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

Scientists have developed SMART (silently mutate and repair template), a strategy that dramatically expands the editable ...

Intellia has leveraged its expertise in Crispr/Cas9 gene editing to advance a pipeline of in vivo and ex vivo therapies for diseases with high unmet medical needs. We believe Intellia's proprietary ...

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

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

CRISPR-Cas9 genome editing exploits the CRISPR-Cas ... while repair pathways can be engineered to introduce specific point mutations or insertions. An inducible CRISPR activation system enables ...

A BABY has had his DNA rewritten to treat his a deadly genetic disorder in a world first. Little KJ Muldoon, now 15 months ...

Using the gene scissors CRISPR and stem cells, researchers at Stockholm University and the UK Dementia Research Institute (UK DRI) at King's College ...

Ask scientists which gene-editing tool is most needed to advance gene therapy, and they'd probably describe a system that's ...

The gene editor -- called evoCAST -- goes a long way toward solving a problem that has confounded the development of gene therapies from the field's beginnings: How to add long stretches of DNA to ...

Innovative delivery techniques, including high-tech nanoparticles and electroporationdevices, may convey more gene therapies ...