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Correction: Elucidating time-dependent changes in the urinary metabolome of renal transplant patients by a combined 1H NMR and GC-MS approach.
Mol Biosyst. 2017 Jan 31;13(2):432. doi: 10.1039/c7mb90005h.
Mol Biosyst. 2017.
PMID: 28102871
Endogenous metabolites that are substrates of organic anion transporter's (OATs) predict methotrexate clearance.
Muhrez K, Benz-de Bretagne I, Nadal-Desbarats L, Blasco H, Gyan E, Choquet S, Montigny F, Emond P, Barin-Le Guellec C.
Muhrez K, et al.
Pharmacol Res. 2017 Apr;118:121-132. doi: 10.1016/j.phrs.2016.05.021. Epub 2016 May 19.
Pharmacol Res. 2017.
PMID: 27210722
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Single nucleotide polymorphisms of ABCC2 modulate renal secretion of endogenous organic anions.
Muhrez K, Largeau B, Emond P, Montigny F, Halimi JM, Trouillas P, Barin-Le Guellec C.
Muhrez K, et al.
Biochem Pharmacol. 2017 Sep 15;140:124-138. doi: 10.1016/j.bcp.2017.05.012. Epub 2017 May 19.
Biochem Pharmacol. 2017.
PMID: 28532626
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Endogenous Metabolites-Mediated Communication Between OAT1/OAT3 and OATP1B1 May Explain the Association Between SLCO1B1 SNPs and Methotrexate Toxicity.
Martinez D, Muhrez K, Woillard JB, Berthelot A, Gyan E, Choquet S, Andrès CR, Marquet P, Barin-Le Guellec C.
Martinez D, et al. Among authors: muhrez k.
Clin Pharmacol Ther. 2018 Oct;104(4):687-698. doi: 10.1002/cpt.1008. Epub 2018 Jan 31.
Clin Pharmacol Ther. 2018.
PMID: 29285751
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