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Disease Info Card
Muscular Dystrophy, Duchenne
Information about Muscular Dystrophy, Duchenne: 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 Muscular Dystrophy, Duchenne
Most recent studies have shown that Muscular Dystrophy, Duchenne shares some biological mechanisms with atrophy, becker-muscular-dystrophy, cardiomyopathies, cardiomyopathy-dilated, dystrophy, fibrosis, heart-failure, hereditary-diseases, muscle-degeneration, muscle-weakness, muscular-atrophy, muscular-dystrophies-limb-girdle, muscular-dystrophy, muscular-dystrophy-animal, myopathy, neuromuscular-diseases, scoliosis-unspecified, spinal-muscular-atrophy, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Muscular Dystrophy, Duchenne, and have been seen in publications frequently: Aging, Cell Death, Cell Proliferation, Excretion, Immune Response, Inflammatory Response, Innervation, Localization, Muscle Atrophy, Muscle Contraction, Muscle Hypertrophy, Myoblast Fusion, Pathogenesis, Proteolysis, Regeneration, Reverse Transcription, Secretion, Senescence, Translation, Transport
Quite a number of genes have been found to play important roles in Muscular Dystrophy, Duchenne, such as AQP4, BEST1, CAV3, CHKA, CHKB, DAG1, DMD, GK, GLB1, MB, MSTN, MYOD1, NOS1, SGCA, TNF, UTRN. 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.