FHL1 reduces dystrophy in transgenic mice overexpressing FSHD muscular dystrophy region gene 1 (FRG1).

Dystrophin expression in muscles of duchenne muscular dystrophy patients after high-density injections of normal myogenic cells. Viral vectors in gene

Compelling evidence indicates that adult satellite cells rep- resent a heterogeneous population of stem cells and com- mitted myogenic progenitors in skeletal muscle. At the

induced in both human DMD and mouse models of muscular dystrophy, we attempted to model this increase by creating skeletal muscle-specific transgenic mice with increased

Therefore, we examined satellite stem cells immediately after the first round of cell division in isolated myofibers that were cultured for 42 h, and we observed an 80% reduction

Early transplantation of human immature dental pulp stem cells from baby teeth to golden retriever muscular dystrophy (GRMD) dogs: Local or systemic. Journal of

Table 3 — Results of electromyographies and muscle biopsies grouped according to the pathology: PHMD, pseudo­hypertrophic muscular dystrophy; LGMD, limb­girdle muscular dystrophy

Normal and dystrophin deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy.. Comi G, Comola M,

Dystrophin, which is usually distributed in the subsarco- lemmal zone of skeletal muscle fibers, is absent in Duchenne muscular dystrophy (DMD) and present in variable amounts with