Modulation of oral bioavailability of anticancer drugs: from mouse to man
- 1 December 2000
- journal article
- review article
- Published by Elsevier in European Journal of Pharmaceutical Sciences
- Vol. 12 (2) , 103-110
- https://doi.org/10.1016/s0928-0987(00)00153-6
Abstract
No abstract availableKeywords
This publication has 54 references indexed in Scilit:
- Oral chemotherapy: rationale and future directions.Journal of Clinical Oncology, 1998
- Topoisomerase I inhibitors: the relevance of prolonged exposure for present clinical developmentBritish Journal of Cancer, 1997
- The bioavailability of oral GI147211 (GG211), a new topoisomerase I inhibitorBritish Journal of Cancer, 1997
- Suppression of intestinal and hepatic cytochrome P4503A in murineToxoplasma infection. Effects ofN-acetylcysteine andNG-monomethyl-L-arginine on the hepatic suppressionXenobiotica, 1996
- BIOCHEMISTRY OF MULTIDRUG RESISTANCE MEDIATED BY THE MULTIDRUG TRANSPORTERAnnual Review of Biochemistry, 1993
- Overexpression of a Transporter Gene in a Multidrug-Resistant Human Lung Cancer Cell LineScience, 1992
- Two members of the mouse mdr gene family confer multidrug resistance with overlapping but distinct drug specificities.Molecular and Cellular Biology, 1990
- The three mouse multidrug resistance (mdr) genes are expressed in a tissue-specific manner in normal mouse tissues.Molecular and Cellular Biology, 1989
- Multidrug-resistance gene (P-glycoprotein) is expressed by endothelial cells at blood-brain barrier sites.Proceedings of the National Academy of Sciences, 1989
- Internal duplication and homology with bacterial transport proteins in the mdr1 (P-glycoprotein) gene from multidrug-resistant human cellsCell, 1986