Use of the nuclear receptor PXR to predict drug interactions
- 20 November 2000
- journal article
- review article
- Published by Elsevier in Toxicology
- Vol. 153 (1-3) , 1-10
- https://doi.org/10.1016/s0300-483x(00)00300-0
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Orphan Nuclear Receptors: From Gene to FunctionEndocrine Reviews, 1999
- SXR, a novel steroid and xenobioticsensing nuclear receptorGenes & Development, 1998
- The Novel Cholesterol-lowering Drug SR-12813 Inhibits Cholesterol Synthesis via an Increased Degradation of 3-Hydroxy-3-methylglutaryl-coenzyme A ReductasePublished by Elsevier ,1996
- The RXR heterodimers and orphan receptorsPublished by Elsevier ,1995
- Nonsteroid nuclear receptors: What Are genetic studies telling us about their role in real life?Cell, 1995
- A conserved carboxy-terminal subdomain is important for ligand interpretation and transactivation by nuclear receptorsEndocrinology, 1994
- Gene structure of CYP3A4, an adult‐specific form of cytochrome P450 in human livers, and its transcriptional controlEuropean Journal of Biochemistry, 1993
- Regulation of Phenobarbital-Inducible Cytochrome-P450 2B1/2 mRNA by Lovastatin and Oxysterols in Primary Cultures of Adult Rat HepatocytesToxicology and Applied Pharmacology, 1993
- Retinoid X receptor is an auxiliary protein for thyroid hormone and retinoic acid receptorsNature, 1992
- Substrate specificities and functions of the P450 cytochromesLife Sciences, 1990