Identification of Three Tyrosine Residues of Glycoprotein Ibα with Distinct Roles in von Willebrand Factor and α-Thrombin Binding
Open Access
- 1 April 1995
- journal article
- Published by Elsevier BV
- Vol. 270 (16), 9571-9578
- https://doi.org/10.1074/jbc.270.16.9571
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Point mutation in a leucine-rich repeat of platelet glycoprotein Ib alpha resulting in the Bernard-Soulier syndrome.JCI Insight, 1993
- Expression of the phenotypic abnormality of platelet-type von Willebrand disease in a recombinant glycoprotein Ib alpha fragment.JCI Insight, 1993
- The Structure of a Complex of Recombinant Hirudin and Human α-ThrombinScience, 1990
- Variant Bernard-Soulier syndrome type bolzano. A congenital bleeding disorder due to a structural and functional abnormality of the platelet glycoprotein Ib-IX complex.JCI Insight, 1990
- Characterization of sites of tyrosine sulfation in proteins and criteria for predicting their occurrenceBiochemical and Biophysical Research Communications, 1986
- The complete amino acid sequence of hirudin, a thrombin specific inhibitorFEBS Letters, 1984
- Improved technique utilizing nonfat dry milk for analysis of proteins and nucleic acids transferred to nitrocelluloseGene Analysis Techniques, 1984
- Platelets have more than one binding site for von Willebrand factor.JCI Insight, 1983
- Isolation of pure IgG1, IgG2a and IgG2b immunoglobulins from mouse serum using protein A-SepharoseImmunochemistry, 1978
- Protein and cell membrane iodinations with a sparingly soluble chloroamide, 1,3,4,6-tetrachloro-3a,6a-diphenylglycolurilBiochemical and Biophysical Research Communications, 1978