Gene Ontology annotation by the MGI curatorial staff, curated orthology
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Annotation inferences using phylogenetic trees
Automated transfer of experimentally-verified manual GO annotation data to mouse-rat orthologs
Electronic Gene Ontology annotations created by ARBA machine learning models
Automated transfer of experimentally-verified manual GO annotation data to mouse-human orthologs
Combined Automated Annotation using Multiple IEA Methods
Persistence of platelet thrombus formation in arterioles of mice lacking both von Willebrand factor and fibrinogen.
Platelets adhere to and translocate on von Willebrand factor presented by endothelium in stimulated veins.
Insights from von Willebrand disease animal models.
Thrombin-initiated platelet activation in vivo is vWF independent during thrombus formation in a laser injury model.
Mice lacking the extracellular matrix protein MAGP1 display delayed thrombotic occlusion following vessel injury.
Key role of glycoprotein Ib/V/IX and von Willebrand factor in platelet activation-dependent fibrin formation at low shear flow.
The matrisome: in silico definition and in vivo characterization by proteomics of normal and tumor extracellular matrices.
Extracellular matrix secretion by cardiac fibroblasts: role of microRNA-29b and microRNA-30c.
Quantitative proteomic profiling of the extracellular matrix of pancreatic islets during the angiogenic switch and insulinoma progression.
Tspan18 is a novel regulator of the Ca(2+) channel Orai1 and von Willebrand factor release in endothelial cells.
MatrisomeDB 2.0: 2023 updates to the ECM-protein knowledge database.
Scatter factor/hepatocyte growth factor is essential for liver development.
Heat stable antigen (mouse CD24) supports myeloid cell binding to endothelial and platelet P-selectin.
A mouse model of severe von Willebrand disease: defects in hemostasis and thrombosis.
Defect in regulated secretion of P-selectin affects leukocyte recruitment in von Willebrand factor-deficient mice.
Localized reduction of atherosclerosis in von Willebrand factor-deficient mice.
Hyaluronan mixed esters of butyric and retinoic acid affording myocardial survival and repair without stem cell transplantation.
Crystal structure of the wild-type von Willebrand factor A1-glycoprotein Ibalpha complex reveals conformation differences with a complex bearing von Willebrand disease mutations.
von Willebrand factor, Jedi knight of the bloodstream.
150-kD von Willebrand factor binding protein extracted from human vascular subendothelium is type VI collagen.
Biochemistry and genetics of von Willebrand factor.
The affinity and stoichiometry of binding of human factor VIII to von Willebrand factor.
Two Cys residues essential for von Willebrand factor multimer assembly in the Golgi.
A novel von Willebrand disease-causing mutation (Arg273Trp) in the von Willebrand factor propeptide that results in defective multimerization and secretion.
Inducible secretion of large, biologically potent von Willebrand factor multimers.
Immunolocalization of von Willebrand protein in Weibel-Palade bodies of human endothelial cells.
ADAMTS13 substrate recognition of von Willebrand factor A2 domain.
Binding of ADAMTS13 to von Willebrand factor.
The relationship of N-linked glycosylation and heavy chain-binding protein association with the secretion of glycoproteins.
von Willebrand factor (VWF)-dependent human platelet activation: porcine VWF utilizes different transmembrane signaling pathways than does thrombin to activate platelets, but both require protein phosphatase function.
Glycoproteins VI and Ib-IX-V stimulate tyrosine phosphorylation of tyrosine kinase Syk and phospholipase Cgamma2 at distinct sites.
Vwf UniProt record (Q8CIZ8)
Human VWF UniProt record (P04275)
Manual literature research for mouse Vwf