The discovery of Cat1 reveals how CARF effectors use complex structures to inhibit viral replication, advancing our ...

This is the first gene editor to use a CRISPR-associated transposase to make targeted edits at therapeutically useful levels in humans.

Two years after the primary legislation was passed in March 2023, England’s implementing rules for the cultivation of gene edited crops were signed into law by the responsible minister on May 13, 2025 ...

The gene editor -- called evoCAST -- goes a long way toward solving a problem that has confounded the development of gene therapies from the field's beginnings: How to add long stretches of DNA to ...

A baby born with a rare and dangerous genetic disease is growing and thriving after getting an experimental gene editing ...

A CRISPR treatment seems to have been effective for a baby’s devastating disease, but it is not clear whether such bespoke ...

An infant with a rare urea cycle disorder became the first patient to receive a personalized gene-editing therapy. His care ...

KJ Muldoon became the first patient to undergo personalized CRISPR treatment, a therapy that found the one uniquely mutated gene out of 20,000 in his little body, and fixed it.

In a medical first that could revolutionize treatment for thousands of rare genetic diseases, doctors have successfully used ...

complex ethics of genetic engineering, including safety, social justice, and regulation, to understand how this technology ...

A nine-month-old baby who was born with a rare genetic disorder is the first person to be successfully treated with ...

A US infant with a rare condition has become history's first patient to be treated with a personalized gene-editing technique that raises hopes for other people with obscure illnesses, doctors ...