Chronic cholestatic diseases
- 1 January 2000
- journal article
- review article
- Published by Elsevier in Journal of Hepatology
- Vol. 32, 129-140
- https://doi.org/10.1016/s0168-8278(00)80421-3
Abstract
No abstract availableKeywords
This publication has 104 references indexed in Scilit:
- In situ nucleic acid detection of PDC-E2, BCOADC-E2, OGDC-E2, PDC-E1α, BCOADC-E1α, OGDC-E1,and the E3 binding protein (protein X) in primary biliary cirrhosisHepatology, 1999
- Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1Nature Genetics, 1997
- Ursodiol for Primary Sclerosing CholangitisNew England Journal of Medicine, 1997
- Familial primary biliary cirrhosisJournal of Hepatology, 1994
- Genetic factors in primary biliary cirrhosisJournal of Hepatology, 1994
- The Molecular Genetics of Autoimmune Liver DiseaseHepatology, 1994
- Primary Autoimmune CholangitisThe American Journal of Surgical Pathology, 1994
- T lymphocytes from patients with primary biliary cirrhosis produce reduced amounts of lymphotoxin, tumor necrosis factor and interferon-γ upon mitogen stimulationJournal of Hepatology, 1992
- Tauroursodeoxycholate prevents taurocholate induced cholestasisLife Sciences, 1982
- Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmurThe Journal of Pediatrics, 1975