scholarly article | Q13442814 |
P2093 | author name string | M Murata | |
J Ware | |||
Z M Ruggeri | |||
S R Russell | |||
P2860 | cites work | Human blood platelet adhesion to artery subendothelium is mediated by factor VIII-Von Willebrand factor bound to the subendothelium | Q40713235 |
Isolation and functional characterization of the von Willebrand factor-binding domain located between residues His1-Arg293 of the alpha-chain of glycoprotein Ib. | Q43567942 | ||
Identification of a site in the alpha chain of platelet glycoprotein Ib that participates in von Willebrand factor binding | Q43643833 | ||
Development of an inhibitor specific to factor VIII: coagulant activity in a patient with platelet-type von Willebrand's disease | Q45862191 | ||
Site-directed mutagenesis of a soluble recombinant fragment of platelet glycoprotein Ib alpha demonstrating negatively charged residues involved in von Willebrand factor binding | Q46469598 | ||
Ristocetin and botrocetin involve two distinct domains of von Willebrand factor for binding to platelet membrane glycoprotein Ib | Q55042554 | ||
Identification of discontinuous von Willebrand factor sequences involved in complex formation with botrocetin. A model for the regulation of von Willebrand factor binding to platelet glycoprotein Ib | Q68010632 | ||
Modulation of platelet function through adhesion receptors. A dual role for glycoprotein IIb-IIIa (integrin alpha IIb beta 3) mediated by fibrinogen and glycoprotein Ib-von Willebrand factor | Q68142029 | ||
Role of botrocetin in platelet agglutination: formation of an activated complex of botrocetin and von Willebrand factor | Q69086903 | ||
The von Willebrand factor-binding domain of platelet membrane glycoprotein Ib. Characterization by monoclonal antibodies and partial amino acid sequence analysis of proteolytic fragments | Q70010199 | ||
Dimeric ristocetin flocculates proteins, binds to platelets, and mediates von Willebrand factor-dependent agglutination of platelets | Q70144037 | ||
Platelet-type von Willebrand's disease: characterization of a new bleeding disorder | Q72939306 | ||
Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease | Q24561673 | ||
High-efficiency transformation of mammalian cells by plasmid DNA | Q27860469 | ||
Rapid and efficient site-specific mutagenesis without phenotypic selection | Q27860628 | ||
The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domain | Q28776603 | ||
Molecular basis of von Willebrand disease type IIB. Candidate mutations cluster in one disulfide loop between proposed platelet glycoprotein Ib binding sequences | Q28776606 | ||
An LFA-3 cDNA encodes a phospholipid-linked membrane protein homologous to its receptor CD2 | Q29614365 | ||
Protein and cell membrane iodinations with a sparingly soluble chloroamide, 1,3,4,6-tetrachloro-3a,6a-diphenylglycoluril | Q29618344 | ||
Effect of shear rate on platelet interaction with subendothelium in citrated and native blood. I. Shear rate--dependent decrease of adhesion in von Willebrand's disease and the Bernard-Soulier syndrome | Q33446498 | ||
Decreased adhesion of giant (Bernard-Soulier) platelets to subendothelium. Further implications on the role of the von Willebrand factor in hemostasis | Q33463842 | ||
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 | ||
The role of von Willebrand factor and fibrinogen in platelet aggregation under varying shear stress | Q34182746 | ||
The platelet glycoprotein Ib-IX complex | Q37167635 | ||
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 | Q37470139 | ||
Developing relationships: arterial platelet adhesion, glycoprotein Ib, and leucine-rich glycoproteins. | Q37619389 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 2133-2137 | |
P577 | publication date | 1993-05-01 | |
P1433 | published in | Journal of Clinical Investigation | Q3186904 |
P1476 | title | Expression of the phenotypic abnormality of platelet-type von Willebrand disease in a recombinant glycoprotein Ib alpha fragment | |
P478 | volume | 91 |
Q36407260 | Adhesive properties of the isolated amino-terminal domain of platelet glycoprotein Ibalpha in a flow field |
Q30482774 | Flow-induced structural transition in the beta-switch region of glycoprotein Ib |
Q93138681 | Hyperactive GPIb-von Willebrand factor interaction as cause of thrombocytopenia: altered platelet formation versus clearance |
Q24314966 | Identification of three tyrosine residues of glycoprotein Ib alpha with distinct roles in von Willebrand factor and alpha-thrombin binding |
Q41125713 | Immunocytochemical aspects of platelet membrane glycoproteins and adhesive proteins during activation. |
Q33493973 | Low shear stress can initiate von Willebrand factor-dependent platelet aggregation in patients with type IIB and platelet-type von Willebrand disease |
Q33499298 | Megakaryocytes and inherited thrombocytopenias |
Q36559664 | Platelet dysfunction and a high bone mass phenotype in a murine model of platelet-type von Willebrand disease |
Q40789645 | Platelet type von Willebrand disease and registry report: communication from the SSC of the ISTH. |
Q41954139 | Shear-stress-induced von Willebrand factor binding to platelets causes the activation of tyrosine kinase(s) |
Q72124489 | Structural implications of the substitution of Val for Met at residue 239 in the alpha chain of human platelet glycoprotein Ib |
Q33560436 | Visualizing the von Willebrand factor/glycoprotein Ib-IX axis with a platelet-type von Willebrand disease mutation |
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