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Disease Info Card
Saethre-chotzen Syndrome
Information about Saethre-chotzen 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 Saethre-chotzen Syndrome
Most recent studies have shown that Saethre-chotzen Syndrome shares some biological mechanisms with acrocephalosyndactylia, acrocephaly, apert-syndrome, blepharoptosis, brachycephaly, congenital-abnormal-synostosis, congenital-abnormality, craniofacial-abnormalities, craniofacial-dysostosis, craniosynostosis, facial-asymmetry, haploinsufficiency, hypoplasia, intracranial-hypertension, malignant-neoplasms, muenke-syndrome, orbital-separation-excessive, pfeiffer-syndrome, syndactyly.
Among the many pathways, these few ones have gauged particular interests from scientists studying Saethre-chotzen Syndrome, and have been seen in publications frequently: Cell Cycle, Cell Cycle Arrest, Cell Differentiation, Cell Growth, Cell Migration, Cell Proliferation, Chemotaxis, Limb Development, Localization, Mesoderm Formation, Neural Crest Cell Migration, Neural Tube Closure, Neurogenesis, Ossification, Osteoblast Differentiation, Osteoblast Proliferation, Protein Phosphorylation, Stem Cell Differentiation, Tube Formation, Tube Morphogenesis
Quite a number of genes have been found to play important roles in Saethre-chotzen Syndrome, such as ARID1B, BGLAP, CDKN1A, CDKN2B, ELSPBP1, FGFR1, FGFR2, FGFR3, HAND2, MRPL28, MSX2, NSG1, NXT1, PLA2G15, RUNX2, SLC22A3, SUB1, TCEAL1, TCF3, 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.