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Orthogonal Cas9-Cas9 chimeras provide a versatile platform for genome editing.Academic Article Why?
Publisher Correction: Orthogonal Cas9-Cas9 chimeras provide a versatile platform for genome editing.Academic Article Why?
Cas9-mediated allelic exchange repairs compound heterozygous recessive mutations in mice.Academic Article Why?
CNS-restricted Transduction and CRISPR/Cas9-mediated Gene Deletion with an Engineered AAV Vector.Academic Article Why?
CRISPR/Cas9-mediated genome editing induces exon skipping by alternative splicing or exon deletion.Academic Article Why?
Cytosolic and Nuclear Delivery of CRISPR/Cas9-ribonucleoprotein for Gene Editing Using Arginine Functionalized Gold Nanoparticles.Academic Article Why?
Direct Cytosolic Delivery of CRISPR/Cas9-Ribonucleoprotein for Efficient Gene Editing.Academic Article Why?
Functional annotation of native enhancers with a Cas9-histone demethylase fusion.Academic Article Why?
Genomic Access to Monarch Migration Using TALEN and CRISPR/Cas9-Mediated Targeted Mutagenesis.Academic Article Why?
Adenovirus-Mediated Somatic Genome Editing of Pten by CRISPR/Cas9 in Mouse Liver in Spite of Cas9-Specific Immune Responses.Academic Article Why?
Transcriptional Regulation with CRISPR/Cas9 Effectors in Mammalian Cells.Academic Article Why?
A Broad-Spectrum Inhibitor of CRISPR-Cas9.Academic Article Why?
A Compact, High-Accuracy Cas9 with a Dinucleotide PAM for In Vivo Genome Editing.Academic Article Why?
Advances in CRISPR/Cas9 Technology for in Vivo Translation.Academic Article Why?
All-in-one adeno-associated virus delivery and genome editing by Neisseria meningitidis Cas9 in vivo.Academic Article Why?
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