Analysis of structural features of dihydropyridine analogs needed to reverse multidrug resistance and to inhibit photoaffinity labeling of P-glycoprotein
- 1 February 1989
- journal article
- research article
- Published by Elsevier in Biochemical Pharmacology
- Vol. 38 (3), 519-527
- https://doi.org/10.1016/0006-2952(89)90393-6
Abstract
No abstract availableThis publication has 36 references indexed in Scilit:
- Potentiation of vincristine by vitamin A against drug-resistant mouse leukaemia cellsBritish Journal of Cancer, 1987
- Homology between P-glycoprotein and a bacterial haemolysin transport protein suggests a model for multidrug resistanceNature, 1986
- Internal duplication and homology with bacterial transport proteins in the mdr1 (P-glycoprotein) gene from multidrug-resistant human cellsCell, 1986
- Mammalian multidrug resistance gene: Complete cDNA sequence indicates strong homology to bacterial transport proteinsCell, 1986
- Human Multidrug-Resistant Cell Lines: Increased mdr 1 Expression Can Precede Gene AmplificationScience, 1986
- Lysosomotropic agents reverse multiple drug resistance in human cancer cellsCancer Letters, 1986
- Isolation and genetic characterization of human KB cell lines resistant to multiple drugsSomatic Cell and Molecular Genetics, 1985
- DNA-mediated transfer of multiple drug resistance and plasma membrane glycoprotein expression.Molecular and Cellular Biology, 1982
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976