Disruption of a transcription network controlled by MEF2 in heart tissue of people with myotonic dystrophy type 1 – an inherited form of muscular dystrophy with symptoms starting in early adulthood – affects activity ...
Jan 9, 2014
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Scientists from the Florida campus of The Scripps Research Institute have revealed an atomic-level view of a genetic defect that causes a form of muscular dystrophy, myotonic dystrophy type 2, and have used this information ...
Jan 2, 2014
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Scientists have found that cells known primarily for tempering immune response also exist in injured muscle tissue, an unexpected role for regulatory T cells.
Dec 6, 2013
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(Medical Xpress)—Reviving a gene which is 'turned down' after birth could be the key to treating Duchenne muscular dystrophy (DMD), an incurable muscle-wasting condition that affects one in every 3,500 boys.
Dec 2, 2013
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Researchers at McMaster University have discovered a protein that is only detectable after muscle damage, and it may serve as a way to measure injury.
Nov 11, 2013
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(Medical Xpress)—For decades, scientists have searched for treatments for myopathies – genetic muscular diseases such as muscular dystrophy and ALS, also called Lou Gehrig's disease. Now, an interdisciplinary team of ...
Nov 4, 2013
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About 3,000 people in Denmark suffer from one of the serious muscle-related diseases that come under the heading of muscular dystrophy. Some patients diagnosed with muscular dystrophy die shortly after birth, others become ...
Oct 31, 2013
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Scientists in The Research Institute at Nationwide Children's Hospital have found a way to overcome one of the biggest obstacles to using viruses to deliver therapeutic genes: how to keep the immune system from neutralizing ...
Oct 30, 2013
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A large scale scientific collaboration led by France's Pierre and Marie Curie University and national institute of health and medical research has generated significant advances in treatment for muscular dystrophies by targeting ...
Oct 25, 2013
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A preclinical study led by researchers in the United States has found that a new oral drug shows early promise for the treatment of muscular dystrophy. The results, which are published today in EMBO Molecular Medicine, show ...
Sep 9, 2013
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