Hepatic protoporphyria in weanling pigs.
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Alkanes↗
Biomedical subjects
D A Roe
Publications and source records attributed to D A Roe.
Factors affecting the induction of porphyria in the laboratory rat. Biochemical and photobiological studies using diethyl 1,4-dihydro-2,4,6-trimethyl-pyridine-3,5-dicarboxylate (DDC) as a porphyrogenic agent.
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Animals↗
Sulphur metabolism in relation to cutaneous disease.
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Chondroitin↗
Body composition of pre-adolescent and adolescent girls. IV. Total body water and creatinine excretion.
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Adipose Tissue↗
Essential hyperlipemia with xanthomatosis: effects of cholestyramine and clofibrate.
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Adult↗
Body composition of pre-adolescent and adolescent girls.
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Adipose Tissue↗
Body composition of pre-adolescent and adolescent girls. II. Anthropometric measurements.
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Adolescent↗
Body composition studies of pre-adolescent and adolescent girls. 3. Predicting specific gravity.
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Adolescent↗
Nutrition reports.
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Drug-Related Side Effects and Adverse Reactions↗
Homeostatic mechanisms for the compensation of cutaneous sulfur losses.
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Adult↗
Nutrient losses from the skin in health and disease.
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Humans↗
Estimation of sulfur in biological materials by atomic absorption spectrometry.
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Methionine↗
Objective clinical methods used in the evaluation of skin disease.
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Dermatology↗
The effect of hypocholesteremic agents on the skin.
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Acanthosis Nigricans↗
Taurine intolerance in psoriasis.
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Humans↗
Pharmacokinetics of ethanol in the ferret.
Select doses of ethanol (25%, W/V) were administered to female ferrets (Mustela putorius) by gastric intubation to determine dosage corresponding to peak blood alcohol levels (BAL) greater than 100 mg/100 ml of blood (mg%) for an extended duration. Low doses (6 ml/kg) resulted in peak BAL of 202 mg% in 1.5 hr and 50 mg% after 12 hr. Intermediate doses (8 ml/kg) resulted in peak BAL of 253 mg% in 1.4 hr and 89 mg% after 12 hr. High doses (12 ml/kg) did not increase peak BAL proportionately, resulted in BAL of 128 mg% after 12 hr, and increased the volume of distribution significantly. A computer-based estimate of kinetic parameters led to the conclusion that metabolism in this range of BAL was not a first order process. Moreover, a decreasing enzyme velocity with increasing substrate concentration precluded calculation of Michaelis-Menten parameters and suggested possible substrate inhibition effects.
Animals↗