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Disease Info Card
Mouth Abnormalities
Information about Mouth Abnormalities: 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 Mouth Abnormalities
Most recent studies have shown that Mouth Abnormalities shares some biological mechanisms with cleft-lip, cleft-palate, congenital-abnormality, congenital-hand-deformities, congenital-heart-defects, cytogenetic-abnormality, developmental-absence-of-tooth, down-syndrome, dysplasia, ectodermal-dysplasia, eye-abnormalities, hypoplasia, jaw-abnormalities, limb-deformities-congenital, malocclusion, micrognathism, mouth-diseases, mouth-neoplasms, tooth-abnormalities.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mouth Abnormalities, and have been seen in publications frequently: Aging, Amelogenesis, Cell Activation, Cell Adhesion, Cell Cycle, Cell Migration, Dentinogenesis, Dna Repair, Excretion, Fertilization, Hypersensitivity, Limb Development, Localization, Mitosis, Ossification, Pathogenesis, Pigmentation, Reflex, Tooth Eruption, Translation
Quite a number of genes have been found to play important roles in Mouth Abnormalities, such as APEX1, CKAP4, ERCC2, EVC, FGFR2, GLI3, GNAI1, IRF6, MSX1, NOD2, OFD1, RPE65, SHH, TIE1, TP63, UVRAG. 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.