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Disease Info Card
Ullrich Congenital Muscular Dystrophy
Information about Ullrich Congenital Muscular 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 Ullrich Congenital Muscular Dystrophy
Most recent studies have shown that Ullrich Congenital Muscular Dystrophy shares some biological mechanisms with collagen-diseases, congenital-muscular-dystrophy-(disorder), connective-tissue-diseases, dystrophy, generalized-muscle-weakness, muscle-contracture, muscle-weakness, muscular-atrophy, muscular-dystrophies-limb-girdle, muscular-dystrophy, myopathy, myotonic-dystrophy, neuromuscular-diseases, posttransfusion-purpura, respiratory-failure, sclerosis, scoliosis-unspecified, tissue-adhesions, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Ullrich Congenital Muscular Dystrophy, and have been seen in publications frequently: Aging, Autophagy, Cell Activation, Cell Adhesion, Cell Death, Excretion, Glycosylation, Localization, Mitochondrial Depolarization, Pathogenesis, Protein Folding, Regeneration, Rna Splicing, Secretion, T Cell Activation, Tissue Homeostasis, Translation
Quite a number of genes have been found to play important roles in Ullrich Congenital Muscular Dystrophy, such as ARHGAP4, CAPN3, CCDC6, COL6A1, COL6A2, COL6A3, COL6A5, CSPG4, F9, HNRNPC, PPID, PPIF, PTCH1, PTPRU, REG1A, RET, SGCA, SLC25A3, TAS2R38, UPF1. 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.