Role of P-glycoprotein-mediated secretion in absorptive drug permeability: An approach using passive membrane permeability and affinity to P-glycoprotein.
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Nanotechnology Formulations for Antibacterial Free Fatty Acids and MonoglyceridesPrediction of promiscuous p-glycoprotein inhibition using a novel machine learning schemeFitting the elementary rate constants of the P-gp transporter network in the hMDR1-MDCK confluent cell monolayer using a particle swarm algorithmQuantitative visualization of passive transport across bilayer lipid membranes.P-Glycoprotein- and cytochrome P-450-mediated herbal drug interactions.Relevance of multidrug resistance proteins for intestinal drug absorption in vitro and in vivo.Hydrogel-assisted functional reconstitution of human P-glycoprotein (ABCB1) in giant liposomes.Simulations of the nonlinear dose dependence for substrates of influx and efflux transporters in the human intestineDiverse approaches for the enhancement of oral drug bioavailability.P-glycoprotein Inhibition for Optimal Drug Delivery.The elementary mass action rate constants of P-gp transport for a confluent monolayer of MDCKII-hMDR1 cells.Verapamil hepatic clearance in four preclinical rat models: towards activity-based scaling.Cell-based multiscale computational modeling of small molecule absorption and retention in the lungs.Revisiting atenolol as a low passive permeability marker.Resolution of P-glycoprotein and non-P-glycoprotein effects on drug permeability using intestinal tissues from mdr1a (-/-) mice.The impact of P-glycoprotein efflux on enterocyte residence time and enterocyte-based metabolism of verapamil.The effect of quercetin on the pharmacokinetics of verapamil and its major metabolite, norverapamil, in rabbits.In silico model for P-glycoprotein substrate prediction: insights from molecular dynamics and in vitro studies.Antimicrobial activity of monocaprin: a monoglyceride with potential use as a denture disinfectant.Classification analysis of P-glycoprotein substrate specificity.In-vitro mutagenic potential and effect on permeability of co-administered drugs across Caco-2 cell monolayers of Rubus idaeus and its fortified fractions.Effect of five novel 5-substituted tetrandrine derivatives on P-glycoprotein-mediated inhibition and transport in Caco-2 cells
P2860
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P2860
Role of P-glycoprotein-mediated secretion in absorptive drug permeability: An approach using passive membrane permeability and affinity to P-glycoprotein.
description
1999 nî lūn-bûn
@nan
1999 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Role of P-glycoprotein-mediate ...... nd affinity to P-glycoprotein.
@ast
Role of P-glycoprotein-mediate ...... nd affinity to P-glycoprotein.
@en
type
label
Role of P-glycoprotein-mediate ...... nd affinity to P-glycoprotein.
@ast
Role of P-glycoprotein-mediate ...... nd affinity to P-glycoprotein.
@en
prefLabel
Role of P-glycoprotein-mediate ...... nd affinity to P-glycoprotein.
@ast
Role of P-glycoprotein-mediate ...... nd affinity to P-glycoprotein.
@en
P2093
P356
P1476
Role of P-glycoprotein-mediate ...... nd affinity to P-glycoprotein.
@en
P2093
Döppenschmitt S
Langguth P
Regårdh CG
Spahn-Langguth H
P304
P356
10.1021/JS980378J
P407
P577
1999-10-01T00:00:00Z