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Pharmaceutical Research|May 17, 2008
The quantitative prediction of CYP-mediated drug interaction by physiologically based pharmacokinetic modelingMotohiro Kato, Yoshihisa Shitara, Hitoshi Sato, et al.Drug Metabolism and Pharmacokinetics|January 23, 2017
Increase in the systemic exposure of primary metabolites of Midazolam in rat arising from CYP inhibition or hepatic dysfunctionTsubasa Hasegawa, Satomi Nakanishi, Keiko Minami, et al.Drug Metabolism and Pharmacokinetics|December 25, 2004
Function of uptake transporters for taurocholate and estradiol 17beta-D-glucuronide in cryopreserved human hepatocytesYoshihisa Shitara, Albert P Li, Yukio Kato, et al.Journal of Pharmaceutical Sciences|October 15, 2020
Improved Prediction of the Drug-Drug Interactions of Pemafibrate Caused by Cyclosporine A and Rifampicin via PBPK Modeling: Consideration of the Albumin-Mediated Hepatic Uptake of Pemafibrate and Inhibition Constants With Preincubation Against OATP1BJi Eun Park, Yoshihisa Shitara, Wooin Lee, et al.The Journal of Pharmacology and Experimental Therapeutics|April 22, 2006
Vectorial transport of enalapril by Oatp1a1/Mrp2 and OATP1B1 and OATP1B3/MRP2 in rat and human liversLichuan Liu, Yunhai Cui, Alfred Y Chung, et al.CPT: Pharmacometrics & Systems Pharmacology|April 1, 2023
Model-based simulation to support the approval of isatuximab alone or with dexamethasone for the treatment of relapsed/refractory multiple myeloma in Japanese patientsHoai-Thu Thai, Kimiko Koiwai, Yoshihisa Shitara, et al.Pharmaceutical Research|March 9, 2002
Comparative inhibitory effects of different compounds on rat oatpl (slc21a1)- and Oatp2 (Slc21a5)-mediated transportYoshihisa Shitara, Daisuke Sugiyama, Hiroyuki Kusuhara, et al.Transplantation|January 29, 2013
CYP3A5 gene variation influences cyclosporine A metabolite formation and renal cyclosporine dispositionSongmao Zheng, Yasar Tasnif, Mary F Hebert, et al.Pageof 4