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 new study that provides a strong indication that a lifesaving treatment may be in the pipeline.
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Researchers followed 400,000 kids for 20 years and found a lasting pre-K advantage
A 20-year study of 400,000 students found that children who attended public school pre-K earned better grades and test scores through high s...
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Two of the traits that set modern humans apart from non-human primates are taller stature and a higher basal metabolic rate. Researchers hav...
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