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Disease Info Card
Exencephaly
Information about Exencephaly: 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 Exencephaly
Most recent studies have shown that Exencephaly shares some biological mechanisms with anencephaly, anophthalmos, cleft-palate, congenital-abnormality, congenital-absence, congenital-cerebral-hernia, congenital-heart-defects, crest-syndrome, edema, fetal-death, fetal-resorption, growth-retardation, hemorrhage, hydrocephalus, hypoplasia, maternal-exposure, microphthalmos, nervousness, spina-bifida, teratogenic-effect.
Among the many pathways, these few ones have gauged particular interests from scientists studying Exencephaly, and have been seen in publications frequently: Brain Development, Cell Cycle, Cell Death, Cell Proliferation, Gastrulation, Localization, Mating, Methylation, Neural Tube Closure, Neural Tube Development, Neural Tube Formation, Neurogenesis, Neuropore Closure, Ossification, Pathogenesis, Posterior Neuropore Closure, Transport, Tube Closure, Tube Development, Tube Formation
Quite a number of genes have been found to play important roles in Exencephaly, such as AFP, CASP3, CDKN1A, CITED2, CSRP3, CTLA4, ERMAP, FGF8, FUZ, HLA-DQA1, NOD2, PAEP, PAX3, SHH, SS18L1, TFF2, TP53. 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.