Researchers at the Max Planck Institute for Evolutionary Anthropology have addressed a longstanding challenge in CRISPR ...

A new gene editor takes advantage of CRISPR-associated proteins to insert whole genes into the genome, scientists report.

Scientists have used personalised gene-editing therapy to successfully treat a baby with a rare genetic condition. Could this ...

The personalized CRISPR treatment could be the future of gene therapy, but hurdles remain before everyone has access.

Genetic medicine reaches a major milestone with a system capable of inserting entire genes into human DNA. This breakthrough ...

In a world first, scientists used CRISPR to fix a baby's unique genetic mutation. The report offers hope for personalized treatments of rare diseases.

Once a cut is made, it is a multistep, imperfect process of cellular DNA repair. CRISPR can be used to make other types of edits too, such as increasing or decreasing the effects of a gene ...

Researchers have used a personalised base-editing gene therapy to successfully treat an infant with carbamoyl-phosphate ...

introduces double-strand breaks that recruit DNA repair machinery. Despite its successes, the CRISPR-Cas9 system has several limitations, including off-target cutting. Over the years, scientists have ...

Globally, people get animal protein mostly from chickens, with pigs and cattle in second and third place. A 2023 report ...