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Disease Info Card
Trigonocephaly
Information about Trigonocephaly: 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 Trigonocephaly
Most recent studies have shown that Trigonocephaly shares some biological mechanisms with brachycephaly, congenital-abnormal-synostosis, congenital-abnormality, congenital-absence, craniofacial-abnormalities, craniofacial-dysostosis, craniosynostosis, cytogenetic-abnormality, developmental-disabilities, hypoplasia, hypotelorism-of-orbit, interfrontal-craniofaciosynostosis, monosomy, muscle-hypotonia, orbital-separation-excessive, plagiocephaly, scaphycephaly, trigonocephaly-syndrome, trisomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Trigonocephaly, and have been seen in publications frequently: Bone Remodeling, Brain Development, Cell Adhesion, Cell Growth, Central Nervous System Myelination, Chromosome Breakage, Developmental Growth, Fertilization, Hypersensitivity, Interphase, Localization, Metaphase, Methylation, Myelination, Ossification, Osteoblast Differentiation, Pathogenesis, Pigmentation, Translation, Transposition
Quite a number of genes have been found to play important roles in Trigonocephaly, such as CDK5R1, CER1, CHP1, CSF2, DCTN3, DYNC1H1, FGFR1, FGFR2, FGFR3, GLI3, LAMC2, PHB2, PTGES3, RRAS, TMED10, TPT1, 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.