Overexpression of MDR1 in an Intestinal Cell Line Results in Increased Cholesterol Uptake from Micelles
- 19 January 2000
- journal article
- Published by Elsevier BV in Biochemical and Biophysical Research Communications
- Vol. 267 (2), 565-571
- https://doi.org/10.1006/bbrc.1999.1996
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- BIOCHEMICAL, CELLULAR, AND PHARMACOLOGICAL ASPECTS OF THE MULTIDRUG TRANSPORTERAnnual Review of Pharmacology and Toxicology, 1999
- Contribution of the murine mdr1a P-glycoprotein to hepatobiliary and intestinal elimination of cationic drugs as measured in mice with anmdr1agene disruptionHepatology, 1998
- Search for specific inhibitors of multidrug resistance in cancerSeminars in Cancer Biology, 1997
- The physiological function of drug-transporting P-glycoproteinsSeminars in Cancer Biology, 1997
- Biophysical Aspects of P-Glycoprotein-Mediated Multidrug ResistanceInternational Review of Cytology, 1997
- Hepatocellular Transport: Role of ATP-Binding Cassette ProteinsSeminars in Liver Disease, 1996
- Absence of the mdr1a P-Glycoprotein in mice affects tissue distribution and pharmacokinetics of dexamethasone, digoxin, and cyclosporin A.JCI Insight, 1995
- Multidrug resistance and the role of P-glycoprotein knockout miceEuropean Journal of Cancer, 1995
- Disruption of the mouse mdr1a P-glycoprotein gene leads to a deficiency in the blood-brain barrier and to increased sensitivity to drugsCell, 1994
- BIOCHEMISTRY OF MULTIDRUG RESISTANCE MEDIATED BY THE MULTIDRUG TRANSPORTERAnnual Review of Biochemistry, 1993