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Beisha Tang

Showing results (211-220 of 514) with videos related to

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Frontiers in Aging Neuroscience|March 31, 2023
Bidirectional Mendelian randomization study of psychiatric disorders and Parkinson's diseaseQi Wu, Shulin Liu, Xiurong Huang, et al.
Annals of Clinical and Translational Neurology|September 17, 2020
Association of rare variants in neurodegenerative genes with familial Alzheimer's diseaseWeiwei Zhang, Bin Jiao, Tingting Xiao, et al.
Brain Communications|June 12, 2025
Phenotypic and genotypic characterization of familial adult myoclonus epilepsy in a Chinese case seriesSheng Zeng, Yao Zhou, Yuwen Zhao, et al.
Frontiers in Neurology|November 12, 2020
Olfactory Dysfunction and Its Relationship With Clinical Features of Parkinson's DiseaseYangjie Zhou, Runcheng He, Yuwen Zhao, et al.
Neurobiology of Aging|April 6, 2019
Genetic analysis of DNA methylation and hydroxymethylation genes in Parkinson's diseaseLi Shu, Lixia Qin, Shishi Min, et al.
Plos One|January 30, 2014
BAG5 protects against mitochondrial oxidative damage through regulating PINK1 degradationXuejing Wang, Jifeng Guo, Erkang Fei, et al.
Neuroimmunomodulation|November 17, 2012
Serum uric acid in patients with Parkinson's disease and vascular parkinsonism: a cross-sectional studyMengqiu Pan, Huimin Gao, Ling Long, et al.
NPJ Parkinson'S Disease|January 3, 2024
Risk factors associated with age at onset of Parkinson's disease in the UK BiobankYuanfeng Huang, Qian Chen, Zheng Wang, et al.
Neural Regeneration Research|July 25, 2023
The <i>MORC2</i> p.S87L mutation reduces proliferation of pluripotent stem cells derived from a patient with the spinal muscular atrophy-like phenotype by inhibiting proliferation-related signaling pathwaysSen Zeng, Honglan Yang, Binghao Wang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 26, 2025
Assessment of Piezo1 Expression in Urinary Exfoliated Cells as a Diagnostic Indicator for Multiple System AtrophyHan Liu, Qingyong Zhu, Jiuqi Wang, et al.
Pageof 52

Showing results (211-220 of 514) with videos related to

Sort By:
Pageof 52
Frontiers in Aging Neuroscience|March 31, 2023
Bidirectional Mendelian randomization study of psychiatric disorders and Parkinson's diseaseQi Wu, Shulin Liu, Xiurong Huang, et al.
Annals of Clinical and Translational Neurology|September 17, 2020
Association of rare variants in neurodegenerative genes with familial Alzheimer's diseaseWeiwei Zhang, Bin Jiao, Tingting Xiao, et al.
Brain Communications|June 12, 2025
Phenotypic and genotypic characterization of familial adult myoclonus epilepsy in a Chinese case seriesSheng Zeng, Yao Zhou, Yuwen Zhao, et al.
Frontiers in Neurology|November 12, 2020
Olfactory Dysfunction and Its Relationship With Clinical Features of Parkinson's DiseaseYangjie Zhou, Runcheng He, Yuwen Zhao, et al.
Neurobiology of Aging|April 6, 2019
Genetic analysis of DNA methylation and hydroxymethylation genes in Parkinson's diseaseLi Shu, Lixia Qin, Shishi Min, et al.
Plos One|January 30, 2014
BAG5 protects against mitochondrial oxidative damage through regulating PINK1 degradationXuejing Wang, Jifeng Guo, Erkang Fei, et al.
Neuroimmunomodulation|November 17, 2012
Serum uric acid in patients with Parkinson's disease and vascular parkinsonism: a cross-sectional studyMengqiu Pan, Huimin Gao, Ling Long, et al.
NPJ Parkinson'S Disease|January 3, 2024
Risk factors associated with age at onset of Parkinson's disease in the UK BiobankYuanfeng Huang, Qian Chen, Zheng Wang, et al.
Neural Regeneration Research|July 25, 2023
The <i>MORC2</i> p.S87L mutation reduces proliferation of pluripotent stem cells derived from a patient with the spinal muscular atrophy-like phenotype by inhibiting proliferation-related signaling pathwaysSen Zeng, Honglan Yang, Binghao Wang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 26, 2025
Assessment of Piezo1 Expression in Urinary Exfoliated Cells as a Diagnostic Indicator for Multiple System AtrophyHan Liu, Qingyong Zhu, Jiuqi Wang, et al.
Pageof 52