Structural implications of the substitution of Val for Met at residue 239 in the alpha chain of human platelet glycoprotein Ib.

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作者信息

Pincus M R, Carty R P, Miller J L

机构信息

Department of Pathology, SUNY Health Science Center, Syracuse.

出版信息

J Protein Chem. 1994 Oct;13(7):629-33. doi: 10.1007/BF01890461.

DOI:10.1007/BF01890461

PMID:7702744

Abstract

摘要

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Structural implications of the substitution of Val for Met at residue 239 in the alpha chain of human platelet glycoprotein Ib.

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本文引用的文献

Expression of the phenotypic abnormality of platelet-type von Willebrand disease in a recombinant glycoprotein Ib alpha fragment.

J Clin Invest. 1993 May;91(5):2133-7. doi: 10.1172/JCI116438.

Pseudo-von Willebrand disease: a mutation in the platelet glycoprotein Ib alpha gene associated with a hyperactive surface receptor.假性血管性血友病：血小板糖蛋白Ibα基因的一种突变，与表面受体活性过高相关。

Blood. 1993 Apr 1;81(7):1787-91.

Pseudo-von Willebrand's disease. An intrinsic platelet defect with aggregation by unmodified human factor VIII/von Willebrand factor and enhanced adsorption of its high-molecular-weight multimers.假性血管性血友病。一种血小板内在缺陷，其表现为未修饰的人凝血因子VIII/血管性血友病因子可引起血小板聚集，且其高分子量多聚体的吸附增强。

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Thromb Res. 1980 Sep 15;19(6):857-67. doi: 10.1016/0049-3848(80)90013-4.

von Willebrand factor binds to platelets and induces aggregation in platelet-type but not type IIB von Willebrand disease.血管性血友病因子与血小板结合，并在血小板型而非IIB型血管性血友病中诱导血小板聚集。

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