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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?
Development of Humanized Mice in the Age of Genome Editing.Academic Article Why?
Heavily and fully modified RNAs guide efficient SpyCas9-mediated genome editing.Academic Article Why?
In vivo Genome Editing Partially Restores Alpha1-Antitrypsin in a Murine Model of AAT Deficiency.Academic Article Why?
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