Pub. Date : 1998 Apr 7
PMID : 9535788
7 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
1 | Expression of multidrug resistance (mdr) genes encoding the P-glycoprotein (P-gp) drug efflux pump was analysed in cultured rat liver epithelial cells acutely treated by the DNA-damaging agent methyl methanesulfonate (MMS). | Methyl Methanesulfonate | ATP-binding cassette, subfamily B (MDR/TAP), member 1B | Rattus norvegicus |
2 | Expression of multidrug resistance (mdr) genes encoding the P-glycoprotein (P-gp) drug efflux pump was analysed in cultured rat liver epithelial cells acutely treated by the DNA-damaging agent methyl methanesulfonate (MMS). | Methyl Methanesulfonate | ATP-binding cassette, subfamily B (MDR/TAP), member 1B | Rattus norvegicus |
3 | Expression of multidrug resistance (mdr) genes encoding the P-glycoprotein (P-gp) drug efflux pump was analysed in cultured rat liver epithelial cells acutely treated by the DNA-damaging agent methyl methanesulfonate (MMS). | Methyl Methanesulfonate | ATP-binding cassette, subfamily B (MDR/TAP), member 1B | Rattus norvegicus |
4 | Expression of multidrug resistance (mdr) genes encoding the P-glycoprotein (P-gp) drug efflux pump was analysed in cultured rat liver epithelial cells acutely treated by the DNA-damaging agent methyl methanesulfonate (MMS). | Methyl Methanesulfonate | ATP-binding cassette, subfamily B (MDR/TAP), member 1B | Rattus norvegicus |
5 | In addition, the DNA-damaging agent was found to enhance in a dose-dependent manner cellular efflux of the P-gp substrate rhodamine 123, which was inhibited by the P-gp inhibitor verapamil, thus providing evidence that exposure to MMS led to increased P-gp-related drug transport in rat liver cells. | Methyl Methanesulfonate | ATP-binding cassette, subfamily B (MDR/TAP), member 1B | Rattus norvegicus |
6 | In addition, the DNA-damaging agent was found to enhance in a dose-dependent manner cellular efflux of the P-gp substrate rhodamine 123, which was inhibited by the P-gp inhibitor verapamil, thus providing evidence that exposure to MMS led to increased P-gp-related drug transport in rat liver cells. | Methyl Methanesulfonate | ATP-binding cassette, subfamily B (MDR/TAP), member 1B | Rattus norvegicus |
7 | In addition, the DNA-damaging agent was found to enhance in a dose-dependent manner cellular efflux of the P-gp substrate rhodamine 123, which was inhibited by the P-gp inhibitor verapamil, thus providing evidence that exposure to MMS led to increased P-gp-related drug transport in rat liver cells. | Methyl Methanesulfonate | ATP-binding cassette, subfamily B (MDR/TAP), member 1B | Rattus norvegicus |