| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0046-8177(87)80332-5 |
| P698 | PubMed publication ID | 3100416 |
| P2093 | author name string | T S Zimmerman | |
| Z M Ruggeri | |||
| P2860 | cites work | Molecular cloning of a cDNA encoding human antihaemophilic factor | Q28268498 |
| Structure of human factor VIII | Q28630991 | ||
| Decreased adhesion of giant (Bernard-Soulier) platelets to subendothelium. Further implications on the role of the von Willebrand factor in hemostasis | Q33463842 | ||
| Platelet aggregation induced by 1-desamino-8-D-arginine vasopressin (DDAVP) in Type IIB von Willebrand's disease | Q33478045 | ||
| Properties of human asialo-factor VIII. A ristocetin-independent platelet-aggregating agent | Q33481601 | ||
| 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 | Q33481677 | ||
| Platelets have more than one binding site for von Willebrand factor | Q33821754 | ||
| A murine monoclonal antibody that completely blocks the binding of fibrinogen to platelets produces a thrombasthenic-like state in normal platelets and binds to glycoproteins IIb and/or IIIa | Q33821916 | ||
| Immunologic differentiation of classic hemophilia (factor 8 deficiency) and von Willebrand's dissase, with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V) and on an acquired circulating anticoagulant agains | Q34055947 | ||
| Preparation and properties of bovine factor VIII (antihemophilic factor). | Q34285283 | ||
| Studies of the human factor VIII/von Willebrand factor protein. III. Qualitative defects in von Willebrand's disease | Q34482682 | ||
| Antihemophilic factor antigen. Localization in endothelial cells by immunofluorescent microscopy | Q34512963 | ||
| Synthesis of Antihemophilic Factor Antigen by Cultured Human Endothelial Cells | Q34513117 | ||
| Asialo von Willebrand factor interactions with platelets. Interdependence of glycoproteins Ib and IIb/IIIa for binding and aggregation | Q34521638 | ||
| Independent modulation of von Willebrand factor and fibrinogen binding to the platelet membrane glycoprotein IIb/IIIa complex as demonstrated by monoclonal antibody | Q34565552 | ||
| Interaction of von Willebrand factor with human platelets in the plasma milieu | Q34602783 | ||
| Functional domains on von Willebrand factor. Recognition of discrete tryptic fragments by monoclonal antibodies that inhibit interaction of von Willebrand factor with platelets and with collagen | Q34613209 | ||
| Carbohydrate moiety of von Willebrand factor is not necessary for maintaining multimeric structure and ristocetin cofactor activity but protects from proteolytic degradation | Q34622020 | ||
| Interaction of asialo von Willebrand factor with glycoprotein Ib induces fibrinogen binding to the glycoprotein IIb/IIIa complex and mediates platelet aggregation | Q34624945 | ||
| Cultured aortic endothelial cells from pigs with von Willebrand disease: in vitro model for studying the molecular defect(s) of the disease | Q35054070 | ||
| Factor VIII recombination after dissociation by CaCl12. | Q35110177 | ||
| Studies on human antihemophilic factor. Evidence for a covalently linked subunit structure | Q35199709 | ||
| Immunologic studies in von Willebrand's disease. Evidence that the antihemophilic factor (AHF) produced after transfusions lacks an antigen associated with normal AHF and the inactive material produced by patients with classic hemophilia | Q35897508 | ||
| The subunit structure of normal and hemophilic factor VIII | Q35899324 | ||
| Biosynthesis of von Willebrand protein by human endothelial cells: processing steps and their intracellular localization | Q36212119 | ||
| Von Willebrand protein binds to extracellular matrices independently of collagen | Q36247327 | ||
| Characterization of the human factor VIII procoagulant protein with a heterologous precipitating antibody | Q36285769 | ||
| Glanzmann thrombasthenia: deficient binding of von Willebrand factor to thrombin-stimulated platelets | Q36314768 | ||
| Cloning and characterization of two cDNAs coding for human von Willebrand factor. | Q36413864 | ||
| Molecular cloning of cDNA for human von Willebrand factor: authentication by a new method | Q36487544 | ||
| Construction of cDNA coding for human von Willebrand factor using antibody probes for colony-screening and mapping of the chromosomal gene. | Q36487665 | ||
| Detection of heterozygotes in both parents of homozygous patients with Von Willebrand's disease | Q36589298 | ||
| Thrombin-induced exposure and prostacyclin inhibition of the receptor for factor VIII/von Willebrand factor on human platelets | Q36983829 | ||
| Aberrant multimeric structure of von Willebrand factor in a new variant of von Willebrand's disease (type IIC) | Q36988093 | ||
| Carbohydrate of the Factor VIII/von Willebrand Factor in von Willebrand's Disease | Q37017221 | ||
| Variant von Willebrand's disease: characterization of two subtypes by analysis of multimeric composition of factor VIII/von Willebrand factor in plasma and platelets | Q37023086 | ||
| Factor VIII/von Willebrand factor protein. Galactose a cryptic determinant of von Willebrand factor activity | Q37031115 | ||
| Disulfide Bonds and the Quaternary Structure of Factor VIII/von Willebrand Factor | Q37031904 | ||
| Immunoradiometric measurement of the factor VIII procoagulant antigen | Q37033265 | ||
| Active release of human platelet factor VIII-related antigen by adenosine diphosphate, collagen, and thrombin | Q37034062 | ||
| Stabilization 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 | Q37046074 | ||
| Synthesis of Factor VIII Antigen by Cultured Guinea Pig Megakaryocytes | Q37047673 | ||
| Factor-VIII-related antigen: multiple molecular forms in human plasma | Q37466525 | ||
| 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 | Q37554183 | ||
| Biosynthesis of the subunits of factor VIIIR by bovine aortic endothelial cells | Q37610888 | ||
| Role of carbohydrate in multimeric structure of factor VIII/von Willebrand factor protein | Q37611058 | ||
| 1-Deamino-8-d-arginine vasopressin: a new pharmacological approach to the management of haemophilia and von Willebrands' diseases | Q39433082 | ||
| Immunoradiometric assay of procoagulant factor-VIII antigen in plasma and serum and its reduction in haemophilia. Preliminary studies on adult and fetal blood | Q39480417 | ||
| Platelet factor VIII-related antigen: Immunofluorescent localization | Q39530860 | ||
| The effects of neuraminidase treatment on the biological activities of factor VIII | Q39685981 | ||
| Von Willebrand's disease: combined qualitative and quantitative abnormalities | Q40644015 | ||
| DDAVP: alternative to replacement treatment in mild haemophilia A and von Willebrand-Jürgens syndrome (author's transl) | Q40661868 | ||
| Acquired von Willebrand's disease. Evidence for a quantitative and qualitative factor VIII disorder | Q40674913 | ||
| Acquired von Willebrand's disease, platelet-release defect and angiodysplasia | Q40687284 | ||
| Radioimmunoassay for coagulant factor VIII-related antigen (VIII:CAg) | Q40705110 | ||
| Two Populations of Factor VIII-Related Antigen in a Family with von Willebrand's Disease | Q40705767 | ||
| Human blood platelet adhesion to artery subendothelium is mediated by factor VIII-Von Willebrand factor bound to the subendothelium | Q40713235 | ||
| The Factor VIII Abnormality in Severe von Willebrand's Disease | Q40726737 | ||
| Studies on factor VIII-related protein. II. Estimation of molecular size differences between factor VIII oligomers | Q41669423 | ||
| Subcellular platelet factor VIII antigen and von Willebrand factor | Q42940232 | ||
| Failure of AHF concentrate to control bleeding in von Willebrand's disease | Q43665677 | ||
| Diagnosis of von Willebrand's disease. A comparative study of diagnostic tests on nine families with von Willebrand's disease and its differential diagnosis from hemophilia and thrombocytopathy | Q43996336 | ||
| A variant of factor 8 related antigen | Q45855059 | ||
| Factor VIII antigen in the vessel walls in von Willebrand's disease and haemophilia A. | Q45855991 | ||
| Response of factor VIII/von Willebrand factor to DDAVP in healthy subjects and patients with haemophilia A and von Willebrand's disease | Q45863842 | ||
| Studies on the relationship between factor VIII related antigen (VIIIRAg) and factor VIII clotting antigen (VIIICAg) by immunoelectrophoresis and autoradiography using 125I anti VIIICAg | Q45864085 | ||
| Acquired von Willebrand Syndrome with Inhibitors Both to Factor VIII Clotting Activity and Ristocetin-Induced Platelet Aggregation | Q45878307 | ||
| A Method for Detecting Factor-VIII Clotting Activity Associated with Factor VIII-related Antigen in Agarose Gels | Q45878671 | ||
| Von Willebrand factor: dissociation from antihemophilic factor procoagulant activity | Q45890237 | ||
| Factor VIII of small molecular weight and its aggregation | Q47359177 | ||
| Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization | Q48377892 | ||
| Characterization of the human factor VIII gene | Q48385931 | ||
| Detection of Heterozygotes for Recessive von Willebrand's Disease by the Assay of Antihemophilic-Factor-like Antigen | Q54384588 | ||
| Spectrum of von Willebrand's Disease: a study of 100 cases. Italian Working Group | Q66875981 | ||
| Urinary excretion of factor VIII after renal transplantation | Q66892653 | ||
| The Chromatographic Separation of Factor VIII on Aminohexyl Sepharose | Q66984431 | ||
| Factor VIII, a series of homologous oligomers and a complex of two proteins | Q67289767 | ||
| von Willebrand disease type IIC with different abnormalities of von Willebrand factor in the same sibship | Q68792876 | ||
| Inherited variants of factor-VIII-related protein in von Willebrand's disease | Q69135742 | ||
| 1-Deamino-8-D-arginine vasopressin and cryoprecipitate in variant von Willebrand disease | Q69962767 | ||
| Pool's cryoprecipitate and exhausted plasma in the treatment of von Willebrand's disease and factor-XI deficiency | Q70067523 | ||
| Structure determination of the major asparagine-linked sugar chain of human factor VIII--von Willebrand factor | Q70426198 | ||
| Von Willebrand factor multimer patterns in von Willebrand's disease | Q70454272 | ||
| Congenital bleeding disorders with long bleeding time and normal platelet count. II. Von Willebrand's disease (report of thirty-seven patients) | Q71106834 | ||
| Molecular Forms of Antihaemophilic Globulin in Plasma, Cryoprecipitate and after Thrombin Activation | Q71426909 | ||
| Heightened interaction between platelets and factor VIII/von Willebrand factor in a new subtype of von Willebrand's disease | Q71498185 | ||
| Binding and release of factor VIII/von Willebrand's factor by human endothelial cells | Q71520196 | ||
| Synthesis and release of factor VIII by cultured human endothelial cells | Q71540905 | ||
| Studies on the pathophysiology and treatment of von Willebrand's disease. V. Properties of factor VIII after DDAVP infusion in variant von Willebrand's disease | Q71565187 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 140-152 | |
| P577 | publication date | 1987-02-01 | |
| P1433 | published in | Human Pathology | Q15756731 |
| P1476 | title | von Willebrand disease | |
| P478 | volume | 18 |
| Q35250259 | Autosomal dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome 4p16, in the region containing the Ellis-van Creveld syndrome locus |
| Q33838757 | Effect of recombinant factor VIIa on the hemostatic defect in dogs with hemophilia A, hemophilia B, and von Willebrand disease |
| Q44662705 | Inheritance and prevalence of von Willebrand's disease severe form in a Brazilian population |
| Q37576572 | Laboratory testing for von Willebrand disease: toward a mechanism-based classification |
| Q33847858 | Mediation of fibrin-induced release of von Willebrand factor from cultured endothelial cells by the fibrin beta chain |
| Q34366855 | Prevention of occlusive coronary artery thrombosis by a murine monoclonal antibody to porcine von Willebrand factor |
| Q37054000 | Regulated Secretion in Vascular Endothelium |
| Q68178306 | Significance and quantitative analysis of von Willebrand factor in human platelets |
| Q45873991 | Two sisters with multiple sclerosis, lamellar ichthyosis, beta thalassaemia minor and a deficiency of factor VIII. |
| Q53061821 | Unravelling the mechanism and significance of thrombin binding to platelet glycoprotein Ib |
| Q67276057 | von Willebrand disease |
| Q41043544 | von Willebrand disease: pathogenesis, classification, and management |
| Q41157159 | von Willebrand's disease in the dog and cat. |
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