New CRISPR/Cas9 technique corrects cystic fibrosis in cultured human stem cells

Researchers corrected mutations that cause cystic fibrosis in cultured human stem cells. They used a technique called prime editing to replace the 'faulty' piece of DNA with a healthy piece. The study shows that prime editing is safer than the conventional CRISPR/Cas9 technique.

from Latest Science News -- ScienceDaily https://www.sciencedaily.com/releases/2021/08/210809105908.htm
New CRISPR/Cas9 technique corrects cystic fibrosis in cultured human stem cells New CRISPR/Cas9 technique corrects cystic fibrosis in cultured human stem cells Reviewed by cmakigo on August 09, 2021 Rating: 5

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