Gene-edited cell lines could be compatible with 90% of the world
Genome-editing strategies are being explored which could mean that just 12 lines of next-generation therapeutic iPSCs could treat 90% of the world's population.
Please sign in or register for FREE
Sign in to RegMedNet
Not yet a member? Become a member FREE to:
- Get unlimited access to ALL CONTENT
- Read selected articles from journals such as Regenerative Medicine FREE
- Receive a weekly email roundup of the latest news and expert opinions
Did you know?
Your RegMedNet account also gives you access to communities on drug discovery, real-world evidence and 3D printing in medicine. Find out more>>