Interaction between mesenchymal stem cells and myoblasts in the context of facioscapulohumeral muscular dystrophy contributes to the disease phenotype
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DOI: 10.1002/jcp.30789
Abstract: Facioscapulohumeral muscular dystrophy (FSHD) is a genetic disease associated with ectopic expression of the DUX4 gene in skeletal muscle. Muscle degeneration in FSHD is accompanied by muscle tissue replacement with fat and connective tissue. Expression… read more here.
Keywords: interaction; facioscapulohumeral muscular; cxcr4; muscular dystrophy ... See more keywords