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Journal of Biochemical Toxicology
|
January 1, 1989
Comparison of the formation of benzo[a]pyrene diolepoxide-DNA adducts in vitro by rat and human microsomes: evidence for the involvement of P-450IA1 and P-450IA2
K Vähäkangas, H Raunio, M Pasanen, et al.
Biokhimiia (Moscow, Russia)
|
May 1, 1990
[Cholesterol-hydroxylating cytochrome P-450 from bovine adrenal cortex mitochondria and human placenta: immunochemical properties and structural characteristics]
S A Usanov, A A Chernogolov, P Honkakoski, et al.
Clinical Pharmacology and Therapeutics
|
November 3, 1998
CYP2D6 polymorphism is not crucial for the disposition of selegiline
H Scheinin, M Anttila, M L Dahl, et al.
European Journal of Pharmacology
|
January 3, 1994
Cocaine N-demethylation and the metabolism-related hepatotoxicity can be prevented by cytochrome P450 3A inhibitors
P Pellinen, P Honkakoski, F Stenbäck, et al.
Acta Medica Scandinavica
|
January 1, 1983
Plasma high-density lipoproteins and liver lipids and proteins in man. Relation to hepatic histology and microsomal enzyme induction
P V Luoma, M J Savolainen, E A Sotaniemi, et al.
British Journal of Clinical Pharmacology
|
December 1, 1984
Drug metabolism in diabetic subjects with fatty livers
H I Pirttiaho, P I Salmela, E A Sotaniemi, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
July 1, 1997
Cytochrome P450 isozymes responsible for the metabolism of toluene and styrene in human liver microsomes
H Kim, R S Wang, E Elovaara, et al.
Pharmacology & Toxicology
|
February 1, 1993
Cytochrome P4502A-mediated coumarin 7-hydroxylation and testosterone hydroxylation in mouse and rat lung
P Honkakoski, J Mäenpää, J Leikola, et al.
Clinical Pharmacology and Therapeutics
|
July 1, 1986
Fibrotic process and drug metabolism in alcoholic liver disease
E A Sotaniemi, O Niemelä, L Risteli, et al.
British Journal of Pharmacology
|
February 28, 2007
New potent and selective cytochrome P450 2B6 (CYP2B6) inhibitors based on three-dimensional quantitative structure-activity relationship (3D-QSAR) analysis
L E Korhonen, M Turpeinen, M Rahnasto, et al.
Page
of 28
Search research articles
Search
Showing results (231-240 of 275) with videos related to
Sort By:
Page
of 28
Journal of Biochemical Toxicology
|
January 1, 1989
Comparison of the formation of benzo[a]pyrene diolepoxide-DNA adducts in vitro by rat and human microsomes: evidence for the involvement of P-450IA1 and P-450IA2
K Vähäkangas, H Raunio, M Pasanen, et al.
Biokhimiia (Moscow, Russia)
|
May 1, 1990
[Cholesterol-hydroxylating cytochrome P-450 from bovine adrenal cortex mitochondria and human placenta: immunochemical properties and structural characteristics]
S A Usanov, A A Chernogolov, P Honkakoski, et al.
Clinical Pharmacology and Therapeutics
|
November 3, 1998
CYP2D6 polymorphism is not crucial for the disposition of selegiline
H Scheinin, M Anttila, M L Dahl, et al.
European Journal of Pharmacology
|
January 3, 1994
Cocaine N-demethylation and the metabolism-related hepatotoxicity can be prevented by cytochrome P450 3A inhibitors
P Pellinen, P Honkakoski, F Stenbäck, et al.
Acta Medica Scandinavica
|
January 1, 1983
Plasma high-density lipoproteins and liver lipids and proteins in man. Relation to hepatic histology and microsomal enzyme induction
P V Luoma, M J Savolainen, E A Sotaniemi, et al.
British Journal of Clinical Pharmacology
|
December 1, 1984
Drug metabolism in diabetic subjects with fatty livers
H I Pirttiaho, P I Salmela, E A Sotaniemi, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
July 1, 1997
Cytochrome P450 isozymes responsible for the metabolism of toluene and styrene in human liver microsomes
H Kim, R S Wang, E Elovaara, et al.
Pharmacology & Toxicology
|
February 1, 1993
Cytochrome P4502A-mediated coumarin 7-hydroxylation and testosterone hydroxylation in mouse and rat lung
P Honkakoski, J Mäenpää, J Leikola, et al.
Clinical Pharmacology and Therapeutics
|
July 1, 1986
Fibrotic process and drug metabolism in alcoholic liver disease
E A Sotaniemi, O Niemelä, L Risteli, et al.
British Journal of Pharmacology
|
February 28, 2007
New potent and selective cytochrome P450 2B6 (CYP2B6) inhibitors based on three-dimensional quantitative structure-activity relationship (3D-QSAR) analysis
L E Korhonen, M Turpeinen, M Rahnasto, et al.
Page
of 28