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341 related items for PubMed ID: 9184419

  • 1. von Willebrand factor without the A2 domain is resistant to proteolysis.
    Lankhof H, Damas C, Schiphorst ME, Ijsseldijk MJ, Bracke M, Furlan M, Tsai HM, de Groot PG, Sixma JJ, Vink T.
    Thromb Haemost; 1997 May; 77(5):1008-13. PubMed ID: 9184419
    [Abstract] [Full Text] [Related]

  • 2. Recombinant vWF type 2A mutants R834Q and R834W show a defect in mediating platelet adhesion to collagen, independent of enhanced sensitivity to a plasma protease.
    Lankhof H, Damas C, Schiphorst ME, Ijsseldijk MJ, Bracke M, Furlan M, de Groot PG, Sixma JJ, Vink T.
    Thromb Haemost; 1999 Jun; 81(6):976-83. PubMed ID: 10404778
    [Abstract] [Full Text] [Related]

  • 3. A3 domain is essential for interaction of von Willebrand factor with collagen type III.
    Lankhof H, van Hoeij M, Schiphorst ME, Bracke M, Wu YP, Ijsseldijk MJ, Vink T, de Groot PG, Sixma JJ.
    Thromb Haemost; 1996 Jun; 75(6):950-8. PubMed ID: 8822592
    [Abstract] [Full Text] [Related]

  • 4. Purified A2 domain of von Willebrand factor binds to the active conformation of von Willebrand factor and blocks the interaction with platelet glycoprotein Ibalpha.
    Martin C, Morales LD, Cruz MA.
    J Thromb Haemost; 2007 Jul; 5(7):1363-70. PubMed ID: 17389010
    [Abstract] [Full Text] [Related]

  • 5. Conformational stability and domain unfolding of the Von Willebrand factor A domains.
    Auton M, Cruz MA, Moake J.
    J Mol Biol; 2007 Feb 23; 366(3):986-1000. PubMed ID: 17187823
    [Abstract] [Full Text] [Related]

  • 6. Laboratory diagnosis and molecular classification of von Willebrand disease.
    Gadisseur A, Hermans C, Berneman Z, Schroyens W, Deckmyn H, Michiels JJ.
    Acta Haematol; 2009 Feb 23; 121(2-3):71-84. PubMed ID: 19506352
    [Abstract] [Full Text] [Related]

  • 7. Identification of a novel 14-3-3zeta binding site within the cytoplasmic domain of platelet glycoprotein Ibalpha that plays a key role in regulating the von Willebrand factor binding function of glycoprotein Ib-IX.
    Yuan Y, Zhang W, Yan R, Liao Y, Zhao L, Ruan C, Du X, Dai K.
    Circ Res; 2009 Dec 04; 105(12):1177-85. PubMed ID: 19875727
    [Abstract] [Full Text] [Related]

  • 8. Type 2M vWD resulting from a lysine deletion within a four lysine residue repeat in the A1 loop of von Willebrand factor.
    Hilbert L, Jenkins PV, Gaucher C, Meriane E, Collins PW, Pasi KJ, Mazurier C.
    Thromb Haemost; 2000 Aug 04; 84(2):188-94. PubMed ID: 10959688
    [Abstract] [Full Text] [Related]

  • 9. The interaction of von Willebrand factor-A1 domain with collagen: mutation G1324S (type 2M von Willebrand disease) impairs the conformational change in A1 domain induced by collagen.
    Morales LD, Martin C, Cruz MA.
    J Thromb Haemost; 2006 Feb 04; 4(2):417-25. PubMed ID: 16420575
    [Abstract] [Full Text] [Related]

  • 10. Analysis of the structure and function of the von Willebrand factor A1 domain using targeted deletions and alanine-scanning mutagenesis.
    Kroner PA, Frey AB.
    Biochemistry; 1996 Oct 15; 35(41):13460-8. PubMed ID: 8873615
    [Abstract] [Full Text] [Related]

  • 11. Mapping and functional studies of two alloantibodies developed in patients with type 3 von Willebrand disease.
    Tout H, Obert B, Houllier A, Fressinaud E, Rothschild C, Meyer D, Girma JP.
    Thromb Haemost; 2000 Feb 15; 83(2):274-81. PubMed ID: 10739386
    [Abstract] [Full Text] [Related]

  • 12. Molecular genetics of von Willebrand disease.
    Mazurier C, Ribba AS, Gaucher C, Meyer D.
    Ann Genet; 1998 Feb 15; 41(1):34-43. PubMed ID: 9599650
    [Abstract] [Full Text] [Related]

  • 13. von Willebrand factor A1 domain can adequately substitute for A3 domain in recruitment of flowing platelets to collagen.
    Bonnefoy A, Romijn RA, Vandervoort PA, VAN Rompaey I, Vermylen J, Hoylaerts MF.
    J Thromb Haemost; 2006 Oct 15; 4(10):2151-61. PubMed ID: 16805860
    [Abstract] [Full Text] [Related]

  • 14. Aurin tricarboxylic acid inhibits platelet adhesion to collagen by binding to the 509-695 disulphide loop of von Willebrand factor and competing with glycoprotein Ib.
    Girma JP, Fressinaud E, Christophe O, Rouault C, Obert B, Takahashi Y, Meyer D.
    Thromb Haemost; 1992 Dec 07; 68(6):707-13. PubMed ID: 1287886
    [Abstract] [Full Text] [Related]

  • 15. Platelet activation and aggregation induced by recombinant von Willebrand factors reproducing four type 2B von Willebrand disease missense mutations.
    de Romeuf C, Hilbert L, Mazurier C.
    Thromb Haemost; 1998 Jan 07; 79(1):211-6. PubMed ID: 9459349
    [Abstract] [Full Text] [Related]

  • 16. Ser968Thr mutation within the A3 domain of von Willebrand factor (VWF) in two related patients leads to a defective binding of VWF to collagen.
    Ribba AS, Loisel I, Lavergne JM, Juhan-Vague I, Obert B, Cherel G, Meyer D, Girma JP.
    Thromb Haemost; 2001 Sep 07; 86(3):848-54. PubMed ID: 11583318
    [Abstract] [Full Text] [Related]

  • 17. Binding of von Willebrand factor to collagen type III: role of specific amino acids in the collagen binding domain of vWF and effects of neighboring domains.
    van der Plas RM, Gomes L, Marquart JA, Vink T, Meijers JC, de Groot PG, Sixma JJ, Huizinga EG.
    Thromb Haemost; 2000 Dec 07; 84(6):1005-11. PubMed ID: 11154106
    [Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. von Willebrand factor contained in a high purity FVIII concentrate (Fanhdi) binds to platelet glycoproteins and supports platelet adhesion to subendothelium under flow conditions.
    Rivera J, Escolar G, Casamiquela R, Bravo MI, Jorquera JI, Castillo R, Ordinas A, Vicente V.
    Haematologica; 1999 Jan 01; 84(1):5-11. PubMed ID: 10091386
    [Abstract] [Full Text] [Related]

  • 20. Platelet-vessel wall interactions in thrombosis and restenosis role of von Willebrand factor.
    Hoylaerts MF.
    Verh K Acad Geneeskd Belg; 1997 Jan 01; 59(3):161-83. PubMed ID: 9490916
    [Abstract] [Full Text] [Related]

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