- CRISPR gene-editing machinery could transform medicine but is difficult to get into tissues and disease-relevant cells
- New delivery system loads CRISPR machinery inside spherical nucleic acid (SNA) nanoparticles
- Particles entered cells three times more effectively, tripled gene-editing efficiency, and decreased toxicity compared to current delivery methods
With the power to rewrite the genetic code underlying countless diseases, CRISPR holds immense promise to revolutionize…
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News Source: www.sciencedaily.com

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