In 2019, the first CRISPR clinical trials were conducted to treat sickle cell diseases and in 2020, this treatment was ...

Australian cancer researchers are the first to establish a next-generation gene-editing tool for modeling and interrogating human disease.

Complementary discoveries have the potential to enhance treatment options for antibiotic-resistant infections. Researchers at ...

The most complex engineering of human cell lines ever has been achieved by scientists, revealing that our genomes are more resilient to significant structural changes than was previously thought.

CRISPR, short for Clustered Regularly Interspaced Short Palindromic Repeats, is a groundbreaking gene-editing technology that ...

"This type of gene editing should also allow for the treatment of diseases whose origin is not genetic or whose origin cannot ...

New research reveals that bacteria form species and maintain cohesion through frequent DNA exchange within species. This ...

It’s a new way to create “bi-paternal” mice that can survive to adulthood—but human applications are still a long way off.