| scholarly article | Q13442814 |
| P2093 | author name string | A Girolami | |
| T S Zimmerman | |||
| Z M Ruggeri | |||
| L De Marco | |||
| P2860 | cites work | Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 | Q25938983 |
| Protein and cell membrane iodinations with a sparingly soluble chloroamide, 1,3,4,6-tetrachloro-3a,6a-diphenylglycoluril | Q29618344 | ||
| Platelet aggregation induced by 1-desamino-8-D-arginine vasopressin (DDAVP) in Type IIB von Willebrand's disease | Q33478045 | ||
| von Willebrand factor binds to platelets and induces aggregation in platelet-type but not type IIB von Willebrand disease | Q33478102 | ||
| 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 | ||
| Asialo von Willebrand factor interactions with platelets. Interdependence of glycoproteins Ib and IIb/IIIa for binding and aggregation | Q34521638 | ||
| Interaction of asialo von Willebrand factor with glycoprotein Ib induces fibrinogen binding to the glycoprotein IIb/IIIa complex and mediates platelet aggregation | Q34624945 | ||
| Studies on human antihemophilic factor. Evidence for a covalently linked subunit structure | Q35199709 | ||
| Thrombin-induced exposure and prostacyclin inhibition of the receptor for factor VIII/von Willebrand factor on human platelets | Q36983829 | ||
| 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 | ||
| ADP-dependent common receptor mechanism for binding of von Willebrand factor and fibrinogen to human platelets | Q37562150 | ||
| Isolation of pure IgG1, IgG2a and IgG2b immunoglobulins from mouse serum using protein A-Sepharose | Q39218339 | ||
| Factor VIII-related properties in platelets from patients with von Willebrand's disease | Q40664491 | ||
| One-step purification of mouse monoclonal antibodies from ascitic fluid by DEAE Affi-Gel blue chromatography. | Q50932733 | ||
| Monoclonal dinitrophenyl-specific murine IgE antibody: preparation, isolation, and characterization | Q61140921 | ||
| Metabolism and function of human platelets washed by albumin density gradient separation | Q67584447 | ||
| The formation of Ca++-dependent complexes of platelet membrane glycoproteins IIb and IIIa in solution as determined by crossed immunoelectrophoresis | Q70549345 | ||
| Isoelectric focusing of human von Willebrand factor in urea-agarose gels | Q70982062 | ||
| Heightened interaction between platelets and factor VIII/von Willebrand factor in a new subtype of von Willebrand's disease | Q71498185 | ||
| The complex multimeric composition of factor VIII/von Willebrand factor | Q71545501 | ||
| Multimeric composition of factor VIII/von Willebrand factor following administration of DDAVP: implications for pathophysiology and therapy of von Willebrand's disease subtypes | Q71604615 | ||
| Methods for the production of clinically effective intermediate- and high-purity factor-VIII concentrates | Q71793955 | ||
| Platelet-type von Willebrand's disease: characterization of a new bleeding disorder | Q72939306 | ||
| THE PREPARATION AND SOME PROPERTIES OF FIBRINOGEN PRECIPITATED FROM HUMAN PLASMA BY GLYCINE | Q76588314 | ||
| EVIDENCE FOR LINKAGE OF UNIVALENT FRAGMENTS OR HALF-MOLECULES OF RABBIT GAMMA-GLOBULIN BY THE SAME DISULFIDE BOND | Q77065154 | ||
| P433 | issue | 21 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 5 | |
| P304 | page(s) | 7424-7428 | |
| P577 | publication date | 1985-11-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | 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 | |
| P478 | volume | 82 |
| Q44480816 | 14-3-3 zeta mediates integrin-induced activation of Cdc42 and Rac. Platelet glycoprotein Ib-IX regulates integrin-induced signaling by sequestering 14-3-3 zeta |
| Q43720106 | A mitogen-activated protein kinase-dependent signaling pathway in the activation of platelet integrin alpha IIbbeta3. |
| Q73289093 | Adrenaline potentiates type 2B von Willebrand factor-induced activation of human platelets by enhancing both the formation and action of thromboxanes |
| Q36316299 | Analysis of the roles of 14-3-3 in the platelet glycoprotein Ib-IX-mediated activation of integrin alpha(IIb)beta(3) using a reconstituted mammalian cell expression model |
| Q24319306 | Crystal structure of the wild-type von Willebrand factor A1-glycoprotein Ibalpha complex reveals conformation differences with a complex bearing von Willebrand disease mutations |
| Q34260216 | Distinct abnormalities in the interaction of purified types IIA and IIB von Willebrand factor with the two platelet binding sites, glycoprotein complexes Ib-IX and IIb-IIIa |
| Q37377651 | Distinct mechanisms of platelet aggregation as a consequence of different shearing flow conditions |
| Q45883711 | Factor VIII/von Willebrand factor. Structure and function |
| Q36925330 | Functional analysis of a type IIB von Willebrand disease missense mutation: increased binding of large von Willebrand factor multimers to platelets |
| Q34045064 | Hemorrhagic problems in obstetrics, exclusive of disseminated intravascular coagulation |
| Q33447346 | IIB von Willebrand's disease: pathogenetic and therapeutic studies |
| Q61914402 | Identification of Domains Responsible for von Willebrand Factor Type VI Collagen Interaction Mediating Platelet Adhesion under High Flow |
| Q28278900 | Identification of a binding sequence for the 14-3-3 protein within the cytoplasmic domain of the adhesion receptor, platelet glycoprotein Ib alpha |
| Q34974088 | Identification of a juxtamembrane mechanosensitive domain in the platelet mechanosensor glycoprotein Ib-IX complex |
| Q37470139 | Identification of a point mutation in type IIB von Willebrand disease illustrating the regulation of von Willebrand factor affinity for the platelet membrane glycoprotein Ib-IX receptor |
| Q33355405 | Interaction of porcine von Willebrand factor with the platelet glycoproteins Ib and IIb/IIIa complex |
| Q38295551 | Interaction of the von Willebrand factor (vWF) with collagen. Localization of the primary collagen-binding site by analysis of recombinant vWF a domain polypeptides |
| Q33422250 | Investigation of platelet function and platelet disorders using flow cytometry |
| Q28216733 | Lateral clustering of platelet GP Ib-IX complexes leads to up-regulation of the adhesive function of integrin alpha IIbbeta 3 |
| Q34360160 | Mapping the N-glycome of human von Willebrand factor |
| Q22253890 | Mapping the glycoprotein Ib-binding site in the von willebrand factor A1 domain |
| Q37196287 | Microfluidic devices for studies of shear-dependent platelet adhesion |
| Q28776606 | Molecular basis of von Willebrand disease type IIB. Candidate mutations cluster in one disulfide loop between proposed platelet glycoprotein Ib binding sequences |
| Q72270527 | Optimization of a recombinant von Willebrand factor fragment as an antagonist of the platelet glycoprotein Ib receptor |
| Q40999861 | Pathogenesis, clinical picture and treatment of von Willebrand's disease |
| Q33373902 | Platelet activation and alpha granule secretion in type IIB von Willebrand's disease |
| Q33436733 | Platelet aggregation induced by type IIb platelet von Willebrand factor |
| Q28115401 | Self-assembly and supramolecular organization of EMILIN |
| Q36835135 | Src family tyrosine kinase Lyn mediates VWF/GPIb-IX-induced platelet activation via the cGMP signaling pathway |
| Q34528381 | 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). |
| Q33838840 | Syk Activity Is Dispensable for Platelet GP1b-IX-V Signaling |
| Q28776603 | The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domain |
| Q36384795 | The role of Akt in the signaling pathway of the glycoprotein Ib-IX induced platelet activation |
| Q42131574 | The role of Rac1 in glycoprotein Ib-IX-mediated signal transduction and integrin activation |
| Q73069293 | Thrombocytopenia in pregnancy |
| Q33442910 | Type 2B von Willebrand disease with or without large multimers: A distinction of the two sides of the disorder is long overdue |
| Q35577294 | Type IIB von Willebrand factor with normal sialic acid content induces platelet aggregation in the absence of ristocetin. Role of platelet activation, fibrinogen, and two distinct membrane receptors |
| Q33452682 | Type IIB von Willebrand's disease with probable autosomal recessive inheritance and presenting as thrombocytopenia in infancy |
| Q33355402 | Type IIB von Willebrand's disease: gene mutations and clinical presentation in nine families from Denmark, Germany and Sweden |
| Q70321843 | von Willebrand disease |
| Q37255563 | von Willebrand disease type B: a missense mutation selectively abolishes ristocetin-induced von Willebrand factor binding to platelet glycoprotein Ib |
| Q47925382 | von Willebrand factor and urinary albumin excretion are possible indicators of endothelial dysfunction in cardiopulmonary bypass |
| Q34574601 | von Willebrand factor interaction with the glycoprotein IIb/IIa complex. Its role in platelet function as demonstrated in patients with congenital afibrinogenemia |
| Q33899746 | von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure |
| Q33858605 | von Willebrand factor synthesized by endothelial cells from a patient with type IIB von Willebrand disease supports platelet adhesion normally but has an increased affinity for platelets |
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