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Disease Info Card
Von Willebrand Disease
Information about Von Willebrand Disease: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Von Willebrand Disease
Most recent studies have shown that Von Willebrand Disease shares some biological mechanisms with atherosclerosis, bleeding-tendency, blood-coagulation-disorders, blood-platelet-disorders, cardiovascular-diseases, diabetes-mellitus, hemophilia-a, hemorrhage, hypertensive-disease, inflammation, neoplasms, pathologic-neovascularization, purpura, purpura-thrombotic-thrombocytopenic, thrombocytopenic-purpura, thrombosis, thrombus, tissue-adhesions, tumor-angiogenesis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Von Willebrand Disease, and have been seen in publications frequently: Angiogenesis, Blood Coagulation, Cell Activation, Cell Adhesion, Cell Proliferation, Coagulation, Endothelial Cell Activation, Excretion, Exocytosis, Fibrinolysis, Hemostasis, Inflammatory Response, Localization, Pathogenesis, Platelet Activation, Platelet Aggregation, Proteolysis, Regeneration, Secretion, Transport
Quite a number of genes have been found to play important roles in Von Willebrand Disease, such as ADAMTS13, CRP, F2, F8, FN1, HBA1, IL6, PECAM1, PLAT, PLG, RNF130, SELP, SERPINE1, THBD, TNC, VEGFA, VWF. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.