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Disease Info Card
Costello Syndrome (disorder)
Information about Costello Syndrome (disorder): 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 Costello Syndrome (disorder)
Most recent studies have shown that Costello Syndrome (disorder) shares some biological mechanisms with cardio-facio-cutaneous-syndrome, cardiomyopathies, congenital-abnormality, congenital-heart-defects, craniofacial-abnormalities, cutis-laxa, developmental-delay-(disorder), developmental-disabilities, dwarfism, failure-to-thrive, growth-disorders, hypertrophic-cardiomyopathy, hypertrophy, macrocephaly, malignant-neoplasms, neoplasms, noonan-syndrome, papilloma, skin-abnormalities.
Among the many pathways, these few ones have gauged particular interests from scientists studying Costello Syndrome (disorder), and have been seen in publications frequently: Anagen, Brain Development, Cell Cycle, Cell Cycle Arrest, Cell Differentiation, Cell Migration, Cell Proliferation, Cellular Senescence, Gliogenesis, Hypersensitivity, Myoblast Differentiation, Neural Precursor Cell Proliferation, Neurogenesis, Oncogene-induced Senescence, Pathogenesis, Pigmentation, Secretion, Senescence, Sulfation, Translation
Quite a number of genes have been found to play important roles in Costello Syndrome (disorder), such as BRAF, CS, ELN, EPHB2, GNL3, HRAS, KRAS, MAP2K1, MAP2K2, MAPK1, PTPN11, RAF1, SOS1, ZHX2. 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.