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Disease Info Card
Epidermolysis Bullosa Junctionalis With Pyloric Atresia
Information about Epidermolysis Bullosa Junctionalis With Pyloric Atresia: 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 Epidermolysis Bullosa Junctionalis With Pyloric Atresia
Most recent studies have shown that Epidermolysis Bullosa Junctionalis With Pyloric Atresia shares some biological mechanisms with aplasia-nos, atresia, bulla, congenital-digestive-system-anomalies, dermatologic-disorders, dystrophy, ectodermal-dysplasia, epidermolysis-bullosa, fetal-diseases, gastric-dilatation, hereditary-diseases, herlitz-disease, junctional-epidermolysis-bullosa, muscular-dystrophy, polyhydramnios, skin-diseases-genetic, tissue-adhesions.
Among the many pathways, these few ones have gauged particular interests from scientists studying Epidermolysis Bullosa Junctionalis With Pyloric Atresia, and have been seen in publications frequently: Cell Adhesion, Cell Cycle, Hemidesmosome Assembly, Localization, Proteolysis
Quite a number of genes have been found to play important roles in Epidermolysis Bullosa Junctionalis With Pyloric Atresia, such as ACHE, AFP, AMY2A, BLOC1S6, COL17A1, CTLA4, DST, EPB42, FN1, HDAC1, HLA-DQA1, ITGA6, ITGB4, NOD2, PLEC, PRH1, VCL. 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.
Pathways Related to Epidermolysis Bullosa Junctionalis With Pyloric Atresia
This information is being compiled and will come in a future update
| Cell Adhesion | Cell Cycle | Hemidesmosome Assembly |
| Localization | Proteolysis |