DMD is a rare disorder characterized by progressive muscle degeneration and premature
death. Therapy development is delayed by difficulties to monitor efficacy non‐invasively in …

Background Transforming growth factor‐β‐activated kinase 1 (TAK1) plays a key role in
regulating fibroblast and myoblast proliferation and differentiation. However, the TAK1 …

Studies reveal a linkage of miR-29s in aging and Parkinson's disease (PD). Here we show
that the serum levels of miR-29s in 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP) …

Duchenne muscular dystrophy (DMD) is a rare genetic disorder affecting paediatric patients.
The disease course is characterized by loss of muscle mass, which is rapidly substituted by …

Duchenne muscular dystrophy (DMD) is a severe X-linked inherited muscular disorder
characterized by the loss of dystrophin. We have previously shown that monogene therapy …

Antisense oligonucleotide (AO)‐mediated exon‐skipping therapies show promise in
Duchenne muscular dystrophy (DMD), a devastating muscular disease caused by frame …

Duchenne muscular dystrophy (DMD) is a genetic neuromuscular disorder caused by
mutations in the gene encoding dystrophin located on chromosome Xp21. The absence of …

Materials and methods Mice. All mice involved in the experiments were males and they were
housed in individually ventilated cages. Five groups of mice were included in the …

The extracellular matrix (ECM) of the skeletal muscle provides the framework for the muscle
structure and plays a key role in the repair and maintenance of myofibers through the …