Two research groups are independently pioneering a groundbreaking gene-editing treatment for severe immunodeficiencies, potentially transforming the...

Gene-editing systems, especially CRISPR-Cas9, have revolutionised genome editing, offering potential cures for genetic disorders, cancers, and other...

Researchers at Ulsan National Institute of Science and Technology in South Korea have developed a CRISPR-Cas9-based method to eliminate tumour cells....

Researchers at Texas Biomedical Research Institute in San Antonio, Texas have developed a novel strategy to inhibit human immunodeficiency virus (HIV)...

At a time where base-editing technology is set to enter the clinic, researchers from Rahul Kohli’s lab at the University of Pennsylvania have made a...

This week’s update looks at a CRISPR-edited CAR T-cell therapy in clinical development for the treatment of a range of B cell cancers.

DNA repair by a hitherto overlooked mechanism - non-homologous blunt-end joining – might lead to a new therapeutic strategy for Duchenne muscular...

Leber congenital amaurosis is a group of rare inherited retinal diseases that lead to blindness over time. Treatment options are limited,...