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Disease Info Card
Junctional Epidermolysis Bullosa
Information about Junctional Epidermolysis Bullosa: 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 Junctional Epidermolysis Bullosa
Most recent studies have shown that Junctional Epidermolysis Bullosa shares some biological mechanisms with atresia, atrophy, bulla, bullous-pemphigoid, cicatrix, dental-enamel-hypoplasia, dermatologic-disorders, dystrophy, epidermolysis-bullosa, epidermolysis-bullosa-dystrophica, epidermolysis-bullosa-junctionalis-with-pyloric-atresia, herlitz-disease, mucinous-adenocarcinoma, skin-diseases-genetic, systemic-infection, tissue-adhesions.
Among the many pathways, these few ones have gauged particular interests from scientists studying Junctional Epidermolysis Bullosa, and have been seen in publications frequently: Ameloblast Differentiation, Amelogenesis, Bone Mineralization, Cell Adhesion, Cell Migration, Cell Proliferation, Cell-matrix Adhesion, Glycosylation, Hemidesmosome Assembly, Immune Response, Keratinocyte Migration, Localization, Pathogenesis, Pigmentation, Proteolysis, Regeneration, Reverse Transcription, Secretion, Translation, Wound Healing
Quite a number of genes have been found to play important roles in Junctional Epidermolysis Bullosa, such as CCDC6, COL17A1, CTLA4, DST, F9, HLA-DQA1, ITGA6, ITGB4, LAMA3, LAMA4, LAMB3, LAMC2, NOD2, PLEC, PTCH1, RET, TAS2R38. 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.