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Pharmacological Reviews
|
June 1, 1981
The use of stable isotopes in pharmacological research
T A Baillie
Pharmaceutisch Weekblad. Scientific Edition
|
June 19, 1992
Metabolism of valproate to hepatotoxic intermediates
T A Baillie
Chemical Research in Toxicology
|
July 1, 1988
Metabolic activation of valproic acid and drug-mediated hepatotoxicity. Role of the terminal olefin, 2-n-propyl-4-pentenoic acid
T A Baillie
Advances in Experimental Medicine and Biology
|
January 5, 2002
Biological reactive intermediates in drug discovery and development: a perspective from the pharmaceutical industry
T A Baillie, K Kassahun
The American Journal of Gastroenterology
|
September 1, 1992
Re:Incidental microvesicular steatosis due to valproic acid anticonvulsant therapy
J Baillie, T A Baillie
Advances in Pharmacology (San Diego, Calif.)
|
January 1, 1994
Reversibility in glutathione-conjugate formation
T A Baillie, K Kassahun
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
March 1, 1993
Cytochrome P-450-mediated dehydrogenation of 2-n-propyl-2(E)-pentenoic acid, a pharmacologically-active metabolite of valproic acid, in rat liver microsomal preparations
K Kassahun, T A Baillie
Chemical Research in Toxicology
|
March 1, 1997
Metabolism of the chemoprotective agent diallyl sulfide to glutathione conjugates in rats
L Jin, T A Baillie
FEBS Letters
|
October 15, 1975
Role of the site of sulpho-conjugation on the formation of hydroxylated corticosterone metabolites in the rat
T A Baillie, H Eriksson
Biomedical Mass Spectrometry
|
July 1, 1984
Evidence for the in vitro metabolism of allylisopropylacetamide to reactive intermediates. Mechanistic studies with oxygen-18
K S Prickett, T A Baillie
Page
of 13
Search research articles
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Showing results (1-10 of 128) with videos related to
Sort By:
Page
of 13
Pharmacological Reviews
|
June 1, 1981
The use of stable isotopes in pharmacological research
T A Baillie
Pharmaceutisch Weekblad. Scientific Edition
|
June 19, 1992
Metabolism of valproate to hepatotoxic intermediates
T A Baillie
Chemical Research in Toxicology
|
July 1, 1988
Metabolic activation of valproic acid and drug-mediated hepatotoxicity. Role of the terminal olefin, 2-n-propyl-4-pentenoic acid
T A Baillie
Advances in Experimental Medicine and Biology
|
January 5, 2002
Biological reactive intermediates in drug discovery and development: a perspective from the pharmaceutical industry
T A Baillie, K Kassahun
The American Journal of Gastroenterology
|
September 1, 1992
Re:Incidental microvesicular steatosis due to valproic acid anticonvulsant therapy
J Baillie, T A Baillie
Advances in Pharmacology (San Diego, Calif.)
|
January 1, 1994
Reversibility in glutathione-conjugate formation
T A Baillie, K Kassahun
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
March 1, 1993
Cytochrome P-450-mediated dehydrogenation of 2-n-propyl-2(E)-pentenoic acid, a pharmacologically-active metabolite of valproic acid, in rat liver microsomal preparations
K Kassahun, T A Baillie
Chemical Research in Toxicology
|
March 1, 1997
Metabolism of the chemoprotective agent diallyl sulfide to glutathione conjugates in rats
L Jin, T A Baillie
FEBS Letters
|
October 15, 1975
Role of the site of sulpho-conjugation on the formation of hydroxylated corticosterone metabolites in the rat
T A Baillie, H Eriksson
Biomedical Mass Spectrometry
|
July 1, 1984
Evidence for the in vitro metabolism of allylisopropylacetamide to reactive intermediates. Mechanistic studies with oxygen-18
K S Prickett, T A Baillie
Page
of 13