Development of an intein-mediated split-Cas9 system for gene therapy
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Genome Engineering with TALE and CRISPR Systems in NeuroscienceCRISPR/Cas9 and cancer targets: future possibilities and present challengesResources for the design of CRISPR gene editing experimentsApplication of CRISPR/Cas9 Technology to HBVA new age in functional genomics using CRISPR/Cas9 in arrayed library screeningLigand-binding domains of nuclear receptors facilitate tight control of split CRISPR activityImproved bi-allelic modification of a transcriptionally silent locus in patient-derived iPSC by Cas9 nickaseCRISPR/Cas9: Transcending the Reality of Genome Editing.Integrase-Deficient Lentiviral Vector as an All-in-One Platform for Highly Efficient CRISPR/Cas9-Mediated Gene EditingA Split Staphylococcus aureus Cas9 as a Compact Genome-Editing Tool in Plants.Genetic and epigenetic control of gene expression by CRISPR-Cas systems.In vivo genome editing with a small Cas9 orthologue derived from Campylobacter jejuniProfiling of engineering hotspots identifies an allosteric CRISPR-Cas9 switchReconfigurable hybrid interface for molecular marker diagnostics and in-situ reportingGenome Engineering Using Adeno-associated Virus: Basic and Clinical Research Applications.Gene Editing for Treatment of Neurological Infections.Integration and exchange of split dCas9 domains for transcriptional controls in mammalian cells.A multifunctional AAV-CRISPR-Cas9 and its host response.Creating and evaluating accurate CRISPR-Cas9 scalpels for genomic surgery.CRISPR-Cas orthologues and variants: optimizing the repertoire, specificity and delivery of genome engineering tools.Therapeutic genome engineering via CRISPR-Cas systems.CRISPR-Cas9 technology: applications and human disease modelling.CRISPR-Based Technologies for the Manipulation of Eukaryotic Genomes.Genome Editing for the Study of Cardiovascular Diseases.Non-viral and viral delivery systems for CRISPR-Cas9 technology in the biomedical field.Emerging Gene Therapies for Genetic Hearing Loss.Evaluating Efficiencies of Dual AAV Approaches for Retinal Targeting.Inducible CRISPR genome-editing tool: classifications and future trends.Synthetic Gene Expression Circuits for Designing Precision Tools in Oncology.Rapid, Selection-Free, High-Efficiency Genome Editing in Protozoan Parasites Using CRISPR-Cas9 Ribonucleoproteins.From Reductionism to Holism: Toward a More Complete View of Development Through Genome Engineering.A Protocol for the Production of Integrase-deficient Lentiviral Vectors for CRISPR/Cas9-mediated Gene Knockout in Dividing Cells.Synthetic Gene Expression Circuits for Designing Precision Tools in Oncology.Genetically engineered pigs as models for human disease.Oligonucleotide conjugated multi-functional adeno-associated viruses.Genome Surgery and Gene Therapy in Retinal Disorders.In Situ Gene Therapy via AAV-CRISPR-Cas9-Mediated Targeted Gene Regulation.VSV-G-Enveloped Vesicles for Traceless Delivery of CRISPR-Cas9.Delivering CRISPR: a review of the challenges and approachesProtein Engineering Strategies to Expand CRISPR-Cas9 Applications
P2860
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P2860
Development of an intein-mediated split-Cas9 system for gene therapy
description
2015 nî lūn-bûn
@nan
2015 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Development of an intein-mediated split-Cas9 system for gene therapy
@ast
Development of an intein-mediated split-Cas9 system for gene therapy
@en
Development of an intein-mediated split-Cas9 system for gene therapy
@nl
type
label
Development of an intein-mediated split-Cas9 system for gene therapy
@ast
Development of an intein-mediated split-Cas9 system for gene therapy
@en
Development of an intein-mediated split-Cas9 system for gene therapy
@nl
prefLabel
Development of an intein-mediated split-Cas9 system for gene therapy
@ast
Development of an intein-mediated split-Cas9 system for gene therapy
@en
Development of an intein-mediated split-Cas9 system for gene therapy
@nl
P2093
P2860
P356
P1476
Development of an intein-mediated split-Cas9 system for gene therapy
@en
P2093
Dong-Jiunn Jeffery Truong
Karin Kühner
Oskar Ortiz
Stanislas Werfel
Wolfgang Wurst
P2860
P304
P356
10.1093/NAR/GKV601
P407
P577
2015-06-16T00:00:00Z