找回密码
 To register

QQ登录

只需一步,快速开始

扫一扫,访问微社区

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

[复制链接]
楼主: frustrate
发表于 2025-3-26 21:17:49 | 显示全部楼层
发表于 2025-3-27 03:57:46 | 显示全部楼层
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.
发表于 2025-3-27 07:50:01 | 显示全部楼层
发表于 2025-3-27 12:00:43 | 显示全部楼层
发表于 2025-3-27 17:27:47 | 显示全部楼层
发表于 2025-3-27 18:11:30 | 显示全部楼层
发表于 2025-3-27 23:24:43 | 显示全部楼层
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.
发表于 2025-3-28 03:21:21 | 显示全部楼层
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.
发表于 2025-3-28 08:46:23 | 显示全部楼层
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.
发表于 2025-3-28 10:34:16 | 显示全部楼层
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.
 关于派博传思  派博传思旗下网站  友情链接
派博传思介绍 公司地理位置 论文服务流程 影响因子官网 SITEMAP 大讲堂 北京大学 Oxford Uni. Harvard Uni.
发展历史沿革 期刊点评 投稿经验总结 SCIENCEGARD IMPACTFACTOR 派博系数 清华大学 Yale Uni. Stanford Uni.
|Archiver|手机版|小黑屋| 派博传思国际 ( 京公网安备110108008328) GMT+8, 2025-5-19 21:55
Copyright © 2001-2015 派博传思   京公网安备110108008328 版权所有 All rights reserved
快速回复 返回顶部 返回列表