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Hepatology (Baltimore, Md.)|March 19, 2026
Liver transcriptome sequencing contributes to the molecular diagnosis of genetic liver diseasesYe Cheng, Zhong-Die Li, Zhi-Hong Guan, et al.World Journal of Gastroenterology|September 27, 2018
Infant cholestasis patient with a novel missense mutation in the AKR1D1 gene successfully treated by early adequate supplementation with chenodeoxycholic acid: A case report and review of the literatureHui-Hui Wang, Fei-Qiu Wen, Dong-Ling Dai, et al.Liver International : Official Journal of the International Association for the Study of the Liver|November 23, 2021
MYO5B-associated diseases: Novel liver-related variants and genotype-phenotype correlationLi Wang, Yi-Ling Qiu, Hong-Mei Xu, et al.The Journal of Biological Chemistry|June 16, 2019
Increased sulfation of bile acids in mice and human subjects with sodium taurocholate cotransporting polypeptide deficiencyFengfeng Mao, Teng Liu, Xinfeng Hou, et al.Cancer Biomarkers : Section a of Disease Markers|December 11, 2023
A new immune-related gene signature predicts the prognosis and immune escape of bladder cancerYang Liu, Yan-Song Han, Jin-Feng Wang, et al.Hepatology (Baltimore, Md.)|November 22, 2019
A Molecular Mechanism Underlying Genotype-Specific Intrahepatic Cholestasis Resulting From MYO5B MutationsArend W Overeem, Qinghong Li, Yi-Ling Qiu, et al.Journal of Cellular Physiology|May 27, 2022
Association of novel TMEM67 variants with mild phenotypes of high gamma-glutamyl transpeptidase cholestasis and congenital hepatic fibrosisYi-Ling Qiu, Li Wang, Min Huang, et al.Scientific Reports|November 15, 2018
Serum Golgi protein 73 is a marker comparable to APRI for diagnosing significant fibrosis in children with liver diseaseLangli Liu, Jianwen Wang, Jiayan Feng, et al.Plos One|October 6, 2016
A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/DeletionsNeng-Li Wang, Yu-Lan Lu, Ping Zhang, et al.Liver International : Official Journal of the International Association for the Study of the Liver|March 4, 2020
Low-GGT intrahepatic cholestasis associated with biallelic USP53 variants: Clinical, histological and ultrastructural characterizationJing Zhang, Ye Yang, Jing-Yu Gong, et al.Pageof 13