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Beisha Tang

Showing results (191-200 of 514) with videos related to

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Frontiers in Neuroscience|April 25, 2022
Association Study of <i>TAF1</i> Variants in Parkinson's DiseaseQian Zeng, Hongxu Pan, Yuwen Zhao, et al.
Neurobiology of Aging|May 29, 2014
Investigation of TREM2, PLD3, and UNC5C variants in patients with Alzheimer's disease from mainland ChinaBin Jiao, Xiaoyan Liu, Beisha Tang, et al.
Cerebellum (London, England)|April 15, 2015
High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease ProgressionYuting Shi, Chunrong Wang, Fengzhen Huang, et al.
Journal of Alzheimer'S Disease : JAD|August 6, 2025
Immune system-associated genes in patients with Alzheimer's diseaseRui Yao, Ziyu Ouyang, Tianyan Xu, et al.
Neurobiology of Aging|June 18, 2016
Analyses MAPT, GRN, and C9orf72 mutations in Chinese patients with frontotemporal dementiaMin Tang, Xiaohua Gu, Jingya Wei, et al.
Annals of Clinical and Translational Neurology|July 21, 2023
Microdeletion in distal PLP1 enhancers causes hereditary spastic paraplegia 2Xun Zhou, Yige Wang, Runcheng He, et al.
Journal of Neurology|July 11, 2023
Efficacy of cerebellar transcranial magnetic stimulation in spinocerebellar ataxia type 3: a randomized, single-blinded, controlled trialYuting Shi, Guangdong Zou, Zhao Chen, et al.
Neurology|June 17, 2015
A SIGMAR1 splice-site mutation causes distal hereditary motor neuropathyXiaobo Li, Zhengmao Hu, Lei Liu, et al.
Neurobiology of Aging|May 7, 2020
Genetic analysis of N6-methyladenosine modification genes in Parkinson's diseaseLixia Qin, Shishi Min, Li Shu, et al.
Epigenomics|May 31, 2019
Identification of a potential exosomal biomarker in spinocerebellar ataxia Type 3/Machado-Joseph diseaseXiaocan Hou, Xuan Gong, Longbo Zhang, et al.
Pageof 52

Showing results (191-200 of 514) with videos related to

Sort By:
Pageof 52
Frontiers in Neuroscience|April 25, 2022
Association Study of <i>TAF1</i> Variants in Parkinson's DiseaseQian Zeng, Hongxu Pan, Yuwen Zhao, et al.
Neurobiology of Aging|May 29, 2014
Investigation of TREM2, PLD3, and UNC5C variants in patients with Alzheimer's disease from mainland ChinaBin Jiao, Xiaoyan Liu, Beisha Tang, et al.
Cerebellum (London, England)|April 15, 2015
High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease ProgressionYuting Shi, Chunrong Wang, Fengzhen Huang, et al.
Journal of Alzheimer'S Disease : JAD|August 6, 2025
Immune system-associated genes in patients with Alzheimer's diseaseRui Yao, Ziyu Ouyang, Tianyan Xu, et al.
Neurobiology of Aging|June 18, 2016
Analyses MAPT, GRN, and C9orf72 mutations in Chinese patients with frontotemporal dementiaMin Tang, Xiaohua Gu, Jingya Wei, et al.
Annals of Clinical and Translational Neurology|July 21, 2023
Microdeletion in distal PLP1 enhancers causes hereditary spastic paraplegia 2Xun Zhou, Yige Wang, Runcheng He, et al.
Journal of Neurology|July 11, 2023
Efficacy of cerebellar transcranial magnetic stimulation in spinocerebellar ataxia type 3: a randomized, single-blinded, controlled trialYuting Shi, Guangdong Zou, Zhao Chen, et al.
Neurology|June 17, 2015
A SIGMAR1 splice-site mutation causes distal hereditary motor neuropathyXiaobo Li, Zhengmao Hu, Lei Liu, et al.
Neurobiology of Aging|May 7, 2020
Genetic analysis of N6-methyladenosine modification genes in Parkinson's diseaseLixia Qin, Shishi Min, Li Shu, et al.
Epigenomics|May 31, 2019
Identification of a potential exosomal biomarker in spinocerebellar ataxia Type 3/Machado-Joseph diseaseXiaocan Hou, Xuan Gong, Longbo Zhang, et al.
Pageof 52