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Journal of Medical Genetics|August 2, 2020
Biallelic loss-of-function ZFYVE19 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.Liver International : Official Journal of the International Association for the Study of the Liver|February 8, 2018
Comprehensive bile acid profiling in hereditary intrahepatic cholestasis: Genetic and clinical correlationsTeng Liu, Ren-Xue Wang, Jun Han, 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.Pageof 3