Experts hailed exciting news for some people with sickle cell disease in England as the health watchdog decided to grant ...

How CRISPR and AI Destroy the World Imagine a world where the genetic code is as easy to edit as a simple copy-and-paste.

Australian cancer researchers are the first to establish a next-generation gene-editing tool for modeling and interrogating ...

Complementary discoveries have the potential to enhance treatment options for antibiotic-resistant infections. Researchers at ...

The most complex engineering of human cell lines ever has been achieved by scientists, revealing that our genomes are more ...

It’s a new way to create “bi-paternal” mice that can survive to adulthood—but human applications are still a long way off.

Australian cancer researchers are the first to establish a next-generation gene-editing tool for modeling and interrogating human disease.

A GROUNDBREAKING genetic treatment with the potential to cure sickle cell disease will be rolled out on the NHS. The one-off ...

Researchers use CRISPR to overcome seemingly insurmontable reproductive barriers — but that doesn't mean this could work for ...

A £1.65 million treatment has been approved for use for some NHS patients, offering some with an inherited blood disorder ...

Vertex Pharmaceuticals (VRTX) stock gains as England opts to reimburse its CRSPR (CRSP)-partnered gene therapy Casgevy to ...