A 19-year-old Canadian man becomes the first human cured through prime gene editing after doctors corrected a rare genetic ...

A new method for safely inserting large chunks of DNA into genomes has now measured up in mice, potentially paving the way ...

After teasing a new regulatory process for personalized genetic medicines at the end of last year, the FDA today unveiled draft guidance for an approval pathway that could see custom CRISPR therapies, ...

Lipid nanoparticles, or LNPs, best known as the delivery vehicle for the COVID-19 mRNA vaccines received by billions of people, are now at the center of a much larger medical revolution. Researchers ...

Gene editing, a set of techniques used to alter sections of an organism's DNA, is helping scientists cure diseases previously ...

Prime Medicine's application will test an FDA that has promised to speed new gene-editing treatments but has recently spurned ...

The U.S. Food and Drug Administration approved the first cell-based gene therapies for sickle cell disease, including the ...

Multiplex gene-editing is gaining popularity due to the flexibility and safety provided by double-strand break-independent base and prime editing technologies, but assays to accurately quantify ...

Drug delivery researchers have vastly improved the potential of genetic therapies by overcoming the challenge of consistently getting genes and gene-editing tools where they need to be within cells.

Scientists at Texas A&M are turning an everyday pick-me-up into a high-tech medical switch. By combining caffeine with CRISPR ...

"2025 proved that our technology delivers, not in the distant future, but right now," says Tropic CEO Gilad Gershon.