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Underlying Causes of Impaired Brain Function in Muscular Dystrophy Revealed
August 8, 2012 The molecular missteps that disrupt brain function in the most common form of adult-onset muscular dystrophy have been revealed in a new study. Myotonic dystrophy is marked by progressive muscle ... > full story -
Possible Muscle Disease Therapeutic Target Found
August 6, 2012 The study of muscular system protein myostatin has been of great interest to researchers as a potential therapeutic target for people with muscular disorders. Although much is known about how ... > full story -
Promising Step Forward Toward Muscular Dystrophy Treatment: Symptoms Reversed in Mice
August 1, 2012 Scientists have reversed symptoms of myotonic muscular dystrophy in mice by eliminating a buildup of toxic RNA in muscle cells. After experimental antisense compounds were administered to mice twice ... > full story -
New Gene Mutation Associated With Congenital Myopathy
July 25, 2012 Researchers have discovered a new cause of congenital myopathy: a mutation in a previously uncharacterized ... > full story -
Rapamycin Effective in Mouse Model of Inherited Heart Disease and Muscular Dystrophies
July 25, 2012 Rapamycin, an FDA-approved immunosuppressant drug under study in aging research labs, improved function and extended survival in mice suffering from a genetic mutation which leads to dilated ... > full story -
Protein Found in Spider Venom Could Treat Muscular Dystrophy
July 16, 2012 When a stockbroker from the Buffalo suburbs discovered that his grandson had Duchenne muscular dystrophy, he turned to medical researchers for help in developing a treatment. He found a promising new ... > full story -
Strong Communication Between Brain and Muscle Requires Both Having the Protein LRP4
July 11, 2012 Communication between the brain and muscle must be strong for us to eat, breathe or walk. Now scientists have found that a protein known to be on the surface of muscle cells must be present in both ... > full story -
New Gene Transfer Strategy Shows Promise for Limb Girdle and Other Muscular Dystrophies
July 9, 2012 The challenge of treating patients with genetic disorders in which a single mutated gene is simply too large to be replaced using traditional gene therapy techniques may soon be a thing of the past. ... > full story -
New Compound Holds Promise for Treating Duchenne MD, Other Inherited Diseases
June 27, 2012 Scientistshave identified a new compound that could treat certain types of genetic disorders in muscles. It is a first, big step in what they hope will lead to human clinical trials for Duchenne ... > full story -
Successful Transplant of Patient-Derived Stem Cells Into Mice With Muscular Dystrophy
June 27, 2012 Stem cells from patients with a rare form of muscular dystrophy have been successfully transplanted into mice affected by the same form of dystrophy, according to a new ... > full story
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