Aurora Therapeutics, cofounded by Nobel Prize–winning scientist Jennifer Doudna, plans to use gene editing and a new FDA ...

Scientists have discovered a new CRISPR mechanism with precise activity, expanding the potential applications of the existing ...

As CRISPR moves from lab success to real-world medicine, 2026 will test whether these revolutionary gene-editing therapies ...

Gene editing has moved from theory to bedside with a speed that would have seemed impossible a decade ago. A new wave of ...

Victoria Gray spent 34 years battling the debilitating pain of sickle cell disease. Then she volunteered to be the world's first "prototype" for a CRISPR therapy, based on technology invented at UC ...

He Jiankui spent three years in prison after creating gene-edited babies. Now back at work, he sees a greater opening for ...

Head and neck cancers often begin in the mouth, throat, or voice box. They're among the most common cancers in the world, affecting over half a million people each year and causing about 300,000 ...

A large genetic screen has revealed how stem cells transform into brain cells, exposing hundreds of genes that make this ...

Innovative research into the gene-editing tool targets influenza’s ability to replicate—stopping it in its tracks.

The study used large-scale CRISPR gene-editing technology to systematically determine which genes are required as embryonic ...

An infant with a rare metabolic disease became the world’s first patient to be treated with a personalized CRISPR gene-editing treatment in a landmark study between Penn Medicine and the Children’s ...

Scientists are testing CRISPR gene editing as a potential HIV cure after successfully removing the virus from infected cells ...