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Disease Info Card
Crest Syndrome
Information about Crest 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 Crest Syndrome
Most recent studies have shown that Crest Syndrome shares some biological mechanisms with alveolar-bone-loss, carcinoma, congenital-abnormality, diffuse-scleroderma, fracture, hemorrhage, malignant-neoplasms, malignant-paraganglionic-neoplasm, melanoma, neoplasm-metastasis, neoplasms, nervousness, neuroblastoma, osteopenia, osteoporosis, pain, raynaud-disease, scleroderma, sclerosis, tissue-adhesions.
Among the many pathways, these few ones have gauged particular interests from scientists studying Crest Syndrome, and have been seen in publications frequently: Bone Remodeling, Bone Resorption, Cell Adhesion, Cell Cycle, Cell Death, Cell Development, Cell Differentiation, Cell Migration, Cell Proliferation, Gastrulation, Innervation, Localization, Neural Crest Cell Migration, Neurogenesis, Ossification, Pathogenesis, Pigmentation, Regeneration, Secretion, Segmentation
Quite a number of genes have been found to play important roles in Crest Syndrome, such as BMP2, BMP4, EDN3, EDNRB, FGF2, FN1, PAX3, PTH, RET, SHH, SLC12A3, SNAI2, SOX10, SOX9, SS18L1, TH. 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.