P-glycoprotein possesses A 1,4-dihydropyridine-selective drug acceptor site which is alloserically coupled to a vinca-alkaloid-selective binding site
- 1 October 1992
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 188 (1) , 440-445
- https://doi.org/10.1016/0006-291x(92)92404-l
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Azidopine noncompetitively interacts with vinblastine and cyclosporin A binding to P-glycoprotein in multidrug resistant cells.Journal of Biological Chemistry, 1991
- Sites for Antagonism on the N-Methyl-D-Aspartate Receptor Channel ComplexAnnual Review of Pharmacology and Toxicology, 1991
- Amplification and expression of mdr1 gene in a multidrug resistant variant of small cell lung cancer cell line NCI-H69British Journal of Cancer, 1989
- THE BIOCHEMISTRY OF P-GLYCOPROTEIN-MEDIATED MULTIDRUG RESISTANCEAnnual Review of Biochemistry, 1989
- Structure and Function of Voltage-Sensitive Ion ChannelsScience, 1988
- Understanding the GABAA receptor: a chemically gated ion channelBiochemical Journal, 1988
- Identification of the multidrug resistance-related membrane glycoprotein as an acceptor for calcium channel blockers.Journal of Biological Chemistry, 1987
- Derivation and preliminary characterisation of adriamycin resistant lines of human lung cancer cellsBritish Journal of Cancer, 1986
- Acetylcholine Receptor: An Allosteric ProteinScience, 1984
- Evidence for multiple receptor sites within the putative calcium channelNaunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1982