Thursday, August 30, 2018

CRISPR halts Duchenne muscular dystrophy progression in dogs

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.

from Top Health News -- ScienceDaily https://ift.tt/2wszm9W

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A protein older than blood circulation could transform cancer immunotherapy

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