Gene Editing Has Struggled To Go Commercial. This Nobel Laureate Has A $1 Billion Plan To Fix That.

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

CRISPR breakthrough: Scientists from China remove HIV DNA from infected cells

Scientists in China report removing HIV from human DNA using gene-editing technology. Experts say the findings are promising but still far from a confirmed cure.

Nanoparticle-Mediated Photodynamic Therapy Takes on Triple-negative Breast Cancer

GA, UNITED STATES, February 4, 2026 / EINPresswire.com / — Researchers have developed a new biomimetic nanocomposite ...
Business Wire

Scribe Therapeutics Highlights Data Underpinning its Comprehensive Strategy Targeting Key Lipid Drivers of ASCVD at American Heart Association (AHA) Scientific Sessions 2025

ALAMEDA, Calif.--(BUSINESS WIRE)--Scribe Therapeutics Inc. (“Scribe”), a genetic medicines company pioneering next-generation in vivo CRISPR-based medicines designed to be safe, durable, and effective ...

CRISPR Meets Caffeine: Scientists Develop New Approach to Cancer Treatment

Researchers at Texas A&M are pairing a widely used ingredient with advanced medical technology to develop new treatments for ...