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CRISPR-Cas9
Research
CRISPR gene therapy for deafness works in young adult mice
The gene therapy takes advantage of a "window of opportunity" in the progressive disease to stop deafness before it's fully set in.
Helen Floersh
Jul 11, 2024 9:15am
Intellia showcases durability of one-and-done HAE option
Jun 2, 2024 8:00am
Intellia opts out of hemophilia gene editing work with Regeneron
Mar 22, 2024 11:21am
Vertex pays Editas $100M to use gene-editing tech
Dec 13, 2023 12:46pm
CRISPR Therapeutics laid off staff a week after positive AdComm
Nov 22, 2023 1:36pm
FDA advisers wave through first CRISPR-based therapy
Nov 1, 2023 11:07am