Associated Papers
Lack of association between UCHL1 S18Y gene polymorphism and Parkinson's disease in the Asian population: a meta-analysis.
Sun S et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2014
UCH-L1 S18Y variant and risk of Parkinson's disease in Asian populations: an updated meta-analysis.
Zhu R et al.
Neuro-degenerative Diseases, 2014
Case-control study of the UCH-L1 S18Y variant in sporadic Parkinson's disease in the Chinese population.
Wang L et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia, 2011
Ubiquitin carboxy-terminal hydrolase L1 (UCHL1) S18Y polymorphism in Alzheimer's disease.
Zetterberg M et al.
Molecular Neurodegeneration, 2010
Polymorphism of HD and UCHL-1 genes in Huntington's disease.
Xu EH et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia, 2009
[Association of the ubiquitin carboxy-terminal hydrolase-L1 genetic polymorphism with the susceptibility of Parkinson's disease].
Xiao Y et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2008
[Association of two polymorphisms in ubiquitin carboxy-terminal hydrolase-L1 gene with Parkinson's disease in Shanghai].
Hao YX et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2008
[Association between interleukin-1 alpha-889 C/T polymorphism and Alzheimer's disease in Chinese Han population].
Zhou YT et al.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae, 2006
ACT and UCH-L1 polymorphisms in Parkinson's disease and age of onset.
Wang J et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2002
No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease.
Levecque C et al.
Journal of Neural Transmission (vienna, Austria : 1996), 2001
The ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism does not confer protection against idiopathic Parkinson's disease.
Mellick GD et al.
Neuroscience Letters, 2000
Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients.
Wintermeyer P et al.
Neuroreport, 2000
A nonpathogenic GAAGGA repeat in the Friedreich gene: implications for pathogenesis.
Ohshima K et al.
Neurology, 1999
Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease.
Lincoln S et al.
Neuroreport, 1999
UCHL1 is associated with Parkinson's disease: a case-unaffected sibling and case-unrelated control study.
Facheris M et al.
Neuroscience Letters, 0