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Beisha Tang

Showing results (461-470 of 515) with videos related to

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Parkinsonism & Related Disorders|July 20, 2021
Genetic etiology of a Chinese ataxia cohort: Expanding the mutational spectrum of hereditary ataxiasNa Wan, Zhao Chen, Linlin Wan, et al.
Neurobiology of Disease|July 16, 2022
Genetics of progressive supranuclear palsy in a Chinese populationXuewen Xiao, Qijie Yang, Yafei Wen, et al.
Neuroscience Bulletin|November 10, 2018
Standardized Operational Protocol for Human Brain Banking in ChinaWenying Qiu, Hanlin Zhang, Aimin Bao, et al.
Frontiers in Aging Neuroscience|August 16, 2023
Evaluation of the role of <i>FMR1</i> CGG repeat allele in Parkinson's disease from the Chinese populationJuan Chen, Yuwen Zhao, Xun Zhou, et al.
Nature Communications|January 12, 2026
Precise excision of expanded GGC repeats in NOTCH2NLC via CRISPR/Cas9 for treating neuronal intranuclear inclusion diseaseNina Xie, Yongcheng Pan, Huichun Tong, et al.
Frontiers in Neuroscience|May 13, 2021
Gene4PD: A Comprehensive Genetic Database of Parkinson's DiseaseBin Li, Guihu Zhao, Qiao Zhou, et al.
Cell Reports|August 1, 2019
Distinct Connectivity and Functionality of Aldehyde Dehydrogenase 1a1-Positive Nigrostriatal Dopaminergic Neurons in Motor LearningJunbing Wu, Justin Kung, Jie Dong, et al.
Brain : a Journal of Neurology|March 24, 2017
Ubiquitin-related network underlain by (CAG)n loci modulate age at onset in Machado-Joseph diseaseZhao Chen, Chunrong Wang, Caifa Zheng, et al.
European Journal of Neurology|July 13, 2021
Genotype and phenotype distribution of 435 patients with Charcot-Marie-Tooth disease from central south ChinaYongzhi Xie, Zhiqiang Lin, Lei Liu, et al.
Neurology|August 21, 2020
Association of serum neurofilament light and disease severity in patients with spinocerebellar ataxia type 3Yun Peng, Youming Zhang, Zhao Chen, et al.
Pageof 52

Showing results (461-470 of 515) with videos related to

Sort By:
Pageof 52
Parkinsonism & Related Disorders|July 20, 2021
Genetic etiology of a Chinese ataxia cohort: Expanding the mutational spectrum of hereditary ataxiasNa Wan, Zhao Chen, Linlin Wan, et al.
Neurobiology of Disease|July 16, 2022
Genetics of progressive supranuclear palsy in a Chinese populationXuewen Xiao, Qijie Yang, Yafei Wen, et al.
Neuroscience Bulletin|November 10, 2018
Standardized Operational Protocol for Human Brain Banking in ChinaWenying Qiu, Hanlin Zhang, Aimin Bao, et al.
Frontiers in Aging Neuroscience|August 16, 2023
Evaluation of the role of <i>FMR1</i> CGG repeat allele in Parkinson's disease from the Chinese populationJuan Chen, Yuwen Zhao, Xun Zhou, et al.
Nature Communications|January 12, 2026
Precise excision of expanded GGC repeats in NOTCH2NLC via CRISPR/Cas9 for treating neuronal intranuclear inclusion diseaseNina Xie, Yongcheng Pan, Huichun Tong, et al.
Frontiers in Neuroscience|May 13, 2021
Gene4PD: A Comprehensive Genetic Database of Parkinson's DiseaseBin Li, Guihu Zhao, Qiao Zhou, et al.
Cell Reports|August 1, 2019
Distinct Connectivity and Functionality of Aldehyde Dehydrogenase 1a1-Positive Nigrostriatal Dopaminergic Neurons in Motor LearningJunbing Wu, Justin Kung, Jie Dong, et al.
Brain : a Journal of Neurology|March 24, 2017
Ubiquitin-related network underlain by (CAG)n loci modulate age at onset in Machado-Joseph diseaseZhao Chen, Chunrong Wang, Caifa Zheng, et al.
European Journal of Neurology|July 13, 2021
Genotype and phenotype distribution of 435 patients with Charcot-Marie-Tooth disease from central south ChinaYongzhi Xie, Zhiqiang Lin, Lei Liu, et al.
Neurology|August 21, 2020
Association of serum neurofilament light and disease severity in patients with spinocerebellar ataxia type 3Yun Peng, Youming Zhang, Zhao Chen, et al.
Pageof 52