In vitro correction of the abnormal multimeric structure of von Willebrand factor in type IIa von Willebrand's disease.
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Investigation of a large kindred with type IIB von Willebrand's disease, dominant inheritance and age-dependent thrombocytopenia.Identification of a cleavage site directing the immunochemical detection of molecular abnormalities in type IIA von Willebrand factor.Molecular basis of human von Willebrand disease: analysis of platelet von Willebrand factor mRNA.Heterogeneity of plasma von Willebrand factor multimers resulting from proteolysis of the constituent subunit.Expression of abnormal von Willebrand factor by endothelial cells from a patient with type IIA von Willebrand disease.Subunit composition of plasma von Willebrand factor. Cleavage is present in normal individuals, increased in IIA and IIB von Willebrand disease, but minimal in variants with aberrant structure of individual oligomers (types IIC, IID, and IIE).Epitope mapping of the von Willebrand factor subunit distinguishes fragments present in normal and type IIA von Willebrand disease from those generated by plasminGenetic linkage of two intragenic restriction fragment length polymorphisms with von Willebrand's disease type IIA. Evidence for a defect in the von Willebrand factor geneUptake of plasma fibrinogen into the alpha granules of human megakaryocytes and platelets.Unique expression of von Willebrand factor by type IIA von Willebrand's disease endothelial cells.Von Willebrand factor collagen binding activity in the diagnosis of von Willebrand disease: an alternative to ristocetin co-factor activity?L1503R is a member of group I mutation and has dominant-negative effect on secretion of full-length VWF multimers: an analysis of two patients with type 2A von Willebrand disease.Factor VIII/von Willebrand factor. Structure and function.The inheritance and molecular genetics of von Willebrand's disease.Porcine platelets contain an increased quantity of ultra-high molecular weight von Willebrand factor and numerous alpha-granular tubular structures.Characterization of Von Willebrand Factor Multimer Structure in Patients With Severe Aortic Stenosis.
P2860
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P2860
In vitro correction of the abnormal multimeric structure of von Willebrand factor in type IIa von Willebrand's disease.
description
article científic
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article scientifique
@fr
articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on September 1985
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
In vitro correction of the abn ...... IIa von Willebrand's disease.
@en
In vitro correction of the abn ...... IIa von Willebrand's disease.
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type
label
In vitro correction of the abn ...... IIa von Willebrand's disease.
@en
In vitro correction of the abn ...... IIa von Willebrand's disease.
@nl
prefLabel
In vitro correction of the abn ...... IIa von Willebrand's disease.
@en
In vitro correction of the abn ...... IIa von Willebrand's disease.
@nl
P2093
P2860
P356
P1476
In vitro correction of the abn ...... IIa von Willebrand's disease.
@en
P2093
Gralnick HR
Maisonneuve P
McKeown LP
Williams SB
P2860
P304
P356
10.1073/PNAS.82.17.5968
P407
P577
1985-09-01T00:00:00Z