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Muscular Dystrophy


— Science

Telomere-lengthening procedure turns clock back years in human cells

By - January 28, 2015 1 Picture
Researchers at the Stanford University School of Medicine have developed a new procedure to increase the length of human telomeres. This increases the number of times cells are able to divide, essentially making the cells many years younger. This not only has useful applications for laboratory work, but may point the way to treating various age-related disorders – or even muscular dystrophy. Read More
— Medical

New combination of drugs slows heart decline in muscular dystrophy patients

By - December 29, 2014 1 Picture
Signs of Duchenne muscular dystrophy (DMD) can start to appear in boys as young as six, leading to deterioration of the heart muscles and ultimately death. Pharmaceuticals aimed at controlling high blood pressure have been used to treat the one in 3,500 young males suffering from the condition, but a new study suggests that a novel combination of these drugs could slow the decline in heart function earlier on, and in promising new ways. Read More
— Science

Researchers create "mighty mouse" with gene tweak that doubles muscle strength

By - December 18, 2011 2 Pictures
He can't fly just yet, but a team of scientists have made a big step towards creating a real-life Mighty Mouse. Researchers at the Salk Institute for Biological Studies, along with two Swiss institutions, Ecole Polytechnique Federale de Lausanne (EPFL) and the University of Lausanne, created a batch of super-strong mice and worms by tweaking a gene that normally inhibits muscle growth. Read More
— Health and Wellbeing

Human protein may help muscular dystrophy patients

By - December 30, 2010 1 Picture
Duchenne Muscular Dystrophy is the most common and severe childhood form of muscular dystrophy (MD), affecting one in 3,500 boys. The disease progressively weakens muscles cells and tissues until muscle degradation is so severe that the patient dies, most often in their late teens or twenties. Scientists at Brown University in Providence, Rhode Island and the University of Pennsylvania, hope their research into the human protein, biglycan, will ultimately improve the condition of muscular dystrophy sufferers. Their studies have shown that biglycan significantly slows muscle damage and improves function in mice with the Duchenne genetic mutation. Human clinical trials will be the next step. Read More
— Robotics

REX robotic exoskeleton gets wheelchair users back on their feet

By - July 16, 2010 4 Pictures
Seemingly simple things like talking to people at eye level and reaching things on shelves can be a huge drawback for those in wheelchairs. Sitting in a wheelchair for extended periods can also lead to the increased risk of certain infections and blood circulation problems. A robotic exoskeleton called REX puts wheelchair users back on their feet, enabling a person to stand, walk and go up and down stairs and slopes. Read More
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