Studies on human antihemophilic factor. Evidence for a covalently linked subunit structure.
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von Willebrand factor binds to platelets and induces aggregation in platelet-type but not type IIB von Willebrand diseaseProperties of human asialo-factor VIII. A ristocetin-independent platelet-aggregating agent.Platelets have more than one binding site for von Willebrand factor.Platelet receptors for human Factor VIII/von Willebrand protein: functional correlation of receptor occupancy and ristocetin-induced platelet aggregation.Heparin inhibition of von Willebrand factor-dependent platelet function in vitro and in vivo.Effects of plasmin on von Willebrand factor multimers. Degradation in vitro and stimulation of release in vivo.Epitope mapping of the von Willebrand factor subunit distinguishes fragments present in normal and type IIA von Willebrand disease from those generated by plasminIndependent modulation of von Willebrand factor and fibrinogen binding to the platelet membrane glycoprotein IIb/IIIa complex as demonstrated by monoclonal antibody.Synthesis and expression of the fibroblast fibronectin receptor in human monocytesCarbohydrate moiety of von Willebrand factor is not necessary for maintaining multimeric structure and ristocetin cofactor activity but protects from proteolytic degradationInteraction of asialo von Willebrand factor with glycoprotein Ib induces fibrinogen binding to the glycoprotein IIb/IIIa complex and mediates platelet aggregation.Analysis of factor VIII coagulant antigen in normal, thrombin-treated, and hemophilic plasmaElectron microscopy of human factor VIII/Von Willebrand glycoprotein: effect of reducing reagents on structure and functionPurification and characterization of a highly purified human factor VIII consisting of a single type of polypeptide chain.Demonstration and characterization of specific binding sites for factor VIII/von Willebrand factor on human plateletsStabilization of factor VIII in plasma by the von Willebrand factor. Studies on posttransfusion and dissociated factor VIII and in patients with von Willebrand's disease.Some effects of calcium on the activation of human factor VIII/Von Willebrand factor protein by thrombinThe properties of immune complexes formed by human antibodies to factor VIII.Interaction of purified type IIB von Willebrand factor with the platelet membrane glycoprotein Ib induces fibrinogen binding to the glycoprotein IIb/IIIa complex and initiates aggregation.Macromolecular factor VIII complex: functional and structural heterogeneity observed in von Willebrand swine with transfusion.Life in the shadow of a dominant partner: the FVIII-VWF association and its clinical implications for hemophilia A.Interaction of factor VIII antigen in hemophilic plasmas with human antibodies to factor VIII.Interaction of factor VIII-von Willebrand Factor with phospholipid vesicles.
P2860
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P2860
Studies on human antihemophilic factor. Evidence for a covalently linked subunit structure.
description
1976 nî lūn-bûn
@nan
1976 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1976 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1976年の論文
@ja
1976年論文
@yue
1976年論文
@zh-hant
1976年論文
@zh-hk
1976年論文
@zh-mo
1976年論文
@zh-tw
1976年论文
@wuu
name
Studies on human antihemophili ...... ntly linked subunit structure.
@ast
Studies on human antihemophili ...... ntly linked subunit structure.
@en
type
label
Studies on human antihemophili ...... ntly linked subunit structure.
@ast
Studies on human antihemophili ...... ntly linked subunit structure.
@en
prefLabel
Studies on human antihemophili ...... ntly linked subunit structure.
@ast
Studies on human antihemophili ...... ntly linked subunit structure.
@en
P2860
P356
P1476
Studies on human antihemophili ...... ntly linked subunit structure.
@en
P2093
P2860
P304
P356
10.1172/JCI108369
P407
P577
1976-04-01T00:00:00Z