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Disease Info Card
Behcet Syndrome
Information about Behcet 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 Behcet Syndrome
Most recent studies have shown that Behcet Syndrome shares some biological mechanisms with aneurysm, aphthous-stomatitis, arthritis, autoimmune-diseases, autoimmune-reaction, disorder-of-eye, erythema, inflammation, inflammatory-disorder, lupus-erythematosus-systemic, nervousness, oral-ulcer, rheumatoid-arthritis, sarcoidosis, thrombosis, ulcer, uveitis, vasculitis, venous-thrombosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Behcet Syndrome, and have been seen in publications frequently: Angiogenesis, Cell Activation, Cell Adhesion, Chemotaxis, Coagulation, Cytokine Production, Dehiscence, Excretion, Fibrinolysis, Hemostasis, Hypersensitivity, Immune Response, Inflammatory Response, Localization, Neutrophil Chemotaxis, Pathogenesis, Phagocytosis, Reflex, Secretion, T Cell Activation
Quite a number of genes have been found to play important roles in Behcet Syndrome, such as C3, CRP, CSF2, CSRP1, CTLA4, ESR1, HLA-B, HLA-DQA1, HLA-DRB4, IFNG, IL10, IL2, IL4, IL6, LAMC2, MEFV, NOD2, TNF. 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.