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Efficient genome engineering in human pluripotent stem cells using Cas9 from Neisseria meningitidis.
CRISPR/Cas9-mediated genome editing induces exon skipping by alternative splicing or exon deletion.
Orthogonal Cas9-Cas9 chimeras provide a versatile platform for genome editing.
Heavily and fully modified RNAs guide efficient SpyCas9-mediated genome editing.
The NIH Somatic Cell Genome Editing program.