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Biopharmaceutics & Drug Disposition|July 6, 2016
In vivo use of the CYP inhibitor 1-aminobenzotriazole to increase long-term exposure in miceAyahisa Watanabe, Kei Mayumi, Kyohei Nishimura, et al.
Biopharmaceutics & Drug Disposition|September 30, 2017
Prediction of drug-drug interactions using physiologically-based pharmacokinetic models of CYP450 modulators included in Simcyp softwareNiloufar Marsousi, Jules A Desmeules, Serge Rudaz, et al.
Biopharmaceutics & Drug Disposition|October 25, 2006
Stereoselective pharmacokinetic analysis of tramadol and its main phase I metabolites in healthy subjects after intravenous and oral administration of racemic tramadolEmilio García Quetglas, Jose Ramón Azanza, Ernesto Cardenas, et al.
Biopharmaceutics & Drug Disposition|February 23, 2007
Effects of morin on the pharmacokinetics of etoposide in ratsXiuguo Li, Jae-Kyung Yun, Jun-Shik Choi
Biopharmaceutics & Drug Disposition|September 5, 2006
Pharmacogenomics of cancer chemopreventive isothiocyanate compound sulforaphane in the intestinal polyps of ApcMin/+ miceTin Oo Khor, Rong Hu, Guoxiang Shen, et al.
Biopharmaceutics & Drug Disposition|December 19, 2006
Comparative in vitro degradation of the human hemorphin LVV-H7 in mammalian plasma analysed by capillary zone electrophoresis and mass spectrometryHarald John, Stefanie Schulz, Wolf-Georg Forssmann
Biopharmaceutics & Drug Disposition|July 28, 2007
Pharmacokinetics of intravenous methotrexate in mutant Nagase analbuminemic ratsYoung H Choi, Soo K Bae, Jung M Oh, et al.
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