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W F Trager

Showing results (31-40 of 85) with videos related to

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The Journal of Clinical Investigation|March 1, 1980
Stereoselective interaction of phenylbutazone with [12C/13C]warfarin pseudoracemates in manR A O'Reilly, W F Trager, C H Motley, et al.
Chirality|January 1, 1991
Metabolic enantiomeric interactions: the inhibition of human (S)-warfarin-7-hydroxylase by (R)-warfarinK L Kunze, A C Eddy, M Gibaldi, et al.
Journal of Pharmaceutical Sciences|October 1, 1985
Metabolic fate of phenprocoumon in humansS Toon, L D Heimark, W F Trager, et al.
Chemical Research in Toxicology|September 1, 1990
Studies on the cytochrome P-450 catalyzed ring alpha-carbon oxidation of the nigrostriatal toxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)S Ottoboni, T J Carlson, W F Trager, et al.
Biomedical Mass Spectrometry|February 1, 1975
The rapid identification of a new metabolite of warfarin via a chemical ionization mass spectrometry ion doublet techniqueL R Pohl, S D Nelson, W A Garland, et al.
Biochemistry|June 10, 1997
Intramolecular isotope effects for benzylic hydroxylation of isomeric xylenes and 4,4'-dimethylbiphenyl by cytochrome P450: relationship between distance of methyl groups and masking of the intrinsic isotope effectK R Iyer, J P Jones, J F Darbyshire, et al.
Chirality|January 1, 1990
Chemical synthesis, absolute configuration, and stereochemistry of formation of 10-hydroxywarfarin: a major oxidative metabolite of (+)-(R)-warfarin from hepatic microsomal preparationsR F Lawrence, A E Rettie, A C Eddy, et al.
Journal of Pharmaceutical Sciences|August 1, 1977
Quantification of lidocaine and several metabolites utilizing chemical-ionization mass spectrometry and stable isotope labelingS D Nelson, W A Garland, G D Breck, et al.
Journal of Medicinal Chemistry|November 1, 1977
Structure of warfarin in solutionE J Valente, E C Lingafelter, W R Porter, et al.
Journal of Pharmaceutical Sciences|October 1, 1980
Simultaneous analysis of phenobarbital and p-hydroxyphenobarbital in biological fluids by GLC-chemical-ionization mass spectrometryI H Patel, R H Levy, J M Neal, et al.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
The Journal of Clinical Investigation|March 1, 1980
Stereoselective interaction of phenylbutazone with [12C/13C]warfarin pseudoracemates in manR A O'Reilly, W F Trager, C H Motley, et al.
Chirality|January 1, 1991
Metabolic enantiomeric interactions: the inhibition of human (S)-warfarin-7-hydroxylase by (R)-warfarinK L Kunze, A C Eddy, M Gibaldi, et al.
Journal of Pharmaceutical Sciences|October 1, 1985
Metabolic fate of phenprocoumon in humansS Toon, L D Heimark, W F Trager, et al.
Chemical Research in Toxicology|September 1, 1990
Studies on the cytochrome P-450 catalyzed ring alpha-carbon oxidation of the nigrostriatal toxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)S Ottoboni, T J Carlson, W F Trager, et al.
Biomedical Mass Spectrometry|February 1, 1975
The rapid identification of a new metabolite of warfarin via a chemical ionization mass spectrometry ion doublet techniqueL R Pohl, S D Nelson, W A Garland, et al.
Biochemistry|June 10, 1997
Intramolecular isotope effects for benzylic hydroxylation of isomeric xylenes and 4,4'-dimethylbiphenyl by cytochrome P450: relationship between distance of methyl groups and masking of the intrinsic isotope effectK R Iyer, J P Jones, J F Darbyshire, et al.
Chirality|January 1, 1990
Chemical synthesis, absolute configuration, and stereochemistry of formation of 10-hydroxywarfarin: a major oxidative metabolite of (+)-(R)-warfarin from hepatic microsomal preparationsR F Lawrence, A E Rettie, A C Eddy, et al.
Journal of Pharmaceutical Sciences|August 1, 1977
Quantification of lidocaine and several metabolites utilizing chemical-ionization mass spectrometry and stable isotope labelingS D Nelson, W A Garland, G D Breck, et al.
Journal of Medicinal Chemistry|November 1, 1977
Structure of warfarin in solutionE J Valente, E C Lingafelter, W R Porter, et al.
Journal of Pharmaceutical Sciences|October 1, 1980
Simultaneous analysis of phenobarbital and p-hydroxyphenobarbital in biological fluids by GLC-chemical-ionization mass spectrometryI H Patel, R H Levy, J M Neal, et al.
Pageof 9