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Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivo.Academic Article Why?
Rapid modelling of cooperating genetic events in cancer through somatic genome editing.Academic Article Why?
CRISPRseek: a bioconductor package to identify target-specific guide RNAs for CRISPR-Cas9 genome-editing systems.Academic Article Why?
Streamlined ex vivo and in vivo genome editing in mouse embryos using recombinant adeno-associated viruses.Academic Article Why?
A co-CRISPR strategy for efficient genome editing in Caenorhabditis elegans.Academic Article Why?
NmeCas9 is an intrinsically high-fidelity genome-editing platform.Academic Article Why?
Genome editing with Cas9 in adult mice corrects a disease mutation and phenotype.Academic Article Why?
The Bacterial Origins of the CRISPR Genome-Editing Revolution.Academic Article Why?
Precision cancer mouse models through genome editing with CRISPR-Cas9.Academic Article Why?
All-in-one adeno-associated virus delivery and genome editing by Neisseria meningitidis Cas9 in vivo.Academic Article Why?
CRISPR/Cas9-mediated genome editing induces exon skipping by alternative splicing or exon deletion.Academic Article Why?
A Compact, High-Accuracy Cas9 with a Dinucleotide PAM for In Vivo Genome Editing.Academic Article Why?
Anti-CRISPR AcrIIA5 Potently Inhibits All Cas9 Homologs Used for Genome Editing.Academic Article Why?
Development of Humanized Mice in the Age of Genome Editing.Academic Article Why?
Genome editing of HBG1 and HBG2 to induce fetal hemoglobin.Academic Article Why?
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