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Bei Sha

Showing results (51-60 of 236) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|October 12, 2013
Increase of the plasma α-synuclein levels in patients with multiple system atrophyZhan-Fang Sun, Xiao-Shuang Xiang, Zhao Chen, et al.
Zoological Research|December 1, 2025
Modeling neuronal intranuclear inclusion disease: A review of animal and human-derived cellular models and mechanistic insightsXin-Hui Wang, Ying Jiang, Hong Jiang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 11, 2007
[Gene screening in five Chinese families with hereditary spastic paraplegia with thin corpus callosum]Guo-hua Zhao, Peng Guo, Zhi-jun Ren, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 9, 2005
[Distribution of genotype and allele frequencies of dopamine D4 receptor gene 48 bp variable number tandem repeat polymorphism in Chinese Han population in Hunan]Ai-ling Zhao, Jing-ping Zhao, Yu-hu Zhang, et al.
Neuroscience Letters|August 5, 2015
Exon dosage analysis of parkin gene in Chinese sporadic Parkinson's diseaseJi-Feng Guo, Xiao-Li Dong, Qian Xu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 12, 2003
[A novel mutation of KCNQ2 gene in a Chinese family with benign familial neonatal convulsions]Hai-yan Li, Bei-sha Tang, Ai-mei Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 7, 2009
[Mutation analysis of ATP13A2 gene in Chinese patients with familial autosomal recessive early-onset parkinsonism]Dan He, Ji-feng Guo, Lei Wang, et al.
Zhonghua Yi Xue Za Zhi|April 12, 2012
[Roles of axonal transport affected by K141N mutant HSP22 in the pathogenesis of CMT2L]Fu-Feng Zhang, Xiao-Qin Lu, Ya-Fang Zhou, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|May 20, 2006
[Construction of the eukaryotic expression vector of MJD1 and its expression in SH-SY5Y cells]Jian-guang Tang, Bei-sha Tang, Lu Shen, et al.
The International Journal of Neuroscience|May 23, 2015
Effects of simvastatin on the expression of inducible nitric oxide synthase and brain-derived neurotrophic factor in a lipopolysaccharide-induced rat model of Parkinson diseaseWang Tan, Cao Xue-bin, Zhang Tian, et al.
Pageof 24

Showing results (51-60 of 236) with videos related to

Sort By:
Pageof 24
Movement Disorders : Official Journal of the Movement Disorder Society|October 12, 2013
Increase of the plasma α-synuclein levels in patients with multiple system atrophyZhan-Fang Sun, Xiao-Shuang Xiang, Zhao Chen, et al.
Zoological Research|December 1, 2025
Modeling neuronal intranuclear inclusion disease: A review of animal and human-derived cellular models and mechanistic insightsXin-Hui Wang, Ying Jiang, Hong Jiang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 11, 2007
[Gene screening in five Chinese families with hereditary spastic paraplegia with thin corpus callosum]Guo-hua Zhao, Peng Guo, Zhi-jun Ren, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 9, 2005
[Distribution of genotype and allele frequencies of dopamine D4 receptor gene 48 bp variable number tandem repeat polymorphism in Chinese Han population in Hunan]Ai-ling Zhao, Jing-ping Zhao, Yu-hu Zhang, et al.
Neuroscience Letters|August 5, 2015
Exon dosage analysis of parkin gene in Chinese sporadic Parkinson's diseaseJi-Feng Guo, Xiao-Li Dong, Qian Xu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 12, 2003
[A novel mutation of KCNQ2 gene in a Chinese family with benign familial neonatal convulsions]Hai-yan Li, Bei-sha Tang, Ai-mei Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 7, 2009
[Mutation analysis of ATP13A2 gene in Chinese patients with familial autosomal recessive early-onset parkinsonism]Dan He, Ji-feng Guo, Lei Wang, et al.
Zhonghua Yi Xue Za Zhi|April 12, 2012
[Roles of axonal transport affected by K141N mutant HSP22 in the pathogenesis of CMT2L]Fu-Feng Zhang, Xiao-Qin Lu, Ya-Fang Zhou, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|May 20, 2006
[Construction of the eukaryotic expression vector of MJD1 and its expression in SH-SY5Y cells]Jian-guang Tang, Bei-sha Tang, Lu Shen, et al.
The International Journal of Neuroscience|May 23, 2015
Effects of simvastatin on the expression of inducible nitric oxide synthase and brain-derived neurotrophic factor in a lipopolysaccharide-induced rat model of Parkinson diseaseWang Tan, Cao Xue-bin, Zhang Tian, et al.
Pageof 24