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Titlebook: Bradykinin, Kallidin and Kallikrein; Ervin G. Erdös,Anne F. Wilde Book 1970 Springer-Verlag Berlin · Heidelberg 1970 Respiration.antibody.

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Assay Methods in the Kinin Systemd potent kinin hormones was discovered. The pioneers in the field of this subdivision of tissue hormones used essentially the same assay methods for the detection of the kinins that we do today. . and . (1928) demonstrated by intravenous injection of urine in the dog the vasodilator activity of kall
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Kallikreins in Glandular Tissuess more comprehensively they might be defined as those proteolytic enzymes of animal origin which release a kinin from kininogen but, as far as is known, do not readily cleave peptide bonds in other proteins. The term kininogenase is a general one which has been applied to any enzyme that liberates a
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Snake Venoms necessary in enzymatic studies, and enzymes from snake venoms are used in some of these methods. These enzymes include phospholipase A (EC 3.1.1.4), L-amino-acid oxidase (EC 1.4.3.2), phosphodiesterase (EC 3.1.4.1), and 5′-nucleotidase (EC 3.1.3.5). Much of the literature on these has been reviewed
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Kallikrein Inhibitorstion of the active principles. The activity of kininogenases can be controlled either by blocking with inhibitors or by degradation with enzymes. Under normal conditions the system is regulated with remarkable precision; in pathological states the mechanism may be overwhelmed.
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Discovery of the Most Important Kallikreins and Kallikrein Inhibitors trained in this field; he therefore asked a well-known physiological chemist to isolate and chemically characterize this substance. But the chemist, who was pharmacologically well informed, declined, since he thought the action of urine on blood pressure would be the sum of the actions of substance
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