Title : MRP4: A previously unidentified factor in resistance to nucleoside-based antiviral drugs.

Pub. Date : 1999 Sep

PMID : 10470083






5 Functional Relationships(s)
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1 In our study of alternative or additional mechanisms of resistance operating during antiviral therapy, overexpression and amplification of the MRP4 gene correlated with ATP-dependent efflux of PMEA (9-(2-phosphonylmethoxyethyl)adenine) and azidothymidine monophosphate from cells and, thus, with resistance to these drugs. adefovir ATP binding cassette subfamily C member 4 Homo sapiens
2 In our study of alternative or additional mechanisms of resistance operating during antiviral therapy, overexpression and amplification of the MRP4 gene correlated with ATP-dependent efflux of PMEA (9-(2-phosphonylmethoxyethyl)adenine) and azidothymidine monophosphate from cells and, thus, with resistance to these drugs. adefovir ATP binding cassette subfamily C member 4 Homo sapiens
3 Overexpression of MRP4 mRNA and MRP4 protein severely impaired the antiviral efficacy of PMEA, azidothymidine and other nucleoside analogs. adefovir ATP binding cassette subfamily C member 4 Homo sapiens
4 Overexpression of MRP4 mRNA and MRP4 protein severely impaired the antiviral efficacy of PMEA, azidothymidine and other nucleoside analogs. adefovir ATP binding cassette subfamily C member 4 Homo sapiens
5 Increased resistance to PMEA and amplification of the MRP4 gene correlated with enhanced drug efflux; transfer of chromosome 13 containing the amplified MRP4 gene conferred resistance to PMEA. adefovir ATP binding cassette subfamily C member 4 Homo sapiens