THE METABOLISM OF DRUGS BY LIVER MICROSOMES FROM ALLOXAN-DIABETIC RATS: LONG TERM DIABETES.
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Alloxan↗
Biomedical subjects
J R FOUTS
Publications and source records attributed to J R FOUTS.
Inhibition of microsomal drug metabolic pathways by chloramphenicol.
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Chloramphenicol↗
Stimulation of hepatic microsomal drug metabolism in the newborn and fetal rabbit.
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Aminopyrine↗
The metabolism of drugs by subfractions of hepatic microsomes.
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Humans↗
The metabolism of drugs by regenerating liver.
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Enzymes↗
The neuromuscular blocking action of paromomycin.
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Anti-Bacterial Agents↗
The metabolism of drugs by liver microsomes from alloxan-diabetic rats.
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Alloxan↗
A classroom demonstration of some pharmacological properties of antibiotics.
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Anti-Bacterial Agents↗
Factors affecting drug metabolism by liver microsomes. IV. Starvation.
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Humans↗
A mammalian thioglycosidase.
A thioglycosidase capable of catalyzing the hydrolysis of 6-purine beta-d-glucothiopyranoside and other thioglycosides has been found in a number of mammalian tissues (including tumors) as well as in almond emulsin. The substrate specificity of mammalian thioglycosidase involves both the aglycone and the glycosyl moieties.
Glycoside Hydrolases↗
Drug metabolism in the newborn rabbit.
A number of drugs that are metabolized through the action of enzymes present in liver microsomes in the adult rabbit are not metabolized in livers of newborn rabbits. The development of metabolic pathways during a period of 4 weeks is presented. Evidence is given for the presence in livers of baby rabbits of inhibitors of some of these drug-enzyme systems.
Animals↗
Enzymatic metabolism of strychnine.
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Strychnine↗
Report on the use of closed-circuit television in the teaching of pharmacology.
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Communications Media↗
Degradation of mescaline by amine oxidases.
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Humans↗
Amine oxidases. XIII. Monoamines as substrates of diamine oxidase.
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Amine Oxidase (Copper-Containing)↗
The enzymatic reduction of chloramphenicol, p-nitrobenzoic acid and other aromatic nitro compounds in mammals.
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Animals↗
Enzymatic reduction of prontosil and other azo dyes.
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Azo Compounds↗
On the mechanism of drug potentiation by iproniazid (2-isopropyl-1-isonicotinyl hydrazine).
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Barbiturates↗