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Scientists for the first time have used CRISPR gene editing to halt the progression of Duchenne muscular dystrophy (DMD) in a large mammal, according to a study by UT Southwestern that provides a strong indication that a lifesaving treatment may be in the pipeline.The research published in Science documents unprecedented improvement in the muscle fibers of dog <a href=https://www.adidas-yeezys.es>adidas yeezy</a> s with DMD 鈥?the most common fatal genetic disease in children, caused by a mutation that inhibits the production of dystrophin, a protein critical for muscle function.Researchers used a single-cut gene-editing technique to restore dystrophin in muscle and heart tissue by up to 92 percent of normal levels. Scientists have estimated a 15 percent threshold is needed to significantly help patients.鈥淐hildren with DMD often die either because their heart loses the strength to pump <a href=https://www.dunks.fr>nike dunk</a> , or their diaphragm becomes <a href=https://www.nbbalance.de>nbbalance</a> too weak to breathe,鈥?said Dr. Eric Olson, Director of UT Southwestern鈥檚 Hamon Center for Regenerative Science and Medicine. 鈥淭hi LAHORE:A 35-year-old rickshaw dri <a href=https://www.campusadidas.fr>adidas campus noir</a> ver died in a road-accident near Badami Bagh police station on Saturday. Police <a href=https://www.campusadidas.fr>adidas campus</a> said Muhammad Ashfaq, son of Muhammad Boota, had an accident near Ring Road when he was hit by a car. <a href=https://www.adidas-samba-adidas.it>adidas samba bianche</a> They said he died on the spot.Published in The Express Tribune, March 27th, 2016.

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