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Disease Info Card
Complete Hearing Loss
Information about Complete Hearing Loss: 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 Complete Hearing Loss
Most recent studies have shown that Complete Hearing Loss shares some biological mechanisms with atrophy, blind-vision, conductive-hearing-loss, congenital-abnormality, deafness-congenital, deafness-sudden, diabetes-mellitus, ear-diseases, ear-inflammation, hearing-problem, labyrinthine-disorder, meniere-disease, meningitis, neoplasms, noise-induced-hearing-loss, otitis-media, otosclerosis, sensorineural-hearing-loss-(disorder), vertigo.
Among the many pathways, these few ones have gauged particular interests from scientists studying Complete Hearing Loss, and have been seen in publications frequently: Aging, Cell Death, Cell Development, Cognition, Ear Development, Excretion, Inner Ear Development, Innervation, Insulin Secretion, Localization, Ossification, Oxidative Phosphorylation, Pathogenesis, Pigmentation, Reflex, Regeneration, Secretion, Short-term Memory, Translation, Transport
Quite a number of genes have been found to play important roles in Complete Hearing Loss, such as ABR, ADSL, ASL, BDNF, CAT, CSF2, GJB2, GJB3, GJB6, HES1, HMGCL, INS, KCNQ1, LAMC2, LIPC, MYO7A, NDUFB6, OTOF, SGPL1, SLC26A4. 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.