Heterogeneity of plasma von Willebrand factor multimers resulting from proteolysis of the constituent subunit.
about
ADAMTS-13 metalloprotease interacts with the endothelial cell-derived ultra-large von Willebrand factorIdentification of strain-specific variants of mouse Adamts13 gene encoding von Willebrand factor-cleaving proteaseSingle particle tracking of ADAMTS13 (a disintegrin and metalloprotease with thrombospondin type-1 repeats) molecules on endothelial von Willebrand factor stringsCurrent understanding of the pathophysiology of thrombotic thrombocytopenic purpura.In vitro bleeding time test can diagnose thrombotic thrombocytopenia purpura and can possibly monitor therapeutic plasma apheresis.Systemic antithrombotic effects of ADAMTS13.Diagnosis and follow-up of thrombotic thrombocytopenic purpura by means of von Willebrand factor collagen binding assay.Degradation of circulating von Willebrand factor and its regulator ADAMTS13 implicates secreted Bacillus anthracis metalloproteases in anthrax consumptive coagulopathy.Reduced survival of type 2B von Willebrand factor, irrespective of large multimer representation or thrombocytopeniaThrombotic microangiopathies: multimers, metalloprotease, and beyond.Crystal structure and enzymatic activity of an ADAMTS-13 mutant with the East Asian-specific P475S polymorphism.A comparison of nano-electrospray gas-phase electrophoretic mobility macromolecular analysis and matrix-assisted laser desorption/ionization linear time-of-flight mass spectrometry for the characterization of the recombinant coagulation glycoproteinThe molecular basis of von Willebrand disease.In vivo imaging analysis of the interaction between unusually large von Willebrand factor multimers and platelets on the surface of vascular wall.Third Åland islands conference on von Willebrand disease, 26-28 September 2012: meeting report.Von Willebrand factor and von Willebrand disease.The role of von Willebrand factor in thrombus formation.Platelet adhesion under flow.Successful aortic aneurysm repair in a woman with severe von Willebrand (type 3) disease.von Willebrand factor and factor VIII are independently required to form stable occlusive thrombi in injured veinsRecombinant CUB-1 domain polypeptide inhibits the cleavage of ULVWF strings by ADAMTS13 under flow conditions.Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival.Modulation of the von Willebrand factor-dependent platelet adhesion through alternative proteolytic pathwaysGeneration of Anti-Murine ADAMTS13 Antibodies and Their Application in a Mouse Model for Acquired Thrombotic Thrombocytopenic Purpura.Triplet structure of von Willebrand factor reflects proteolytic degradation of high molecular weight multimers.Autosomal dominant C1149R von Willebrand disease: phenotypic findings and their implications.Collagen binding provides a sensitive screen for variant von Willebrand disease.Endothelial cell ADAMTS-13 and VWF: production, release, and VWF string cleavage.Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease.Role of von Willebrand factor in the haemostasis.Current management of patients with severe von Willebrand disease type 3: a 2012 update.von Willebrand factor: biological function and molecular defects.Triplet structure of human von Willebrand factor.Cleavage of ultralarge multimers of von Willebrand factor by C-terminal-truncated mutants of ADAMTS-13 under flow.The role of von Willebrand factor in the hemostatic defect of acute promyelocytic leukemia.Plasma levels of active Von Willebrand factor are increased in patients with first ST-segment elevation myocardial infarction: a multicenter and multiethnic study.In vivo von Willebrand factor size heterogeneity in spite of the clinical deficiency of ADAMTS-13.Native multimer analysis of plasma and platelet von Willebrand factor compared to denaturing separation: implication for the interpretation of satellite bands.
P2860
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P2860
Heterogeneity of plasma von Willebrand factor multimers resulting from proteolysis of the constituent subunit.
description
1991 nî lūn-bûn
@nan
1991 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Heterogeneity of plasma von Wi ...... is of the constituent subunit.
@ast
Heterogeneity of plasma von Wi ...... is of the constituent subunit.
@en
Heterogeneity of plasma von Wi ...... is of the constituent subunit.
@nl
type
label
Heterogeneity of plasma von Wi ...... is of the constituent subunit.
@ast
Heterogeneity of plasma von Wi ...... is of the constituent subunit.
@en
Heterogeneity of plasma von Wi ...... is of the constituent subunit.
@nl
prefLabel
Heterogeneity of plasma von Wi ...... is of the constituent subunit.
@ast
Heterogeneity of plasma von Wi ...... is of the constituent subunit.
@en
Heterogeneity of plasma von Wi ...... is of the constituent subunit.
@nl
P2093
P2860
P356
P1476
Heterogeneity of plasma von Wi ...... is of the constituent subunit.
@en
P2093
M Galbusera
Z M Ruggeri
P2860
P304
P356
10.1172/JCI115376
P407
P577
1991-09-01T00:00:00Z