Relationship between drug/metabolite exposure and impairment of excretory transport function.
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ITC recommendations for transporter kinetic parameter estimation and translational modeling of transport-mediated PK and DDIs in humansMembrane transporters in drug developmentPredicting the outer boundaries of P-glycoprotein (P-gp)-based drug interactions at the human blood-brain barrier based on rat studies.Pitavastatin is a more sensitive and selective organic anion-transporting polypeptide 1B clinical probe than rosuvastatin.Species differences in hepatobiliary disposition of taurocholic acid in human and rat sandwich-cultured hepatocytes: implications for drug-induced liver injuryEffects of uremic toxins on transport and metabolism of different biopharmaceutics drug disposition classification system xenobioticsHepatic basolateral efflux contributes significantly to rosuvastatin disposition II: characterization of hepatic elimination by basolateral, biliary, and metabolic clearance pathways in rat isolated perfused liver.Trimethoprim-metformin interaction and its genetic modulation by OCT2 and MATE1 transporters.Intracellular drug concentrations and transporters: measurement, modeling, and implications for the liver.An experimental approach to evaluate the impact of impaired transport function on hepatobiliary drug disposition using Mrp2-deficient TR- rat sandwich-cultured hepatocytes in combination with Bcrp knockdown.Understanding the critical disposition pathways of statins to assess drug-drug interaction risk during drug development: it's not just about OATP1B1.Species differences in drug transporters and implications for translating preclinical findings to humans.Why clinical modulation of efflux transport at the human blood-brain barrier is unlikely: the ITC evidence-based position.Prediction of pharmacokinetics and drug-drug interactions when hepatic transporters are involved.Mechanisms and therapeutic potential of inhibiting drug efflux transporters.A Comprehensive Review of Drug-Drug Interactions with Metformin.The Antimicrobial Agent Fusidic Acid Inhibits Organic Anion Transporting Polypeptide-Mediated Hepatic Clearance and May Potentiate Statin-Induced Myopathy.Fractional dynamics pharmacokinetics-pharmacodynamic models.The elimination of MTC-220, a novel anti-tumor agent of conjugate of paclitaxel and muramyl dipeptide analogue, in rats.Cellular Pharmacokinetic Model-Based Analysis of Genistein, Glyceollin, and MK-571 Effects on 5 (and 6)-Carboxy-2',7'-Dichloroflourescein Disposition in Caco-2 Cells.Brain and Testis Accumulation of Regorafenib is Restricted by Breast Cancer Resistance Protein (BCRP/ABCG2) and P-glycoprotein (P-GP/ABCB1).Role of Hepatic Drug Transporters in Drug Development.
P2860
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P2860
Relationship between drug/metabolite exposure and impairment of excretory transport function.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
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2008年學術文章
@zh-hant
name
Relationship between drug/meta ...... excretory transport function.
@en
Relationship between drug/meta ...... excretory transport function.
@nl
type
label
Relationship between drug/meta ...... excretory transport function.
@en
Relationship between drug/meta ...... excretory transport function.
@nl
prefLabel
Relationship between drug/meta ...... excretory transport function.
@en
Relationship between drug/meta ...... excretory transport function.
@nl
P2093
P2860
P356
P1476
Relationship between drug/meta ...... f excretory transport function
@en
P2093
Gary M Pollack
J Cory Kalvass
Maciej J Zamek-Gliszczynski
P2860
P304
P356
10.1124/DMD.108.023648
P50
P577
2008-11-20T00:00:00Z