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G S Marks

Showing results (41-50 of 185) with videos related to

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Pharmacological Research Communications|February 1, 1975
Isolation of a protein-2-halogenoethylamine complex from rabbit aortic tissueJ Boegman, J Elliott, V Krupa, et al.
Canadian Journal of Physiology and Pharmacology|October 16, 2001
Isolation of regioisomers of N-alkylprotoporphyrin IX from chick embryo liver after treatment with porphyrinogenic xenobioticsS M Kobus, S G Wong, G S Marks
Biochemical Pharmacology|March 15, 1988
Xenobiotic mediated inhibition of hepatic uroporphyrinogen decarboxylase activity in 17-day-old chick embryo liver cells in cultureM E Lyon, J A Owen, G S Marks
Circulation|December 1, 1982
Arterial-venous nitroglycerin gradient during intravenous infusion in manP W Armstrong, J A Moffat, G S Marks
Molecular Pharmacology|July 1, 1980
Association between the membrane-fluidizing properties and porphyrin-inducing activity of alfaxolone and related steroidsI R Neilson, M A Singer, G S Marks
Molecular Pharmacology|July 1, 1978
Effect of varying the insulin to glucagon ratio on porphyrin biosynthesis in chick embryo liver cellsP W Fischer, J K Stephens, G S Marks
Journal of Chromatography|February 29, 1980
Second derivative-high-performance liquid chromatographic-fluorometric detection of porphyrins in chick embryo liver cell culture mediumD T Zelt, J A Owen, G S Marks
Molecular Pharmacology|September 1, 1981
Ferrochelatase-inhibitory and porphyrin-inducing properties of 3,5-diethoxycarbonyl-1, 4-dihydro-2,4,6-trimethylpyridine and its analogues in chick embryo liver cellsS P Cole, R A Whitney, G S Marks
Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 22, 2000
N-Methylprotoporphyrin is a more potent inhibitor of recombinant human than of recombinant chicken ferrochelataseJ T Gamble, H A Dailey, G S Marks
Drug Metabolism and Disposition: the Biological Fate of Chemicals|August 26, 1999
Cytochrome CYP sources of N-alkylprotoporphyrin IX after administration of porphyrinogenic xenobiotics to ratsS G Wong, E H Lin, G S Marks
Pageof 19

Showing results (41-50 of 185) with videos related to

Sort By:
Pageof 19
Pharmacological Research Communications|February 1, 1975
Isolation of a protein-2-halogenoethylamine complex from rabbit aortic tissueJ Boegman, J Elliott, V Krupa, et al.
Canadian Journal of Physiology and Pharmacology|October 16, 2001
Isolation of regioisomers of N-alkylprotoporphyrin IX from chick embryo liver after treatment with porphyrinogenic xenobioticsS M Kobus, S G Wong, G S Marks
Biochemical Pharmacology|March 15, 1988
Xenobiotic mediated inhibition of hepatic uroporphyrinogen decarboxylase activity in 17-day-old chick embryo liver cells in cultureM E Lyon, J A Owen, G S Marks
Circulation|December 1, 1982
Arterial-venous nitroglycerin gradient during intravenous infusion in manP W Armstrong, J A Moffat, G S Marks
Molecular Pharmacology|July 1, 1980
Association between the membrane-fluidizing properties and porphyrin-inducing activity of alfaxolone and related steroidsI R Neilson, M A Singer, G S Marks
Molecular Pharmacology|July 1, 1978
Effect of varying the insulin to glucagon ratio on porphyrin biosynthesis in chick embryo liver cellsP W Fischer, J K Stephens, G S Marks
Journal of Chromatography|February 29, 1980
Second derivative-high-performance liquid chromatographic-fluorometric detection of porphyrins in chick embryo liver cell culture mediumD T Zelt, J A Owen, G S Marks
Molecular Pharmacology|September 1, 1981
Ferrochelatase-inhibitory and porphyrin-inducing properties of 3,5-diethoxycarbonyl-1, 4-dihydro-2,4,6-trimethylpyridine and its analogues in chick embryo liver cellsS P Cole, R A Whitney, G S Marks
Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 22, 2000
N-Methylprotoporphyrin is a more potent inhibitor of recombinant human than of recombinant chicken ferrochelataseJ T Gamble, H A Dailey, G S Marks
Drug Metabolism and Disposition: the Biological Fate of Chemicals|August 26, 1999
Cytochrome CYP sources of N-alkylprotoporphyrin IX after administration of porphyrinogenic xenobiotics to ratsS G Wong, E H Lin, G S Marks
Pageof 19