Currently, the researchers are using CRISPR-TO to move endogenous RNAs – RNA molecules that are naturally produced within the ...

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

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

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 ...

For Uditi’s parents, reading about use of CRISPR tech, or ‘genetic scissors’, to treat baby KJ, diagnosed with severe genetic ...

A “genetic surgery” or “interventional genetics” system for individualized treatments would be a marriage of drug development ...

KJ Muldoon — who was diagnosed with CPS1 deficiency at one week old — received the first-ever custom gene-editing infusion to ...

A personalized gene editing therapy was successfully used to treat an infant with CPS1 deficiency, a disease that causes ...

Discover how scientists essentially added a guide molecule to the gene editor to help it insert an entire gene into the most ...

US infant KJ Muldoon makes history as first patient treated with personalized gene-editing, offering hope for rare illnesses.

Global health stories including rare illnesses, climate change, hypertension, and more, with a focus on little KJ Muldoon's ...