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Gene
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August 19, 2015
MMACHC gene mutation in familial hypogonadism with neurological symptoms
Changhe Shi, Dandan Shang, Shilei Sun, et al.
Frontiers in Neurology
|
April 26, 2021
Analysis of 12 GWAS-Linked Loci With Parkinson's Disease in the Chinese Han Population
Liyuan Fan, Changhe Shi, Xinchao Hu, et al.
Molecular Biology Reports
|
June 12, 2017
CADASIL mutant NOTCH3(R90C) decreases the viability of HS683 oligodendrocytes via apoptosis
Mibo Tang, Changhe Shi, Bo Song, et al.
Frontiers in Neuroscience
|
June 3, 2026
Genetic and clinical investigation of insulin-degrading enzyme in Parkinson's disease within the Chinese Han population
Huimin Zheng, Yu Guo, Lue Zhou, et al.
Frontiers in Neurology
|
January 31, 2020
New Insights Into the Pathogenesis of Alzheimer's Disease
Liyuan Fan, Chengyuan Mao, Xinchao Hu, et al.
Gene
|
March 22, 2015
A novel compound WISP3 mutation in a Chinese family with progressive pseudorheumatoid dysplasia
Haiyang Luo, Changhe Shi, Chengyuan Mao, et al.
Stem Cell Research
|
February 7, 2021
Generation of an induced pluripotent stem cell line (ZZUi022-A) from a paroxysmal kinesigenic dyskinesia individual carrying the PRRT2 gene mutation
Liyuan Fan, Chengyuan Mao, Changhe Shi, et al.
The Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry
|
July 31, 2020
α-Synuclein in Parkinson's Disease: Does a Prion-Like Mechanism of Propagation from Periphery to the Brain Play a Role?
Huimin Zheng, Changhe Shi, Haiyang Luo, et al.
Frontiers in Neurology
|
September 8, 2025
Correction: Peripheral cutaneous synucleinopathy characteristics in genetic Parkinson's disease
Yanpeng Yuan, Yangyang Wang, Minglei Liu, et al.
NPJ Parkinson'S Disease
|
October 20, 2024
Human midbrain organoids: a powerful tool for advanced Parkinson's disease modeling and therapy exploration
Xin Cui, Xinwei Li, Huimin Zheng, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 53) with videos related to
Sort By:
Page
of 6
Gene
|
August 19, 2015
MMACHC gene mutation in familial hypogonadism with neurological symptoms
Changhe Shi, Dandan Shang, Shilei Sun, et al.
Frontiers in Neurology
|
April 26, 2021
Analysis of 12 GWAS-Linked Loci With Parkinson's Disease in the Chinese Han Population
Liyuan Fan, Changhe Shi, Xinchao Hu, et al.
Molecular Biology Reports
|
June 12, 2017
CADASIL mutant NOTCH3(R90C) decreases the viability of HS683 oligodendrocytes via apoptosis
Mibo Tang, Changhe Shi, Bo Song, et al.
Frontiers in Neuroscience
|
June 3, 2026
Genetic and clinical investigation of insulin-degrading enzyme in Parkinson's disease within the Chinese Han population
Huimin Zheng, Yu Guo, Lue Zhou, et al.
Frontiers in Neurology
|
January 31, 2020
New Insights Into the Pathogenesis of Alzheimer's Disease
Liyuan Fan, Chengyuan Mao, Xinchao Hu, et al.
Gene
|
March 22, 2015
A novel compound WISP3 mutation in a Chinese family with progressive pseudorheumatoid dysplasia
Haiyang Luo, Changhe Shi, Chengyuan Mao, et al.
Stem Cell Research
|
February 7, 2021
Generation of an induced pluripotent stem cell line (ZZUi022-A) from a paroxysmal kinesigenic dyskinesia individual carrying the PRRT2 gene mutation
Liyuan Fan, Chengyuan Mao, Changhe Shi, et al.
The Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry
|
July 31, 2020
α-Synuclein in Parkinson's Disease: Does a Prion-Like Mechanism of Propagation from Periphery to the Brain Play a Role?
Huimin Zheng, Changhe Shi, Haiyang Luo, et al.
Frontiers in Neurology
|
September 8, 2025
Correction: Peripheral cutaneous synucleinopathy characteristics in genetic Parkinson's disease
Yanpeng Yuan, Yangyang Wang, Minglei Liu, et al.
NPJ Parkinson'S Disease
|
October 20, 2024
Human midbrain organoids: a powerful tool for advanced Parkinson's disease modeling and therapy exploration
Xin Cui, Xinwei Li, Huimin Zheng, et al.
Page
of 6