174 related articles for article (PubMed ID: 10923647)
1. Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients.
Wintermeyer P; Krüger R; Kuhn W; Müller T; Woitalla D; Berg D; Becker G; Leroy E; Polymeropoulos M; Berger K; Przuntek H; Schöls L; Epplen JT; Riess O
Neuroreport; 2000 Jul; 11(10):2079-82. PubMed ID: 10923647
[TBL] [Abstract][Full Text] [Related]
2. The ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism does not confer protection against idiopathic Parkinson's disease.
Mellick GD; Silburn PA
Neurosci Lett; 2000 Oct; 293(2):127-30. PubMed ID: 11027850
[TBL] [Abstract][Full Text] [Related]
3. No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease.
Levecque C; Destée A; Mouroux V; Becquet E; Defebvre L; Amouyel P; Chartier-Harlin MC
J Neural Transm (Vienna); 2001; 108(8-9):979-84. PubMed ID: 11716150
[TBL] [Abstract][Full Text] [Related]
4. The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease.
Harhangi BS; Farrer MJ; Lincoln S; Bonifati V; Meco G; De Michele G; Brice A; Dürr A; Martinez M; Gasser T; Bereznai B; Vaughan JR; Wood NW; Hardy J; Oostra BA; Breteler MM
Neurosci Lett; 1999 Jul; 270(1):1-4. PubMed ID: 10454131
[TBL] [Abstract][Full Text] [Related]
5. Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease.
Lincoln S; Vaughan J; Wood N; Baker M; Adamson J; Gwinn-Hardy K; Lynch T; Hardy J; Farrer M
Neuroreport; 1999 Feb; 10(2):427-9. PubMed ID: 10203348
[TBL] [Abstract][Full Text] [Related]
6. A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population.
Satoh J; Kuroda Y
J Neurol Sci; 2001 Aug; 189(1-2):113-7. PubMed ID: 11535241
[TBL] [Abstract][Full Text] [Related]
7. UCHL1 S18Y variant is a risk factor for Parkinson's disease in Japan.
Miyake Y; Tanaka K; Fukushima W; Kiyohara C; Sasaki S; Tsuboi Y; Yamada T; Oeda T; Shimada H; Kawamura N; Sakae N; Fukuyama H; Hirota Y; Nagai M;
BMC Neurol; 2012 Jul; 12():62. PubMed ID: 22839974
[TBL] [Abstract][Full Text] [Related]
8. An Ile93Met substitution in the UCH-L1 gene is not a disease-causing mutation for idiopathic Parkinson's disease.
Shi Q; Tao E
Chin Med J (Engl); 2003 Feb; 116(2):312-3. PubMed ID: 12775255
[TBL] [Abstract][Full Text] [Related]
9. Association between ubiquitin carboxy-terminal hydrolase-L1 S18Y variant and risk of Parkinson's disease: the impact of ethnicity and onset age.
Liu Y; Chen YY; Liu H; Yao CJ; Zhu XX; Chen DJ; Yang J; Lu YJ; Cao JY
Neurol Sci; 2015 Feb; 36(2):179-88. PubMed ID: 25370916
[TBL] [Abstract][Full Text] [Related]
10. Case-control study of UCHL1 S18Y variant in Parkinson's disease.
Tan EK; Puong KY; Fook-Chong S; Chua E; Shen H; Yuen Y; Pavanni R; Wong MC; Puvan K; Zhao Y
Mov Disord; 2006 Oct; 21(10):1765-8. PubMed ID: 16941465
[TBL] [Abstract][Full Text] [Related]
11. ACT and UCH-L1 polymorphisms in Parkinson's disease and age of onset.
Wang J; Zhao CY; Si YM; Liu ZL; Chen B; Yu L
Mov Disord; 2002 Jul; 17(4):767-71. PubMed ID: 12210873
[TBL] [Abstract][Full Text] [Related]
12. Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease.
Maraganore DM; Farrer MJ; Hardy JA; Lincoln SJ; McDonnell SK; Rocca WA
Neurology; 1999 Nov; 53(8):1858-60. PubMed ID: 10563640
[TBL] [Abstract][Full Text] [Related]
13. Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese.
Tan EK; Lu CS; Peng R; Teo YY; Wu-Chou YH; Chen RS; Weng YH; Chen CM; Fung HC; Tan LC; Zhang ZJ; An XK; Lee-Chen GJ; Lee MC; Fook-Chong S; Burgunder JM; Wu RM; Wu YR
Neurobiol Aging; 2010 Dec; 31(12):2194-6. PubMed ID: 19329225
[TBL] [Abstract][Full Text] [Related]
14. UCHL1 is a Parkinson's disease susceptibility gene.
Maraganore DM; Lesnick TG; Elbaz A; Chartier-Harlin MC; Gasser T; Krüger R; Hattori N; Mellick GD; Quattrone A; Satoh J; Toda T; Wang J; Ioannidis JP; de Andrade M; Rocca WA;
Ann Neurol; 2004 Apr; 55(4):512-21. PubMed ID: 15048890
[TBL] [Abstract][Full Text] [Related]
15. Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease.
Hutter CM; Samii A; Factor SA; Nutt JG; Higgins DS; Bird TD; Griffith A; Roberts JW; Leis BC; Montimurro JS; Kay DM; Edwards KL; Payami H; Zabetian CP
Eur J Neurol; 2008 Feb; 15(2):134-9. PubMed ID: 18093156
[TBL] [Abstract][Full Text] [Related]
16. Importance of familial Parkinson's disease and parkinsonism to the understanding of nigral degeneration in sporadic Parkinson's disease.
Hattori N; Shimura H; Kubo S; Wang M; Shimizu N; Tanaka K; Mizuno Y
J Neural Transm Suppl; 2000; (60):101-16. PubMed ID: 11205133
[TBL] [Abstract][Full Text] [Related]
17. Complex interactions in Parkinson's disease: a two-phased approach.
Maraganore DM; de Andrade M; Lesnick TG; Farrer MJ; Bower JH; Hardy JA; Rocca WA
Mov Disord; 2003 Jun; 18(6):631-6. PubMed ID: 12784265
[TBL] [Abstract][Full Text] [Related]
18. Ubiquitin specific proteases USP24 and USP40 and ubiquitin thiolesterase UCHL1 polymorphisms have synergic effect on the risk of Parkinson's disease among Taiwanese.
Wu YR; Chen CM; Chen YC; Chao CY; Ro LS; Fung HC; Hsiao YC; Hu FJ; Lee-Chen GJ
Clin Chim Acta; 2010 Jul; 411(13-14):955-8. PubMed ID: 20302855
[TBL] [Abstract][Full Text] [Related]
19. S18Y in ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) associated with decreased risk of Parkinson's disease in Sweden.
Carmine Belin A; Westerlund M; Bergman O; Nissbrandt H; Lind C; Sydow O; Galter D
Parkinsonism Relat Disord; 2007 Jul; 13(5):295-8. PubMed ID: 17287139
[TBL] [Abstract][Full Text] [Related]
20. UCHL1 is associated with Parkinson's disease: a case-unaffected sibling and case-unrelated control study.
Facheris M; Strain KJ; Lesnick TG; de Andrade M; Bower JH; Ahlskog JE; Cunningham JM; Lincoln S; Farrer MJ; Rocca WA; Maraganore DM
Neurosci Lett; 2005 Jun 10-17; 381(1-2):131-4. PubMed ID: 15882803
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]