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Beisha Tang

Showing results (221-230 of 514) with videos related to

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Nature Communications|August 24, 2023
Human forebrain organoid-based multi-omics analyses of PCCB as a schizophrenia associated gene linked to GABAergic pathwaysWendiao Zhang, Ming Zhang, Zhenhong Xu, et al.
Frontiers in Neurology|June 30, 2023
Characteristics of autonomic dysfunction in neuronal intranuclear inclusion diseaseLu Zhou, Yun Tian, Sizhe Zhang, et al.
Human Molecular Genetics|June 6, 2022
Altered hydroxymethylome in the substantia nigra of Parkinson's diseaseShishi Min, Qian Xu, Lixia Qin, et al.
Parkinsonism & Related Disorders|September 25, 2010
Genetic analysis of Spinocerebellar ataxia type 17 in Parkinson's disease in Mainland ChinaQian Xu, Dandan Jia, Junling Wang, et al.
Nature Communications|October 26, 2017
DNA N6-methyladenine is dynamically regulated in the mouse brain following environmental stressBing Yao, Ying Cheng, Zhiqin Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 29, 2005
[Studies on PANK2 gene mutations in Chinese patients with Hallervorden-Spatz syndrome]Yuhu Zhang, Beisha Tang, Jifeng Guo, et al.
Parkinsonism & Related Disorders|November 15, 2019
Clinical findings of autosomal-dominant striatal degeneration and PDE8B mutation screening in parkinsonism and related disordersJie Ni, Xiaoping Yi, Zhen Liu, et al.
Parkinsonism & Related Disorders|October 6, 2009
Genetic screening for mutations in the Nrdp1 gene in Parkinson disease patients in a Chinese populationXiaoyun Mo, Deyuan Liu, Wei Li, et al.
Neurobiology of Aging|January 27, 2018
Mutation analysis of the TIA1 gene in Chinese patients with amyotrophic lateral sclerosis and frontotemporal dementiaZhenhua Yuan, Bin Jiao, Lihua Hou, et al.
The International Journal of Neuroscience|December 19, 2017
Association of TNF-α rs1799964 and IL-1β rs16944 polymorphisms with multiple system atrophy in Chinese Han populationXin Zhou, Chunrong Wang, Zhao Chen, et al.
Pageof 52

Showing results (221-230 of 514) with videos related to

Sort By:
Pageof 52
Nature Communications|August 24, 2023
Human forebrain organoid-based multi-omics analyses of PCCB as a schizophrenia associated gene linked to GABAergic pathwaysWendiao Zhang, Ming Zhang, Zhenhong Xu, et al.
Frontiers in Neurology|June 30, 2023
Characteristics of autonomic dysfunction in neuronal intranuclear inclusion diseaseLu Zhou, Yun Tian, Sizhe Zhang, et al.
Human Molecular Genetics|June 6, 2022
Altered hydroxymethylome in the substantia nigra of Parkinson's diseaseShishi Min, Qian Xu, Lixia Qin, et al.
Parkinsonism & Related Disorders|September 25, 2010
Genetic analysis of Spinocerebellar ataxia type 17 in Parkinson's disease in Mainland ChinaQian Xu, Dandan Jia, Junling Wang, et al.
Nature Communications|October 26, 2017
DNA N6-methyladenine is dynamically regulated in the mouse brain following environmental stressBing Yao, Ying Cheng, Zhiqin Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 29, 2005
[Studies on PANK2 gene mutations in Chinese patients with Hallervorden-Spatz syndrome]Yuhu Zhang, Beisha Tang, Jifeng Guo, et al.
Parkinsonism & Related Disorders|November 15, 2019
Clinical findings of autosomal-dominant striatal degeneration and PDE8B mutation screening in parkinsonism and related disordersJie Ni, Xiaoping Yi, Zhen Liu, et al.
Parkinsonism & Related Disorders|October 6, 2009
Genetic screening for mutations in the Nrdp1 gene in Parkinson disease patients in a Chinese populationXiaoyun Mo, Deyuan Liu, Wei Li, et al.
Neurobiology of Aging|January 27, 2018
Mutation analysis of the TIA1 gene in Chinese patients with amyotrophic lateral sclerosis and frontotemporal dementiaZhenhua Yuan, Bin Jiao, Lihua Hou, et al.
The International Journal of Neuroscience|December 19, 2017
Association of TNF-α rs1799964 and IL-1β rs16944 polymorphisms with multiple system atrophy in Chinese Han populationXin Zhou, Chunrong Wang, Zhao Chen, et al.
Pageof 52