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Frontiers in Neurology
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March 3, 2020
Corrigendum: Gene-Related Cerebellar Neurodegeneration in SCA3/MJD: A Case-Controlled Imaging-Genetic Study
Huirong Peng, Xiaochun Liang, Zhe Long, et al.
Neurobiology of Aging
|
August 10, 2020
No genetic evidence for the involvement of GGC repeat expansions of the NOTCH2NLC gene in Chinese patients with multiple system atrophy
Keqin Xu, Linlin Wan, Zhao Chen, et al.
Scientific Reports
|
February 6, 2016
Identification of a de novo DYNC1H1 mutation via WES according to published guidelines
Dongxue Ding, Zhao Chen, Kai Li, et al.
Journal of the Peripheral Nervous System : JPNS
|
January 24, 2016
MFN2-related genetic and clinical features in a cohort of Chinese CMT2 patients
Yongzhi Xie, Xiaobo Li, Lei Liu, et al.
Plos One
|
October 7, 2015
Targeted Next-Generation Sequencing Revealed Novel Mutations in Chinese Ataxia Telangiectasia Patients: A Precision Medicine Perspective
Zhao Chen, Wei Ye, Zhe Long, et al.
Cellular and Molecular Life Sciences : CMLS
|
April 7, 2025
Loss of NgBR causes neuronal damage through decreasing KAT7-mediated RFX1 acetylation and FGF1 expression
Yuwei Hu, Yanni Ma, Lele Liu, et al.
Neuroscience Letters
|
May 15, 2012
Spinocerebellar ataxia type 27 (SCA27) is an uncommon cause of dominant ataxia among Chinese Han population
Zhao Chen, Xiaohui Li, Beisha Tang, et al.
Journal of the Peripheral Nervous System : JPNS
|
September 14, 2013
Two novel MPZ mutations in Chinese CMT patients
Lei Liu, Xiaobo Li, Xiaohong Zi, et al.
Human Molecular Genetics
|
March 22, 2021
Downregulation of TOP2 modulates neurodegeneration caused by GGGGCC expanded repeats
Bin Jiao, Mengli Wang, Hao Feng, et al.
Frontiers in Aging Neuroscience
|
November 3, 2022
The effect of regional white matter hyperintensities on essential tremor subtypes and severity
Runcheng He, Yan Qin, Xun Zhou, et al.
Page
of 52
Search research articles
Search
Showing results (181-190 of 514) with videos related to
Sort By:
Page
of 52
Frontiers in Neurology
|
March 3, 2020
Corrigendum: Gene-Related Cerebellar Neurodegeneration in SCA3/MJD: A Case-Controlled Imaging-Genetic Study
Huirong Peng, Xiaochun Liang, Zhe Long, et al.
Neurobiology of Aging
|
August 10, 2020
No genetic evidence for the involvement of GGC repeat expansions of the NOTCH2NLC gene in Chinese patients with multiple system atrophy
Keqin Xu, Linlin Wan, Zhao Chen, et al.
Scientific Reports
|
February 6, 2016
Identification of a de novo DYNC1H1 mutation via WES according to published guidelines
Dongxue Ding, Zhao Chen, Kai Li, et al.
Journal of the Peripheral Nervous System : JPNS
|
January 24, 2016
MFN2-related genetic and clinical features in a cohort of Chinese CMT2 patients
Yongzhi Xie, Xiaobo Li, Lei Liu, et al.
Plos One
|
October 7, 2015
Targeted Next-Generation Sequencing Revealed Novel Mutations in Chinese Ataxia Telangiectasia Patients: A Precision Medicine Perspective
Zhao Chen, Wei Ye, Zhe Long, et al.
Cellular and Molecular Life Sciences : CMLS
|
April 7, 2025
Loss of NgBR causes neuronal damage through decreasing KAT7-mediated RFX1 acetylation and FGF1 expression
Yuwei Hu, Yanni Ma, Lele Liu, et al.
Neuroscience Letters
|
May 15, 2012
Spinocerebellar ataxia type 27 (SCA27) is an uncommon cause of dominant ataxia among Chinese Han population
Zhao Chen, Xiaohui Li, Beisha Tang, et al.
Journal of the Peripheral Nervous System : JPNS
|
September 14, 2013
Two novel MPZ mutations in Chinese CMT patients
Lei Liu, Xiaobo Li, Xiaohong Zi, et al.
Human Molecular Genetics
|
March 22, 2021
Downregulation of TOP2 modulates neurodegeneration caused by GGGGCC expanded repeats
Bin Jiao, Mengli Wang, Hao Feng, et al.
Frontiers in Aging Neuroscience
|
November 3, 2022
The effect of regional white matter hyperintensities on essential tremor subtypes and severity
Runcheng He, Yan Qin, Xun Zhou, et al.
Page
of 52