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Beisha Tang

Showing results (161-170 of 514) with videos related to

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Archives of Neurology|January 21, 2004
Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegiaBeisha Tang, Guohua Zhao, Kun Xia, et al.
Epilepsy Research|February 6, 2008
A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsionsHaiyan Li, Nan Li, Lu Shen, et al.
Scientific Reports|July 7, 2016
Genome-wide analysis of DNA methylation during antagonism of DMOG to MnCl2-induced cytotoxicity in the mouse substantia nigraNannan Yang, Yang Wei, Tan Wang, et al.
Neurobiology of Aging|March 22, 2014
Mutational analysis in early-onset familial Alzheimer's disease in Mainland ChinaBin Jiao, Beisha Tang, Xiaoyan Liu, et al.
European Journal of Nuclear Medicine and Molecular Imaging|February 8, 2026
Beyond nigrostriatal dopamine transporter loss: whole-brain DAT depletion patterns discriminate PD phenotypesJian Li, Xuan Guo, Yaqin Xiang, et al.
Journal of the Neurological Sciences|July 18, 2016
The rs3756063 polymorphism is associated with SNCA methylation in the Chinese Han populationYang Wei, Nannan Yang, Qian Xu, et al.
Biochemical and Biophysical Research Communications|January 3, 2014
The BAG2 protein stabilises PINK1 by decreasing its ubiquitinationXiangqian Che, Beisha Tang, Xuejing Wang, et al.
Gene|April 12, 2025
Pathogenicity analysis of three SCA14-associated missense mutations in PRKCG gene of Chinese patients with ataxiaHongyu Yuan, Zhao Chen, Linlin Wan, et al.
Frontiers in Neurology|June 6, 2019
Factors Associated With Dyskinesia in Parkinson's Disease in Mainland ChinaXun Zhou, Jifeng Guo, Qiying Sun, et al.
Frontiers in Neurology|October 17, 2019
Gene-Related Cerebellar Neurodegeneration in SCA3/MJD: A Case-Controlled Imaging-Genetic StudyHuirong Peng, Xiaochun Liang, Zhe Long, et al.
Pageof 52

Showing results (161-170 of 514) with videos related to

Sort By:
Pageof 52
Archives of Neurology|January 21, 2004
Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegiaBeisha Tang, Guohua Zhao, Kun Xia, et al.
Epilepsy Research|February 6, 2008
A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsionsHaiyan Li, Nan Li, Lu Shen, et al.
Scientific Reports|July 7, 2016
Genome-wide analysis of DNA methylation during antagonism of DMOG to MnCl2-induced cytotoxicity in the mouse substantia nigraNannan Yang, Yang Wei, Tan Wang, et al.
Neurobiology of Aging|March 22, 2014
Mutational analysis in early-onset familial Alzheimer's disease in Mainland ChinaBin Jiao, Beisha Tang, Xiaoyan Liu, et al.
European Journal of Nuclear Medicine and Molecular Imaging|February 8, 2026
Beyond nigrostriatal dopamine transporter loss: whole-brain DAT depletion patterns discriminate PD phenotypesJian Li, Xuan Guo, Yaqin Xiang, et al.
Journal of the Neurological Sciences|July 18, 2016
The rs3756063 polymorphism is associated with SNCA methylation in the Chinese Han populationYang Wei, Nannan Yang, Qian Xu, et al.
Biochemical and Biophysical Research Communications|January 3, 2014
The BAG2 protein stabilises PINK1 by decreasing its ubiquitinationXiangqian Che, Beisha Tang, Xuejing Wang, et al.
Gene|April 12, 2025
Pathogenicity analysis of three SCA14-associated missense mutations in PRKCG gene of Chinese patients with ataxiaHongyu Yuan, Zhao Chen, Linlin Wan, et al.
Frontiers in Neurology|June 6, 2019
Factors Associated With Dyskinesia in Parkinson's Disease in Mainland ChinaXun Zhou, Jifeng Guo, Qiying Sun, et al.
Frontiers in Neurology|October 17, 2019
Gene-Related Cerebellar Neurodegeneration in SCA3/MJD: A Case-Controlled Imaging-Genetic StudyHuirong Peng, Xiaochun Liang, Zhe Long, et al.
Pageof 52