which makes the process of gene editing faster and easier for researchers, including those developing treatments for genetic conditions such as sickle cell disease or cystic fibrosis. The CRISPRware ...

From the internet to the ozone layer, AI to the human genome, UC scientists have turned federal research funding into history ...

Investors say genetic prediction services for embryos, used by Elon Musk and others, are a trust fund for future children.

Today, the Cystic Fibrosis Foundation announced an additional investment of up to $24 million in Prime Medicine to continue the development of a gene editing therapy for people with cystic ...

Today, the Cystic Fibrosis Foundation announced an additional investment of up to $24 million in Prime Medicine to continue the development of a gene editing ...

Hundreds of people with cystic fibrosis are to be offered a once-a-day pill which has been hailed as “life changing” by health experts.

Prime Medicine secures up to $24 million from the CF Foundation to advance Prime Editors for cystic fibrosis treatment.

CAMBRIDGE, Mass., July 16, 2025 (GLOBE NEWSWIRE) -- Prime Medicine, Inc. (Nasdaq: PRME), a biotechnology company committed to delivering a new class of differentiated one-time curative genetic ...

Prime Medicine will initially focus on targeting G542X, one of the most prevalent cystic fibrosis-causing nonsense mutations for which no therapies are currently available.

Hundreds of cystic fibrosis patients become eligible for ‘life-changing’ therapy - Some people with the rarest forms of the disease have been unable to access the latest medicines.

SUNY Cortland Men’s Soccer Coach paddleboards 80 miles to raise awareness for Cystic Fibrosis Axtell spent 15 hours paddling from The Bahamas to Florida.

Ayodeji Adegunsoye, MD, PhD, MSc, highlights how the underrepresentation of minority populations in pulmonary fibrosis genetic studies hinders accurate disease risk prediction and broader clinical ...