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Published in 2020 at "Nature Communications"
DOI: 10.1038/s41467-020-17952-5
Abstract: Precise genome editing using CRISPR-Cas9 is a promising therapeutic avenue for genetic diseases, although off-target editing remains a significant safety concern. Guide RNAs shorter than 16 nucleotides in length effectively recruit Cas9 to complementary sites…
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Keywords:
crispr guard;
guide rnas;
target;
activity ... See more keywords