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Drug Metabolism and Disposition: the Biological Fate of Chemicals|September 17, 2004
Assessment of catechol induction and glucuronidation in rat liver microsomesEivor Elovaara, Jouni Mikkola, Leena Luukkanen, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 14, 2008
Regio- and stereospecific N-glucuronidation of medetomidine: the differences between UDP glucuronosyltransferase (UGT) 1A4 and UGT2B10 account for the complex kinetics of human liver microsomesSanna Kaivosaari, Päivi Toivonen, Olli Aitio, et al.The Journal of Biological Chemistry|November 19, 2002
Expression and characterization of recombinant human UDP-glucuronosyltransferases (UGTs). UGT1A9 is more resistant to detergent inhibition than other UGTs and was purified as an active dimeric enzymeMika Kurkela, J Arturo García-Horsman, Leena Luukkanen, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 17, 2002
Characterization of catechol glucuronidation in rat liverLaurence Antonio, Joël-Paul Grillasca, Jyrki Taskinen, et al.Bioorganic & Medicinal Chemistry Letters|September 29, 2022
Development of benzodioxine-heteroarylpiperazines as highly potent and selective α2c antagonistsShouming Wang, Anssi Haikarainen, Antti Pohjakallio, et al.Bioorganic & Medicinal Chemistry Letters|May 15, 2022
2,3-Dihydrobenzo-dioxine piperidine derivatives as potent and selective α2c antagonistsShouming Wang, Anssi Haikarainen, Antti Pohjakallio, et al.Pageof 2