Aug. 9, 2016 Maintaining proper levels of an essential helper molecule is crucial for optimal muscle function. Some athletes are already taking supplements to increase synthesis of this compound, called NAD, with ...
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July 21, 2016 A key gene enables the repair of injured muscle throughout life, according to a study in mice. The study results further suggest that this "overlooked" gene may play an important role in ...
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June 16, 2016 The cause of heart arrhythmia in myotonic dystrophy was RNA abnormalities in the sodium channel in the heart, clarifying the symptom's mechanism, an international joint research group found. ...
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June 1, 2016 Certain stem cells in our bodies have the potential to turn into either fat or muscle. Experiments in mice suggest prospective drugs that manipulate these cells' fate could make it possible to ...
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Feb. 18, 2016 Researchers have identified pecific ways in which fetal muscle stem cells remodel their environment to support their enhanced capacity for regeneration, which could lead to targets for therapies to ...
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Feb. 12, 2016 Scientists have developed a new approach that could eventually be used to treat Duchenne muscular dystrophy. The stem cell gene therapy could be applicable for 60 percent of people with Duchenne, ...
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Jan. 22, 2016 Researchers have developed the A-Gear: a robotic arm that can support the daily activities of people suffering the muscular disease Duchenne Muscular Dystrophy. They recently put the final touches to ...
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Jan. 6, 2016 A drug commonly used to treat leukemia is showing potential as a treatment that could slow the progression of the muscle-wasting condition, Duchenne muscular ...
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Dec. 10, 2015 A drug used to treat cancer can neutralize the toxic RNA that causes the prolonged muscle contractions and other symptoms of myotonic dystrophy type 1, the most common form of adult-onset muscular ...
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Nov. 30, 2015 Researchers have identified the role of TNF receptor-associated factor 6 (TRAF6), an adaptor protein and E3 ubiquitin ligase, in ensuring the vitality of stem cells that regenerate muscle ...
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Nov. 18, 2015 A new study of individuals with myotonic dystrophy type 2 -- a rare form of muscular dystrophy -- has helped pinpoint the symptoms of the disease that are most important to patients. These findings ...
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Nov. 16, 2015 For nearly 20 years, scientists have thought that the muscle weakness observed in patients with Duchenne muscular dystrophy is primarily due to problems in their muscle fibers, but new research shows ...
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Nov. 12, 2015 Researchers have shown that a gene called Jagged1, or JAG1 for short, could be a target for the development of new approaches to treat Duchenne muscular dystrophy, a genetic disorder characterized by ...
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Oct. 26, 2015 Researchers report on their discovery of a way to bypass faculty cell signalling that leads to muscle damage in Duchene muscular dystrophy. This work suggests a new therapeutic strategy for patients ...
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Oct. 13, 2015 Genetic ablation of P2RX7 can improve muscle function and partially correct cognitive impairment and bone loss in a mouse model of Duchenne muscular dystrophy, according to a new study. The research ...
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Oct. 13, 2015 New research has demonstrated a new method for observing the behavior of the protein Dystrophin in a living animal cell, in real-time. This breakthrough may provide a key to understanding how to ...
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Oct. 12, 2015 An RNA editing technique called 'exon skipping' has shown preliminary success in treating a rare and severe form of muscular dystrophy that currently has no treatment. The discovery stems ...
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Sep. 22, 2015 Researchers have successfully isolated human muscle stem cells and shown that the cells could robustly replicate and repair damaged muscles when grafted onto an injured ...
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Aug. 20, 2015 Duchenne muscular dystrophy (DMD) is disease that leads to the degeneration of muscle due to dysfunctional expression of the protein dystrophin. A new iPS cell model found that the early stages of ...
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Aug. 6, 2015 Lack of microinvaginations in the cell membrane, caveolae, can cause serious diseases such as lipodystrophy and muscular dystrophy. Researchers have now discovered a “main switch” that regulates ...
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