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Disease Info Card
Thanatophoric Dysplasia
Information about Thanatophoric Dysplasia: 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 Thanatophoric Dysplasia
Most recent studies have shown that Thanatophoric Dysplasia shares some biological mechanisms with achondroplasia, bone-diseases-developmental, congenital-abnormality, craniofacial-dysostosis, craniosynostosis, dwarfism, dysplasia, fetal-death, fetal-diseases, hydrocephalus, hypochondroplasia-(disorder), hypoplasia, macrocephaly, osteochondrodysplasias, osteogenesis-imperfecta, polyhydramnios, skeletal-dysplasia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Thanatophoric Dysplasia, and have been seen in publications frequently: Angiogenesis, Bone Development, Cell Adhesion, Cell Cycle, Cell Growth, Chondrocyte Differentiation, Chondrocyte Proliferation, Endochondral Bone Growth, Endochondral Ossification, Glycosylation, Localization, Neurogenesis, Oncogenesis, Ossification, Pathogenesis, Proteolysis, Secondary Growth, Secretory Pathway, Transport, Wound Healing
Quite a number of genes have been found to play important roles in Thanatophoric Dysplasia, such as CDKN1A, CDKN2A, FGF1, FGF2, FGF3, FGFR1, FGFR2, FGFR3, IHH, MAPK1, MAPK3, PTH, PTHLH, PTK2B, SOX9, STAT1, STAT5B. 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.