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- Table of Contents
Information about Shortened Trunk: 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.
Most recent studies have shown that Shortened Trunk shares some biological mechanisms with acquired-kyphosis, bone-diseases-developmental, cleft-palate, dwarfism, dyggve-melchior-clausen-syndrome, dysostoses, dysplasia, hypogonadism, hypoplasia, jarcho-levin-syndrome, kyphoscoliosis-deformity-of-spine, late-spondyloepiphyseal-dysplasia, lordosis, mucopolysaccharidoses, mucopolysaccharidosis-iv, osteochondrodysplasias, scoliosis-unspecified, skeletal-dysplasia, spondyloepiphyseal-dysplasia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Shortened Trunk, and have been seen in publications frequently: Bone Development, Chondrocyte Differentiation, Convergent Extension, Dna Repair, Embryo Development, Embryonic Morphogenesis, Endochondral Ossification, Excretion, Gastrulation, Lung Growth, Mastication, Menarche, Notch Signaling Pathway, Ossification, Pathogenesis, Secretion, Segmentation, Somitogenesis, Translation
Quite a number of genes have been found to play important roles in Shortened Trunk, such as COL2A1, DLL3, DYM, GALNS, GLB1, IGF1, IGFBP3, LFNG, MTSS1, SS18L1, TRAPPC2, TRPV4. 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.