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Factor VIIIa

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  • An engineered interdomain disulfide bond stabilizes human blood coagulation factor viiia  Academic Article
  • Anticoagulant dysfunction of human Arg352Trp-activated protein C caused by defective factor Va inactivation  Academic Article
  • Blood coagulation: The outstanding hydrophobic residues  Academic Article
  • Cathepsin g, a leukocyte protease, activates coagulation factorviii  Academic Article
  • Detailed mechanisms of the inactivation of factor viiia by activated protein c in the presence of its cofactors, protein s and factor v  Academic Article
  • Factor V is an anticoagulant cofactor for activated protein C during inactivation of factor Va  Academic Article
  • Function of the activated protein c (apc) autolysis loop in activated fviii inactivation  Academic Article
  • Identification of a sequence of human activated protein-C (residues 390-404) essential for its anticoagulant activity  Academic Article
  • Intrinsic stability and functional properties of disulfide bond-stabilized coagulation factor VIIIa variants  Academic Article
  • Prothrombin amino terminal region helps protect coagulation factor Va from proteolytic inactivation by activated protein C  Academic Article
  • Selective factor VIII activation by the tissue factor-factor VIIa-factor Xa complex  Academic Article

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