Novel nanoparticles deliver CRISPR gene editing tools into the cell with much higher efficiency
Mon, 07/15/2019 – 11:46
Researchers have developed a significantly improved delivery mechanism for the CRISPR/Cas9 gene editing method in the liver using biodegradable synthetic lipid nanoparticles. Read more at Tufts Now.
Source: National Institute of Biomedical Imaging and Biomedical Engineering- News