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 ...

Beginning a chain of events that will presumably lead to the origin of our universe's Spider-Man, researchers in Germany have ...

CRISPR-Cas9 is a powerful gene editing system that has revolutionized our ability to treat disease and probe the human genome. CRISPR has been used to edit the genomes of animals, plants, and microbes ...

The only gene-editing therapy currently on the market is a CRISPR–Cas9-based treatment for two blood disorders, sickle-cell ...

Researchers have completed a first-in-human clinical trial testing a CRISPR/Cas9 gene-editing technique to help the immune system fight advanced gastrointestinal (GI) cancers. The results show ...

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

Researchers at the University of Minnesota have completed a first-in-human clinical trial testing a CRISPR/Cas9 gene-editing technique to help the immune system fight advanced gastrointestinal (GI ...

Due to its efficiency, CRISPR-Cas9 has already been used in numerous ... solution that included the components of the gene-editing system as well as a gene sequence for a red fluorescent protein.

Researchers at the University of Minnesota have completed a first-in-human clinical trial testing a CRISPR/Cas9 gene-editing technique to help the immune system fight advanced gastrointestinal (GI ...

A favorable appeals court ruling repositioned a coalition of universities and Nobel laureates to win credit for inventing a ...

A team of researchers at Columbia, Harvard and University of Minnesota has developed a gene editing technique they say could ...

Cas9, the University of Bayreuth’s Biomaterials research group was able to bioengineer a common house spider to produce glowing red silk. Professor Thomas Scheibel and doctoral student Edgardo ...