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4. Analysis of the coding and the 5' flanking regions of the alpha-synuclein gene in patients with Parkinson's disease. Pastor P; Muñoz E; Ezquerra M; Obach V; Martí MJ; Valldeoriola F; Tolosa E; Oliva R Mov Disord; 2001 Nov; 16(6):1115-9. PubMed ID: 11748744 [TBL] [Abstract][Full Text] [Related]
5. Developmentally regulated expression of persyn, a member of the synuclein family, in skin. Ninkina NN; Privalova EM; Pinõn LG; Davies AM; Buchman VL Exp Cell Res; 1999 Feb; 246(2):308-11. PubMed ID: 9925745 [TBL] [Abstract][Full Text] [Related]
6. Low frequency of alpha-synuclein mutations in familial Parkinson's disease. Farrer M; Wavrant-De Vrieze F; Crook R; Boles L; Perez-Tur J; Hardy J; Johnson WG; Steele J; Maraganore D; Gwinn K; Lynch T Ann Neurol; 1998 Mar; 43(3):394-7. PubMed ID: 9506559 [TBL] [Abstract][Full Text] [Related]
7. Evaluation of the gamma-synuclein gene in German Parkinson's disease patients. Krüger R; Schöls L; Müller T; Kuhn W; Woitalla D; Przuntek H; Epplen JT; Riess O Neurosci Lett; 2001 Sep; 310(2-3):191-3. PubMed ID: 11585599 [TBL] [Abstract][Full Text] [Related]
9. Mutation, sequence analysis, and association studies of alpha-synuclein in Parkinson's disease. Parsian A; Racette B; Zhang ZH; Chakraverty S; Rundle M; Goate A; Perlmutter JS Neurology; 1998 Dec; 51(6):1757-9. PubMed ID: 9855543 [TBL] [Abstract][Full Text] [Related]
10. Association analysis of polymorphisms in VMAT2 and TMEM106B genes for Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy. Hu T; Chen Y; Ou R; Wei Q; Cao B; Zhao B; Wu Y; Song W; Chen X; Shang HF J Neurol Sci; 2017 Jun; 377():65-71. PubMed ID: 28477711 [TBL] [Abstract][Full Text] [Related]
12. Genetic polymorphism in the persyn (gamma-synuclein) gene and the risk of Alzheimer's disease. Luedecking EK; Ganguli M; DeKosky ST; Kamboh MI Neurosci Lett; 1999 Feb; 261(3):186-8. PubMed ID: 10081980 [TBL] [Abstract][Full Text] [Related]
13. Sequence of the superoxide dismutase 1 (SOD 1) gene in familial Parkinson's disease. Bandmann O; Davis MB; Marsden CD; Harding AE J Neurol Neurosurg Psychiatry; 1995 Jul; 59(1):90-1. PubMed ID: 7608718 [TBL] [Abstract][Full Text] [Related]
14. Persyn, a member of the synuclein family, has a distinct pattern of expression in the developing nervous system. Buchman VL; Hunter HJ; Pinõn LG; Thompson J; Privalova EM; Ninkina NN; Davies AM J Neurosci; 1998 Nov; 18(22):9335-41. PubMed ID: 9801372 [TBL] [Abstract][Full Text] [Related]
15. No pathogenic mutations in the beta-synuclein gene in Parkinson's disease. Lincoln S; Crook R; Chartier-Harlin MC; Gwinn-Hardy K; Baker M; Mouroux V; Richard F; Becquet E; Amouyel P; Destée A; Hardy J; Farrer M Neurosci Lett; 1999 Jul; 269(2):107-9. PubMed ID: 10430516 [TBL] [Abstract][Full Text] [Related]
16. An association analysis of the rs1572931 polymorphism of the RAB7L1 gene in Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy in China. Guo XY; Chen YP; Song W; Zhao B; Cao B; Wei QQ; Ou RW; Yang Y; Yuan LX; Shang HF Eur J Neurol; 2014 Oct; 21(10):1337-43. PubMed ID: 25040112 [TBL] [Abstract][Full Text] [Related]
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18. [Study on gamma-synuclein gene in patients with idiopathic Parkinson's disease]. Su JJ; Xie HJ; Zhao WW; Han HX; Gao T; Xu L; Tang GM; Ren DM Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Oct; 20(5):444-6. PubMed ID: 14556204 [TBL] [Abstract][Full Text] [Related]
19. alpha-Synuclein gene haplotypes are associated with Parkinson's disease. Farrer M; Maraganore DM; Lockhart P; Singleton A; Lesnick TG; de Andrade M; West A; de Silva R; Hardy J; Hernandez D Hum Mol Genet; 2001 Aug; 10(17):1847-51. PubMed ID: 11532993 [TBL] [Abstract][Full Text] [Related]
20. Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD). Vaughan JR; Farrer MJ; Wszolek ZK; Gasser T; Durr A; Agid Y; Bonifati V; DeMichele G; Volpe G; Lincoln S; Breteler M; Meco G; Brice A; Marsden CD; Hardy J; Wood NW Hum Mol Genet; 1998 Apr; 7(4):751-3. PubMed ID: 9499430 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]