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Disease Info Card
Telangiectasis
Information about Telangiectasis: 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 Telangiectasis
Most recent studies have shown that Telangiectasis shares some biological mechanisms with arteriovenous-malformation, ataxia, ataxia-telangiectasia, atrophy, calcinosis, dermatologic-disorders, diffuse-scleroderma, edema, epistaxis, erythema, gastrointestinal-hemorrhage, hemangioma, hemorrhage, hereditary-hemorrhagic-telangiectasia, malignant-neoplasms, neoplasms, raynaud-disease, retinal-diseases, skin-neoplasms, vascular-anomaly.
Among the many pathways, these few ones have gauged particular interests from scientists studying Telangiectasis, and have been seen in publications frequently: Aging, Angiogenesis, Cell Cycle, Cell Cycle Arrest, Cell Cycle Checkpoint, Cell Death, Cell Proliferation, Coagulation, Dna Damage Checkpoint, Dna Repair, Dna Replication, Hypersensitivity, Localization, Metaphase, Mitosis, Pathogenesis, Pigmentation, Response To Ionizing Radiation, S Phase, Senescence
Quite a number of genes have been found to play important roles in Telangiectasis, such as ACVRL1, ANTXR1, ATM, ATR, CDKN1A, CHEK1, CHEK2, CTLA4, ENG, HLA-DQA1, MMAB, NBN, NOD2, PRKDC, SLPI, SS18L1, TP53, 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.