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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
August 8, 2007
[Mutation detection of parkin gene by denaturing high performance liquid chromatography]
Jing Li, Bei-sha Tang, Ji-feng Guo, et al.
NPJ Parkinson'S Disease
|
July 23, 2024
High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson's disease
Chaodong Wang, Hankui Liu, Xu-Ying Li, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences
|
February 19, 2005
Mutation screening of Cx32 in Han Chinese patients with Charcot-Marie-Tooth disease
Ru-xu Zhang, Wei Luo, Xiao-hong Zi, et al.
Chinese Medical Journal
|
September 29, 2009
Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Chinese Han patients with hereditary spastic paraplegia
Juan Du, Lu Shen, Guo-hua Zhao, et al.
Journal of the Neurological Sciences
|
December 12, 2013
Hypomethylation of SNCA in blood of patients with sporadic Parkinson's disease
San-xi Ai, Qian Xu, Ya-cen Hu, et al.
CNS Neuroscience & Therapeutics
|
January 3, 2013
Simvastatin induces neuroprotection in 6-OHDA-lesioned PC12 via the PI3K/AKT/caspase 3 pathway and anti-inflammatory responses
Yun-Qi Xu, Ling Long, Jun-Qiang Yan, et al.
Neuroscience Letters
|
March 13, 2012
Lower serum UA levels in Parkinson's disease patients in the Chinese population
Hai-nan Zhang, Ji-feng Guo, Dan He, et al.
Biochemical and Biophysical Research Communications
|
December 5, 2012
Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis
Wen-Juan Guan, Jun-Ling Wang, Yu-Tao Liu, et al.
Frontiers in Cellular Neuroscience
|
September 27, 2013
C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China
Bin Jiao, Ji-Feng Guo, Ya-Qin Wang, et al.
Scientific Reports
|
October 4, 2016
RAB39B gene mutations are not linked to familial Parkinson's disease in China
Ji-Feng Kang, Yang Luo, Bei-Sha Tang, et al.
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Showing results (141-150 of 236) with videos related to
Sort By:
Page
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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
August 8, 2007
[Mutation detection of parkin gene by denaturing high performance liquid chromatography]
Jing Li, Bei-sha Tang, Ji-feng Guo, et al.
NPJ Parkinson'S Disease
|
July 23, 2024
High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson's disease
Chaodong Wang, Hankui Liu, Xu-Ying Li, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences
|
February 19, 2005
Mutation screening of Cx32 in Han Chinese patients with Charcot-Marie-Tooth disease
Ru-xu Zhang, Wei Luo, Xiao-hong Zi, et al.
Chinese Medical Journal
|
September 29, 2009
Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Chinese Han patients with hereditary spastic paraplegia
Juan Du, Lu Shen, Guo-hua Zhao, et al.
Journal of the Neurological Sciences
|
December 12, 2013
Hypomethylation of SNCA in blood of patients with sporadic Parkinson's disease
San-xi Ai, Qian Xu, Ya-cen Hu, et al.
CNS Neuroscience & Therapeutics
|
January 3, 2013
Simvastatin induces neuroprotection in 6-OHDA-lesioned PC12 via the PI3K/AKT/caspase 3 pathway and anti-inflammatory responses
Yun-Qi Xu, Ling Long, Jun-Qiang Yan, et al.
Neuroscience Letters
|
March 13, 2012
Lower serum UA levels in Parkinson's disease patients in the Chinese population
Hai-nan Zhang, Ji-feng Guo, Dan He, et al.
Biochemical and Biophysical Research Communications
|
December 5, 2012
Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis
Wen-Juan Guan, Jun-Ling Wang, Yu-Tao Liu, et al.
Frontiers in Cellular Neuroscience
|
September 27, 2013
C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China
Bin Jiao, Ji-Feng Guo, Ya-Qin Wang, et al.
Scientific Reports
|
October 4, 2016
RAB39B gene mutations are not linked to familial Parkinson's disease in China
Ji-Feng Kang, Yang Luo, Bei-Sha Tang, et al.
Page
of 24