Characterization of the gene encoding human platelet glycoprotein IX.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference52 articles.
1. Characterization of the platelet membrane glycoprotein abnormalities in Bernard-Soulier syndrome and comparison with normal by surface-labeling techniques and high-resolution two-dimensional gel electrophoresis.
2. 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
3. Decreased adhesion of giant (Bernard-Soulier) platelets to subendothelium
4. Periodicity of leucine and tandem repetition of a 24-amino acid segment in the primary structure of leucine-rich alpha 2-glycoprotein of human serum.
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3. Molecular characterization of two mutations in platelet glycoprotein (GP) Ibα in two Finnish Bernard-Soulier syndrome families;European Journal of Haematology;2009-04-24
4. Variant Bernard-Soulier syndrome due to homozygous Asn45Ser mutation in the platelet glycoprotein (GP) IX in seven patients of five unrelated Finnish families;European Journal of Haematology;2009-04-24
5. Vulnerable mutation Trp126 → stop of glycoprotein IX in Japanese Bernard - Soulier syndrome;European Journal of Haematology;2009-04-24
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