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Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
September 3, 2015
The Polymorphic Variant P24T of UDP-Glucuronosyltransferase 1A4 and Its Unusual Consequences
Johanna Troberg, Moshe Finel
British Journal of Clinical Pharmacology
|
February 10, 2019
Case report by Toce and co-authors: Have all the reasons for poor morphine glucuronidation been addressed?
Moshe Finel, Erkka Järvinen
Current Drug Metabolism
|
January 29, 2008
The UDP-glucuronosyltransferases as oligomeric enzymes
Moshe Finel, Mika Kurkela
Molecular Pharmacology
|
March 11, 2010
A molecular model of the human UDP-glucuronosyltransferase 1A1, its membrane orientation, and the interactions between different parts of the enzyme
Liisa Laakkonen, Moshe Finel
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
January 22, 2010
How many and which amino acids are responsible for the large activity differences between the highly homologous UDP-glucuronosyltransferases (UGT) 1A9 and UGT1A10?
Katriina Itäaho, Liisa Laakkonen, Moshe Finel
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
March 26, 2011
N-glucuronidation of drugs and other xenobiotics by human and animal UDP-glucuronosyltransferases
Sanna Kaivosaari, Moshe Finel, Mikko Koskinen
The Journal of Steroid Biochemistry and Molecular Biology
|
November 10, 2019
Human efflux transport of testosterone, epitestosterone and other androgen glucuronides
Erkka Järvinen, Heidi Kidron, Moshe Finel
The Journal of Pharmacy and Pharmacology
|
July 23, 2008
High-throughput screening technologies for drug glucuronidation profiling
Olga Trubetskoy, Moshe Finel, Vladimir Trubetskoy
Biochemical Pharmacology
|
August 5, 2008
The human UDP-glucuronosyltransferase UGT1A3 is highly selective towards N2 in the tetrazole ring of losartan, candesartan, and zolarsartan
Anna Alonen, Moshe Finel, Risto Kostiainen
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
August 23, 2012
UDP-glucuronic acid binds first and the aglycone substrate binds second to form a ternary complex in UGT1A9-catalyzed reactions, in both the presence and absence of bovine serum albumin
Nenad Manevski, Jari Yli-Kauhaluoma, Moshe Finel
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of 13
Search research articles
Search
Showing results (1-10 of 122) with videos related to
Sort By:
Page
of 13
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
September 3, 2015
The Polymorphic Variant P24T of UDP-Glucuronosyltransferase 1A4 and Its Unusual Consequences
Johanna Troberg, Moshe Finel
British Journal of Clinical Pharmacology
|
February 10, 2019
Case report by Toce and co-authors: Have all the reasons for poor morphine glucuronidation been addressed?
Moshe Finel, Erkka Järvinen
Current Drug Metabolism
|
January 29, 2008
The UDP-glucuronosyltransferases as oligomeric enzymes
Moshe Finel, Mika Kurkela
Molecular Pharmacology
|
March 11, 2010
A molecular model of the human UDP-glucuronosyltransferase 1A1, its membrane orientation, and the interactions between different parts of the enzyme
Liisa Laakkonen, Moshe Finel
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
January 22, 2010
How many and which amino acids are responsible for the large activity differences between the highly homologous UDP-glucuronosyltransferases (UGT) 1A9 and UGT1A10?
Katriina Itäaho, Liisa Laakkonen, Moshe Finel
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
March 26, 2011
N-glucuronidation of drugs and other xenobiotics by human and animal UDP-glucuronosyltransferases
Sanna Kaivosaari, Moshe Finel, Mikko Koskinen
The Journal of Steroid Biochemistry and Molecular Biology
|
November 10, 2019
Human efflux transport of testosterone, epitestosterone and other androgen glucuronides
Erkka Järvinen, Heidi Kidron, Moshe Finel
The Journal of Pharmacy and Pharmacology
|
July 23, 2008
High-throughput screening technologies for drug glucuronidation profiling
Olga Trubetskoy, Moshe Finel, Vladimir Trubetskoy
Biochemical Pharmacology
|
August 5, 2008
The human UDP-glucuronosyltransferase UGT1A3 is highly selective towards N2 in the tetrazole ring of losartan, candesartan, and zolarsartan
Anna Alonen, Moshe Finel, Risto Kostiainen
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
August 23, 2012
UDP-glucuronic acid binds first and the aglycone substrate binds second to form a ternary complex in UGT1A9-catalyzed reactions, in both the presence and absence of bovine serum albumin
Nenad Manevski, Jari Yli-Kauhaluoma, Moshe Finel
Page
of 13