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Disease Info Card
Uveitis
Information about Uveitis: 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 Uveitis
Most recent studies have shown that Uveitis shares some biological mechanisms with anterior-uveitis, aqueous-humor-disorders, arthritis, autoimmune-diseases, autoimmune-reaction, behcet-syndrome, blind-vision, cataract, disorder-of-eye, edema, endophthalmitis, glaucoma, inflammation, intraocular-pressure-disorder, macular-retinal-edema, retinal-detachment, retinal-diseases, sarcoidosis, uveitis-posterior.
Among the many pathways, these few ones have gauged particular interests from scientists studying Uveitis, and have been seen in publications frequently: Cell Activation, Cell Adhesion, Cell Proliferation, Chemotaxis, Coagulation, Cytokine Production, Enucleation, Hypersensitivity, Immune Response, Inflammatory Response, Leukocyte Migration, Localization, Lymphocyte Proliferation, Pathogenesis, Pigmentation, Reflex, Secretion, Sensitization, T Cell Activation, Tolerance Induction
Quite a number of genes have been found to play important roles in Uveitis, such as ALB, CCL2, CD4, CTLA4, GRB10, HLA-B, IFNG, IL10, IL2, IL4, IL6, NOD2, NOS2, RBP3, TNF, VEGFA. 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.