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Journal Abstract Search

651 related items for PubMed ID: 27683759

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  • 9. Type 2M von Willebrand disease: F606I and I662F mutations in the glycoprotein Ib binding domain selectively impair ristocetin- but not botrocetin-mediated binding of von Willebrand factor to platelets.
    Hillery CA, Mancuso DJ, Evan Sadler J, Ponder JW, Jozwiak MA, Christopherson PA, Cox Gill J, Paul Scott J, Montgomery RR.
    Blood; 1998 Mar 01; 91(5):1572-81. PubMed ID: 9473222
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  • 10. A new case of platelet-type von Willebrand disease supports the recent findings of gain-of-function GP1BA variants outside the C-terminal disulphide loop enhances affinity for von Willebrand factor.
    Monteiro C, Gonçalves A, Pereira M, Lau C, Morais S, Santos R.
    Br J Haematol; 2023 Nov 01; 203(4):673-677. PubMed ID: 37592722
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  • 11. Molecular genetics of type 2 von Willebrand disease.
    Fressinaud E, Mazurier C, Meyer D.
    Int J Hematol; 2002 Jan 01; 75(1):9-18. PubMed ID: 11843298
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  • 13. Platelet-type von Willebrand disease: new insights into the molecular pathophysiology of a unique platelet defect.
    Othman M, Kaur H, Emsley J.
    Semin Thromb Hemost; 2013 Sep 01; 39(6):663-73. PubMed ID: 23934752
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  • 14. A novel D235Y mutation in the GP1BA gene enhances platelet interaction with von Willebrand factor in an Iranian family with platelet-type von Willebrand disease.
    Enayat S, Ravanbod S, Rassoulzadegan M, Jazebi M, Tarighat S, Ala F, Emsley J, Othman M.
    Thromb Haemost; 2012 Nov 01; 108(5):946-54. PubMed ID: 23014764
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  • 18. Biochemical characterization of a recombinant von Willebrand factor (VWF) with combined type 2B and type 1 defects in the VWF gene in two patients with a type 2A phenotype of von Willebrand disease.
    Baronciani L, Federici AB, Cozzi G, Canciani MT, Mannucci PM.
    J Thromb Haemost; 2007 Feb 01; 5(2):282-8. PubMed ID: 17155947
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