The AU-Rich 3′ Untranslated Region of Human MDR1 mRNA Is an Inefficient mRNA Destabilizer
- 11 August 1999
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 261 (3) , 627-634
- https://doi.org/10.1006/bbrc.1999.1101
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Increased P-glycoprotein messenger RNA stability in rat liver tumors in vivoJournal of Cellular Physiology, 1998
- Expression of the multidrug resistance genes in the liverThe FASEB Journal, 1997
- Regulation of mdrlb gene expression in Fischer, Wistar and Sprague-Dawley rats in vivo and in vitroCarcinogenesis: Integrative Cancer Research, 1996
- Induction of P‐Glycorprotein mRNA by protein synthesis inhibition is not controlled by a transcriptional repressor protein in rat and human liver cellsJournal of Cellular Physiology, 1995
- Selective degradation of early-response-gene mRNAs: functional analyses of sequence features of the AU-rich elements.Molecular and Cellular Biology, 1994
- BIOCHEMISTRY OF MULTIDRUG RESISTANCE MEDIATED BY THE MULTIDRUG TRANSPORTERAnnual Review of Biochemistry, 1993
- Regulation of P-glycoprotein gene expression in hepatocyte cultures and liver cell lines by a trans-acting transcriptional repressorNucleic Acids Research, 1992
- THE BIOCHEMISTRY OF P-GLYCOPROTEIN-MEDIATED MULTIDRUG RESISTANCEAnnual Review of Biochemistry, 1989
- Internal duplication and homology with bacterial transport proteins in the mdr1 (P-glycoprotein) gene from multidrug-resistant human cellsCell, 1986
- A conserved AU sequence from the 3′ untranslated region of GM-CSF mRNA mediates selective mRNA degradationCell, 1986