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Disease Info Card
Apert Syndrome
Information about Apert Syndrome: 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 Apert Syndrome
Most recent studies have shown that Apert Syndrome shares some biological mechanisms with acne, acrocephalosyndactylia, acrocephaly, cleft-palate, congenital-abnormal-synostosis, congenital-abnormality, congenital-hand-deformities, craniofacial-abnormalities, craniofacial-dysostosis, craniosynostosis, dysostoses, dysplasia, exophthalmos, hydrocephalus, hypoplasia, intracranial-hypertension, orbital-separation-excessive, pfeiffer-syndrome, syndactyly.
Among the many pathways, these few ones have gauged particular interests from scientists studying Apert Syndrome, and have been seen in publications frequently: Aging, Bone Development, Brain Development, Cell Death, Cell Division, Cell Proliferation, Endochondral Bone Growth, Endochondral Ossification, Limb Morphogenesis, Oncogenesis, Ossification, Osteoblast Differentiation, Pathogenesis, Secretion, Segmentation, Sperm Motility, Spermatogenesis, Tooth Eruption, Transposition, Wound Healing
Quite a number of genes have been found to play important roles in Apert Syndrome, such as FGF10, FGF13, FGF2, FGF7, FGFR1, FGFR2, FGFR3, FN1, FUT3, HPS4, IL6, MAPK1, MAPK3, MPZ, RPLP0, RUNX2, TBPL1, TWIST1, TYRP1. 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.