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Bei Sha

Showing results (61-70 of 236) with videos related to

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Yi Chuan = Hereditas|September 11, 2015
[Molecular mechanism of idiopathic basal ganglia calcification]Cheng Wang, Xuan Xu, Lu-lu Li, et al.
Neuroscience Letters|August 7, 2013
Marginal association between SNP rs2046571 of the HAS2 gene and Parkinson's disease in the Chinese female populationYi Yuan, Bei-sha Tang, Ri-li Yu, et al.
Asian Pacific Journal of Tropical Medicine|April 23, 2015
Influence of simvastatin on dopaminergic neurons of lipopolysaccharide-induced rat model of Parkinson's diseaseTan Wang, Xue-Bin Cao, Xiao-Wu Chen, et al.
Parkinsonism & Related Disorders|March 22, 2016
Safety and efficacy of valproic acid treatment in SCA3/MJD patientsLi-Fang Lei, Guo-Ping Yang, Jun-Ling Wang, et al.
Chinese Medical Journal|July 2, 2005
Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6Hong Jiang, Bei-sha Tang, Bo Xu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 8, 2010
A rare Von Hippel-Lindau disease that mimics acute myelitis: case report and review of the literatureHong Jiang, Yu-ting Shi, Jun-ling Wang, et al.
Parkinson'S Disease|October 1, 2015
Effect of GBA Mutations on Phenotype of Parkinson's Disease: A Study on Chinese Population and a Meta-AnalysisYuan Zhang, Qi-Ying Sun, Yu-Wen Zhao, et al.
Sichuan Da Xue Xue Bao. Yi Xue Ban = Journal of Sichuan University. Medical Science Edition|September 21, 2010
[Protective effect of over-expression OGCP on HEK293 cells treated by rotenone and mutant Parkin protein]Chun-Yu Wang, Bei-Sha Tang, Hai-Nan Zhang, et al.
Brain Research|June 16, 2010
R492X mutation in PTEN-induced putative kinase 1 induced cellular mitochondrial dysfunction and oxidative stressXiang-Li Yuan, Ji-Feng Guo, Zhen-Hua Shi, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 11, 2008
[The clinical characteristics of a pedigree with incompletely penetrated autosomal dominant hereditary spastic paraplegia and its exclusion analysis of genetic loci]Guo-hua Zhao, Zhi-jun Ren, Xiao-min Liu, et al.
Pageof 24

Showing results (61-70 of 236) with videos related to

Sort By:
Pageof 24
Yi Chuan = Hereditas|September 11, 2015
[Molecular mechanism of idiopathic basal ganglia calcification]Cheng Wang, Xuan Xu, Lu-lu Li, et al.
Neuroscience Letters|August 7, 2013
Marginal association between SNP rs2046571 of the HAS2 gene and Parkinson's disease in the Chinese female populationYi Yuan, Bei-sha Tang, Ri-li Yu, et al.
Asian Pacific Journal of Tropical Medicine|April 23, 2015
Influence of simvastatin on dopaminergic neurons of lipopolysaccharide-induced rat model of Parkinson's diseaseTan Wang, Xue-Bin Cao, Xiao-Wu Chen, et al.
Parkinsonism & Related Disorders|March 22, 2016
Safety and efficacy of valproic acid treatment in SCA3/MJD patientsLi-Fang Lei, Guo-Ping Yang, Jun-Ling Wang, et al.
Chinese Medical Journal|July 2, 2005
Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6Hong Jiang, Bei-sha Tang, Bo Xu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 8, 2010
A rare Von Hippel-Lindau disease that mimics acute myelitis: case report and review of the literatureHong Jiang, Yu-ting Shi, Jun-ling Wang, et al.
Parkinson'S Disease|October 1, 2015
Effect of GBA Mutations on Phenotype of Parkinson's Disease: A Study on Chinese Population and a Meta-AnalysisYuan Zhang, Qi-Ying Sun, Yu-Wen Zhao, et al.
Sichuan Da Xue Xue Bao. Yi Xue Ban = Journal of Sichuan University. Medical Science Edition|September 21, 2010
[Protective effect of over-expression OGCP on HEK293 cells treated by rotenone and mutant Parkin protein]Chun-Yu Wang, Bei-Sha Tang, Hai-Nan Zhang, et al.
Brain Research|June 16, 2010
R492X mutation in PTEN-induced putative kinase 1 induced cellular mitochondrial dysfunction and oxidative stressXiang-Li Yuan, Ji-Feng Guo, Zhen-Hua Shi, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 11, 2008
[The clinical characteristics of a pedigree with incompletely penetrated autosomal dominant hereditary spastic paraplegia and its exclusion analysis of genetic loci]Guo-hua Zhao, Zhi-jun Ren, Xiao-min Liu, et al.
Pageof 24