Imagine a world where the genetic code is as easy to edit as a simple copy-and-paste. This is the reality of CRISPR, a revolutionary technology that could cure diseases and save countless lives. But ...

Treatments for rare diseases are hard to create and expensive to deliver, but there is new hope for editing the software of ...

Using CRISPR technology that targets RNA instead of DNA, researchers at New York University and the New York Genome Center ...

A fresh wave of gene-editing therapies is surging to the fore — even as the field wrestles with the challenge of getting the first generation of expensive and complex CRISPR treatments to the ...