Duchenne muscular dystrophy is a severe muscle wasting disease caused by the failure to produce dystrophin. Dystrophic mdx and healthy C57 mice (n=5/group/time point) were subject to 15 stimulated, in vivo lengthening contractions and examined following 0, 3, or 24 hours to determine if the severe dystrophic response to exercise could be reproduced with a moderate volume of contractions. As expected, the mdx mice exhibited greater force loss (pM.Sc
The lack of dystrophin in Duchenne muscular dystrophy (DMD) compromises the integrity and function o...
The mdx mouse is the most frequently used animal model for Duchenne muscular dystrophy (DMD), a fata...
International audienceIt is well known that inactivity/activity influences skeletal muscle physiolog...
Duchenne muscular dystrophy is a severe muscle wasting disease caused by the failure to produce dyst...
Absence of dystrophin in mdx muscles may render the muscle more susceptible to damage when submitted...
Progressive weakness is a typical feature of Duchenne muscular dystrophy (DMD) patients and is exace...
Absence of dystrophin in mdx muscles may render the muscle more susceptible to damage when submitted...
International audienceBackgroundThe greater susceptibility to contraction-induced skeletal muscle in...
Background Preclinical testing of potential therapies for Duchenne muscular dystrophy (DMD) is condu...
International audienceThere is fear that mechanical overloading (OVL; ie, high-force contractions) a...
Progressive weakness is a typical feature of Duchenne muscular dystrophy (DMD) patients and is exace...
Weakness and fatigability, typical features of Duchenne muscular dystrophy, are aggravated in mdx mi...
The diversity of movement in mammals requires three different types of muscle contraction: isometric...
Weakness and fatigability, typical features of Duchenne muscular dystrophy, are aggravated in mdx mi...
It is commonly accepted that skeletal muscles from dystrophin-deficient mdx mice are more susceptibl...
The lack of dystrophin in Duchenne muscular dystrophy (DMD) compromises the integrity and function o...
The mdx mouse is the most frequently used animal model for Duchenne muscular dystrophy (DMD), a fata...
International audienceIt is well known that inactivity/activity influences skeletal muscle physiolog...
Duchenne muscular dystrophy is a severe muscle wasting disease caused by the failure to produce dyst...
Absence of dystrophin in mdx muscles may render the muscle more susceptible to damage when submitted...
Progressive weakness is a typical feature of Duchenne muscular dystrophy (DMD) patients and is exace...
Absence of dystrophin in mdx muscles may render the muscle more susceptible to damage when submitted...
International audienceBackgroundThe greater susceptibility to contraction-induced skeletal muscle in...
Background Preclinical testing of potential therapies for Duchenne muscular dystrophy (DMD) is condu...
International audienceThere is fear that mechanical overloading (OVL; ie, high-force contractions) a...
Progressive weakness is a typical feature of Duchenne muscular dystrophy (DMD) patients and is exace...
Weakness and fatigability, typical features of Duchenne muscular dystrophy, are aggravated in mdx mi...
The diversity of movement in mammals requires three different types of muscle contraction: isometric...
Weakness and fatigability, typical features of Duchenne muscular dystrophy, are aggravated in mdx mi...
It is commonly accepted that skeletal muscles from dystrophin-deficient mdx mice are more susceptibl...
The lack of dystrophin in Duchenne muscular dystrophy (DMD) compromises the integrity and function o...
The mdx mouse is the most frequently used animal model for Duchenne muscular dystrophy (DMD), a fata...
International audienceIt is well known that inactivity/activity influences skeletal muscle physiolog...