Increasing the efficiency of homology-directed repair for CRISPR-Cas9-induced precise gene editing in mammalian cells.
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An Overview of CRISPR-Based Tools and Their Improvements: New Opportunities in Understanding Plant-Pathogen Interactions for Better Crop ProtectionCRISPR/Cas9: Implications for Modeling and Therapy of Neurodegenerative DiseasesCustomizing the genome as therapy for the β-hemoglobinopathiesRNA Interference in the Age of CRISPR: Will CRISPR Interfere with RNAi?The therapeutic potential of genome editing for β-thalassemiaDNA repair targeted therapy: The past or future of cancer treatment?Gene targeting, genome editing: from Dolly to editorsGenome Editing and Its Applications in Model OrganismsResources for the design of CRISPR gene editing experimentsOrigins of Programmable Nucleases for Genome EngineeringEnabling functional genomics with genome engineeringEngineering large animal models of human diseaseDesigned nucleases for targeted genome editingProgress and Prospects of Anti-HBV Gene Therapy DevelopmentUse of designer nucleases for targeted gene and genome editing in plantsCRISPR/Cas9: a powerful genetic engineering tool for establishing large animal models of neurodegenerative diseasesThe CRISPR revolution and its impact on cancer researchExome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and mice.MYBPC1, an Emerging Myopathic Gene: What We Know and What We Need to LearnUsing CRISPR/Cas to study gene function and model disease in vivoCRISPR-Mediated Epigenome EditingPatterns of CRISPR/Cas9 activity in plants, animals and microbesTargeted genome editing in primate embryosSnaps and mends: DNA breaks and chromosomal translocationsHighly efficient CRISPR/Cas9-mediated transgene knockin at the H11 locus in pigsImproved delivery of Cas9 protein/gRNA complexes using lipofectamine CRISPRMAX.A novel two-step genome editing strategy with CRISPR-Cas9 provides new insights into telomerase action and TERT gene expression.Integration-defective lentiviral vector mediates efficient gene editing through homology-directed repair in human embryonic stem cellsTherapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivoCRISPR/Cas9-loxP-Mediated Gene Editing as a Novel Site-Specific Genetic Manipulation Tool.Construction of a highly efficient CRISPR/Cas9-mediated duck enteritis virus-based vaccine against H5N1 avian influenza virus and duck Tembusu virus infectionHighly efficient biallelic genome editing of human ES/iPS cells using a CRISPR/Cas9 or TALEN system.Optimization of a CRISPR/Cas9-mediated Knock-in Strategy at the Porcine Rosa26 Locus in Porcine Foetal Fibroblasts.CRISPR/Cas9 - Mediated Precise Targeted Integration In Vivo Using a Double Cut Donor with Short Homology Arms.CRISPR/Cas9-mediated genome editing via postnatal administration of AAV vector cures haemophilia B mice.Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery.Cloning-free CRISPRPrecision Medicine: Genetic Repair of Retinitis Pigmentosa in Patient-Derived Stem CellsImmunogenomic engineering of a plug-and-(dis)play hybridoma platform.Development of an intein-mediated split-Cas9 system for gene therapy
P2860
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P2860
Increasing the efficiency of homology-directed repair for CRISPR-Cas9-induced precise gene editing in mammalian cells.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh
2015年學術文章
@zh-hant
name
Increasing the efficiency of h ...... ne editing in mammalian cells.
@en
type
label
Increasing the efficiency of h ...... ne editing in mammalian cells.
@en
prefLabel
Increasing the efficiency of h ...... ne editing in mammalian cells.
@en
P2093
P2860
P50
P356
P1433
P1476
Increasing the efficiency of h ...... ene editing in mammalian cells
@en
P2093
Sandrine Sander
Timm Weber
Van Trung Chu
Wolfgang Wurst
P2860
P2888
P304
P356
10.1038/NBT.3198
P577
2015-03-24T00:00:00Z