GPIbα-vWF rolling under shear stress shows differences between type 2B and 2M von Willebrand disease.
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L V McIntire | L. McIntire | S. Eskin | S G Eskin | M. Cruz | L A Coburn | V S Damaraju | S Dozic | M A Cruz | S. Dožić | L. Coburn | V. Damaraju
[1] Jizhong Lou,et al. Platelet glycoprotein Ibalpha forms catch bonds with human WT vWF but not with type 2B von Willebrand disease vWF. , 2008, The Journal of clinical investigation.
[2] Brian Savage,et al. Specific Synergy of Multiple Substrate–Receptor Interactions in Platelet Thrombus Formation under Flow , 1998, Cell.
[3] D. Torney,et al. The reaction-limited kinetics of membrane-to-surface adhesion and detachment , 1988, Proceedings of the Royal Society of London. Series B. Biological Sciences.
[4] Scott L. Diamond,et al. Selectin-Like Kinetics and Biomechanics Promote Rapid Platelet Adhesion in Flow: The GPIbα-vWF Tether Bond , 2002 .
[5] R. Handin,et al. Interaction of the von Willebrand Factor (vWF) with Collagen , 1995, The Journal of Biological Chemistry.
[6] Timothy A. Springer,et al. The Kinetics of L-selectin Tethers and the Mechanics of Selectin-mediated Rolling , 1997, The Journal of cell biology.
[7] R. Romijn,et al. von Willebrand factor A1 domain can adequately substitute for A3 domain in recruitment of flowing platelets to collagen , 2006, Journal of thrombosis and haemostasis : JTH.
[8] Cheng Zhu,et al. Direct observation of catch bonds involving cell-adhesion molecules , 2003, Nature.
[9] J. Moake. Thrombotic thrombocytopenic purpura: the systemic clumping "plague". , 2002, Annual review of medicine.
[10] R. Handin,et al. The interaction of the von Willebrand factor-A1 domain with platelet glycoprotein Ib/IX. The role of glycosylation and disulfide bonding in a monomeric recombinant A1 domain protein. , 1993, The Journal of biological chemistry.
[11] E. Sedlák,et al. Changes in thermodynamic stability of von Willebrand factor differentially affect the force-dependent binding to platelet GPIbalpha. , 2009, Biophysical journal.
[12] S. Diamond,et al. Selectin-like kinetics and biomechanics promote rapid platelet adhesion in flow: the GPIb/spl alpha/-vWF tether bond , 2002, Proceedings of the Second Joint 24th Annual Conference and the Annual Fall Meeting of the Biomedical Engineering Society] [Engineering in Medicine and Biology.
[13] J. Sixma,et al. A3 Domain Is Essential for Interaction of von Willebrand Factor with Collagen Type III , 1996, Thrombosis and Haemostasis.
[14] D. Meyer,et al. Localization of a collagen-interactive domain of human von Willebrand factor between amino acid residues Gly 911 and Glu 1,365 , 1987 .
[15] Cheng Zhu,et al. Low Force Decelerates L-selectin Dissociation from P-selectin Glycoprotein Ligand-1 and Endoglycan* , 2004, Journal of Biological Chemistry.
[16] Larry V. McIntire,et al. Kinetics of GPIbα-vWF-A1 Tether Bond under Flow: Effect of GPIbα Mutations on the Association and Dissociation Rates , 2003 .
[17] R. Liddington,et al. Crystal Structure of the von Willebrand Factor A1 Domain and Implications for the Binding of Platelet Glycoprotein Ib* , 1998, The Journal of Biological Chemistry.
[18] D. Mancuso,et al. von Willebrand disease type B: a missense mutation selectively abolishes ristocetin-induced von Willebrand factor binding to platelet glycoprotein Ib. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[19] M. Hoylaerts,et al. von Willebrand factor binds to native collagen VI primarily via its A1 domain. , 1997, The Biochemical journal.
[20] Daniel A Hammer,et al. Adhesive dynamics simulations of the shear threshold effect for leukocytes. , 2007, Biophysical journal.
[21] José A López,et al. Molecular mechanisms of platelet adhesion and activation. , 1997, The international journal of biochemistry & cell biology.
[22] R. Liddington,et al. Mapping the Glycoprotein Ib-binding Site in the von Willebrand Factor A1 Domain* , 2000, The Journal of Biological Chemistry.
[23] Cheng Zhu,et al. Catch bonds govern adhesion through L-selectin at threshold shear , 2004, The Journal of cell biology.
[24] Kazuo Fujikawa,et al. ADAMTS-13 rapidly cleaves newly secreted ultralarge von Willebrand factor multimers on the endothelial surface under flowing conditions. , 2002, Blood.
[25] M. Crúz,et al. 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 , 2006, Journal of thrombosis and haemostasis : JTH.
[26] C. Mazurier,et al. Platelet Activation and Aggregation Induced by Recombinant von Willebrand Factors Reproducing Four Type 2B von Willebrand Disease Missense Mutations , 1998, Thrombosis and Haemostasis.
[27] J. Sixma,et al. Structures of Glycoprotein Ibα and Its Complex with von Willebrand Factor A1 Domain , 2002, Science.
[28] A. Reininger. Function of von Willebrand factor in haemostasis and thrombosis , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[29] P. Mannucci,et al. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor , 2006, Journal of thrombosis and haemostasis : JTH.
[30] T. Matsushita,et al. Identification of Amino Acid Residues Essential for von Willebrand Factor Binding to Platelet Glycoprotein Ib. , 1995, The Journal of Biological Chemistry.
[31] J. Moake,et al. Conformational stability and domain unfolding of the Von Willebrand factor A domains. , 2007, Journal of molecular biology.