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Disease Info Card
Middle Ear Cholesteatoma
Information about Middle Ear Cholesteatoma: 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 Middle Ear Cholesteatoma
Most recent studies have shown that Middle Ear Cholesteatoma shares some biological mechanisms with abscess, cholesteatoma, conductive-hearing-loss, ear-diseases, ear-inflammation, ear-neoplasms, facial-paralysis, glanders, infection---suppurative, inflammation, otitis-media, otitis-media-chronic, otitis-media-with-effusion, pathologic-fistula, retraction-of-tympanic-membrane, sensorineural-hearing-loss-(disorder), suppurative-otitis-media, tympanic-membrane-perforation.
Among the many pathways, these few ones have gauged particular interests from scientists studying Middle Ear Cholesteatoma, and have been seen in publications frequently: Angiogenesis, Bone Resorption, Cell Adhesion, Cell Cycle, Cell Death, Cell Growth, Cell Proliferation, Dehiscence, Immune Response, Inflammatory Response, Keratinization, Keratinocyte Differentiation, Keratinocyte Proliferation, Localization, Pathogenesis, Regeneration, Secretion, Transposition, Wound Healing
Quite a number of genes have been found to play important roles in Middle Ear Cholesteatoma, such as CYLD, EGF, EGFR, F11, FGF2, FGF7, HES1, HMGCL, IL1A, IL1B, IL6, LIPC, MMP2, MMP9, PCNA, PTCRA, TNF, TNFRSF11B. 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.