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Disease Info Card
Microstomia
Information about Microstomia: 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 Microstomia
Most recent studies have shown that Microstomia shares some biological mechanisms with cicatrix, cleft-palate, congenital-abnormality, dental-caries, diffuse-scleroderma, dysplasia, epidermolysis-bullosa, facial-asymmetry, facial-injuries, fetal-growth-retardation, freeman-sheldon-syndrome, hypoplasia, interosseous-desmitis, malignant-squamous-cell-neoplasm, micrognathism, mouth-diseases, scleroderma, sclerosis, stenosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Microstomia, and have been seen in publications frequently: Aging, Bone Maturation, Cell Death, Dehiscence, Fatty Acid Transport, Innervation, Limb Development, Localization, Mastication, Methylation, Muscle Hypertrophy, Ossification, Pathogenesis, Reflex, Segmentation, Tooth Eruption, Translation, Transport, Transposition, Wound Healing
Quite a number of genes have been found to play important roles in Microstomia, such as ACAT1, ACCS, ACSS2, CDSN, FGF8, FUT3, MB, OTX2, PLA2G15, PRRX1, SLC25A5, SLC27A4, SMG1, SS18L1, TBPL1, TBX1. 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.