Bromocriptine Modulates P-Glycoprotein Function
- 1 March 1998
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 244 (2) , 481-488
- https://doi.org/10.1006/bbrc.1998.8289
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Kinetics of the multidrug transporter (P-glycoprotein) and its reversalPhysiological Reviews, 1997
- Bromocriptine Transcriptionally Activates the Multidrug Resistance Gene (pgp2/mdr1b) by a Novel PathwayPublished by Elsevier ,1997
- Absence of the mdr1a P-Glycoprotein in mice affects tissue distribution and pharmacokinetics of dexamethasone, digoxin, and cyclosporin A.Journal of Clinical Investigation, 1995
- BIOCHEMISTRY OF MULTIDRUG RESISTANCE MEDIATED BY THE MULTIDRUG TRANSPORTERAnnual Review of Biochemistry, 1993
- The Pharmacology of Parkinson's Disease Therapy: An UpdateAnnual Review of Pharmacology and Toxicology, 1993
- Increased mdr-1/P-glycoprotein expression after treatment of human colon carcinoma cells with P-glycoprotein antagonists.Journal of Biological Chemistry, 1993
- The direct activation of human multidrug resistance gene (MDR1) by anticancer agentsBiochemical and Biophysical Research Communications, 1989
- The gene encoding multidrug resistance is induced and expressed at high levels during pregnancy in the secretory epithelium of the uterus.Proceedings of the National Academy of Sciences, 1988
- Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues.Proceedings of the National Academy of Sciences, 1987
- Multiple receptors for dopamineNature, 1979