Disease Info Card

Becker Muscular Dystrophy

Information about Becker 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 Becker Muscular Dystrophy

Most recent studies have shown that Becker Muscular Dystrophy shares some biological mechanisms with atrophy, cardiomyopathies, cardiomyopathy-dilated, congenital-muscular-dystrophy-(disorder), dystrophy, fibrosis, heart-diseases, heart-failure, hereditary-diseases, hypertrophy, muscle-weakness, muscular-atrophy, muscular-dystrophies-limb-girdle, muscular-dystrophy, muscular-dystrophy-duchenne, myopathy, myotonic-dystrophy, neuromuscular-diseases, spinal-muscular-atrophy, weakness.

Among the many pathways, these few ones have gauged particular interests from scientists studying Becker Muscular Dystrophy, and have been seen in publications frequently: Aging, Cell Adhesion, Cell Cycle, Cell Death, Cellular Localization, Coagulation, Dna Amplification, Innervation, Interphase, Localization, Metaphase, Muscle Atrophy, Muscle Hypertrophy, Pathogenesis, Reflex, Regeneration, Reverse Transcription, Signal Transmission, Translation, Transport

Quite a number of genes have been found to play important roles in Becker Muscular Dystrophy, such as ACE, BEST1, CAPN3, CHKA, CHKB, DAG1, DMD, ERG, FKRP, FKTN, GK, KCNH2, MYOD1, SGCA, SGCB, SGCG, 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.