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Importance of the multidrug and toxin extrusion MATE/SLC47A family to pharmacokinetics, pharmacodynamics/toxicodynamics and pharmacogenomics

British journal of pharmacology, 2011-12, Vol.164 (7), p.1817-1825

2011

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Organic Cation Transporter OCTs (SLC22) and MATEs (SLC47) in the Human Kidney

The AAPS journal, 2013-04, Vol.15 (2), p.581-588

2013

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Organic cation transporter OCT/SLC22A and H +/organic cation antiporter MATE/SLC47A are key molecules for nephrotoxicity of platinum agents

Biochemical pharmacology, 2011-03, Vol.81 (5), p.563-568

2011

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THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Transporters

British journal of pharmacology, 2021-10, Vol.178 (S1), p.S412-S513

2021

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Multidrug and toxin extrusion family SLC47: Physiological, pharmacokinetic and toxicokinetic importance of MATE1 and MATE2-K

Molecular aspects of medicine, 2013-04, Vol.34 (2-3), p.661-668

2013

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Disruption of multidrug and toxin extrusion MATE1 potentiates cisplatin-induced nephrotoxicity

Biochemical pharmacology, 2010-12, Vol.80 (11), p.1762-1767

2010

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Inhibitory effects of vandetanib on creatinine transport via renal organic cation transporter OCT2

European journal of pharmaceutical sciences, 2021-03, Vol.158, p.105666-105666, Article 105666

2021

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The Concise Guide to PHARMACOLOGY 2023/24: Transporters

British journal of pharmacology, 2023-10, Vol.180 (S2), p.S374-S469

2023

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Physiological and pharmacokinetic roles of H +/organic cation antiporters (MATE/SLC47A)

Biochemical pharmacology, 2008-05, Vol.75 (9), p.1689-1696

2008

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Cisplatin and oxaliplatin, but not carboplatin and nedaplatin, are substrates for human organic cation transporters (SLC22A1-3 and multidrug and toxin extrusion family)

The Journal of pharmacology and experimental therapeutics, 2006-11, Vol.319 (2), p.879-886

2006

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Precise comparison of protein localization among OCT, OAT, and MATE in human kidney

Journal of pharmaceutical sciences, 2013-09, Vol.102 (9), p.3302-3308

2013

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Substrate specificity of MATE1 and MATE2-K, human multidrug and toxin extrusions/H +-organic cation antiporters

Biochemical pharmacology, 2007-07, Vol.74 (2), p.359-371

2007

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Identification and functional characterization of a new human kidney-specific H+/organic cation antiporter, kidney-specific multidrug and toxin extrusion 2

Journal of the American Society of Nephrology, 2006-08, Vol.17 (8), p.2127-2135

2006

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Involvement of autophagy in the pharmacological effects of the mTOR inhibitor everolimus in acute kidney injury

European journal of pharmacology, 2012-12, Vol.696 (1-3), p.143-154

2012

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Involvement of human multidrug and toxin extrusion 1 in the drug interaction between cimetidine and metformin in renal epithelial cells

The Journal of pharmacology and experimental therapeutics, 2009-04, Vol.329 (1), p.185-191

2009

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Identification and Comparative Functional Characterization of a New Human Riboflavin Transporter hRFT3 Expressed in the Brain

The Journal of nutrition, 2010-07, Vol.140 (7), p.1220-1226

2010

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Targeted Disruption of the Multidrug and Toxin Extrusion 1 (Mate1) Gene in Mice Reduces Renal Secretion of Metformin

Molecular pharmacology, 2009-06, Vol.75 (6), p.1280-1286

2009

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Novel drug transporter substrates identification: An innovative approach based on metabolomic profiling, in silico ligand screening and biological validation

Pharmacological research, 2023-10, Vol.196, p.106941-106941, Article 106941

2023

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Identification and functional characterization of a novel human and rat riboflavin transporter, RFT1

American Journal of Physiology: Cell Physiology, 2008-09, Vol.295 (3), p.C632-C641

2008

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Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B

Human mutation, 2011-01, Vol.32 (1), p.E1976-E1984

2011

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Differential contribution of organic cation transporters, OCT2 and MATE1, in platinum agent-induced nephrotoxicity

Biochemical pharmacology, 2007-08, Vol.74 (3), p.477-487

2007

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Impact of Genetic Variation in Breast Cancer Resistance Protein (BCRP/ABCG2) on Sunitinib Pharmacokinetics

DRUG METABOLISM AND PHARMACOKINETICS, 2012, Vol.27 (6), p.631-639

2012

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Metformin is a Superior Substrate for Renal Organic Cation Transporter OCT2 rather than Hepatic OCT1

DRUG METABOLISM AND PHARMACOKINETICS, 2005, Vol.20 (5), p.379-386

2005

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Renal transport of adefovir, cidofovir, and tenofovir by SLC22A family members (hOAT1, hOAT3, and hOCT2)

Pharmaceutical research, 2007-04, Vol.24 (4), p.811-815

2007

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Management of dose variability and side effects for individualized cancer pharmacotherapy with tyrosine kinase inhibitors

Pharmacology & therapeutics (Oxford), 2015-08, Vol.152, p.125-134

2015

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Importance of the multidrug and toxin extrusion MATE/SLC47A family to pharmacokinetics, pharmacodynamics/toxicodynamics and pharmacogenomics

Organic Cation Transporter OCTs (SLC22) and MATEs (SLC47) in the Human Kidney

Organic cation transporter OCT/SLC22A and H +/organic cation antiporter MATE/SLC47A are key molecules for nephrotoxicity of platinum agents

THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Transporters

Multidrug and toxin extrusion family SLC47: Physiological, pharmacokinetic and toxicokinetic importance of MATE1 and MATE2-K

Disruption of multidrug and toxin extrusion MATE1 potentiates cisplatin-induced nephrotoxicity

Inhibitory effects of vandetanib on creatinine transport via renal organic cation transporter OCT2

The Concise Guide to PHARMACOLOGY 2023/24: Transporters

Physiological and pharmacokinetic roles of H +/organic cation antiporters (MATE/SLC47A)

Cisplatin and oxaliplatin, but not carboplatin and nedaplatin, are substrates for human organic cation transporters (SLC22A1-3 and multidrug and toxin extrusion family)

Precise comparison of protein localization among OCT, OAT, and MATE in human kidney

Substrate specificity of MATE1 and MATE2-K, human multidrug and toxin extrusions/H +-organic cation antiporters

Identification and functional characterization of a new human kidney-specific H+/organic cation antiporter, kidney-specific multidrug and toxin extrusion 2

Involvement of autophagy in the pharmacological effects of the mTOR inhibitor everolimus in acute kidney injury

Involvement of human multidrug and toxin extrusion 1 in the drug interaction between cimetidine and metformin in renal epithelial cells

Identification and Comparative Functional Characterization of a New Human Riboflavin Transporter hRFT3 Expressed in the Brain

Targeted Disruption of the Multidrug and Toxin Extrusion 1 (Mate1) Gene in Mice Reduces Renal Secretion of Metformin

Novel drug transporter substrates identification: An innovative approach based on metabolomic profiling, in silico ligand screening and biological validation

Identification and functional characterization of a novel human and rat riboflavin transporter, RFT1

Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B

Differential contribution of organic cation transporters, OCT2 and MATE1, in platinum agent-induced nephrotoxicity

Impact of Genetic Variation in Breast Cancer Resistance Protein (BCRP/ABCG2) on Sunitinib Pharmacokinetics

Metformin is a Superior Substrate for Renal Organic Cation Transporter OCT2 rather than Hepatic OCT1

Renal transport of adefovir, cidofovir, and tenofovir by SLC22A family members (hOAT1, hOAT3, and hOCT2)

Management of dose variability and side effects for individualized cancer pharmacotherapy with tyrosine kinase inhibitors

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