Muscle susceptibility to lengthening contractions (fragility) in the first series of experiments (A) and utrophin expression (B) in treated mdx mice. Sed: non-treated sedentary mdx mice; Run: exercised and treated with vehicle; Run+CLi-Low: exercised and treated mdx mice with 20 μg/kg CLi; Run+CLi-High: exercised and treated mdx mice with 100 μg/kg CLi. n = 14–18 per group for A; n = 7–9 per group for figure B. b: significantly different from Run mice (p<0.05).</p
Dystrophin, the protein product of the Duchenne muscular dystrophy (DMD) gene, is absent in the skel...
Duchenne muscular dystrophy is a severe muscle wasting disease caused by the failure to produce dyst...
<p>A. Wild type mice were less severely affected than <i>mdx</i> and <i>mdx-Xist</i><sup>Δhs</sup> m...
Muscle tetanic isometric force and muscle susceptibility to lengthening contractions (fragility) in ...
Relative quantification by real-time PCR of genes involved in muscle atrophy (A), muscle fibrosis (B...
Previous studies have shown that proteasome inhibition can have beneficial effects in dystrophic mou...
International audiencePrevious studies have shown that proteasome inhibition can have beneficial eff...
Relative expression of genes involved in cardiac fibrosis (A) and remodeling (B) and catabolism (C) ...
The lack of dystrophin in Duchenne muscular dystrophy (DMD) compromises the integrity and function o...
Dystrophin deficiency leads to increased proteasome activity in skeletal muscle. Previous observatio...
AbstractThe genetic defect of mdx mice resembles that of Duchenne muscular dystrophy, although their...
<p>Five-month-old mdx/utrn+/+ and mdx/utrn+/- mice have a significantly lower treadmill completion r...
Glucocorticoids are clinically used in Duchenne muscular dystrophy although their mechanism of actio...
Weakness and fatigability, typical features of Duchenne muscular dystrophy, are aggravated in mdx mi...
The mdx mouse is the most frequently used animal model for Duchenne muscular dystrophy (DMD), a fata...
Dystrophin, the protein product of the Duchenne muscular dystrophy (DMD) gene, is absent in the skel...
Duchenne muscular dystrophy is a severe muscle wasting disease caused by the failure to produce dyst...
<p>A. Wild type mice were less severely affected than <i>mdx</i> and <i>mdx-Xist</i><sup>Δhs</sup> m...
Muscle tetanic isometric force and muscle susceptibility to lengthening contractions (fragility) in ...
Relative quantification by real-time PCR of genes involved in muscle atrophy (A), muscle fibrosis (B...
Previous studies have shown that proteasome inhibition can have beneficial effects in dystrophic mou...
International audiencePrevious studies have shown that proteasome inhibition can have beneficial eff...
Relative expression of genes involved in cardiac fibrosis (A) and remodeling (B) and catabolism (C) ...
The lack of dystrophin in Duchenne muscular dystrophy (DMD) compromises the integrity and function o...
Dystrophin deficiency leads to increased proteasome activity in skeletal muscle. Previous observatio...
AbstractThe genetic defect of mdx mice resembles that of Duchenne muscular dystrophy, although their...
<p>Five-month-old mdx/utrn+/+ and mdx/utrn+/- mice have a significantly lower treadmill completion r...
Glucocorticoids are clinically used in Duchenne muscular dystrophy although their mechanism of actio...
Weakness and fatigability, typical features of Duchenne muscular dystrophy, are aggravated in mdx mi...
The mdx mouse is the most frequently used animal model for Duchenne muscular dystrophy (DMD), a fata...
Dystrophin, the protein product of the Duchenne muscular dystrophy (DMD) gene, is absent in the skel...
Duchenne muscular dystrophy is a severe muscle wasting disease caused by the failure to produce dyst...
<p>A. Wild type mice were less severely affected than <i>mdx</i> and <i>mdx-Xist</i><sup>Δhs</sup> m...