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Disease Info Card
Bernard-soulier Syndrome
Information about Bernard-soulier Syndrome: 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 Bernard-soulier Syndrome
Most recent studies have shown that Bernard-soulier Syndrome shares some biological mechanisms with bleeding-tendency, blood-coagulation-disorders, blood-coagulation-disorders-inherited, blood-platelet-disorders, epistaxis, gray-platelet-syndrome, hemophilia-a, hemorrhage, hemorrhagic-disorders, menorrhagia, platelet-storage-pool-deficiency, pregnancy-complications-hematologic, purpura, purpura-thrombocytopenic-idiopathic, thrombasthenia, thrombocytopenic-purpura, thrombosis, thrombus, tissue-adhesions, von-willebrand-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Bernard-soulier Syndrome, and have been seen in publications frequently: Blood Coagulation, Cell Adhesion, Coagulation, Exocytosis, Glycosylation, Hemostasis, Immune Response, Localization, Menarche, Pathogenesis, Platelet Activation, Platelet Aggregation, Platelet Formation, Platelet Morphogenesis, Protein Phosphorylation, Proteolysis, Response To Heparin, Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in Bernard-soulier Syndrome, such as ABCB6, ATP8A2, C4BPA, CARD14, F2, GP1BA, GP9, ITGA2B, ITGB3, MYH9, PRDX2, PRNP, RNF130, THPO, TNC, 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.