Role of Human Organic Cation Transporter 1 (hOCT1) Polymorphisms in Lamivudine (3TC) Uptake and Drug-Drug Interactions-Reference-Cited by-同舟云学术

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Role of Human Organic Cation Transporter 1 (hOCT1) Polymorphisms in Lamivudine (3TC) Uptake and Drug-Drug Interactions

Published:2016-06-24 Issue: Volume:7 Page:
ISSN:1663-9812
Container-title:Frontiers in Pharmacology
language:
Short-container-title:Front. Pharmacol.

Author:

Arimany-Nardi Cristina,Minuesa Gerard,Keller Thorsten,Erkizia Itziar,Koepsell Hermann,Martinez-Picado Javier,Pastor-Anglada Marçal

Funder

Ministerio de Ciencia e Innovación

Deutsche Forschungsgemeinschaft

Publisher

Frontiers Media SA

Subject

Pharmacology (medical),Pharmacology

Reference24 articles.

1. Genotype-dependent effects of inhibitors of the organic cation transporter, OCT1: predictions of metformin interactions;Ahlin;Pharmacogenomics J.,2011

2. Role of SLC22A1 polymorphic variants in drug disposition, therapeutic responses, and drug-drug interactions;Arimany-Nardi;Pharmacogenomics J.,2015a

3. Human organic cation transporter 1 (hOCT1) as a mediator of bendamustine uptake and cytotoxicity in chronic lymphocytic leukemia (CLL) cells;Arimany-Nardi;Pharmacogenomics J.,2015b

4. The cysteines of the extracellular loop are crucial for trafficking of human organic cation transporter 2 to the plasma membrane and are involved in oligomerization;Brast;FASEB J.,2012

5. Genetic variants of organic cation transporter 1 (OCT1) and OCT2 significantly reduce lamivudine uptake;Choi;Biopharm. Drug Dispos.,2012

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