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Disease Info Card
Jeune Thoracic Dystrophy
Information about Jeune Thoracic Dystrophy: 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 Jeune Thoracic Dystrophy
Most recent studies have shown that Jeune Thoracic Dystrophy shares some biological mechanisms with asphyxia, asphyxia-neonatorum, bone-diseases-developmental, congenital-abnormality, dwarfism, dysplasia, dystrophy, ellis-van-creveld-syndrome, fibrosis, kidney-diseases, kidney-failure, kidney-failure-chronic, osteochondrodysplasias, polydactyly, respiratory-distress, respiratory-failure, short-rib-polydactyly-syndrome, thoracic-diseases.
Among the many pathways, these few ones have gauged particular interests from scientists studying Jeune Thoracic Dystrophy, and have been seen in publications frequently: Artery Development, Bone Maturation, Cell Cycle, Cell Differentiation, Cell Proliferation, Endochondral Ossification, Excretion, Intraflagellar Transport, Intrahepatic Bile Duct Development, Localization, Lung Development, Lung Growth, Ossification, Osteoblast Differentiation, Pathogenesis, Protein Transport, Rna Interference, Swimming, Transport, Wound Healing
Quite a number of genes have been found to play important roles in Jeune Thoracic Dystrophy, such as ARL13B, ASAH1, ATM, BBS2, CD55, DYNC2H1, FOXM1, HNF1B, IFT80, INVS, NPHP1, ONECUT1, PKHD1, SHH, SMS, TCN2, UCN2, WDR19. 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.