SpaceX on the Moon, the Oldest Fossils on Earth, a Cryogenic Breakthrough, and More.
This could prevent neurological disorders, such as Leigh Syndrome.
Editing genes is still risky business.
This new way of delivering repaired genes could prevent cancer.
The first FDA-approved gene therapy could cure inherited retinal defects.
The first gene therapy for children is coming to Europe.
A new breakthrough gene therapy could be made available to children suffering from a rare genetic disorder.
“If you could do one action that might save a thousand, a million or a billion people—but you might die from doing it? Why would you take the risk?”
Gene edited immune cells from a healthy donor saves the life of one-year-old child dying of leukemia.
Biotech startup Editas Medicine intends to begin using CRISPR in human trials to treat a rare form of blindness by 2017.
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