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C. Flood, … , S. A. S. Tait, S. Willoughby
Citation Information: J Clin Invest. 1967;46(5):717-727. https://doi.org/10.1172/JCI105572.
C. Flood, … , S. A. S. Tait, S. Willoughby
Published May 1, 1967
Citation Information: J Clin Invest. 1967;46(5):717-727. https://doi.org/10.1172/JCI105572.
Abstract
After intravenous and oral administration of radioactive aldosterone to normal subjects, 7.3 ± 0.4 (SE) and 5.4 ± 0.5 (SE)%, respectively, of the dose was recovered from a 48-hour collection of urine as aldosterone released by mild acid hydrolysis (from aldosterone 18-glucuronide), and 35 ± 5 (SE) and 39 ± 4 (SE)%, respectively, was recovered as tetrahydroaldosterone after incubation with β-glucuronidase.
Authors
C. Flood, G. Pincus, J. F. Tait, S. A. S. Tait, S. Willoughby
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