Lv11
40 积分 2024-04-16 加入
Biallelic loss-of-function ZFYVE19 mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasis
4小时前
已完结
Gene therapy for liver diseases — progress and challenges
9天前
已完结
Clinical Features, Diagnosis, and Treatment of Congenital and Neonatal Tuberculosis: A Retrospective Study
13天前
已完结
A LIMA1 variant promotes low plasma LDL cholesterol and decreases intestinal cholesterol absorption
1个月前
已完结
Combining Panel-Based Next-Generation Sequencing and Exome Sequencing for Genetic Liver Diseases
1个月前
已完结
Large Scale Genomic Investigation of Pediatric Cholestasis Reveals a Novel Hepatorenal Ciliopathy Caused by PSKH1 Mutations
1个月前
已完结
Unexplained cholestasis in adults and adolescents: diagnostic benefit of genetic examination
1个月前
已完结
MGA loss-of-function variants cause premature ovarian insufficiency
1个月前
已完结
Bile acids and the gut microbiota: metabolic interactions and impacts on disease
1个月前
已完结
Direct Reprogramming of Human Fibroblasts to Functional and Expandable Hepatocytes
1个月前
已完结
皖公网安备34019202002308
