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Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 4, 2011
Reevaluation of the microsomal metabolism of montelukast: major contribution by CYP2C8 at clinically relevant concentrationsAnne M Filppula, Jouko Laitila, Pertti J Neuvonen, et al.
Pediatric Nephrology (Berlin, Germany)|March 18, 2005
Cyclosporine A monitoring--how to account for twice and three times daily dosingSamuel Fanta, Janne T Backman, Paula Seikku, et al.
Basic & Clinical Pharmacology & Toxicology|September 24, 2005
Metabolism of repaglinide by CYP2C8 and CYP3A4 in vitro: effect of fibrates and rifampicinLauri I Kajosaari, Jouko Laitila, Pertti J Neuvonen, et al.
Pharmacological Reviews|January 2, 2016
Role of Cytochrome P450 2C8 in Drug Metabolism and InteractionsJanne T Backman, Anne M Filppula, Mikko Niemi, et al.
Clinical Pharmacology and Therapeutics|September 28, 2021
Performance of Plasma Coproporphyrin I and III as OATP1B1 Biomarkers in HumansMikko Neuvonen, Aleksi Tornio, Päivi Hirvensalo, et al.
European Journal of Clinical Pharmacology|May 4, 2006
Montelukast and zafirlukast do not affect the pharmacokinetics of the CYP2C8 substrate pioglitazoneTiina Jaakkola, Janne T Backman, Mikko Neuvonen, et al.
European Journal of Clinical Pharmacology|November 24, 2011
Fluconazole but not the CYP3A4 inhibitor, itraconazole, increases zafirlukast plasma concentrationsTiina Karonen, Jouko Laitila, Mikko Niemi, et al.
European Journal of Clinical Pharmacology|June 10, 2011
No significant effect of the SLCO1B1 polymorphism on the pharmacokinetics of ursodeoxycholic acidXiaoqiang Xiang, Juha Vakkilainen, Janne T Backman, et al.
Pharmacogenetics and Genomics|November 16, 2012
SLCO2B1 c.935G>A single nucleotide polymorphism has no effect on the pharmacokinetics of montelukast and aliskirenTuija Tapaninen, Tiina Karonen, Janne T Backman, et al.
British Journal of Clinical Pharmacology|January 5, 2006
Effect of rifampicin on the pharmacokinetics of pioglitazoneTiina Jaakkola, Janne T Backman, Mikko Neuvonen, et al.
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