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Disease Info Card
Hemophilia B
Information about Hemophilia B: 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 Hemophilia B
Most recent studies have shown that Hemophilia B shares some biological mechanisms with acquired-immunodeficiency-syndrome, arthropathy, bleeding-tendency, blood-coagulation-disorders, factor-vii-deficiency, factor-xi-deficiency, hemarthrosis, hematoma, hemophilia-a, hemophilic-arthritis, hemorrhage, hemorrhagic-disorders, hepatitis, hepatitis-b, hepatitis-c, hiv-infections, immunologic-deficiency-syndromes, severe-hereditary-factor-viii-deficiency-disease, thrombosis, von-willebrand-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hemophilia B, and have been seen in publications frequently: Anaphylaxis, Angiogenesis, Blood Coagulation, Coagulation, Dna Amplification, Fibrinolysis, Hemostasis, Hypersensitivity, Immune Response, Localization, Methylation, Pathogenesis, Platelet Aggregation, Proteolysis, Secretion, Sex Determination, Tolerance Induction, Translation, Tropism, Wound Healing
Quite a number of genes have been found to play important roles in Hemophilia B, such as ALB, AMBP, CD4, EGF, F10, F2, F3, F8, F9, SERPINC1, TF, TMSB4X, TSTA3, 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.