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Times Co-cited
Similarity
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In Vivo CRISPR/Cas9 Gene Editing Corrects Retinal Dystrophy in the S334ter-3 Rat Model of Autosomal Dominant Retinitis Pigmentosa.
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In vivo genome editing with a small Cas9 orthologue derived from Campylobacter jejuni.
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Development of a gene-editing approach to restore vision loss in Leber congenital amaurosis type 10.
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In vivo Editing of the Human Mutant Rhodopsin Gene by Electroporation of Plasmid-based CRISPR/Cas9 in the Mouse Retina.
Maria Carmela Latella, Maria Teresa Di Salvo, Fabienne Cocchiarella, Daniela Benati, Giulia Grisendi, Antonella Comitato, Valeria Marigo, Alessandra Recchia. Mol Ther Nucleic Acids 2016
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RNA-guided human genome engineering via Cas9.
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A dual AAV system enables the Cas9-mediated correction of a metabolic liver disease in newborn mice.
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High-fidelity CRISPR-Cas9 nucleases with no detectable genome-wide off-target effects.
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CRISPR/Cas9-Mediated Genome Editing as a Therapeutic Approach for Leber Congenital Amaurosis 10.
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In vivo genome editing via CRISPR/Cas9 mediated homology-independent targeted integration.
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Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage.
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Postnatal genome editing partially restores dystrophin expression in a mouse model of muscular dystrophy.
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Cationic lipid-mediated delivery of proteins enables efficient protein-based genome editing in vitro and in vivo.
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In vivo gene editing in dystrophic mouse muscle and muscle stem cells.
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Cas9/sgRNA selective targeting of the P23H Rhodopsin mutant allele for treating retinitis pigmentosa by intravitreal AAV9.PHP.B-based delivery.
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Clustered Regularly Interspaced Short Palindromic Repeats-Based Genome Surgery for the Treatment of Autosomal Dominant Retinitis Pigmentosa.
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Rationally engineered Cas9 nucleases with improved specificity.
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Genome editing with Cas9 in adult mice corrects a disease mutation and phenotype.
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AAV-Mediated CRISPR/Cas Gene Editing of Retinal Cells In Vivo.
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Nanoparticle delivery of Cas9 ribonucleoprotein and donor DNA in vivo induces homology-directed DNA repair.
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Genome surgery using Cas9 ribonucleoproteins for the treatment of age-related macular degeneration.
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DNA targeting specificity of RNA-guided Cas9 nucleases.
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CRISPR RNA maturation by trans-encoded small RNA and host factor RNase III.
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In vivo genome editing improves muscle function in a mouse model of Duchenne muscular dystrophy.
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Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage.
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Identification of preexisting adaptive immunity to Cas9 proteins in humans.
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A Single Administration of CRISPR/Cas9 Lipid Nanoparticles Achieves Robust and Persistent In Vivo Genome Editing.
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Non-Viral CRISPR/Cas Gene Editing In Vitro and In Vivo Enabled by Synthetic Nanoparticle Co-Delivery of Cas9 mRNA and sgRNA.
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Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy.
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Gene and mutation independent therapy via CRISPR-Cas9 mediated cellular reprogramming in rod photoreceptors.
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In Situ Gene Therapy via AAV-CRISPR-Cas9-Mediated Targeted Gene Regulation.
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A non-viral CRISPR/Cas9 delivery system for therapeutically targeting HBV DNA and pcsk9 in vivo.
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CRISPR-LbCpf1 prevents choroidal neovascularization in a mouse model of age-related macular degeneration.
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In vivo-directed evolution of a new adeno-associated virus for therapeutic outer retinal gene delivery from the vitreous.
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Genome editing abrogates angiogenesis in vivo.
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Somatic Gene Editing of GUCY2D by AAV-CRISPR/Cas9 Alters Retinal Structure and Function in Mouse and Macaque.
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Search-and-replace genome editing without double-strand breaks or donor DNA.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.