Monday, 24 March 2014

Researchers discover molecular basis of muscle atrophy party Belt

By targeting the cellular and molecular mechanisms responsible for creating this protein, scientists can develop new drugs to stop muscle wasting by the belt muscular dystrophy and other conditions.

"Unfortunately, rare diseases like limb-girdle muscular dystrophy do not get the attention it deserves or funding," said Gerald Weissmann, MD, Editor-in-Chief FASEB Journal. "I hope that the breakthrough described in this study is to discover what regulates a protein that determines the muscle tissue stays and goes in our leadership, and the bodies of a group of new drugs for this type of muscular dystrophy and many others."Get more Tips Here http://www.venusfactoreviewscam.com/john-barban/


To determine C - FLIP as the guilty party in the belt of muscular dystrophy, the researchers used tissue from human biopsies to analyze the molecular pathways involved in every step of progress in this disorder. The researchers found that does not produce the protein C - FLIP, which is responsible for blocking the death of muscle cells, as it should in people with limb-girdle muscular dystrophy, which is controlled by the establishment of protein C - FLIP another protein called calpain.. According to the book, may have implications of this result for other types of muscular dystrophy and other situations that cause the death of muscle fibers, such as long-term paralysis, denervation, aging, or cachexia.

"Limb-girdle muscular dystrophy is a rare condition and the devastating robs people of movements that the rest of us take for granted," said Wiseman. "Fortunately, this study should provide researchers with the goal of much-needed for the development of drugs to treat at least one of these conditions."

According to the American Association of muscular dystrophy, limb-girdle muscular dystrophy is a group of disorders that affect the voluntary muscles around the hips and shoulders, and is caused by mutations of at least 15 genes responsible for making proteins needed for normal muscle function. As the disease progresses, people with limb-girdle muscular dystrophy may lose their ability to walk, and out of chairs, comb hair, and feed them.

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