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Disease Info Card
Thrombasthenia
Information about Thrombasthenia: 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 Thrombasthenia
Most recent studies have shown that Thrombasthenia shares some biological mechanisms with afibrinogenemia, bernard-soulier-syndrome, bleeding-tendency, blood-coagulation-disorders, blood-platelet-disorders, epistaxis, factor-vii-deficiency, hemophilia-a, hemorrhage, hemorrhagic-disorders, menorrhagia, platelet-storage-pool-deficiency, pregnancy-complications-hematologic, purpura, purpura-thrombocytopenic-idiopathic, thrombocytopenic-purpura, thrombosis, thrombus, tissue-adhesions, von-willebrand-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Thrombasthenia, and have been seen in publications frequently: Bone Resorption, Cell Adhesion, Coagulation, Fibrinolysis, Hemostasis, Immune Response, Integrin Activation, Intracellular Transport, Localization, Menarche, Mrna Splicing, Pathogenesis, Platelet Activation, Platelet Aggregation, Protein Phosphorylation, Proteolysis, Secretion, Sensitization, Translation, Transport
Quite a number of genes have been found to play important roles in Thrombasthenia, such as ATP8A2, CTLA4, DUSP2, F2, FABP6, FN1, HLA-DQA1, ITGA2B, ITGB3, NOD2, PSMG1, RALGDS, RNF130, TNC, VTN, 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.