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@engadget.com
5 months ago
UK authorizes first gene therapy for treating sickle cell disease
@slashgear.com
2 years ago
Human proteins enable researchers to deliver medication directly to the cells
@digitaltrends.com
4 years ago
CRISPR-Cas9 gene editing could one day ‘turn off’ HIV virus in the body
@xconomy.com
5 years ago
RNAi Hits Europe as EMA Follows FDA, Approves Alnylam Drug
@xconomy.com
5 years ago
CRISPR Risks? Researchers Stoke Fears of Cancer in Gene-Edited Cells
@techcrunch.com
6 years ago
With $250 million, Peter Diamandis’ new startup is all about taking stem cells from placentas
@WIRED
6 years ago
Medical researchers have the cargo they need to test genetic therapies. Now they just need to figure out how to deliver it.
@theverge.com
7 years ago
Gene-editing tool CRISPR may soon be used to treat humans for the first time
@theverge.com
9 years ago
Scientists are one step closer to replacing mechanical pacemakers with biological ones