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Regulation of Factor VIIIa in the Intrinsic Factor Xase
Thrombosis and Haemostasis, 1999IntroductionHemophilia A, the most common of the severe, inherited bleeding disorders, results from a deficiency or defect in the plasma protein factor VIII. The activated form of the protein serves as an essential cofactor for factor IXa in the conversion of factor X to factor Xa. This surface-bound complex of enzyme and cofactor is referred to as the
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Assay of intrinsic factor with anti-intrinsic factor serum in vitro
Biochimica et Biophysica Acta, 1963J, ABELS, W, BOUMA, H O, NIEWEG
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A Synthetic Factor XIIa Inhibitor Blocks Selectively Intrinsic Coagulation Initiation.
ACS Chemical Biology, 2015Vanessa Baeriswyl +6 more
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Structural basis for receptor recognition of vitamin-B12–intrinsic factor complexes
Nature, 2010C. Andersen +4 more
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