Researchers have now achieved the highest reported rates of inserting genes into human cells with the CRISPR-Cas9 gene-editing system, a necessary step for harnessing CRISPR for clinical gene-therapy applications. By chemically tweaking the ends of the DNA to be inserted, the new technique is up to five times more efficient than current approaches.
from Diseases and Conditions News -- ScienceDaily https://ift.tt/2tEtXhx
Monday, 23 December 2019
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment