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(1953)
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Skeggs Lt, Kahn, Marsh Wh (1953)
A method of assaying small amounts of hypertensin.Laboratory investigation; a journal of technical methods and pathology, 2 2
(1955)
A factor in plasma that enhances contraction produced by angiotonin on rabbit aortic strips, Fed
L. Skeggs, W. Marsh, J. Kahn, N. Shumway (1955)
AMINO ACID COMPOSITION AND ELECTROPHORETIC PROPERTIES OF HYPERTENSIN IThe Journal of Experimental Medicine, 102
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Chemistry and Methods of EnzymesNature, 154
L. Skeggs, W. Marsh, J. Kahn, N. Shumway (1954)
THE EXISTENCE OF TWO FORMS OF HYPERTENSINThe Journal of Experimental Medicine, 99
L. Skeggs, W. Marsh, J. Kahn, N. Shumway (1954)
THE PURIFICATION OF HYPERTENSIN IThe Journal of Experimental Medicine, 100
L. Skeggs, J. Leonards, C. Heisler (1949)
Artificial Kidney. II. Construction and Operation of an Improved Continuous Dialyzer.∗Proceedings of the Society for Experimental Biology and Medicine, 72
S. Moore, W. Stein (1954)
A modified ninhydrin reagent for the photometric determination of amino acids and related compounds.The Journal of biological chemistry, 211 2
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It has been shown by use of isolated, perfused rat kidneys that hypertensin II is a potent vasoconstrictor substance while hypertensin I is not. Hence it would appear that in intact animals the pressor activity of hypertensin I results from its rapid conversion to hypertensin II. An enzyme which effects this conversion has been procured from horse plasma in a semipurified form by means of ammonium sulfate fractionation and isoelectric precipitation. A method is described for estimating the activity of the enzyme. An example of the use of the preparation in converting purified hypertensin I to hypertensin II has been described. Footnotes Submitted: 13 November 1955
The Journal of Experimental Medicine – Rockefeller University Press
Published: Mar 1, 1956
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