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With a sizable grant from the TED Audacious Project, scientists at UC Davis, UC Berkeley and UC San Francisco are using the Nobel-Prize-winning gene editing tool known as CRISPR to attempt to reduce the methane released by dairy cows.
Vertex Pharmaceuticals and CRISPR Therapeutics's one-dose gene editing therapy for sickle cell disease would be cost effective if priced at up to $1.9 million, an influential US drug pricing group said on Wednesday.
Mutations in the identical genes lead to diverse subtypes of tumors in different individuals. Scientists have identified a new way to generate tumor subtypes.
In the face of safety risks, experts have tightened the reins on heritable genome editing—but haven’t ruled out using it someday.
A new CRISPR technique was employed by Chinese scientists to successfully restore vision in mice. Researchers in China have announced a groundbreaking discovery in the treatment of retinitis pigmentosa, a leading cause of blindness in humans.