CRISPR Gene Editing Shows Promise for Treating a Fatal Muscle Disease temim 12:02 AM temim Results from a dog trial may help push new Duchenne muscular dystrophy therapy toward human trials -- Read more on ScientificAmerican.com from Scientific American News https://ift.tt/2PR5YlV via IFTTT Twitter Facebook Google Tumblr Pinterest Artikel Menarik Lainnya Notre Dame's Architectural LegacyThis religious center, cultural icon and UNESCO World Heritage Site is also an engineering marvel How We Roll: Study Shows We're More Lone Wolves Than Team PlayersResults may explain why collective action on climate change and health policy is so difficult -- RWatching Apollo 11 with NASA Historian Bill BarryThe agency’s chief historian discusses the film and what the moon missions can teach us about globaCaffeine Peps Up Solar EnergyThe human energizer can also improve the efficiency and stability of perovskite solar cells -- ReaCan Robots Help Pick Up after the Recycling Crisis?They will have to overcome the challenges of America’s convenient single-stream recycling system -Are We More Attracted to People Who Look like Our Parents?Though we might be drawn to people who have physical commonalities with us and therefore our parent
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