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Journal Abstract Search

173 related items for PubMed ID: 21043709

  • 1. Inhibition of Binding of von Willebrand Factor to the Platelet Glycoprotein Ib-IX Complex, Heparin and Sulfatides by Polyanionic Compounds. The Mechanism of Modulation of the Adhesive Function of von Willebrand Factor.
    Andrews RK, Bendall LJ, Booth WJ, Berndt MC.
    Platelets; 1995; 6(5):252-8. PubMed ID: 21043709
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  • 2. The amino Acid sequence glutamine-628 to valine-646 within the A1 repeat domain mediates binding of von Willebrand factor to bovine brain sulfatides and equine tendon collagen.
    Andrews RK, Booth WJ, Bendall LJ, Berndt MC.
    Platelets; 1995; 6(5):245-51. PubMed ID: 21043708
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  • 3. Purification of botrocetin from Bothrops jararaca venom. Analysis of the botrocetin-mediated interaction between von Willebrand factor and the human platelet membrane glycoprotein Ib-IX complex.
    Andrews RK, Booth WJ, Gorman JJ, Castaldi PA, Berndt MC.
    Biochemistry; 1989 Oct 17; 28(21):8317-26. PubMed ID: 2557900
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  • 8. Evidence from limited proteolysis of a ristocetin-induced conformational change in human von Willebrand factor that promotes its binding to platelet glycoprotein Ib-IX-V.
    Kang M, Wilson L, Kermode JC.
    Blood Cells Mol Dis; 2008 Oct 17; 40(3):433-43. PubMed ID: 17977030
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  • 10. 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
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  • 11. 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 07; 84(1):5-11. PubMed ID: 10091386
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  • 12. 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
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  • 13. Mocarhagin, a novel cobra venom metalloproteinase, cleaves the platelet von Willebrand factor receptor glycoprotein Ibalpha. Identification of the sulfated tyrosine/anionic sequence Tyr-276-Glu-282 of glycoprotein Ibalpha as a binding site for von Willebrand factor and alpha-thrombin.
    Ward CM, Andrews RK, Smith AI, Berndt MC.
    Biochemistry; 1996 Apr 16; 35(15):4929-38. PubMed ID: 8664285
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  • 14. Binding of the von Willebrand factor A1 domain to histone.
    Ward CM, Tetaz TJ, Andrews RK, Berndt MC.
    Thromb Res; 1997 Jun 15; 86(6):469-77. PubMed ID: 9219327
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  • 18. Cytoplasmic truncation of glycoprotein Ib alpha weakens its interaction with von Willebrand factor and impairs cell adhesion.
    Schade AJ, Arya M, Gao S, Diz-Küçükkaya R, Anvari B, McIntire LV, López JA, Dong JF.
    Biochemistry; 2003 Feb 25; 42(7):2245-51. PubMed ID: 12590614
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  • 19. Ristocetin and botrocetin involve two distinct domains of von Willebrand factor for binding to platelet membrane glycoprotein Ib.
    Girma JP, Takahashi Y, Yoshioka A, Diaz J, Meyer D.
    Thromb Haemost; 1990 Oct 22; 64(2):326-32. PubMed ID: 1702906
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  • 20. Distinct abnormalities in the interaction of purified types IIA and IIB von Willebrand factor with the two platelet binding sites, glycoprotein complexes Ib-IX and IIb-IIIa.
    De Marco L, Mazzucato M, De Roia D, Casonato A, Federici AB, Girolami A, Ruggeri ZM.
    J Clin Invest; 1990 Sep 22; 86(3):785-92. PubMed ID: 2394830
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