A new CRISPR breakthrough shows scientists can turn genes back on without cutting DNA, by removing chemical tags that act ...

As CRISPR moves from lab success to real-world medicine, 2026 will test whether these revolutionary gene-editing therapies ...

Innovative research into the gene-editing tool targets influenza’s ability to replicate—stopping it in its tracks.

Gene editing has moved from theory to bedside with a speed that would have seemed impossible a decade ago. A new wave of ...

CHANGE-seq-BE was developed to enable scientists to better understand base editors, an important class of CRISPR precise genome editors.

By editing thousands of genes in mouse stem cells, the scientists identified a list of over 300 that are crucial for neural differentiation.

Head and neck cancers often begin in the mouth, throat, or voice box. They're among the most common cancers in the world, affecting over half a million people each year and causing about 300,000 ...

A sweeping genetic screen reveals how the brain is built and exposes a hidden gene behind a newly discovered childhood brain ...

An infant with a rare metabolic disease became the world’s first patient to be treated with a personalized CRISPR gene-editing treatment in a landmark study between Penn Medicine and the Children’s ...

Which genes are required for turning embryonic stem cells into brain cells, and what happens when this process goes wrong? In ...

CRISPR became big in 2025, bringing advances for serious Indian health risks, which will continue in the coming year ...