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Showing results (91-100 of 248) with videos related to

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Xenobiotica; the Fate of Foreign Compounds in Biological Systems|April 5, 2013
A high throughput assay for the glucuronidation of 7-hydroxy-4-trifluoromethylcoumarin by recombinant human UDP-glucuronosyltransferases and liver microsomesTuomas Rahikainen, Merja R Häkkinen, Moshe Finel, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|April 2, 2005
Kinetic characterization of the 1A subfamily of recombinant human UDP-glucuronosyltransferasesLeena Luukkanen, Jyrki Taskinen, Mika Kurkela, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|December 31, 2014
Differences in the glucuronidation of bisphenols F and S between two homologous human UGT enzymes, 1A9 and 1A10Darja Gramec Skledar, Johanna Troberg, Jason Lavdas, et al.
Journal of Visceral Surgery|February 14, 2015
Acute mesenteric ischemia of arterial origin: importance of early revascularizationF Plumereau, S Mucci, P Le Naoures, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|June 5, 2012
Role of human UDP-glucuronosyltransferases in the biotransformation of the triazoloacridinone and imidazoacridinone antitumor agents C-1305 and C-1311: highly selective substrates for UGT1A10Barbara Fedejko-Kap, Stacie M Bratton, Moshe Finel, et al.
The FEBS Journal|February 1, 2007
Substrate specificity of the human UDP-glucuronosyltransferase UGT2B4 and UGT2B7. Identification of a critical aromatic amino acid residue at position 33Lydia Barre, Sylvie Fournel-Gigleux, Moshe Finel, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|May 19, 2009
Synthesis, structure characterization, and enzyme screening of clenbuterol glucuronidesAnna Alonen, Minna Gartman, Olli Aitio, et al.
International Journal of Pharmaceutics|September 8, 2009
Caco-2 cell monolayers as a tool to study simultaneous phase II metabolism and metabolite efflux of indomethacin, paracetamol and 1-naphtholSanna Siissalo, Laura Laine, Ari Tolonen, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|November 22, 2008
UDP-glucuronosyltransferases (UGTs) 2B7 and UGT2B17 display converse specificity in testosterone and epitestosterone glucuronidation, whereas UGT2A1 conjugates both androgens similarlyTaina Sten, Ingo Bichlmaier, Tiia Kuuranne, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|August 23, 2008
The configuration of the 17-hydroxy group variably influences the glucuronidation of beta-estradiol and epiestradiol by human UDP-glucuronosyltransferasesKatriina Itäaho, Peter I Mackenzie, Shin-ichi Ikushiro, et al.
Pageof 25

Showing results (91-100 of 248) with videos related to

Sort By:
Pageof 25
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|April 5, 2013
A high throughput assay for the glucuronidation of 7-hydroxy-4-trifluoromethylcoumarin by recombinant human UDP-glucuronosyltransferases and liver microsomesTuomas Rahikainen, Merja R Häkkinen, Moshe Finel, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|April 2, 2005
Kinetic characterization of the 1A subfamily of recombinant human UDP-glucuronosyltransferasesLeena Luukkanen, Jyrki Taskinen, Mika Kurkela, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|December 31, 2014
Differences in the glucuronidation of bisphenols F and S between two homologous human UGT enzymes, 1A9 and 1A10Darja Gramec Skledar, Johanna Troberg, Jason Lavdas, et al.
Journal of Visceral Surgery|February 14, 2015
Acute mesenteric ischemia of arterial origin: importance of early revascularizationF Plumereau, S Mucci, P Le Naoures, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|June 5, 2012
Role of human UDP-glucuronosyltransferases in the biotransformation of the triazoloacridinone and imidazoacridinone antitumor agents C-1305 and C-1311: highly selective substrates for UGT1A10Barbara Fedejko-Kap, Stacie M Bratton, Moshe Finel, et al.
The FEBS Journal|February 1, 2007
Substrate specificity of the human UDP-glucuronosyltransferase UGT2B4 and UGT2B7. Identification of a critical aromatic amino acid residue at position 33Lydia Barre, Sylvie Fournel-Gigleux, Moshe Finel, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|May 19, 2009
Synthesis, structure characterization, and enzyme screening of clenbuterol glucuronidesAnna Alonen, Minna Gartman, Olli Aitio, et al.
International Journal of Pharmaceutics|September 8, 2009
Caco-2 cell monolayers as a tool to study simultaneous phase II metabolism and metabolite efflux of indomethacin, paracetamol and 1-naphtholSanna Siissalo, Laura Laine, Ari Tolonen, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|November 22, 2008
UDP-glucuronosyltransferases (UGTs) 2B7 and UGT2B17 display converse specificity in testosterone and epitestosterone glucuronidation, whereas UGT2A1 conjugates both androgens similarlyTaina Sten, Ingo Bichlmaier, Tiia Kuuranne, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|August 23, 2008
The configuration of the 17-hydroxy group variably influences the glucuronidation of beta-estradiol and epiestradiol by human UDP-glucuronosyltransferasesKatriina Itäaho, Peter I Mackenzie, Shin-ichi Ikushiro, et al.
Pageof 25