The Constitutive Androstane Receptor and Pregnane X Receptor Function Coordinately to Prevent Bile Acid-induced Hepatotoxicity
Open Access
- 1 November 2004
- journal article
- Published by Elsevier BV
- Vol. 279 (47), 49517-49522
- https://doi.org/10.1074/jbc.m409041200
Abstract
No abstract availableKeywords
This publication has 41 references indexed in Scilit:
- Deoxycholic Acid Activates the c-Jun N-terminal Kinase Pathway via FAS Receptor Activation in Primary HepatocytesJournal of Biological Chemistry, 2004
- A Novel Constitutive Androstane Receptor-Mediated and CYP3A-Independent Pathway of Bile Acid DetoxificationMolecular Pharmacology, 2004
- Protective Role of Hydroxysteroid Sulfotransferase in Lithocholic Acid-induced Liver ToxicityJournal of Biological Chemistry, 2003
- A G Protein-coupled Receptor Responsive to Bile AcidsJournal of Biological Chemistry, 2003
- Identification of membrane-type receptor for bile acids (M-BAR)Biochemical and Biophysical Research Communications, 2002
- Vitamin D Receptor As an Intestinal Bile Acid SensorScience, 2002
- Regulation of Multidrug Resistance-associated Protein 2 (ABCC2) by the Nuclear Receptors Pregnane X Receptor, Farnesoid X-activated Receptor, and Constitutive Androstane ReceptorJournal of Biological Chemistry, 2002
- The Farnesoid X-activated Receptor Mediates Bile Acid Activation of Phospholipid Transfer Protein Gene ExpressionPublished by Elsevier BV ,2000
- Humanized xenobiotic response in mice expressing nuclear receptor SXRNature, 2000
- 6α-Hydroxylation of taurochenodeoxycholic acid and lithocholic acid by CYP3A4 in human liver microsomesBiochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, 1999