CRISPR is a technology that can be used to edit genes and, as such, will likely change the world. The essence of CRISPR is simple: it’s a way of finding a specific bit of DNA inside a cell. After that ...

NtRON Bio announced today, following its recent U.S. patent application related to colorectal cancer using the IMPA™ phage engineering technology, it has now completed the filing of two patents for a ...

CRISPR uncovers gene that supercharges vitamin D—and stops tumors in their tracks Scientists hail key gene with promising ‘new avenues’ for precision medicine through CRISPR/Cas9.

The new tool, CRISPRware, takes its name from CRISPR-Cas9, the workhorse of modern genome editing. At its core, Cas9 is a protein that binds with a short RNA sequence designed to be complementary to a ...

A research team headed by the University of Zurich has developed a powerful new method to precisely edit DNA by combining cutting-edge genetic engineering with artificial intelligence. The work has ...

For years, researchers have been trying to figure out how to treat inherited blood disorders like sickle cell disease without ...

A team from UC San Diego, John Hopkins and UC Berkeley Universities found a way to edit a single gene in a mosquito that prevented it from transmitting malaria.

CRISPR Therapeutics reports promising Phase 1 clinical data for CTX310™, with significant triglyceride and LDL reductions, and updates on other programs.

CRISPR Therapeutics CRSP and Intellia Therapeutics NTLA are leading developers of therapies that utilize the Nobel Prize-winning CRISPR/Cas9 gene editing technology.