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

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

One of the most commonly used gene-delivery methods relies on engineered viruses to insert stretches of genetic material into ...

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

Discover how scientists essentially added a guide molecule to the gene editor to help it insert an entire gene into the most ...

A US baby with a rare liver disorder is the first to receive a custom CRISPR therapy. Experts say this breakthrough could help treat many untreatable genetic diseases ...

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

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

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