Results 241 to 250 of about 42,048 (270)
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Cytochrome P-450 enzyme system inhibitors/tretinoin interaction
Reactions Weekly, 2022openaire +1 more source
The Cytochrome P-450 Drug Metabolizing Enzyme System
Journal of Head Trauma Rehabilitation, 2002Bruno, Wroblewski, Mel B, Glenn
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Selective damage of ethanol to cytochrome P-450 enzyme system in alcoholics
Journal of Hepatology, 1989D. von Knebel +4 more
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Biokhimiia (Moscow, Russia), 1977
The lipid composition of rat liver microsomes, their "ghosts" and the reconstituted membrane hydroxylation system was investigated. The phospholipid content and composition of the reconstituted membranes were found to depend on the reconstitution method. The reconstituted membranes contained besides phospholipids also cholesterol and gangliosides.
E V, Diatlovitskaia +4 more
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The lipid composition of rat liver microsomes, their "ghosts" and the reconstituted membrane hydroxylation system was investigated. The phospholipid content and composition of the reconstituted membranes were found to depend on the reconstitution method. The reconstituted membranes contained besides phospholipids also cholesterol and gangliosides.
E V, Diatlovitskaia +4 more
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Voprosy onkologii, 1987
Pretreatment of Wistar male rats with antioxidants prevented the toxic effect of diethylnitrosamine (DENA) at LD50. Six-fold acceleration of DENA excretion and significant increase of maximum plasma concentration of a DENA metabolite nitrite were, also observed after antioxidants treatment. Liver microsomal metabolism of DNA was altered by pretreatment
T S, Shuliakovskaia +4 more
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Pretreatment of Wistar male rats with antioxidants prevented the toxic effect of diethylnitrosamine (DENA) at LD50. Six-fold acceleration of DENA excretion and significant increase of maximum plasma concentration of a DENA metabolite nitrite were, also observed after antioxidants treatment. Liver microsomal metabolism of DNA was altered by pretreatment
T S, Shuliakovskaia +4 more
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Neurotoxicology, 1984
The biological oxidation of several tributyltin derivatives, by a cytochrome P-450 dependent monooxygenase enzyme system with reduced nicotinamideadeninedinucleotidephosphate as the essential cofactor, produced carbon-hydroxylated compounds identified as alpha-, beta-, gamma- and delta-hydroxybutyldibutyltin derivatives.
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The biological oxidation of several tributyltin derivatives, by a cytochrome P-450 dependent monooxygenase enzyme system with reduced nicotinamideadeninedinucleotidephosphate as the essential cofactor, produced carbon-hydroxylated compounds identified as alpha-, beta-, gamma- and delta-hydroxybutyldibutyltin derivatives.
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