This new tool, known as minimal, versatile genetic perturbation technology (mvGPT), combines the powers of gene editing, ...

Casgevy, also known as exa-cel, was the first treatment to be licensed using gene-editing tool Crispr (Alamy/PA) A £1.65 million treatment has been approved for use for some NHS patients ...

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

Branched endosomal disruptor (BEND) lipids mediate delivery of mRNA and CRISPR-Cas9 ribonucleoprotein complex for hepatic gene editing and T cell engineering. Nature Communications , 2025; 16 (1 ...

Campaigners reacted with joy as health officials approved a gene-editing therapy for certain children and adults with severe sickle cell disorder. It is thought that 1,700 people could be eligible ...

Researchers have developed a gene-editing treatment for prion disease that extends lifespan by about 50 percent in a mouse model of the fatal neurodegenerative condition. The treatment ...

Gene editing using base editing has been shown to extend the lifespan of mice with prion disease by approximately 50%. This approach involves a single-letter DNA change that reduces prion protein ...

Researchers at the Broad Institute of MIT and Harvard have developed a gene-editing treatment for prion disease that extends lifespan by about 50 percent in a mouse model of the fatal ...

If successful, this gene editing approach could provide hope to thousands of people affected by Stargardt disease and potentially other inherited retinal disorders. More information: Alissa Muller ...

Shares of gene editing companies dropped on Friday as Wall Street reacted to Intellia Therapeutics' (NASDAQ:NTLA) plans to lay off 27% of its staff alongside a decision to halt a mid-stage ...