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Antiretroviral Drug Metabolism in Humanized PXR-CAR-CYP3A-NOG Mice
Antiretroviral drug (ARV) metabolism is linked largely to hepatic cytochrome P450 activity. One ARV drug class known to be metabolized by intestinal and hepatic CYP3A are the protease inhibitors (PIs). Plasma drug concentrations are boosted by CYP3A inhibitors such as cobisistat and ritonavir (RTV)....
Tallennettuna:
| Julkaisussa: | J Pharmacol Exp Ther |
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| Päätekijät: | , , , , , , , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
The American Society for Pharmacology and Experimental Therapeutics
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5878674/ https://ncbi.nlm.nih.gov/pubmed/29476044 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1124/jpet.117.247288 |
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