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Beisha Tang

Showing results (261-270 of 514) with videos related to

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Neuromuscular Disorders : NMD|July 23, 2018
A novel AIFM1 mutation in a Chinese family with X-linked Charcot-Marie-Tooth disease type 4Binghao Wang, Xiaobo Li, Junpu Wang, et al.
Gene|April 5, 2020
Corrigendum to "Profiling of mitochondrial genomes in SCA3/MJD patients from mainland China" [Gene 738 (2020) 144487]Hongyu Yuan, Huihua Yang, Linliu Peng, et al.
Gene|February 23, 2020
Profiling of mitochondrial genomes in SCA3/MJD patients from mainland ChinaHongyu Yuan, Huihua Yang, Linliu Peng, et al.
Scientific Reports|October 25, 2016
Insertion of a knockout-first cassette in Ampd1 gene leads to neonatal death by disruption of neighboring genes expressionYongcheng Pan, Lusi Zhang, Qiong Liu, et al.
Human Molecular Genetics|April 25, 2006
Association of PINK1 and DJ-1 confers digenic inheritance of early-onset Parkinson's diseaseBeisha Tang, Hui Xiong, Ping Sun, et al.
Scientific Reports|January 28, 2016
Spinocerebellar ataxia type 21 exists in the Chinese Han populationSheng Zeng, Junsheng Zeng, Miao He, et al.
Frontiers in Neurology|October 12, 2020
Study on the Clinical Features of Parkinson's Disease With Probable Rapid Eye Movement Sleep Behavior DisorderKexin Long, Changmin Wan, Yaqin Xiang, et al.
Frontiers in Neurology|February 14, 2022
One PMP22/MPZ and Three MFN2/GDAP1 Concomitant Variants Occurred in a Cohort of 189 Chinese Charcot-Marie-Tooth FamiliesYongzhi Xie, Zhiqiang Lin, Xiaobo Li, et al.
Biochemical and Biophysical Research Communications|March 15, 2020
Corrigendum to "PRRT2 frameshift mutation reduces its mRNA stability resulting loss of function in paroxysmal kinesigenic dyskinesia"Yongcheng Pan, Qiong Liu, Jennifer Zhang, et al.
Journal of the Neurological Sciences|December 29, 2005
Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasiaHong Jiang, Beisha Tang, Kun Xia, et al.
Pageof 52

Showing results (261-270 of 514) with videos related to

Sort By:
Pageof 52
Neuromuscular Disorders : NMD|July 23, 2018
A novel AIFM1 mutation in a Chinese family with X-linked Charcot-Marie-Tooth disease type 4Binghao Wang, Xiaobo Li, Junpu Wang, et al.
Gene|April 5, 2020
Corrigendum to "Profiling of mitochondrial genomes in SCA3/MJD patients from mainland China" [Gene 738 (2020) 144487]Hongyu Yuan, Huihua Yang, Linliu Peng, et al.
Gene|February 23, 2020
Profiling of mitochondrial genomes in SCA3/MJD patients from mainland ChinaHongyu Yuan, Huihua Yang, Linliu Peng, et al.
Scientific Reports|October 25, 2016
Insertion of a knockout-first cassette in Ampd1 gene leads to neonatal death by disruption of neighboring genes expressionYongcheng Pan, Lusi Zhang, Qiong Liu, et al.
Human Molecular Genetics|April 25, 2006
Association of PINK1 and DJ-1 confers digenic inheritance of early-onset Parkinson's diseaseBeisha Tang, Hui Xiong, Ping Sun, et al.
Scientific Reports|January 28, 2016
Spinocerebellar ataxia type 21 exists in the Chinese Han populationSheng Zeng, Junsheng Zeng, Miao He, et al.
Frontiers in Neurology|October 12, 2020
Study on the Clinical Features of Parkinson's Disease With Probable Rapid Eye Movement Sleep Behavior DisorderKexin Long, Changmin Wan, Yaqin Xiang, et al.
Frontiers in Neurology|February 14, 2022
One PMP22/MPZ and Three MFN2/GDAP1 Concomitant Variants Occurred in a Cohort of 189 Chinese Charcot-Marie-Tooth FamiliesYongzhi Xie, Zhiqiang Lin, Xiaobo Li, et al.
Biochemical and Biophysical Research Communications|March 15, 2020
Corrigendum to "PRRT2 frameshift mutation reduces its mRNA stability resulting loss of function in paroxysmal kinesigenic dyskinesia"Yongcheng Pan, Qiong Liu, Jennifer Zhang, et al.
Journal of the Neurological Sciences|December 29, 2005
Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasiaHong Jiang, Beisha Tang, Kun Xia, et al.
Pageof 52