H
Hong Jiang
Researcher at Central South University
Publications - 393
Citations - 23057
Hong Jiang is an academic researcher from Central South University. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 51, co-authored 280 publications receiving 18722 citations. Previous affiliations of Hong Jiang include University of Texas at Austin & City University of New York.
Papers
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Journal ArticleDOI
The Role of Glutamine and Glutaminase in Pulmonary Hypertension
Shang Wang,Yi Yan,Weifang Xu,Su-Gang Gong,Xiu-jun Zhong,Q Y An,Ya-Lin Zhao,Jin-Ming Liu,Lan Wang,Ping Yuan,Hong Jiang +10 more
TL;DR: This review aims to explore the special linking among glutamine hydrolysis, glutaminase and PH, so as to provide theoretical basis for clinical precision treatment in PH.
Journal ArticleDOI
Spinocerebellar ataxia type 27 (SCA27) is an uncommon cause of dominant ataxia among Chinese Han population
Zhao Chen,Xiaohui Li,Beisha Tang,Junling Wang,Yuting Shi,Zhanfang Sun,Li Zhang,Qian Pan,Kun Xia,Hong Jiang +9 more
TL;DR: Interestingly, a pair of siblings carried the same heterozygous variation (c.-10delC) characterized by different clinical features, which suggests that SCA27 is a rare subtype in China, probably a novel insertion/deletion (I/D) polymorphism in the 5'UTR region of the exon 1b.
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UQCRC1 variants in Parkinson's disease: a large cohort study in Chinese mainland population.
Yuwen Zhao,Hongxu Pan,Qian Zeng,Zhenghuan Fang,Zhenhua Liu,Yige Wang,Li Jiang,Runcheng He,Xun Zhou,Yangjie Zhou,Qian Xu,Qiying Sun,Bin Li,Guihu Zhao,Yang Yang,Yacen Hu,Ya-Se Chen,Juan Du,Lifang Lei,Hainan Zhang,Chunyu Wang,Xinxiang Yan,Lu Shen,Hong Jiang,Jinchen Li,Beisha Tang,Jieqiong Tan,Jifeng Guo +27 more
Journal Article
Mutation analysis of small heat-shock protein 22 gene in Chinese patients with Charcot-Marie-Tooth disease.
Xiao-min Liu,Beisha Tang,Guohua Zhao,Kun Xia,Fu-feng Zhang,Qian Pan,Fang Cai,Zhengmao Hu,Cheng Zhang,Biao Chen,Lu Shen,Ruxu Zhang,Hong Jiang +12 more
TL;DR: The rate of HSP22 gene mutation in Chinese patients with CMT is as low as 0.87%(1/115), and a 582(C--> T)(T194T)samesense mutation was found in two unrelated families.
Journal ArticleDOI
TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large-Sample Study
Wo-Tu Tian,Fei-Xia Zhan,Zhenhua Liu,Zhe Liu,Qing Liu,Xia-Nan Guo,Zai-Wei Zhou,Shi-Ge Wang,Xiao-Rong Liu,Hong Jiang,Xun-Hua Li,Guohua Zhao,Hai-Yan Li,Jianguang Tang,Guang-Hui Bi,Ping Zhong,Xiao-Meng Yin,Tao-Tao Liu,Rui-Long Ni,Hao-Ran Zheng,Xiaoli Liu,Xiao-Hang Qian,Jingying Wu,Yuwen Cao,Chao Zhang,Shi-Hua Liu,Ying-Ying Wu,Qun-Feng Wang,Ting Xu,Wen-Zhe Hou,Zi-Yi Li,Hui-Yi Ke,Ze-Yu Zhu,Lan Zheng,Tian Wang,Tian-Yi Rong,Li Wu,Yu Zhang,Kan Fang,Zhan-Hang Wang,Ya-Kun Zhang,Mei Zhang,Yu-Wu Zhao,Beisha Tang,Xing-Hua Luan,Xiao-Jun Huang,Li Cao +46 more
TL;DR: In this paper, Transmembrane Protein 151 (TMEM151A) variants were mainly clustered in sporadic paroxysmal kinesigenic dyskinesia (PKD) patients compared with the control groups.