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.

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

A study introduces a CRISPR model that predicts gRNA activity more accurately using chemically synthesized gRNAs. The model ...

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

The baby boy, born with a devastating genetic disease, is thriving after becoming the first known person to receive a bespoke ...

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

A pivotal medical milestone has been reached. For the first time ever, researchers have used a personalized CRISPR-based gene ...

At a gene therapy conference, there was excitement about the first correction of a genetic misspelling, along with questions ...

The goal is to reuse key parts of the treatment and simply swap in a custom set of instructions for each patient's specific ...

Currently, the researchers are using CRISPR-TO to move endogenous RNAs – RNA molecules that are naturally produced within the ...

Scientists have uncovered a critical role for rapid DNA repair in maintaining genome stability. A new study reveals that ...