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Beisha Tang

Showing results (351-360 of 514) with videos related to

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Plos One|February 18, 2015
Two novel SNPs in ATXN3 3' UTR may decrease age at onset of SCA3/MJD in Chinese patientsZhe Long, Zhao Chen, Chunrong Wang, et al.
Frontiers in Neurology|June 26, 2020
The Discriminative Power of Different Olfactory Domains in Parkinson's DiseaseYuwen Zhao, Yan He, Runcheng He, et al.
Genes & Genomics|March 30, 2022
Coffin-Siris syndrome in two chinese patients with novel pathogenic variants of ARID1A and SMARCA4Mingjie Liu, Linlin Wan, Chunrong Wang, et al.
Frontiers in Neuroscience|April 19, 2021
Characterizing the Expression Patterns of Parkinson's Disease Associated GenesBin Li, Guihu Zhao, Kuokuo Li, et al.
Neuro-Degenerative Diseases|October 25, 2014
Mutation and clinical characteristics of autosomal-dominant hereditary spastic paraplegias in ChinaYingying Luo, Chong Chen, Zixiong Zhan, et al.
Frontiers in Genetics|March 8, 2019
Is the High Frequency of Machado-Joseph Disease in China Due to New Mutational Origins?Tianjiao Li, Sandra Martins, Yun Peng, et al.
Annals of Clinical and Translational Neurology|June 26, 2024
The characteristic and biomarker value of transcranial sonography in cerebellar ataxiaSudan Zhu, Yuting Shi, Zhao Chen, et al.
Frontiers in Neurology|July 12, 2021
Evaluation of Peripheral Immune Activation in Amyotrophic Lateral SclerosisMengli Wang, Zhen Liu, Juan Du, et al.
Mechanisms of Ageing and Development|May 16, 2024
Comprehensive variant analysis of phospholipase A2 superfamily genes in large Chinese Parkinson' s disease cohortsJiabin Liu, Yige Wang, Yuwen Zhao, et al.
Pharmacological Research|January 18, 2026
Impaired PARP1-Dependent DNA Repair in MORC2 Mutations Drives Axonal Degeneration in Charcot-Marie-Tooth Disease Subtype 2Z and Spinal Muscular Atrophy-Like Neuromotor disordersMengli Wang, Honglan Yang, Zhongzheng Li, et al.
Pageof 52

Showing results (351-360 of 514) with videos related to

Sort By:
Pageof 52
Plos One|February 18, 2015
Two novel SNPs in ATXN3 3' UTR may decrease age at onset of SCA3/MJD in Chinese patientsZhe Long, Zhao Chen, Chunrong Wang, et al.
Frontiers in Neurology|June 26, 2020
The Discriminative Power of Different Olfactory Domains in Parkinson's DiseaseYuwen Zhao, Yan He, Runcheng He, et al.
Genes & Genomics|March 30, 2022
Coffin-Siris syndrome in two chinese patients with novel pathogenic variants of ARID1A and SMARCA4Mingjie Liu, Linlin Wan, Chunrong Wang, et al.
Frontiers in Neuroscience|April 19, 2021
Characterizing the Expression Patterns of Parkinson's Disease Associated GenesBin Li, Guihu Zhao, Kuokuo Li, et al.
Neuro-Degenerative Diseases|October 25, 2014
Mutation and clinical characteristics of autosomal-dominant hereditary spastic paraplegias in ChinaYingying Luo, Chong Chen, Zixiong Zhan, et al.
Frontiers in Genetics|March 8, 2019
Is the High Frequency of Machado-Joseph Disease in China Due to New Mutational Origins?Tianjiao Li, Sandra Martins, Yun Peng, et al.
Annals of Clinical and Translational Neurology|June 26, 2024
The characteristic and biomarker value of transcranial sonography in cerebellar ataxiaSudan Zhu, Yuting Shi, Zhao Chen, et al.
Frontiers in Neurology|July 12, 2021
Evaluation of Peripheral Immune Activation in Amyotrophic Lateral SclerosisMengli Wang, Zhen Liu, Juan Du, et al.
Mechanisms of Ageing and Development|May 16, 2024
Comprehensive variant analysis of phospholipase A2 superfamily genes in large Chinese Parkinson' s disease cohortsJiabin Liu, Yige Wang, Yuwen Zhao, et al.
Pharmacological Research|January 18, 2026
Impaired PARP1-Dependent DNA Repair in MORC2 Mutations Drives Axonal Degeneration in Charcot-Marie-Tooth Disease Subtype 2Z and Spinal Muscular Atrophy-Like Neuromotor disordersMengli Wang, Honglan Yang, Zhongzheng Li, et al.
Pageof 52