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Disease Info Card
X-linked Emery-dreifuss Muscular Dystrophy
Information about X-linked Emery-dreifuss 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 X-linked Emery-dreifuss Muscular Dystrophy
Most recent studies have shown that X-linked Emery-dreifuss Muscular Dystrophy shares some biological mechanisms with atrophy, autosomal-dominant-emery-dreifuss-muscular-dystrophy-(disorder), cardiac-arrhythmia, cardiomyopathies, dysplasia, dystrophy, lipodystrophy, muscle-contracture, muscle-weakness, muscular-atrophy, muscular-dystrophies-limb-girdle, muscular-dystrophy, muscular-dystrophy-emery-dreifuss, muscular-dystrophy-facioscapulohumeral, myopathy, neuromuscular-diseases, spinal-muscular-atrophy, sudden-cardiac-death, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying X-linked Emery-dreifuss Muscular Dystrophy, and have been seen in publications frequently: Aging, Cardiac Conduction, Cell Cycle, Cell Death, Cell Differentiation, Chromatin Organization, Glycosylation, Interphase, Localization, Mitosis, Mrna Splicing, Muscle Atrophy, Muscle Fiber Development, Myoblast Differentiation, Myoblast Proliferation, Pathogenesis, Regeneration, Rna Interference, Translation
Quite a number of genes have been found to play important roles in X-linked Emery-dreifuss Muscular Dystrophy, such as BANF1, DMD, EMD, HSP90AA1, LEMD3, LMNA, LMNB1, LMNB2, LMO7, MYH7, PLEKHM1, SGCA, TMPO, UBL4A, VCP. 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.