Titlebook: Kinins—II; Biochemistry, Pathop Setsuro Fujii,Hiroshi Moriya,Tomoji Suzuki Book 1979 The Editor(s) (if applicable) and The Author(s), under

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indigenous

A Direct Radioimmunoassay for Human Urinary Kallikreino each tube. The tubes were incubated 18 hr at 4°C, centrifuged 4,000 rpm for 30 min and, after decantation, the precipitate was counted for .I. The RIA reported here is sufficiently sensitive to detect 1 ng of kallikrein and should offer a useful technique to determine alterations of the kallikrein

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Glandular Kallikrein in Plasma and Urine: Evaluation of a Direct RIA for Its Determinationy the direct RIA and by a kininogenase method (r = 0.75, p< 0.001) in both DOCA-salt treated and in the control rats.Although the results obtained by the direct RIA and an esterase method significantly correlate in the control rats (r = 0.67,p <0.001), they did not in the DOCA-salt rats (r = −0.048,

WAG

Fluorogenic Peptide Substrates for Proteases in Blood Coagulation, Kallikrein-Kinin and Fibrinolysisity sequence for enterokinase (Ottesen, 1967). Similarly, Factor Xa is presumed to recognize the tetrapeptide sequence Ile-Glu-Gly-Arg located close to the cleavage site required for the activation of bovine prothrombin (Magnusson et al. 1975). Based on this idea, several peptidyl-p-nitroanilides, s

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Determination of Hageman Factor (HG, Factor XII) and Plasma Prekallikrein (Fletcher Factor) by Radiot difference between the levels of HF and prekallikrein in plasma and those in serum. Both HF and prekallikrein were significantly reduced in plasmas of patients with advanced liver cirrhosis or disseminated intravascular coagulation (DIC) and in cord serums, but they were normal in plasmas obtained

Dorsal-Kyphosis

N. Yanaihara,H. Sato,A. Inoue,N. Sakura,M. Sakagami,T. Mochizuki,H. Nakamura,C. Yanaihara

Leaven

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Keishi Abe,Hisao Kato,Yataka Sakurai,Toru Itoh,Keitaro Saito,Toshiaki Haruyama,Yoichi Otsuka,Kaoru Y

大都市