HIV protease inhibitors are substrates for OATP1A2, OATP1B1 and OATP1B3 and lopinavir plasma concentrations are influenced by SLCO1B1 polymorphisms
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Different interaction profiles of direct-acting anti-hepatitis C virus agents with human organic anion transporting polypeptidesPerspectives on pharmacogenomics of antiretroviral medications and HIV-associated comorbiditiesOATPs, OATs and OCTs: the organic anion and cation transporters of the SLCO and SLC22A gene superfamiliesDrug transporters in tissues and cells relevant to sexual transmission of HIV: Implications for drug deliveryA multi-system approach assessing the interaction of anticonvulsants with P-gpSingle Nucleotide Polymorphisms in Cellular Drug Transporters Are Associated with Intolerance to Antiretroviral Therapy in Brazilian HIV-1 Positive IndividualsGenomewide association study of atazanavir pharmacokinetics and hyperbilirubinemia in AIDS Clinical Trials Group protocol A5202.Phase I safety, pharmacokinetics, and pharmacogenetics study of the antituberculosis drug PA-824 with concomitant lopinavir-ritonavir, efavirenz, or rifampin.Population pharmacokinetic modeling of the association between 63396C->T pregnane X receptor polymorphism and unboosted atazanavir clearance.Gyrase B inhibitor impairs HIV-1 replication by targeting Hsp90 and the capsid protein.Raltegravir is a substrate for SLC22A6: a putative mechanism for the interaction between raltegravir and tenofovirHIV protease inhibitors do not cause the accumulation of prelamin A in PBMCs from patients receiving first line therapy: the ANRS EP45 "aging" studyImpact of body weight and missed doses on lopinavir concentrations with standard and increased lopinavir/ritonavir doses during late pregnancy.Pharmacokinetics and virologic response of zidovudine/lopinavir/ritonavir initiated during the third trimester of pregnancyAssociation of pharmacogenetic markers with premature discontinuation of first-line anti-HIV therapy: an observational cohort study.Pharmacogenomics of antimicrobial agents.Potential role of organic anion transporting polypeptide 1B1 (OATP1B1) in the selective hepatic uptake of hematoporphyrin monomethyl ether isomers.Risk of adverse events among older adults following co-prescription of clarithromycin and statins not metabolized by cytochrome P450 3A4.CYP3A5, ABCB1, and SLCO1B1 polymorphisms and pharmacokinetics and virologic outcome of lopinavir/ritonavir in HIV-infected children.PDZK1 and NHERF1 regulate the function of human organic anion transporting polypeptide 1A2 (OATP1A2) by modulating its subcellular trafficking and stability.Pharmacogenetics in the brazilian population.Organic anion-transporting polypeptide 1b2 (Oatp1b2) is important for the hepatic uptake of unconjugated bile acids: Studies in Oatp1b2-null mice.Pharmacokinetics of lopinavir/ritonavir crushed versus whole tablets in children.Bilirubin-a potential marker of drug exposure in atazanavir-based antiretroviral therapyPharmacogenomics of HIV therapy: summary of a workshop sponsored by the National Institute of Allergy and Infectious Diseases.Population approach to analyze the pharmacokinetics of free and total lopinavir in HIV-infected pregnant women and consequences for dose adjustment.Special populations and pharmacogenetic issues in tuberculosis drug development and clinical researchEstimation of the effect of SLCO1B1 polymorphisms on lopinavir plasma concentration in HIV-infected adults.Pharmacokinetic Interactions Between Quinine and Lopinavir/Ritonavir in Healthy Thai AdultsEffect of SLCO1B1 Polymorphisms on Rifabutin Pharmacokinetics in African HIV-Infected Patients with Tuberculosis.Individualization of antiretroviral therapy.Physiologically Based Modelling of Darunavir/Ritonavir Pharmacokinetics During Pregnancy.Discordant associations between SLCO1B1 521T→C and plasma levels of ritonavir-boosted protease inhibitors in AIDS clinical trials group study A5146.Interaction between HIV protease inhibitors (PIs) and hepatic transporters in sandwich cultured human hepatocytes: implication for PI-based DDIs.Clinical pharmacokinetics of antiretroviral drugs in older persons.Influence of drug transport proteins on the pharmacokinetics and drug interactions of HIV protease inhibitors.Functional analysis of novel polymorphisms in the human SLCO1A2 gene that encodes the transporter OATP1A2Interactions between tenofovir and nevirapine in CD4+ T cells and monocyte-derived macrophages restrict their intracellular accumulation.Rilpivirine inhibits drug transporters ABCB1, SLC22A1, and SLC22A2 in vitroInterindividual variability in hepatic organic anion-transporting polypeptides and P-glycoprotein (ABCB1) protein expression: quantification by liquid chromatography tandem mass spectroscopy and influence of genotype, age, and sex
P2860
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P2860
HIV protease inhibitors are substrates for OATP1A2, OATP1B1 and OATP1B3 and lopinavir plasma concentrations are influenced by SLCO1B1 polymorphisms
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
HIV protease inhibitors are su ...... enced by SLCO1B1 polymorphisms
@en
type
label
HIV protease inhibitors are su ...... enced by SLCO1B1 polymorphisms
@en
prefLabel
HIV protease inhibitors are su ...... enced by SLCO1B1 polymorphisms
@en
P2093
P2860
P50
P1476
HIV protease inhibitors are su ...... enced by SLCO1B1 polymorphisms
@en
P2093
Ammara Chaikan
Chloë E James
David J Back
Deirdre Egan
Enrique Salcedo Sora
Pat G Bray
Sara Gibbons
Saye H Khoo
Victoria Shallcross
Wai San Kwan
P2860
P304
P356
10.1097/FPC.0B013E328335B02D
P577
2010-02-01T00:00:00Z