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Beisha Tang

Showing results (491-500 of 515) with videos related to

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Neurology|April 24, 2021
New Model for Estimation of the Age at Onset in Spinocerebellar Ataxia Type 3Linliu Peng, Zhao Chen, Zhe Long, et al.
Frontiers in Aging Neuroscience|July 22, 2022
The Natural History of Spinocerebellar Ataxia Type 3 in Mainland China: A 2-Year Cohort StudyYun Peng, Linliu Peng, Zhao Chen, et al.
Acta Neuropathologica|February 18, 2021
ATP10B variants in Parkinson's disease: a large cohort study in Chinese mainland populationYuwen Zhao, Hongxu Pan, Yige Wang, et al.
Plos One|December 7, 2013
Identification of CHIP as a novel causative gene for autosomal recessive cerebellar ataxiaYuting Shi, Junling Wang, Jia-Da Li, et al.
Computational and Structural Biotechnology Journal|April 19, 2021
GPCards: An integrated database of genotype-phenotype correlations in human genetic diseasesBin Li, Zheng Wang, Qian Chen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 6, 2023
Synaptic Loss in Spinocerebellar Ataxia Type 3 Revealed by SV2A Positron Emission TomographyZhao Chen, Guang Liao, Na Wan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2020
Prediction of the Age at Onset of Spinocerebellar Ataxia Type 3 with Machine LearningLinliu Peng, Zhao Chen, Tiankai Chen, et al.
Science Advances|June 17, 2026
Haplotype-resolved methylomes reveal parent-of-origin DNA methylation imbalance in autism spectrum disorderLu Xia, Hailiang Guo, Ruiting Liu, et al.
Aging and Disease|May 10, 2023
Age and Sex Affect Essential Tremor (ET) Plus: Clinical Heterogeneity in ET Based on the National Survey in ChinaQiying Sun, Runcheng He, Hongyan Huang, et al.
Human Genetics|October 13, 2020
Biallelic loss-of-function variants in NEMF cause central nervous system impairment and axonal polyneuropathyAshfaque Ahmed, Meng Wang, Gaber Bergant, et al.
Pageof 52

Showing results (491-500 of 515) with videos related to

Sort By:
Pageof 52
Neurology|April 24, 2021
New Model for Estimation of the Age at Onset in Spinocerebellar Ataxia Type 3Linliu Peng, Zhao Chen, Zhe Long, et al.
Frontiers in Aging Neuroscience|July 22, 2022
The Natural History of Spinocerebellar Ataxia Type 3 in Mainland China: A 2-Year Cohort StudyYun Peng, Linliu Peng, Zhao Chen, et al.
Acta Neuropathologica|February 18, 2021
ATP10B variants in Parkinson's disease: a large cohort study in Chinese mainland populationYuwen Zhao, Hongxu Pan, Yige Wang, et al.
Plos One|December 7, 2013
Identification of CHIP as a novel causative gene for autosomal recessive cerebellar ataxiaYuting Shi, Junling Wang, Jia-Da Li, et al.
Computational and Structural Biotechnology Journal|April 19, 2021
GPCards: An integrated database of genotype-phenotype correlations in human genetic diseasesBin Li, Zheng Wang, Qian Chen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 6, 2023
Synaptic Loss in Spinocerebellar Ataxia Type 3 Revealed by SV2A Positron Emission TomographyZhao Chen, Guang Liao, Na Wan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2020
Prediction of the Age at Onset of Spinocerebellar Ataxia Type 3 with Machine LearningLinliu Peng, Zhao Chen, Tiankai Chen, et al.
Science Advances|June 17, 2026
Haplotype-resolved methylomes reveal parent-of-origin DNA methylation imbalance in autism spectrum disorderLu Xia, Hailiang Guo, Ruiting Liu, et al.
Aging and Disease|May 10, 2023
Age and Sex Affect Essential Tremor (ET) Plus: Clinical Heterogeneity in ET Based on the National Survey in ChinaQiying Sun, Runcheng He, Hongyan Huang, et al.
Human Genetics|October 13, 2020
Biallelic loss-of-function variants in NEMF cause central nervous system impairment and axonal polyneuropathyAshfaque Ahmed, Meng Wang, Gaber Bergant, et al.
Pageof 52