Jian-guang Tang

发表

Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasia

K. Xia, Q. Pan, H. Dai, 2006, Journal of the Neurological Sciences.

SUMO-1 Modification on K166 of PolyQ-Expanded aTaxin-3 Strengthens Its Stability and Increases Its Cytotoxicity

K. Xia, B. Tang, Juan Du, 2013, PloS one.

The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China

Huidong Tang, S. Chen, Wotu Tian, 2020, Movement disorders : official journal of the Movement Disorder Society.

The Study of The Interaction Between Parkin and OGCP*: The Study of The Interaction Between Parkin and OGCP*

B. Tang, Ji-feng Guo, Xinxiang Yan, 2010 .

Genetic variations of Omi/HTRA2 in Chinese patients with Parkinson's disease

B. Tang, Ji-feng Guo, Xinxiang Yan, 2011, Brain Research.

TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large‐Sample Study

B. Tang, Qing Liu, Wotu Tian, 2021, Movement disorders : official journal of the Movement Disorder Society.

BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage

B. Tang, Ji-feng Guo, Jiahong Lu, 2017, Oxidative medicine and cellular longevity.

Case Report: Mutant SCN9A Susceptible to Charcot Neuroarthropathy in a Patient With Congenital Insensitivity to Pain

Xiaohui Xie, Jian-guang Tang, Yi-qiao Hu, 2021, Frontiers in Neuroscience.

Preliminary Study of hsa-mir-626 Change in the Cerebrospinal Fluid in Parkinson's Disease.

B. Tang, Ji-feng Guo, Jian-guang Tang, 2021, Neurology India.

Preliminary study of hsa-miR-626 change in the cerebrospinal fluid of Parkinson’s disease patients

Jian-guang Tang, Jie-qiong Tan, Hai-nan Zhang, 2019, Journal of Clinical Neuroscience.

Identification of the core promoter of STK11 gene and its transcriptional regulation by p53

X. Yi, Hongwei Shen, Jian-guang Tang, 2008 .

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24

K. Xia, Q. Pan, H. Dai, 2004, Human Genetics.

Expression and immunogenicity of hepatitis E virus-like particles based on recombinant truncated ORF2 capsid protein.

Xinping Wang, Jian-guang Tang, Yuemin Cao, 2022, Protein expression and purification.

Mutation spectrum of amyotrophic lateral sclerosis in Central South China

B. Tang, Ling Huang, Hong Jiang, 2021, Neurobiology of Aging.

A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Jian-guang Tang, Hui Zeng, Yi-feng Yang, 2017, Cytogenetic and Genome Research.

[Frequency analysis of autosomal dominant spinocerebellar ataxias in Han population in the Chinese mainland and clinical and molecular characterization of spinocerebellar ataxia type 6].

K. Xia, B. Tang, Hong Jiang, 2005, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

[Studies on PANK2 gene mutations in Chinese patients with Hallervorden-Spatz syndrome].

K. Xia, Q. Pan, Zhengmao Hu, 2005, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Mitochondrial genome variations are associated with amyotrophic lateral sclerosis in patients from mainland China

Mingyu Liang, B. Tang, Hong Jiang, 2021, Journal of Neurology.

Research on screening and identification of proteins interacting with ataxin-3.

K. Xia, Q. Pan, B. Tang, 2005, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Jian-guang Tang, Hui Zeng, Yi-feng Yang, 2017, Cytogenetic and Genome Research.