Identification of a site in the alpha chain of platelet glycoprotein Ib that participates in von Willebrand factor binding.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference33 articles.
1. Glycoprotein Ib and glycoprotein IX are fully complexed in the intact platelet membrane
2. Binding of radioiodinated human von Willebrand factor to Bernard-Soulier, thrombasthenic and von Willebrand's disease platelets
3. Studies with a murine monoclonal antibody that abolishes ristocetin- induced binding of von Willebrand factor to platelets: additional evidence in support of GPIb as a platelet receptor for von Willebrand factor
4. Platelets have more than one binding site for von Willebrand factor.
5. Defective Adhesion of Platelets to Subendothelium in von Willebrand’s Disease and Bernard-Soulier Syndrome
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1. Platelet-type Von Willebrand disease: Three decades in the life of a rare bleeding disorder;Blood Reviews;2011-07
2. Inhibitors of Platelet Adhesion: VWF-GP1b/IX and Collagen-GPVI Inhibitors;Fundamental and Clinical Cardiology Series;2009-06
3. An acquired Bernard-Soulier-like platelet defect in a patient with liver cirrhosis;European Journal of Haematology;2009-04-24
4. Decreased clearance of von Willebrand factor in a patient with type 2B von Willebrand disease following development of immune thrombocytopenia;Pediatric Blood & Cancer;2008-05-20
5. Platelet functional implications of glycoprotein Ibα polymorphisms in African Americans;American Journal of Hematology;2007-01
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