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Disease Info Card
Craniosynostosis
Information about Craniosynostosis: 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 Craniosynostosis
Most recent studies have shown that Craniosynostosis shares some biological mechanisms with acrocephalosyndactylia, apert-syndrome, cleft-palate, congenital-abnormal-synostosis, congenital-abnormality, craniofacial-abnormalities, craniofacial-dysostosis, dysplasia, facial-asymmetry, hemorrhage, hydrocephalus, hypoplasia, intracranial-hypertension, orbital-separation-excessive, pfeiffer-syndrome, plagiocephaly, scaphycephaly, syndactyly, trigonocephaly.
Among the many pathways, these few ones have gauged particular interests from scientists studying Craniosynostosis, and have been seen in publications frequently: Bone Development, Bone Remodeling, Brain Development, Cell Differentiation, Cell Growth, Cell Proliferation, Coagulation, Endochondral Ossification, Intramembranous Ossification, Localization, Ossification, Osteoblast Differentiation, Osteoblast Proliferation, Pathogenesis, Regeneration, Secretion, Segmentation, Translation, Transposition, Wound Healing
Quite a number of genes have been found to play important roles in Craniosynostosis, such as BGLAP, BMP2, CS, CSF2, EFNB1, FGF13, FGF2, FGFR1, FGFR2, FGFR3, FUT3, HPS4, LAMC2, MSX2, NLRP5, RUNX2, SPP1, SS18L1, 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.