Advanced non-viral gene delivery systems are expanding the range of indications and therapy modalities possible for the new generation of genetic medicines.

IDT played a pivotal role in manufacturing the personalized gene editing therapy given to baby KJ Muldoon to treat his rare ...

The UK is driving pioneering malaria research in areas including genetic engineering, vaccines, and medicines. In Tanzania, the scientists involved tell Nick Ferris why research to tackle the disease ...

How the UK quietly became a research powerhouse in the fight against malaria - ON THE GROUND: The UK is driving pioneering ...

Creating standardized building blocks, including gene editing proteins, guide RNAs, donor templates, and delivery vehicles, ...

A child known publicly as Baby KJ was celebrated onstage at the twelfth Breakthrough Prize ceremony in Santa Monica last ...

How do our genes determine our appearance and our susceptibility to disease? This question is central to biomedical research, ...

JMIR Publications today featured two new stories in its News and Perspectives section, highlighting a shift toward proactive, ...

India has developed BIRSA 101, its first indigenous CRISPR gene therapy for sickle cell disease, using a more precise ...

A CRISPR Therapy Just Cured A Disease From Inside The Body For The First Time. The Gene-Editing Era Officially Started Monday ...

Intellia Therapeutics, Inc. (Nasdaq: NTLA), a leading biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies, today announced the ...

A $500 million commitment — and a call for the global scientific community to join — aims to unlock predictive models of the human cell to accelerate the cure and prevention of all disease REDWOOD ...