KJ Muldoon recently made history by becoming the first patient to receive a personalized CRISPR gene therapy, designed specifically for the genetic mutations causing his rare metabolic disease. | KJ ...

The organizations launched the center with a $20 million CZI grant to build on the success of the first personalized CRISPR base-editing therapy.

The global CRISPR gene editing market size is calculated at USD 4.77 billion in 2025 and is expected to reach around USD ...

Personalized CRISPR cures for children born with rare genetic diseases are now a step closer to being more widely available.

In vivo base editing enables precise, single-nucleotide changes to DNA without double-strand breaks. A recent application in ...

The global biotechnology market is anticipated to surge to USD 1.78 trillion by 2034, driven by innovations in personalized ...

PR Newswire SAN FRANCISCO, July 8, 2025 SAN FRANCISCO, July 8, 2025 /PRNewswire/ -- Personalized CRISPR cures for children born with rare genetic diseases are now a step closer to ...

Explore the top 10 anticipated scientific breakthroughs and research fields of 2025 every student should know. From AI to space, discover the future of science and technology.

Rare genetic diseases are challenging for patients and their families—made all the more overwhelming because symptoms tend to ...

UCD team uses novel polymer-based system to deliver corrective genes, an approach that appears to be better tolerated by ...

India offers a treasure trove of genetic data for AI-enabled researchers to develop therapies neglected by commercial ...

The gene-editing platform known as Crispr is widely used by researchers in scientific laboratories in their search for new ...