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 An AI System Spontaneously Develops Baby-Like Ability to Gauge Big and SmallOn its own, the neural network seems to recap a process experienced by human infants -- Read more Watch Now: Einstein's Scientific Revolution and the Limits of Quantum TheoryCosmologist Lee Smolin says that at certain key points, the scientific worldview is based on fallacHow Wild Should We Let the Solar System Be?Experts argue that more than 85 percent of the solar system should be left untouched so that we canBrain Restoration System Explores Hazy Territory between Being Dead or AliveAn experiment that restored cellular function to pigs’ brains hours after death holds the potentialHow to Be a Data-Driven ParentEconomist Emily Oster explains how to make the best decisions for your particular child, using the As Pesticide Turns Up in More Places, Safety Concerns MountA growing body of research is challenging the assumption that neonicotinoids are safer and less lik
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