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Disease Info Card
Cleft Face
Information about Cleft Face: 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 Face
Most recent studies have shown that Cleft Face shares some biological mechanisms with amniotic-band-syndrome, amniotic-bands, cleft-lip, cleft-palate, cleft-palate-with-cleft-lip, congenital-abnormality, congenital-cerebral-hernia, craniofacial-abnormalities, craniofacial-dysostosis, cytogenetic-abnormality, dysplasia, epilepsy, eye-abnormalities, fetal-diseases, frontonasal-dysplasia-sequence, holoprosencephaly, hypoplasia, oblique-facial-clefts, orbital-separation-excessive, teratogenic-effect.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cleft Face, and have been seen in publications frequently: Aging, Bone Development, Cell Adhesion, Cell Death, Cell Migration, Cell Proliferation, Coagulation, Gastrulation, Limb Development, Localization, Neural Crest Cell Migration, Neural Tube Closure, Ossification, Palate Development, Pathogenesis, Programmed Cell Death, Regulation Of Gene Expression, Response To Paclitaxel, Skin Development, Transposition
Quite a number of genes have been found to play important roles in Cleft Face, such as BMP2, CALML3, CKAP4, COTL1, CP, CPO, CPOX, CSRP3, DNAJC5, FGFR1, IRF6, PDGFC, RARA, RPE65, SHH, SS18L1, TP53, 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.