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132 related items for PubMed ID: 15606553

  • 1. Impact of O-linked glycosylation of the VWF-A1-domain flanking regions on platelet interaction.
    Schulte am Esch J, Robson SC, Knoefel WT, Eisenberger CF, Peiper M, Rogiers X.
    Br J Haematol; 2005 Jan; 128(1):82-90. PubMed ID: 15606553
    [Abstract] [Full Text] [Related]

  • 2. O-linked glycosylation and functional incompatibility of porcine von Willebrand factor for human platelet GPIb receptors.
    Schulte Am Esch J, Robson SC, Knoefel WT, Hosch SB, Rogiers X.
    Xenotransplantation; 2005 Jan; 12(1):30-7. PubMed ID: 15598271
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 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 15; 5(7):1363-70. PubMed ID: 17389010
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. 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 04; 86(3):848-54. PubMed ID: 11583318
    [Abstract] [Full Text] [Related]

  • 7. Identification of peptide antagonists to glycoprotein Ibalpha that selectively inhibit von Willebrand factor dependent platelet aggregation.
    Benard SA, Smith TM, Cunningham K, Jacob J, DeSilva T, Lin L, Shaw GD, Kriz R, Kelleher KS.
    Biochemistry; 2008 Apr 22; 47(16):4674-82. PubMed ID: 18363340
    [Abstract] [Full Text] [Related]

  • 8. A template-assembled synthetic protein surface mimetic of the von Willebrand factor A1 domain inhibits botrocetin-induced platelet aggregation.
    Hauert J, Fernandez-Carneado J, Michielin O, Mathieu S, Grell D, Schapira M, Spertini O, Mutter M, Tuchscherer G, Kovacsovics T.
    Chembiochem; 2004 Jun 07; 5(6):856-64. PubMed ID: 15174170
    [Abstract] [Full Text] [Related]

  • 9. Inhibition of adhesive and signaling functions of the platelet GPIb-V-IX complex by a cell penetrating GPIbalpha peptide.
    David T, Ohlmann P, Eckly A, Moog S, Cazenave JP, Gachet C, Lanza F.
    J Thromb Haemost; 2006 Dec 07; 4(12):2645-55. PubMed ID: 17100656
    [Abstract] [Full Text] [Related]

  • 10. Structure-function relationship of the A1 domain of von Willebrand factor.
    Girma JP, Ribba AS, Meyer D.
    Thromb Haemost; 1995 Jul 07; 74(1):156-60. PubMed ID: 8578449
    [Abstract] [Full Text] [Related]

  • 11. Identification of the binding site for an alloantibody to von Willebrand factor which inhibits binding to glycoprotein Ib within the amino-terminal region flanking the A1 domain.
    Shibata M, Shima M, Fujimura Y, Takahashi Y, Nakai H, Sakurai Y, Asatani M, Nomura A, Take H, Giddings JC, Yoshioka A.
    Thromb Haemost; 1999 May 07; 81(5):793-8. PubMed ID: 10365755
    [Abstract] [Full Text] [Related]

  • 12. 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 07; 4(2):417-25. PubMed ID: 16420575
    [Abstract] [Full Text] [Related]

  • 13. Autoantibody selectively inhibits binding of von Willebrand factor to glycoprotein ib. Recognition site is located in the A1 loop of von Willebrand factor.
    Mohri H, Yamazaki E, Suzuki Z, Takano T, Yokota S, Okubo T.
    Thromb Haemost; 1997 Apr 07; 77(4):760-6. PubMed ID: 9134656
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Characterization of bitiscetin-2, a second form of bitiscetin from the venom of Bitis arietans : comparison of its binding site with the collagen-binding site on the von Willebrand factor A3-domain.
    Obert B, Romijn RA, Houllier A, Huizinga EG, Girma JP.
    J Thromb Haemost; 2006 Jul 23; 4(7):1596-601. PubMed ID: 16839359
    [Abstract] [Full Text] [Related]

  • 17. The A/T1381 polymorphism in the A1-domain of von Willebrand factor influences the affinity of von Willebrand factor for platelet glycoprotein Ibalpha.
    Szántó T, Schlammadinger A, Staelens S, De Meyer SF, Freson K, Pareyn I, Vauterin S, Hársfalvi J, Deckmyn H, Vanhoorelbeke K.
    Thromb Haemost; 2007 Jul 23; 98(1):178-85. PubMed ID: 17598011
    [Abstract] [Full Text] [Related]

  • 18. Platelet aggregation by membrane-expressed A1 domains of von Willebrand Factor is dependent on residues Asp 560 and Gly 561.
    Schulte am Esch J, Robson SC, Cruz MA.
    Biochem Biophys Res Commun; 2003 Mar 21; 302(4):873-7. PubMed ID: 12646253
    [Abstract] [Full Text] [Related]

  • 19. Expression of the amino-terminal domain of platelet glycoprotein Ib alpha: exploitation of a calmodulin tag for determination of its functional activity.
    Li CQ, Ye P, Cao Zf, Wang H, Lu L, Nicastro P, Wood E, Robert JJ, Ouwehand WH, Hill F, López JA, Wardell MR.
    Protein Expr Purif; 2001 Jul 21; 22(2):200-10. PubMed ID: 11437595
    [Abstract] [Full Text] [Related]

  • 20. 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 21; 4(10):2151-61. PubMed ID: 16805860
    [Abstract] [Full Text] [Related]

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