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Titlebook: Enzyme- and Transporter-Based Drug-Drug Interactions; Progress and Future K. Sandy‘Pang ,A. David‘Rodrigues,Raimund M. Peter Book 2010 Spr

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樓主: frustrate
31#
發(fā)表于 2025-3-26 21:17:49 | 只看該作者
32#
發(fā)表于 2025-3-27 03:57:46 | 只看該作者
Deutsch-Afrikanische Beziehungen 2003osed to improve the accuracy of the prediction. Also, a method to predict the alterations caused by drug–drug interactions mediated by intestinal cytochrome P450 3A4 or P-glycoprotein was introduced. In this chapter, these methods and computerized simulation method are shown.
33#
發(fā)表于 2025-3-27 07:50:01 | 只看該作者
34#
發(fā)表于 2025-3-27 12:00:43 | 只看該作者
35#
發(fā)表于 2025-3-27 17:27:47 | 只看該作者
36#
發(fā)表于 2025-3-27 18:11:30 | 只看該作者
37#
發(fā)表于 2025-3-27 23:24:43 | 只看該作者
Deutsch-afrikanische Beziehungen 1989entary, and sometimes overlapping, functions, a feature which can set the stage for drug–drug interactions. In this chapter, we provide an overview of the phase I and phase II families of detoxification enzymes, their potential for induction and inhibition, and the role of genetic variants in the occurrence of drug–drug interactions.
38#
發(fā)表于 2025-3-28 03:21:21 | 只看該作者
Deutsch-afrikanische Beziehungen 1992er, PXR, CAR, FXR, and VDR form a core group of nuclear receptors that regulate the expression of a number of important drug-metabolizing enzymes and drug transporters. In this chapter, the molecular determinants of adaptive response to drug exposure are detailed in the context of clinical relevance and drug development.
39#
發(fā)表于 2025-3-28 08:46:23 | 只看該作者
Deutsch-Afrikanische Beziehungen 2003osed to improve the accuracy of the prediction. Also, a method to predict the alterations caused by drug–drug interactions mediated by intestinal cytochrome P450 3A4 or P-glycoprotein was introduced. In this chapter, these methods and computerized simulation method are shown.
40#
發(fā)表于 2025-3-28 10:34:16 | 只看該作者
Art and the Ancestor Narrative,lico database of drug–drug interaction have been much wanted. In this chapter, examples of, and prediction methods for, transporter-mediated drug–drug interactions are shown, and a Web-based transporter-mediated drug–drug interaction database in TP-search (./) is also described.
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