Preschool; Collagen Type VII; Data | 2011 |
In this issue: glycine substitution mutations in the COL7A1 gene: implications for inheritance of dystrophic epidermolysis bullosa - dominant vs. recessive.
Topics: Amino Acid Substitution; Collagen Type VII; DNA Mutational Analysis; Epidermolysis Bullosa Dystrophi | 2011 |
Mood and cognition in leucine-rich repeat kinase 2 G2019S Parkinson's disease.
Topics: Aged; Aged, 80 and over; Cognition Disorders; Female; Genetic Predisposition to Disease; Glycine; Hu | 2011 |
The insulin-like growth factor 2 receptor gene Gly1619Arg polymorphism and idiopathic recurrent spontaneous abortion.
Topics: Abortion, Habitual; Abortion, Spontaneous; Adult; Amino Acid Substitution; Arginine; Case-Control St | 2012 |
Frequency of uridine monophosphate synthase Gly(213)Ala polymorphism in Caucasian gastrointestinal cancer patients and healthy subjects, investigated by means of new, rapid genotyping assays.
Topics: Adult; Aged; Aged, 80 and over; Alanine; Amino Acid Substitution; Carcinoma; Chromatography, High Pr | 2011 |
Association study of DRD3 gene in schizophrenia in Mexican sib-pairs.
Topics: Adult; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Glycine; Hu | 2011 |
A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient.
Topics: Adult; Brain; Genetic Predisposition to Disease; Genome-Wide Association Study; Gerstmann-Straussler | 2011 |
Arg16Gly β2-adrenergic receptor gene polymorphism in Japanese patients with aspirin-exacerbated respiratory disease.
Topics: Adult; Aged; Alleles; Amino Acid Substitution; Arginine; Asian People; Asthma, Aspirin-Induced; Fema | 2011 |
Is there any association between GLY82 ser polymorphism of rage gene and Turkish diabetic and non diabetic patients with coronary artery disease?
Topics: Coronary Artery Disease; Demography; Diabetes Complications; Female; Gene Frequency; Genetic Associa | 2012 |
Association of XRCC1, XRCC3, and NAT2 polymorphisms with the risk of oral submucous fibrosis among eastern Indian population.
Topics: Adult; Areca; Arginine; Arylamine N-Acetyltransferase; Case-Control Studies; Codon; DNA Repair; DNA- | 2012 |
SLC6A4 rare variant associated with eating disorders in Mexican patients.
Topics: Adolescent; Alanine; DNA Mutational Analysis; Feeding and Eating Disorders; Female; Gene Frequency; | 2012 |
Dyskinesias in patients with Parkinson's disease: effect of the leucine-rich repeat kinase 2 (LRRK2) G2019S mutation.
Topics: Adult; Aged; Aged, 80 and over; DNA Mutational Analysis; Dyskinesia, Drug-Induced; Female; Gene Freq | 2012 |
CD226 Gly307Ser association with neuromyelitis optica in Southern Han Chinese.
Topics: Adult; Age of Onset; Antigens, Differentiation, T-Lymphocyte; Asian People; Case-Control Studies; Ch | 2012 |
Guanidinoacetate methyltransferase (GAMT) deficiency in two Tunisian siblings: clinical and biochemical features.
Topics: Abnormalities, Multiple; Adolescent; Amino Acid Metabolism, Inborn Errors; Child; Chromatography, Hi | 2012 |
[The absence of the common LRRK2 G2019S mutation in 120 young onset Hungarian Parkinon's disease patients].
Topics: Adult; Age of Onset; Aged; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testin | 2012 |
XRCC1 gene polymorphisms and risk of ameloblastoma.
Topics: Adenine; Adult; Ameloblastoma; Arginine; Codon; DNA Repair; DNA-Binding Proteins; Female; Gene Frequ | 2013 |
Gly1057Asp polymorphism of insulin receptor substrate-2 is associated with coronary artery disease in the Taiwanese population.
Topics: Aged; Alleles; Asian People; Coronary Angiography; Coronary Artery Disease; Female; Gene Frequency; | 2012 |
Novel insertion mutation p.Asp610GlyfsX23 in APC gene causes familial adenomatous polyposis in Chinese families.
Topics: Adenomatous Polyposis Coli; Adolescent; Adult; Asian People; Aspartic Acid; Base Sequence; Case-Cont | 2013 |
Olfaction and imaging biomarkers in premotor LRRK2 G2019S-associated Parkinson disease.
Topics: Aged; Aged, 80 and over; Biomarkers; Chi-Square Distribution; Cohort Studies; Cross-Sectional Studie | 2013 |
Association of the G-250A promoter polymorphism in the hepatic lipase gene with the risk of type 2 diabetes mellitus.
Topics: Adult; Aged; Alanine; Amino Acid Substitution; Asian People; Case-Control Studies; Diabetes Mellitus | 2013 |
Role of toll-like receptor 4 mutations in gram-negative septic shock.
Topics: Aspartic Acid; Confounding Factors, Epidemiologic; Drosophila Proteins; Genetic Predisposition to Di | 2002 |
Lack of association between Alzheimer's disease and Gln-Arg 192 Q/R polymorphism of the PON-1 gene in an Italian population.
Topics: Aged; Alzheimer Disease; Amino Acid Substitution; Arginine; Aryldialkylphosphatase; Case-Control Stu | 2003 |
Influence of interleukin-12 receptor beta1 polymorphisms on tuberculosis.
Topics: Adult; Aged; Alanine; Asian People; Blotting, Western; Case-Control Studies; Cysteine; Female; Genet | 2003 |
[Significance of Factor V gene A506G mutation (Leiden) in the pathogenesis of ischemic stroke].
Topics: Adult; Age of Onset; Alanine; Brain Ischemia; DNA Mutational Analysis; Factor V; Female; Genetic Pre | 2003 |
Investigation of an LDLR gene polymorphism (19p13.2) in susceptibility to migraine without aura.
Topics: Adolescent; Adult; Alanine; Alleles; Child; Chromosome Mapping; Chromosomes, Human, Pair 19; Exons; | 2003 |
A novel genetic variant in the apolipoprotein A5 gene is associated with hypertriglyceridemia.
Topics: Age Factors; Amino Acid Substitution; Apolipoproteins A; Asian People; Body Mass Index; Cholesterol; | 2003 |
Beta 1-adrenergic receptor polymorphisms confer differential function and predisposition to heart failure.
Topics: Adrenergic beta-Antagonists; Animals; Arginine; Cardiac Output, Low; Echocardiography; Genetic Predi | 2003 |
Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease.
Topics: Alleles; Arginine; Charcot-Marie-Tooth Disease; Cysteine; Demyelinating Diseases; DNA Mutational Ana | 2003 |
Alcoholism-related phenotypes and genetic variants of the CB1 receptor.
Topics: Adult; Alanine; Alcoholism; Analysis of Variance; Case-Control Studies; Chitinases; Delirium; Drosop | 2003 |
Support for RGS4 as a susceptibility gene for schizophrenia.
Topics: Adult; Alanine; Alleles; Case-Control Studies; Chi-Square Distribution; Diagnostic and Statistical M | 2004 |
Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alanine; Americas; Asperger Syndrome; Autistic Disorder; | 2004 |
Cu/Zn-superoxide dismutase (GLY93-->ALA) mutation alters AMPA receptor subunit expression and function and potentiates kainate-mediated toxicity in motor neurons in culture.
Topics: Alanine; Amyotrophic Lateral Sclerosis; Animals; Cells, Cultured; Drug Resistance; Fetus; Genetic Pr | 2004 |
Gender in obsessive-compulsive disorder: clinical and genetic findings.
Topics: Adolescent; Adult; Age of Onset; Aged; Case-Control Studies; Comorbidity; Cysteine; Female; Gene Fre | 2004 |
The Toll-like receptor 4 Asp299Gly functional variant is associated with decreased rheumatoid arthritis disease susceptibility but does not influence disease severity and/or outcome.
Topics: Adult; Aged; Arthritis, Rheumatoid; Aspartic Acid; Case-Control Studies; Female; Gene Frequency; Gen | 2004 |
Possible association of interleukin 1 gene locus polymorphisms with low back pain.
Topics: Adult; Alanine; Alleles; Cohort Studies; Cysteine; Finland; Genetic Predisposition to Disease; Genot | 2004 |
Susceptibility to primary sclerosing cholangitis is associated with polymorphisms of intercellular adhesion molecule-1.
Topics: Alleles; Arginine; Case-Control Studies; Cholangitis, Sclerosing; Cohort Studies; Gene Frequency; Ge | 2004 |
Role of alpha-adducin DNA polymorphisms in the genetic predisposition to diabetic nephropathy.
Topics: Adult; Calmodulin-Binding Proteins; Cytoskeletal Proteins; Diabetes Mellitus, Type 1; Diabetic Nephr | 2004 |
The factor V G1691A mutation is a risk for porencephaly: A case-control study.
Topics: Alanine; Brain Diseases; Case-Control Studies; Chi-Square Distribution; Child; Factor V; Female; Gen | 2004 |
Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk.
Topics: Adenomatous Polyposis Coli; Aspartic Acid; Base Pair Mismatch; Biomarkers, Tumor; Case-Control Studi | 2004 |
Toll-like receptor 4 Asp299Gly gene polymorphism and risk of atherothrombosis.
Topics: Amino Acid Substitution; Aspartic Acid; Case-Control Studies; Genetic Predisposition to Disease; Gly | 2005 |
A Gly482Ser polymorphism of the peroxisome proliferator-activated receptor-gamma coactivator-1 (PGC-1) gene is associated with type 2 diabetes in Caucasians.
Topics: Case-Control Studies; Diabetes Mellitus, Type 2; Female; Gene Frequency; Genetic Predisposition to D | 2004 |
Ethnic origin determines the impact of genetic variants in dopamine receptor gene (DRD1) concerning essential hypertension.
Topics: Adult; Aged; Alanine; Blood Pressure; Blood Pressure Monitoring, Ambulatory; Female; Gene Frequency; | 2004 |
Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.
Topics: Aged; Amino Acid Sequence; Animals; Dihydroxyphenylalanine; DNA Mutational Analysis; Family Health; | 2005 |
PGC-1alpha Gly482Ser polymorphism associates with hypertension among Danish whites.
Topics: Adult; Aged; Blood Pressure; Denmark; Female; Genetic Predisposition to Disease; Genotype; Glycine; | 2005 |
A functional interleukin-10 mutation in Dutch patients with Crohn's disease.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Arginine; Crohn Disease; DNA Mutational Analysis; Female | 2005 |
Reduced endocannabinoid immune modulation by a common cannabinoid 2 (CB2) receptor gene polymorphism: possible risk for autoimmune disorders.
Topics: Amino Acid Substitution; Arachidonic Acids; Autoimmune Diseases; Cannabinoid Receptor Modulators; Ce | 2005 |
Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.
Topics: Alanine; Alleles; Autistic Disorder; Blood Platelets; Chromosomes, Human, Pair 17; Compulsive Behavi | 2005 |
CARD15/NOD2 polymorphisms do not explain concordance of Crohn's disease in Swedish monozygotic twins.
Topics: Adolescent; Adult; Arginine; Case-Control Studies; Child; Crohn Disease; Female; Frameshift Mutation | 2005 |
Cardiovascular risk in relation to alpha-adducin Gly460Trp polymorphism and systolic pressure: a prospective population study.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Blood Pressure; Calmodulin-Binding Proteins; Cardiovascu | 2005 |
Association of severe micropenis with Gly146Ala polymorphism in the gene for steroidogenic factor-1.
Topics: Adolescent; Alanine; Child; Child, Preschool; Genetic Predisposition to Disease; Glycine; Homeodomai | 2005 |
Association of the 1438G/A and 102T/C polymorphism of the 5-HT2A receptor gene with irritable bowel syndrome 5-HT2A gene polymorphism in irritable bowel syndrome.
Topics: Alanine; Case-Control Studies; Cysteine; Gene Frequency; Genetic Predisposition to Disease; Genotype | 2005 |
G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort.
Topics: Adult; Aged; Aged, 80 and over; Cohort Studies; DNA Mutational Analysis; Family Health; Female; Gene | 2005 |
A new mutation of the tau gene, G303V, in early-onset familial progressive supranuclear palsy.
Topics: Amino Acid Substitution; Blotting, Northern; Blotting, Western; Brain; Dihydroxyphenylalanine; DNA M | 2005 |
Polymorphism of arylamine-N-acetyltransferase 2 gene is associated with the risk of atopic dermatitis.
Topics: Adolescent; Alleles; Amino Acid Substitution; Arylamine N-Acetyltransferase; Case-Control Studies; C | 2005 |
G2019S LRRK2 mutation in French and North African families with Parkinson's disease.
Topics: Adult; Africa, Northern; Aged; Aged, 80 and over; DNA Mutational Analysis; Family Health; Female; Fr | 2005 |
CD14 and TLR4 gene polymorphisms in adult periodontitis.
Topics: Adult; Age Factors; Aged; Aggregatibacter actinomycetemcomitans; Aspartic Acid; Cytosine; Disease Su | 2005 |
Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics.
Topics: Adolescent; Adult; Age of Onset; Aged; Aged, 80 and over; DNA Mutational Analysis; Family Health; Fe | 2006 |
The Gly482Ser missense mutation of the peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PGC-1 alpha) gene associates with reduced insulin sensitivity in normal and glucose-intolerant obese subjects.
Topics: Adult; Amino Acid Substitution; Female; Genetic Predisposition to Disease; Glucose Intolerance; Glyc | 2005 |
Gingival epithelial cells heterozygous for Toll-like receptor 4 polymorphisms Asp299Gly and Thr399ile are hypo-responsive to Porphyromonas gingivalis.
Topics: Amino Acid Substitution; Aspartic Acid; Cells, Cultured; Gene Expression Profiling; Genetic Predispo | 2006 |
Biochemical and pathological characterization of Lrrk2.
Topics: Adult; Aged; Aged, 80 and over; alpha-Synuclein; Amino Acid Sequence; Animals; Blotting, Western; Br | 2006 |
Protective effect of the G-765C COX-2 polymorphism on subclinical atherosclerosis and inflammatory markers in asymptomatic subjects with cardiovascular risk factors.
Topics: Atherosclerosis; Biomarkers; Cholesterol; Cyclooxygenase 2; Cysteine; Female; Gene Expression Regula | 2006 |
Two Japanese families with hyperekplexia who have a Arg271Gln mutation in the glycine receptor alpha 1 subunit gene.
Topics: Child, Preschool; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glycine; Hip D | 2006 |
LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance.
Topics: Adolescent; Adult; Age of Onset; Aged; Aged, 80 and over; Arginine; Child; Child, Preschool; DNA Mut | 2006 |
The Gly146Ala variation in human SF-1 gene: its association with insulin resistance and type 2 diabetes in Chinese.
Topics: Alanine; Chi-Square Distribution; China; Diabetes Mellitus, Type 2; Female; Gene Frequency; Genetic | 2006 |
Interleukin 6 G-174 C polymorphism and breast cancer risk.
Topics: Aged; Aged, 80 and over; Breast Neoplasms; Cysteine; Female; Genetic Predisposition to Disease; Geno | 2006 |
A functional variant of the dopamine D3 receptor is associated with risk and age-at-onset of essential tremor.
Topics: Adolescent; Adult; Age of Onset; Aged; Aged, 80 and over; Amino Acid Sequence; Case-Control Studies; | 2006 |
CARD15 gene variants in aggressive periodontitis.
Topics: Adult; Arginine; Base Sequence; Case-Control Studies; Cytosine; Disease Susceptibility; DNA Transpos | 2006 |
Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations.
Topics: Aged; DNA Mutational Analysis; Family Health; Female; Gene Frequency; Genetic Predisposition to Dise | 2006 |
Insulin receptor substrate gene polymorphism is associated with obstructive sleep apnea syndrome in men.
Topics: Adult; Arginine; Female; Genetic Predisposition to Disease; Glycine; Humans; Insulin Receptor Substr | 2006 |
Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease.
Topics: Adult; Age of Onset; Aged; Aged, 80 and over; DNA Mutational Analysis; Family Health; Female; Geneti | 2007 |
The G51S purine nucleoside phosphorylase polymorphism is associated with cognitive decline in Alzheimer's disease patients.
Topics: Alleles; Alzheimer Disease; Apolipoprotein E4; Cognition Disorders; Disease Progression; Follow-Up S | 2007 |
Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia.
Topics: Aged; Arginine; Asian People; Female; Genetic Predisposition to Disease; Glycine; Humans; Leucine-Ri | 2007 |
The methionine synthase polymorphism c.2756A>G (D919G) influences diastolic blood pressure.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adult; Aged; Alleles; Antihypertensive Ag | 2007 |
p62 accumulates and enhances aggregate formation in model systems of familial amyotrophic lateral sclerosis.
Topics: Adaptor Proteins, Signal Transducing; Amyotrophic Lateral Sclerosis; Animals; Cell Line; Cell Surviv | 2007 |
R990G polymorphism of calcium-sensing receptor does produce a gain-of-function and predispose to primary hypercalciuria.
Topics: Alleles; Amino Acid Substitution; Blotting, Western; Case-Control Studies; Cell Line; Codon; Electro | 2007 |
Arginine 16 glycine beta2-adrenoceptor polymorphism and cardiovascular structure and function in patients with heart failure.
Topics: Apolipoproteins E; Biomarkers, Tumor; DNA Mutational Analysis; Female; Genetic Predisposition to Dis | 2007 |
Addendum to "Prospective study of the G20210A polymorphism in the prothrombin gene, plasma prothrombin concentration, and incidence of venous thromboembolism".
Topics: Case-Control Studies; Genetic Predisposition to Disease; Glycine; Humans; Incidence; Polymorphism, G | 2007 |
MAPK-pathway activity, Lrrk2 G2019S, and Parkinson's disease.
Topics: Aged; Aged, 80 and over; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glycine | 2007 |
Receptor for advanced glycation end products Glycine 82 Serine polymorphism and risk of cardiovascular events in rheumatoid arthritis.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Arthritis, Rheumatoid; Cardiovascular Diseases; Genetic | 2007 |
Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease.
Topics: Aged; Australia; Cohort Studies; DNA Mutational Analysis; Family Health; Female; Genetic Predisposit | 2007 |
Human KCNQ1 S140G mutation is associated with atrioventricular blocks.
Topics: Animals; Atrial Fibrillation; Atrioventricular Node; China; Chromans; Electrocardiography; Female; G | 2007 |
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 |
P27 V109G Polymorphism is associated with lymph node metastases but not with increased risk of breast cancer.
Topics: Breast Neoplasms; Carcinoma, Ductal, Breast; Case-Control Studies; Cyclin-Dependent Kinase Inhibitor | 2007 |
No association between the DRD3 Ser9Gly polymorphism and schizophrenia.
Topics: Adult; Antipsychotic Agents; Case-Control Studies; Diagnostic and Statistical Manual of Mental Disor | 2008 |
Interleukin-23R Arg381Gln is associated with susceptibility to Crohn's disease but not with phenotype in an Italian population.
Topics: Adolescent; Adult; Arginine; Case-Control Studies; Crohn Disease; Female; Genetic Predisposition to | 2007 |
Association between migraine and the G1246A polymorphism in the hypocretin receptor 2 gene.
Topics: Adult; Alanine; Chi-Square Distribution; DNA Mutational Analysis; Female; Genetic Predisposition to | 2007 |
A novel p.Gly1700Asp mutation in COL7A1 responsible for dominant dystrophic epidermolysis bullosa: more severe phenotype in female members of a Chinese family.
Topics: Adult; Asian People; Aspartic Acid; China; Collagen Type VII; DNA Mutational Analysis; Epidermolysis | 2008 |
Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants?
Topics: Alanine; Arginine; Biomarkers, Tumor; Breast Neoplasms; Centrosome; DNA, Complementary; Factor Analy | 2007 |
Polymorphism of the endothelial nitric oxide synthase gene is associated with diabetic retinopathy in a cohort of West Africans.
Topics: Adult; Aged; Alleles; Black People; Cohort Studies; Diabetes Mellitus, Type 2; Diabetic Retinopathy; | 2007 |
LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China.
Topics: Adult; Aged; Aged, 80 and over; Arginine; Asian People; Chi-Square Distribution; China; Female; Gene | 2008 |
Associations of FcepsilonRIbeta E237G polymorphism with wheezing in Taiwanese schoolchildren.
Topics: Air Pollution; Alleles; Case-Control Studies; Child; Environmental Exposure; Female; Genetic Predisp | 2008 |
The Ser9Gly polymorphism of the dopamine D3 receptor gene and risk of schizophrenia: an association study and a large meta-analysis.
Topics: Adult; Alleles; Case-Control Studies; China; Female; Gene Frequency; Genetic Predisposition to Disea | 2008 |
Essential tremor and the common LRRK2 G2385R variant.
Topics: Adult; Aged; Arginine; Cohort Studies; Confidence Intervals; DNA Mutational Analysis; Essential Trem | 2008 |
Distinct effects of the recurrent Mlh1G67R mutation on MMR functions, cancer, and meiosis.
Topics: Adaptor Proteins, Signal Transducing; Animals; Apoptosis; Cell Line; Chromosomes; Cisplatin; DNA Dam | 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 |
Uncertain pathogenicity of MSH2 variants N127S and G322D challenges their classification.
Topics: Asparagine; Aspartic Acid; Biliary Tract Neoplasms; Blotting, Western; Colorectal Neoplasms, Heredit | 2008 |
The association of genotypic combination of the DRD3 and BDNF polymorphisms on the adhesio interthalamica and medial temporal lobe structures.
Topics: Adolescent; Adult; Brain-Derived Neurotrophic Factor; Dominance, Cerebral; Female; Genetic Predispos | 2008 |
Allosteric regulation of the N-methyl-D-aspartate receptor-linked ion channel complex and effects of ethanol in ethanol-withdrawal seizure-prone and -resistant mice.
Topics: Allosteric Regulation; Animals; Cerebral Cortex; Dizocilpine Maleate; Ethanol; Genetic Predispositio | 1995 |
Mutation screening of dihydropyridine receptor gamma subunit cDNA from malignant hyperthermia susceptible patients.
Topics: Amino Acid Sequence; Base Sequence; Calcium Channels; Calcium Channels, L-Type; Chromosome Mapping; | 1995 |
Association of persistent bronchial hyperresponsiveness with beta2-adrenoceptor (ADRB2) haplotypes. A population study.
Topics: Adolescent; Adult; Allergens; Amino Acid Sequence; Asthma; Bronchial Hyperreactivity; Bronchial Prov | 1998 |
Increased cerebrospinal fluid glycine: a biochemical marker for a leukoencephalopathy with vanishing white matter.
Topics: Adolescent; Adult; Biomarkers; Brain; Brain Diseases; Child; Child, Preschool; Excitatory Amino Acid | 1999 |
Is the Ala138Gly alteration of MEFV gene important for amyloidosis?
Topics: Alanine; Amino Acid Substitution; Amyloidosis; Cytoskeletal Proteins; Familial Mediterranean Fever; | 2001 |
Increased seizure susceptibility in mice lacking metabotropic glutamate receptor 7.
Topics: Animals; Anticonvulsants; Bicuculline; Cerebral Cortex; Convulsants; Drug Resistance; Electroencepha | 2001 |
Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients.
Topics: Adult; Aged; Alanine; Amino Acid Substitution; Child; Child, Preschool; Female; Genetic Predispositi | 2002 |
Intracellular adhesion molecule Gly241Arg polymorphism has no impact on ARDS or septic shock in community-acquired pneumonia.
Topics: Arginine; Community-Acquired Infections; Genetic Predisposition to Disease; Glycine; Humans; Interce | 2002 |
Rheumatoid arthritis in Israeli Jews: shared sequences in the third hypervariable region of DRB1 alleles are associated with susceptibility.
Topics: Alanine; Alleles; Amino Acid Sequence; Arthritis, Rheumatoid; Genetic Predisposition to Disease; Gly | 1991 |