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Disease Info Card
Brachycephaly
Information about Brachycephaly: 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 Brachycephaly
Most recent studies have shown that Brachycephaly shares some biological mechanisms with acrocephalosyndactylia, apert-syndrome, congenital-abnormal-synostosis, congenital-abnormality, congenital-heart-defects, craniofacial-abnormalities, craniofacial-dysostosis, craniosynostosis, cytogenetic-abnormality, developmental-delay-(disorder), dwarfism, hypoplasia, microcephaly, muscle-hypotonia, orbital-separation-excessive, plagiocephaly, plagiocephaly-nonsynostotic, scaphycephaly, trisomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Brachycephaly, and have been seen in publications frequently: Brain Development, Cell Proliferation, Chromatin Remodeling, Dna Methylation, Histone Methylation, Hypersensitivity, Inflammatory Response, Interphase, Limb Development, Localization, Mating, Methylation, Mrna Splicing, Nuclear Export, Ossification, Pathogenesis, Pigmentation, Transposition, Wound Healing
Quite a number of genes have been found to play important roles in Brachycephaly, such as ARID1B, CDKN2B, EHMT1, ENDOU, EXOSC6, FGFR1, FGFR2, FGFR3, MAPK3, NDUFB6, NLRP5, NXT1, PES1, PTER, RAI1, S100A10, SUB1, TWIST1. 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.