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American Journal of Human Genetics|June 20, 2003
A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2Qing-he Xing, Ming-tai Wang, Xiang-dong Chen, et al.Basic & Clinical Pharmacology & Toxicology|March 26, 2018
HLA-A*02:07 Allele Associates with Clarithromycin-Induced Cutaneous Adverse Drug Reactions in Chinese PatientsSheng-An Chen, Li-Rong Zhang, Fan-Ping Yang, et al.Human Mutation|November 8, 2019
TJP2 hepatobiliary disorders: Novel variants and clinical diversityJing Zhang, Lang-Li Liu, Jing-Yu Gong, et al.Neuroscience Letters|February 9, 2007
Response of risperidone treatment may be associated with polymorphisms of HTT gene in Chinese schizophrenia patientsLei Wang, Lan Yu, Guang He, et al.Pharmacogenomics|August 23, 2012
HLA-B*58:01 allele is associated with augmented risk for both mild and severe cutaneous adverse reactions induced by allopurinol in Han ChineseZhi-hao Cao, Zhi-yun Wei, Qin-yuan Zhu, et al.European Archives of Psychiatry and Clinical Neuroscience|December 20, 2005
An association study between the transthyretin (TTR) gene and mental retardationJun Li, Jian-Jun Gao, Fu-Chang Zhang, et al.Journal of Medical Genetics|August 2, 2020
Biallelic loss-of-function <i>ZFYVE19</i> mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasisWeisha Luan, Chen-Zhi Hao, Jia-Qi Li, et al.Hepatology (Baltimore, Md.)|August 19, 2025
A novel mechanism involving USP53-regulated BSEP trafficking underlies low-GGT intrahepatic cholestasisJian Ding, Hui-Yu She, Ye Cheng, et al.Hepatology (Baltimore, Md.)|December 28, 2016
Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ-glutamyltransferase cholestasisYi-Ling Qiu, Jing-Yu Gong, Jia-Yan Feng, et al.Innovation (Cambridge (Mass.))|February 24, 2025
The pharmacogenomic landscape in the Chinese: An analytics of pharmacogenetic variants in 206,640 individualsLei-Yun Wang, Bing Yu, Ying Peng, et al.Pageof 3