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求上油管的加速器
- A study of the effect of cyclosporine on fevipiprant pharmacokinetics and its absolute bioavailability using an intravenous microdose approach
- Application of the Extended Clearance Classification System (ECCS) in Drug Discovery and Development: Selection of Appropriate 快喵Ⅴpn Tools and Clearance Prediction
- Organic cation transporter 1 and 3 contribute to the high accumulation of dehydrocorydaline in the heart
- Preclinical Transplacental Transfer and Pharmacokinetics of Fipronil in Rats
- Detection of Weak Organic Anion-Transporting Polypeptide (OATP) 1B Inhibition by Probenecid (PROB) with Plasma-Based Coproporphyrin in Humans
- Quantification of Neonatal Fc Receptor (FcRn) and Beta-2 Microglobulin (β2M) in Human Liver Tissues by UPLC-MRM-Based Targeted Quantitative Proteomics for Applications in Biotherapeutic PBPK Models
求上油管的加速器
DMD presents important research in pharmacology and toxicology and is a valuable resource in drug design, drug metabolism, drug transport, expression of drug metabolizing enzymes and transporters, and regulation of drug metabolizing enzyme and transporter gene expression.
求上油管的加速器
Drug Metabolism and Disposition
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求上油管的加速器
求上油管的加速器
- Strain-Dependent Variability of Early Discovery Small Molecule Pharmacokinetics in Mice: Does Strain Matter?
- OATP1B3 Expression and Function is Modulated by Coexpression with OCT1, OATP1B1, and NTCP
- Urinary Bile Acid Profile of Newborns Born by Cesarean Section Is Characterized by Oxidative Metabolism of Primary Bile Acids: Limited Roles of Fetal-Specific CYP3A7 in Cholate Oxidations
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- Complete Structural Elucidation of Gemfibrozil Metabolites by Crystalline Sponges
- Metabolism and Disposition of Volanesorsen across Species
- Physiology of the Neonatal Gastrointestinal System
- Liver Zonation Index of Transporters and Enzymes in Mice
- Pharmacokinetics and Disposition of Biologics
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