A Ph.D. student in biomolecular engineering at the University of California, Santa Cruz, has built a software program ...

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

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

Remember "Baby KJ"? Now CRISPR pioneers have partnered with the Chan Zuckerberg Initiative to launch center for curing rare ...

New research has found a novel target with therapeutic potential for metastatic eye melanoma—an aggressive eye cancer—with ...

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

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 ...

Portfolios have building blocks that determine whether family capital survives market shocks, tax‑code changes and ...

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

Disclaimer: AlphaGalileo is not responsible for the accuracy of content posted to AlphaGalileo by contributing institutions ...

Martin Kampmann, PhD, delivers the 2025 Byers Lecture. Photo by Sonya YruelWhen Martin Kampmann, PhD, set out to explore the ...