News

Scientists have achieved the first DNA-free CRISPR gene editing in raspberries, reaching 19% efficiency and opening the door to faster breeding of firmer, more resilient berries — though regenerating ...
A research team headed by the University of Zurich has developed a powerful new method to precisely edit DNA by combining ...
Even CRISPR-Cas9, the groundbreaking technology that earned a Nobel Prize in 2020, has major limitations.
Thanks to new tools based on CRISPR-Cas9 technology, the team led by Dr José Luis Sardina, group leader at the Josep Carreras Institute, has succeeded in controlling the "switch" of the IL1RN ...
The CRISPR/Cas9 technology can be used to make cuts in DNA at specific sites of targeted genes, providing a powerful tool for developing gene editing-based therapeutics.
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.
Dr. Jennifer Domm will offer audience members a grounding in the history of CRSPR Cas 9 and explain how that has led to new therapies for Sickle Cell Disease that can eventually be commercialized and ...
No doubt 2025 will usher in many more advances in CRISPR therapies, thanks to the FDA’s new Platform Technology Designation Program, which will allow innovators to have an easier path to market.
“We wanted to create a technology that could reliably move RNA to where it needs to function.” Qi and his colleagues used a version of the gene-editing tool CRISPR, called CRISPR-Cas13, to target ...