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

In 2012, scientists Jennifer Doudna and Emmanuelle Charpentier replicated this mechanism found in microbes to develop a ...

While the medical world is melting down from the absolute apocalypse that is RFK Jr., it's good to celebrate that (at least ...

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 ...

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

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

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 ...

Excision announces publication highlighting EBT-107 for treatment of chronic hepatitis B in bioRxiv: Watertown, Massachusetts Friday, May 16, 2025, 18:00 Hrs [IST] Excision BioThe ...

The Regents of the University of California v. The Broad Institute, Inc., Appeal Nos. 2022-1594, -1653 (Fed. Cir. May 12, 2025) Must ...

Kashmir University of Agricultural Sciences and Technology (SKUAST-Kashmir) has successfully produced a gene-edited sheep, ...