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Disease Info Card
Cleft Palate
Information about Cleft Palate: 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 Cleft Palate
Most recent studies have shown that Cleft Palate shares some biological mechanisms with bilateral-cleft-lip, cleft-lip, cleft-palate-with-cleft-lip, congenital-abnormality, congenital-heart-defects, craniofacial-abnormalities, cytogenetic-abnormality, dysplasia, hypoplasia, malocclusion, micrognathism, otitis-media, pathologic-fistula, pierre-robin-syndrome, speech-disorders, teratogenic-effect, unilateral-cleft-lip, unilateral-complete-cleft-lip, velopharyngeal-insufficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cleft Palate, and have been seen in publications frequently: Aging, Cell Cycle, Cell Death, Cell Differentiation, Cell Migration, Cell Proliferation, Dehiscence, Localization, Mastication, Mating, Ossification, Palate Development, Pathogenesis, Programmed Cell Death, Reflex, Regeneration, Tooth Eruption, Transport, Transposition, Wound Healing
Quite a number of genes have been found to play important roles in Cleft Palate, such as CALML3, COTL1, CP, CPO, CPOX, CSRP3, FUT3, HPS4, IRF6, MSX1, MTHFR, SS18L1, TBX1, TGFA, TGFB3, TMEM54, TNIP1, TP63. 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.