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Beisha Tang

Showing results (401-410 of 514) with videos related to

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The International Journal of Neuroscience|April 9, 2010
Mutation detection in candidate genes for benign familial infantile seizures on a novel locusNan Li, Haiyan Li, Hong Jiang, et al.
Biological Psychiatry|February 6, 2019
MicroRNA-26a/Death-Associated Protein Kinase 1 Signaling Induces Synucleinopathy and Dopaminergic Neuron Degeneration in Parkinson's DiseaseYing Su, Man-Fei Deng, Wan Xiong, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 15, 2026
Interpretable Machine Learning Model for Individualized Survival Prediction of Multiple System AtrophyXiao Dong, Daji Chen, Linlin Wan, et al.
Alzheimer'S Research & Therapy|April 4, 2025
Evaluating the diagnostic performance of six plasma biomarkers for Alzheimer's disease and other neurodegenerative dementias in a large Chinese cohortBin Jiao, Ziyu Ouyang, Yiliang Liu, et al.
NPJ Parkinson'S Disease|May 25, 2022
The macular inner plexiform layer thickness as an early diagnostic indicator for Parkinson's diseaseXin Wang, Bin Jiao, Xiaoliang Jia, et al.
Acta Neuropathologica|March 17, 2023
Mutations in ARHGEF15 cause autosomal dominant hereditary cerebral small vessel disease and osteoporotic fractureXuebing Ding, Yongkang Chen, Cancan Guo, et al.
Nucleic Acids Research|September 30, 2025
Gene4Denovo2: an updated platform for human de novo mutations discovery and interpretationZhaopo Zhu, Pei Yu, Xinxin Mao, et al.
Frontiers in Aging Neuroscience|September 15, 2023
Clinical features of progressive supranuclear palsyYafei Wen, Qijie Yang, Bin Jiao, et al.
BMC Neurology|June 13, 2026
Natural history and 12-month progression of multiple system atrophy in a Chinese cohortTao Feng, Han Wang, Jian Wang, et al.
Epilepsia|July 17, 2018
A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1BHongying Ma, Shenglei Feng, Xuejun Deng, et al.
Pageof 52

Showing results (401-410 of 514) with videos related to

Sort By:
Pageof 52
The International Journal of Neuroscience|April 9, 2010
Mutation detection in candidate genes for benign familial infantile seizures on a novel locusNan Li, Haiyan Li, Hong Jiang, et al.
Biological Psychiatry|February 6, 2019
MicroRNA-26a/Death-Associated Protein Kinase 1 Signaling Induces Synucleinopathy and Dopaminergic Neuron Degeneration in Parkinson's DiseaseYing Su, Man-Fei Deng, Wan Xiong, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 15, 2026
Interpretable Machine Learning Model for Individualized Survival Prediction of Multiple System AtrophyXiao Dong, Daji Chen, Linlin Wan, et al.
Alzheimer'S Research & Therapy|April 4, 2025
Evaluating the diagnostic performance of six plasma biomarkers for Alzheimer's disease and other neurodegenerative dementias in a large Chinese cohortBin Jiao, Ziyu Ouyang, Yiliang Liu, et al.
NPJ Parkinson'S Disease|May 25, 2022
The macular inner plexiform layer thickness as an early diagnostic indicator for Parkinson's diseaseXin Wang, Bin Jiao, Xiaoliang Jia, et al.
Acta Neuropathologica|March 17, 2023
Mutations in ARHGEF15 cause autosomal dominant hereditary cerebral small vessel disease and osteoporotic fractureXuebing Ding, Yongkang Chen, Cancan Guo, et al.
Nucleic Acids Research|September 30, 2025
Gene4Denovo2: an updated platform for human de novo mutations discovery and interpretationZhaopo Zhu, Pei Yu, Xinxin Mao, et al.
Frontiers in Aging Neuroscience|September 15, 2023
Clinical features of progressive supranuclear palsyYafei Wen, Qijie Yang, Bin Jiao, et al.
BMC Neurology|June 13, 2026
Natural history and 12-month progression of multiple system atrophy in a Chinese cohortTao Feng, Han Wang, Jian Wang, et al.
Epilepsia|July 17, 2018
A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1BHongying Ma, Shenglei Feng, Xuejun Deng, et al.
Pageof 52