Aurora Therapeutics, cofounded by Nobel Prize–winning scientist Jennifer Doudna, plans to use gene editing and a new FDA ...

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

Scientists have discovered a new CRISPR mechanism with precise activity, expanding the potential applications of the existing ...

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

A massive gene experiment exposed how the brain builds itself, and uncovered a hidden cause of severe developmental issues.

Multiple sclerosis (MS) is a chronic neurological disease characterized by nerve damage and consequent impairments in vision, ...

The PINTAR Diagnostics Team from the School of Life Sciences and Technology (SITH), Institut Teknologi Bandung (ITB) won the ...

Scientists are testing CRISPR gene editing as a potential HIV cure after successfully removing the virus from infected cells ...

Victoria Gray spent 34 years battling the debilitating pain of sickle cell disease. Then she volunteered to be the world's first "prototype" for a CRISPR therapy, based on technology invented at UC ...

Illumina on Tuesday unveiled what it calls the world’s largest functional cell dictionary that, when paired with artificial ...

In the twentieth century, identity was something one received and cultivated. Today it is something one produces and displays ...

Therapeutic Potential of CRISPR–Cas3 Genome-Editing System for Transthyretin Amyloidosis. Credit: Institute of Medical ...