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Disease Info Card
Jarcho-levin Syndrome
Information about Jarcho-levin 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 Jarcho-levin Syndrome
Most recent studies have shown that Jarcho-levin Syndrome shares some biological mechanisms with bone-diseases-developmental, congenital-abnormality, congenital-heart-defects, congenital-musculoskeletal-anomalies, diaphragmatic-hernia, dwarfism, dysostoses, dysplasia, fetal-diseases, hernia, kyphoscoliosis-deformity-of-spine, meningomyelocele, osteochondrodysplasias, respiratory-failure, scoliosis-unspecified, shortened-trunk, spina-bifida, spinal-diseases.
Among the many pathways, these few ones have gauged particular interests from scientists studying Jarcho-levin Syndrome, and have been seen in publications frequently: Bone Remodeling, Cell Differentiation, Diaphragm Development, Gastrulation, Glycosylation, Localization, Lung Growth, Mesenchymal Stem Cell Differentiation, Mesenchymal To Epithelial Transition, Neurogenesis, Notch Signaling Pathway, Ossification, Pathogenesis, Regulation Of Mesenchymal Stem Cell Differentiation, Segmentation, Somite Development, Somite Specification, Somitogenesis, Stem Cell Differentiation, Vasculogenesis
Quite a number of genes have been found to play important roles in Jarcho-levin Syndrome, such as AR, AREG, DLL3, EGF, FDXR, FOLH1, HES7, JAG1, LFNG, MESP2, MTSS1, NOTCH1, RBPJ, SCD, SH2B1. 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.