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Signal Transduction and Targeted Therapy
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September 10, 2025
Loss-of-function variations in solute carrier family 38 member 6 are associated with essential tremor
Zhangqi Yuan, Qiying Sun, Junyu Luo, et al.
Translational Neurodegeneration
|
July 2, 2016
The recommendations of Chinese Parkinson's disease and movement disorder society consensus on therapeutic management of Parkinson's disease
Shengdi Chen, Piu Chan, Shenggang Sun, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 5, 2026
Nongenetic Factors Associated with Age at Onset and Disease Severity in Spinocerebellar Ataxia Type 3: A Cross-Sectional Cohort Study
Jiawei He, Zhao Chen, Linyi Zeng, et al.
Annals of Neurology
|
September 17, 2020
Biallelic Intronic AAGGG Expansion of RFC1 is Related to Multiple System Atrophy
Linlin Wan, Zhao Chen, Na Wan, et al.
Frontiers in Genetics
|
May 23, 2022
Profiling the Genome-Wide Landscape of Short Tandem Repeats by Long-Read Sequencing
Zhenhua Liu, Guihu Zhao, Yuhui Xiao, et al.
Science Advances
|
November 23, 2022
Expression of expanded GGC repeats within <i>NOTCH2NLC</i> causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease
Qiong Liu, Kailin Zhang, Yunhee Kang, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 26, 2024
Brain eQTLs of European, African American, and Asian ancestry improve interpretation of schizophrenia GWAS
Yu Chen, Sihan Liu, Zongyao Ren, et al.
Neurobiology of Aging
|
February 22, 2020
Identification of expanded repeats in NOTCH2NLC in neurodegenerative dementias
Bin Jiao, Lu Zhou, Yafang Zhou, et al.
American Journal of Human Genetics
|
October 3, 2024
Cross-ancestry analysis of brain QTLs enhances interpretation of schizophrenia genome-wide association studies
Yu Chen, Sihan Liu, Zongyao Ren, et al.
Journal of Medical Genetics
|
June 4, 2014
SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia
Hui Guo, Xuemin Jin, Tengfei Zhu, et al.
Page
of 52
Search research articles
Search
Showing results (481-490 of 515) with videos related to
Sort By:
Page
of 52
Signal Transduction and Targeted Therapy
|
September 10, 2025
Loss-of-function variations in solute carrier family 38 member 6 are associated with essential tremor
Zhangqi Yuan, Qiying Sun, Junyu Luo, et al.
Translational Neurodegeneration
|
July 2, 2016
The recommendations of Chinese Parkinson's disease and movement disorder society consensus on therapeutic management of Parkinson's disease
Shengdi Chen, Piu Chan, Shenggang Sun, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 5, 2026
Nongenetic Factors Associated with Age at Onset and Disease Severity in Spinocerebellar Ataxia Type 3: A Cross-Sectional Cohort Study
Jiawei He, Zhao Chen, Linyi Zeng, et al.
Annals of Neurology
|
September 17, 2020
Biallelic Intronic AAGGG Expansion of RFC1 is Related to Multiple System Atrophy
Linlin Wan, Zhao Chen, Na Wan, et al.
Frontiers in Genetics
|
May 23, 2022
Profiling the Genome-Wide Landscape of Short Tandem Repeats by Long-Read Sequencing
Zhenhua Liu, Guihu Zhao, Yuhui Xiao, et al.
Science Advances
|
November 23, 2022
Expression of expanded GGC repeats within <i>NOTCH2NLC</i> causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease
Qiong Liu, Kailin Zhang, Yunhee Kang, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 26, 2024
Brain eQTLs of European, African American, and Asian ancestry improve interpretation of schizophrenia GWAS
Yu Chen, Sihan Liu, Zongyao Ren, et al.
Neurobiology of Aging
|
February 22, 2020
Identification of expanded repeats in NOTCH2NLC in neurodegenerative dementias
Bin Jiao, Lu Zhou, Yafang Zhou, et al.
American Journal of Human Genetics
|
October 3, 2024
Cross-ancestry analysis of brain QTLs enhances interpretation of schizophrenia genome-wide association studies
Yu Chen, Sihan Liu, Zongyao Ren, et al.
Journal of Medical Genetics
|
June 4, 2014
SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia
Hui Guo, Xuemin Jin, Tengfei Zhu, et al.
Page
of 52