Analysis of the role of von Willebrand factor, platelet glycoprotein VI-, and α2β1-mediated collagen binding in thrombus formation-Reference-Cited by-同舟云学术

Analysis of the role of von Willebrand factor, platelet glycoprotein VI-, and α2β1-mediated collagen binding in thrombus formation

Published:2014-09-11 Issue:11 Volume:124 Page:1799-1807
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Shida Yasuaki¹,Rydz Natalia¹,Stegner David²,Brown Christine¹,Mewburn Jeffrey³,Sponagle Kate¹,Danisment Ozge¹,Crawford Bredon¹,Vidal Barbara¹,Hegadorn Carol A.¹,Pruss Cynthia M.¹,Nieswandt Bernhard²,Lillicrap David¹

Affiliation:

1. Department of Pathology and Molecular Medicine, Queen’s University, Kingston, ON, Canada;

2. University Hospital and Rudolf Virchow Center for Experimental Biomedicine, University of Würzburg, Würzburg, Germany; and

3. Division of Cancer Biology and Genetics, Queen’s University, Kingston, ON, Canada

Abstract

Key PointsThe robustness of the VWF:collagen-binding assay is confirmed in a comprehensive evaluation of VWD collagen-binding defects. Collagen binding by VWF, GPVI, and α2β1 have major albeit overlapping functions in primary hemostasis.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/124/11/1799/1468817/1799.pdf

Reference44 articles.

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5. Surface-dependent expression in the platelet GPIb binding domain within human von Willebrand factor studied by atomic force microscopy.;Kang;Thromb Res,2007

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