Scripps VIVO scripps research logo

  • Index
  • Log in
  • Home
  • People
  • Organizations
  • Research
  • Events
Search form
As of April 1st VIVO Scientific Profiles will no longer updated for faculty, and the link to VIVO will be removed from the library website. Faculty profile pages will continue to be updated via Interfolio. VIVO will continue being used behind the scenes to update graduate student profiles. Please contact helplib@scripps.edu if you have questions.
How to download citations from VIVO | Alternative profile options

Factor VIII

Concept
uri icon
  • Overview
scroll to property group menus

Overview

subject area of

  • 1-deamino-8-D-arginine vasopressin and cryoprecipitate in variant von Willebrand disease  Academic Article
  • 1-deamino-8-D-arginine vasopressin: a new pharmacological approach to the management of haemophilia and von Willebrands' diseases  Academic Article
  • A Child With Wegener's Granulomatosis and Severe Hemophilia A: Interplay of Disease Processes  Academic Article
  • A direct enzymatic assay for the esterolytic activity of activated hageman factor  Academic Article
  • A genome-wide association study of resistance to HIV infection in highly exposed uninfected individuals with hemophilia A  Academic Article
  • Antigenic liposomes displaying CD22 ligands induce antigen-specific B cell apoptosis  Academic Article
  • Aptamer ARC19499 mediates a procoagulant hemostatic effect by inhibiting tissue factor pathway inhibitor  Academic Article
  • Blood-coagulation factor Va abnormality associated with resistance to activated protein-C in venous thrombophilia  Academic Article
  • Carbohydrate composition and identification of blood group A, B, and H oligosaccharide structures on human Factor VIII/von Willebrand factor  Academic Article
  • Carbohydrate of the factor VIII/von Willebrand factor in von Willebrand's disease  Academic Article
  • Carbohydrate on human factor viii von willebrand factor - impairment of function by removal of specific galactose residues  Academic Article
  • Cathepsin g, a leukocyte protease, activates coagulation factorviii  Academic Article
  • Classification of variant von Willebrand's disease subtypes by analysis of functional characteristics and multimeric composition of factor VIII/von Willebrand factor  Academic Article
  • Clotting factors in von Willebrand's disease  Academic Article
  • Concentrates of clotting-factor IX  Academic Article
  • DDAVP enhances platelet adherence and platelet aggregate growth on human artery subendothelium  Academic Article
  • Determination of the von Willebrand's disease antigen (factor VIII-related antigen) in plasma by quantitative immunoelectrophoresis  Academic Article
  • Development of factor VIII antibody in haemophilic monozygotic twins.  Academic Article
  • Differences between heterozygous dominant and recessive von Willebrand's disease type I expressed by bleeding symptoms and combinations of factor VIII variables  Academic Article
  • Drug-drug interaction of the anti-TFPI aptamer BAX499 and factor VIII: Studies of spatial dynamics of fibrin clot formation in hemophilia A  Academic Article
  • Enhanced factor VIII activity in von Willebrand's disease  Academic Article
  • Evidence of activation of the protein-c pathway during acute vascular damage induced by mediterranean spotted-fever  Academic Article
  • Factor VIII and chronic renal failure  Academic Article
  • Factor VIII antigen in the vessel walls in von Willebrand's disease and haemophilia A  Academic Article
  • Factor VIII coagulant activity and factor VIII-like antigen: independent molecular entities  Academic Article
  • Factor VIII-related properties in platelets from patients with von Willebrand's disease  Academic Article
  • Factor VIII/von Willebrand factor  Academic Article
  • Factor VIII/von Willebrand factor in glomerular nephropathies  Academic Article
  • Familial incidence of precipitating antibodies in von Willebrand's disease: A study of four cases  Academic Article
  • Formation of the fibrin clot: the balance of procoagulant and inhibitory factors  Academic Article
  • Heightened interaction between platelets and factor VIII/von Willebrand factor in a new subtype of von Willebrand's disease  Academic Article
  • Homology models of the C domains of blood coagulation factors V and VIII: A proposed membrane binding mode for FV and FVIII C2 domains  Academic Article
  • Human protein-C and thromboembolic disease  Academic Article
  • Immunoradiometric assay of factor VIII related antigen, with observations in 32 patients with von Willebrand's disease  Academic Article
  • Inhibition of fibrinolysis by recombinant factor viia in plasma from patients with severe hemophilia a  Academic Article
  • Interaction of factor VIII antigen in hemophilic plasmas with human antibodies to factor VIII  Academic Article
  • Intrinsic stability and functional properties of disulfide bond-stabilized coagulation factor VIIIa variants  Academic Article
  • Lymphocyte-instructed monocyte induction of the coagulation pathways parallels the induction of hepatitis by the murine hepatitis-virus  Academic Article
  • Mechanism of action of human activated protein-C, a thrombin-dependent anticoagulant enzyme  Academic Article
  • Molecular immunology of factor VIII  Academic Article
  • Multimeric composition of factor VIII/von Willebrand factor following administration of DDAVP: implications for pathophysiology and therapy of von Willebrand's disease subtypes  Academic Article
  • Nervous regulation of factor-VIII levels in man  Academic Article
  • Pathogenesis of von Willebrand's disease  Academic Article
  • Platelets and von Willebrand disease  Academic Article
  • Precipitating antibodies in von Willebrand's disease  Academic Article
  • Precipitating antibodies to factor VIII/von Willebrand factor in von Willebrand's disease: effects on replacement therapy  Academic Article
  • Preliminary trial of cyclophosphamide in the management of hemophiliacs with factor VIII inhibitors  Academic Article
  • Proteolytic inactivation of human factor-VIII procoagulant protein by activated human protein-C and its analogy with factor-V  Academic Article
  • Selective factor VIII activation by the tissue factor-factor VIIa-factor Xa complex  Academic Article
  • Spectrum of von Willebrand's Disease: a study of 100 cases  Academic Article
  • Structural basis for hemophilia A caused by mutations in the C domains of blood coagulation factor VIII  Academic Article
  • Structure and function of von Willebrand factor: relationship to von Willebrand's disease  Academic Article
  • Studies on the prolonged bleeding time in von Willebrand's disease  Academic Article
  • The complex multimeric composition of factor VIII/von Willebrand factor  Academic Article
  • The defective down regulation of fibrinolysis in haemophilia a can be restored by increasing the tafi plasma concentration  Academic Article
  • The hematological aspects of a case of systemic lupus erythematosus  Academic Article
  • Thrombophilic factors are not the leading cause of thrombosis in Behcet's disease  Academic Article
  • Tissue distribution of factor VIII gene expression in vivo: a closer look  Academic Article
  • Type IIB Tampa: a variant of von Willebrand disease with chronic thrombocytopenia, circulating platelet aggregates, and spontaneous platelet aggregation  Academic Article
  • Urinary excretion of factor VIII after renal transplantation  Academic Article
  • Urinary excretion of factor-VIII-related antigen and fibrin(ogen) degradation fragments D and E after kidney transplantation  Academic Article
  • Variant von Willebrand's disease: characterization of two subtypes by analysis of multimeric composition of factor VIII/von Willebrand factor in plasma and platelets  Academic Article
  • Varied immunological reactivity of factor VIII from animal plasmas  Academic Article
  • Vascular remodeling underlies rebleeding in hemophilic arthropathy  Academic Article
  • [Factor VIII inhibitors][Article in Italian]  Academic Article
  • [Multimeric structure of factor VIII/von Willebrand factor released from human platelets by ADP, collagen and thrombin][Article in Spanish]  Academic Article
  • von Willebrand disease  Academic Article
  • von Willebrand factor  Academic Article
  • von Willebrand factor binds to platelets and induces aggregation in platelet-type but not type IIB von Willebrand disease  Academic Article
  • von Willebrand's Disease  Academic Article
  • von Willebrand's disease  Academic Article

©2022 The Scripps Research Institute | Terms of Use | Powered by VIVO

  • About
  • Contact Us
  • Support