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Beisha Tang

Showing results (181-190 of 514) with videos related to

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Frontiers in Neurology|March 3, 2020
Corrigendum: Gene-Related Cerebellar Neurodegeneration in SCA3/MJD: A Case-Controlled Imaging-Genetic StudyHuirong Peng, Xiaochun Liang, Zhe Long, et al.
Neurobiology of Aging|August 10, 2020
No genetic evidence for the involvement of GGC repeat expansions of the NOTCH2NLC gene in Chinese patients with multiple system atrophyKeqin Xu, Linlin Wan, Zhao Chen, et al.
Scientific Reports|February 6, 2016
Identification of a de novo DYNC1H1 mutation via WES according to published guidelinesDongxue Ding, Zhao Chen, Kai Li, et al.
Journal of the Peripheral Nervous System : JPNS|January 24, 2016
MFN2-related genetic and clinical features in a cohort of Chinese CMT2 patientsYongzhi Xie, Xiaobo Li, Lei Liu, et al.
Plos One|October 7, 2015
Targeted Next-Generation Sequencing Revealed Novel Mutations in Chinese Ataxia Telangiectasia Patients: A Precision Medicine PerspectiveZhao Chen, Wei Ye, Zhe Long, et al.
Cellular and Molecular Life Sciences : CMLS|April 7, 2025
Loss of NgBR causes neuronal damage through decreasing KAT7-mediated RFX1 acetylation and FGF1 expressionYuwei Hu, Yanni Ma, Lele Liu, et al.
Neuroscience Letters|May 15, 2012
Spinocerebellar ataxia type 27 (SCA27) is an uncommon cause of dominant ataxia among Chinese Han populationZhao Chen, Xiaohui Li, Beisha Tang, et al.
Journal of the Peripheral Nervous System : JPNS|September 14, 2013
Two novel MPZ mutations in Chinese CMT patientsLei Liu, Xiaobo Li, Xiaohong Zi, et al.
Human Molecular Genetics|March 22, 2021
Downregulation of TOP2 modulates neurodegeneration caused by GGGGCC expanded repeatsBin Jiao, Mengli Wang, Hao Feng, et al.
Frontiers in Aging Neuroscience|November 3, 2022
The effect of regional white matter hyperintensities on essential tremor subtypes and severityRuncheng He, Yan Qin, Xun Zhou, et al.
Pageof 52

Showing results (181-190 of 514) with videos related to

Sort By:
Pageof 52
Frontiers in Neurology|March 3, 2020
Corrigendum: Gene-Related Cerebellar Neurodegeneration in SCA3/MJD: A Case-Controlled Imaging-Genetic StudyHuirong Peng, Xiaochun Liang, Zhe Long, et al.
Neurobiology of Aging|August 10, 2020
No genetic evidence for the involvement of GGC repeat expansions of the NOTCH2NLC gene in Chinese patients with multiple system atrophyKeqin Xu, Linlin Wan, Zhao Chen, et al.
Scientific Reports|February 6, 2016
Identification of a de novo DYNC1H1 mutation via WES according to published guidelinesDongxue Ding, Zhao Chen, Kai Li, et al.
Journal of the Peripheral Nervous System : JPNS|January 24, 2016
MFN2-related genetic and clinical features in a cohort of Chinese CMT2 patientsYongzhi Xie, Xiaobo Li, Lei Liu, et al.
Plos One|October 7, 2015
Targeted Next-Generation Sequencing Revealed Novel Mutations in Chinese Ataxia Telangiectasia Patients: A Precision Medicine PerspectiveZhao Chen, Wei Ye, Zhe Long, et al.
Cellular and Molecular Life Sciences : CMLS|April 7, 2025
Loss of NgBR causes neuronal damage through decreasing KAT7-mediated RFX1 acetylation and FGF1 expressionYuwei Hu, Yanni Ma, Lele Liu, et al.
Neuroscience Letters|May 15, 2012
Spinocerebellar ataxia type 27 (SCA27) is an uncommon cause of dominant ataxia among Chinese Han populationZhao Chen, Xiaohui Li, Beisha Tang, et al.
Journal of the Peripheral Nervous System : JPNS|September 14, 2013
Two novel MPZ mutations in Chinese CMT patientsLei Liu, Xiaobo Li, Xiaohong Zi, et al.
Human Molecular Genetics|March 22, 2021
Downregulation of TOP2 modulates neurodegeneration caused by GGGGCC expanded repeatsBin Jiao, Mengli Wang, Hao Feng, et al.
Frontiers in Aging Neuroscience|November 3, 2022
The effect of regional white matter hyperintensities on essential tremor subtypes and severityRuncheng He, Yan Qin, Xun Zhou, et al.
Pageof 52