Crispr’s ability to cut genetic code like scissors has just started to turn into medicines. Now, gene editing pioneer ...

Researchers used a virus-based CRISPR system to precisely edit the gatekeeper enzyme HMGR in petunias and lettuce, ...

Scientists are testing an entirely new way to fight heart disease: whether gene editing might offer a one-time fix for high ...

UCLA researchers have developed a lipid nanoparticle-based gene-editing approach capable of inserting an entire healthy gene ...

UCLA researchers have developed a lipid nanoparticle-based gene-editing approach capable of inserting an entire healthy gene into human airway cells, restoring key biological function in a laboratory ...

With a shared purpose, we can realize the true promise of CRISPR and improve healthcare, providing hope to more patients with ...

Researchers develop a single genome-editing strategy to treat multiple disorders caused by nonsense mutations, promising efficient and cost-effective therapies.

Faced with a life-threatening metabolic disease, KJ’s doctors at Children’s Hospital of Philadelphia sprinted to create a ...

These biotech companies have catalysts ahead.

Researchers have developed a single genome-editing strategy, known as PERT, that could potentially treat various diseases caused by nonsense mutations.

China research team at Wuhan University of Science and Technology uses CRISPR to remove HIV DNA from human cells, marking a potential breakthrough in treatment.