Biomedical subjects
J Stewart
Publications and source records attributed to J Stewart.
Genetic variation in patterns of nephron function during natriuresis in mice.
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[Micropuncture study of urine formation. IV. In the mouse undergoing salt diuresis].
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Comparison of the 50 and 100 gram oral glucose tolerance test.
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Free and esterified cholesterol quantitation: human menstrual cycle, rat estrous cycle and pregnancy in the rat.
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Automation in the blood transfusion laboratory. II. ABO grouping, Rh and Kell typing, antibody screening, and VD testing of blood donations in the autoanalyzer.
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Diuretic responses to electrolyte loads in four strains of mice.
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Saphenous-vein arteriovenous fistula in regular dialysis treatment.
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Biometrical genetics with one or two loci. I. The choice of a specific genetic model.
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Biometrical genetics with one or two loci. II. The estimation of linkage.
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Pregnancy-induced changes in rat tissue glucose-6-phosphate dehydrogenase activities and sex chromatin frequencies.
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Studies on syndrome of diabetes insipidus associated with oligosyndactyly in mice.
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Effect of vasopressin on the entry of sodium into the renal tubule.
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IgA and partial deletions of chromosome 18.
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Diuretic responses to water-load in four strains of mice.
1. The kinetics of excretion of water, sodium and potassium following a stomach load of water, with and without an initial injection of vasopressin, are described in each of four strains of mice: RAP, CBA/FaCam, Peru and A/Cam.2. In general there was a diuretic lag followed by an increase in the rate of excretion of water to a maximum, after which the rate of excretion fell again to near resting levels. The rate of excretion of sodium rose to an initial maximum which significantly preceded the maximum rate of water excretion. The rate of excretion of sodium then fell to a minimum at a time not significantly different from the time of maximum rate of water excretion.3. The effect of an initial injection of vasopressin was to increase and to prolong the initial rise in rate of sodium excretion. The maximum rate of water excretion and the minimum sodium concentration were delayed, but the levels eventually reached were not significantly altered, by the vasopressin injection.4. The strains of mice differed significantly in diuretic lag, maximum rate of diuresis, and 3 hr excretion of water and electrolytes.5. The strains also differed significantly in the effects of vasopressin, both in increasing diuretic lag and in increasing sodium excretion. There was no correlation between the antidiuretic and natriuretic effects of vasopressin.
State-dependent learning produced with steroids.
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Genetic variation in diuretic responses: further and correlated responses to selection.
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WHO collaborative study on the sero-epidemiology of rubella.
Under the auspices of WHO an investigation was made by 9 laboratories in different parts of the world on the distribution of rubella antibodies in girls and women of child-bearing age. In the first part of the study the objective was to determine the reliability and reproducibility of the tests employed. It was found that there were no significant differences in the variability of the titres obtained in different laboratories when the results were compared with those obtained by repeatedly testing the same sera in one laboratory.In the second part of the study sera were obtained from girls in schools and women attending clinics and health centres. They were not taken from random samples of the populations. In most of the studies the pattern of development of antibody was similar. About half the persons had antibody at 6-8 years of age and 80%-87% at 17-22 years of age, the percentage remaining relatively constant thereafter. The island populations of Trinidad and Jamaica and a rural area of Japan were, however, found to have significantly fewer women with antibodies than urban areas in Europe or the Americas.