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PUBMED FOR HANDHELDS

Journal Abstract Search


175 related items for PubMed ID: 16706977

  • 1. Intrinsic stability and functional properties of disulfide bond-stabilized coagulation factor VIIIa variants.
    Gale AJ, Radtke KP, Cunningham MA, Chamberlain D, Pellequer JL, Griffin JH.
    J Thromb Haemost; 2006 Jun; 4(6):1315-22. PubMed ID: 16706977
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  • 2. Disulfide bond-stabilized factor VIII has prolonged factor VIIIa activity and improved potency in whole blood clotting assays.
    Radtke KP, Griffin JH, Riceberg J, Gale AJ.
    J Thromb Haemost; 2007 Jan; 5(1):102-8. PubMed ID: 17059431
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  • 4. Structural and functional characterization of platelet receptor-mediated factor VIII binding.
    Ahmad SS, Scandura JM, Walsh PN.
    J Biol Chem; 2000 Apr 28; 275(17):13071-81. PubMed ID: 10777612
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  • 11. A3 domain region 1803-1818 contributes to the stability of activated factor VIII and includes a binding site for activated factor IX.
    Bloem E, Meems H, van den Biggelaar M, Mertens K, Meijer AB.
    J Biol Chem; 2013 Sep 06; 288(36):26105-26111. PubMed ID: 23884417
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  • 12. Binding of factor VIIIa and factor VIII to factor IXa on phospholipid vesicles.
    Duffy EJ, Parker ET, Mutucumarana VP, Johnson AE, Lollar P.
    J Biol Chem; 1992 Aug 25; 267(24):17006-11. PubMed ID: 1512239
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  • 13. Activation of factor VIII by thrombin increases its affinity for binding to synthetic phospholipid membranes and activated platelets.
    Saenko EL, Scandella D, Yakhyaev AV, Greco NJ.
    J Biol Chem; 1998 Oct 23; 273(43):27918-26. PubMed ID: 9774404
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  • 17. Isolation and characterization of thrombin-activated human factor VIII.
    Curtis JE, Helgerson SL, Parker ET, Lollar P.
    J Biol Chem; 1994 Feb 25; 269(8):6246-51. PubMed ID: 8119969
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  • 18. Model for the factor VIIIa-dependent decay of the intrinsic factor Xase. Role of subunit dissociation and factor IXa-catalyzed proteolysis.
    Fay PJ, Beattie TL, Regan LM, O'Brien LM, Kaufman RJ.
    J Biol Chem; 1996 Mar 15; 271(11):6027-32. PubMed ID: 8626386
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  • 20. Mutations associated with hemophilia A in the 558-565 loop of the factor VIIIa A2 subunit alter the catalytic activity of the factor Xase complex.
    Jenkins PV, Freas J, Schmidt KM, Zhou Q, Fay PJ.
    Blood; 2002 Jul 15; 100(2):501-8. PubMed ID: 12091341
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