This little company's scientific breakthrough opened up a whole new sliver of the drug market (although it's still leading ...

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 ...

CRISPR is revolutionizing medicine by enabling precise DNA edits, treating genetic diseases like sickle cell anemia and beta-thalassemia, and pioneering in vivo editing and personalized therapies.

The Food and Drug Administration on Friday approved the first drug that uses this technology to treat an illness, sickle cell disease.

CRISPR technology revolutionizes gene therapy, offering potential treatments for genetic disorders and cancers through precise gene editing techniques.

New CRISPR tool enables more seamless gene editing — and improved disease modeling Yale scientists have developed a CRISPR technology that can assess genetic interactions on a host of immunological ...

CRISPR can be tough to describe, let alone visualize. This powerful gene-editing technique has the potential to change our lives. Here's our take.

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 ...

CRSP is a speculative buy for aggressive investors, driven by the commercial launch and multibillion-dollar potential of ...

The CRISPR gene editing technique, for instance, allows scientists to pinpoint an exact sequence of DNA within a gene, excise it using the Cas9 enzyme, and paste in a new segment of DNA in place ...

The award of the Nobel Prize to CRISPR researchers symbolizes its tremendous promise to medicine. Indeed, scientists are already trying to use this technology to treat people with COVID-19.