Multi-kilobase homozygous targeted gene replacement in human induced pluripotent stem cells. - Wikidata - wikimedia - TriplyDB

Multi-kilobase homozygous targeted gene replacement in human induced pluripotent stem cells.

Multi-kilobase homozygous targeted gene replacement in human induced pluripotent stem cells.

http://www.wikidata.org/entity/Q35088938

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CRISPR/Cas9-mediated gene editing in human tripronuclear zygotes Site-Specific Genome Engineering in Human Pluripotent Stem Cells The therapeutic potential of genome editing for β-thalassemia Resources for the design of CRISPR gene editing experiments Precision cancer mouse models through genome editing with CRISPR-Cas9.An enhanced gene targeting toolkit for Drosophila: Golic+.Efficient inversions and duplications of mammalian regulatory DNA elements and gene clusters by CRISPR/Cas9.CRISPR-Cas9-mediated genome editing and guide RNA design.Annealing of Complementary DNA Sequences During Double-Strand Break Repair in Drosophila Is Mediated by the Ortholog of SMARCAL1.High-Content Analysis of CRISPR-Cas9 Gene-Edited Human Embryonic Stem Cells.Crispr-mediated Gene Targeting of Human Induced Pluripotent Stem Cells Conservative site-specific and single-copy transgenesis in human LINE-1 elements.Precise Correction of Disease Mutations in Induced Pluripotent Stem Cells Derived From Patients With Limb Girdle Muscular Dystrophy Co-incident insertion enables high efficiency genome engineering in mouse embryonic stem cells.Efficient CRISPR/Cas9-Mediated Versatile, Predictable, and Donor-Free Gene Knockout in Human Pluripotent Stem Cells Efficient precise knockin with a double cut HDR donor after CRISPR/Cas9-mediated double-stranded DNA cleavage Human Cell Assays for Synthesis-Dependent Strand Annealing and Crossing over During Double-Strand Break Repair.Creating and evaluating accurate CRISPR-Cas9 scalpels for genomic surgery.Genome Editing in Human Pluripotent Stem Cells: Approaches, Pitfalls, and Solutions.CRISPR/Cas9-Mediated Three Nucleotide Insertion Corrects a Deletion Mutation in MRP1/ABCC1 and Restores Its Proper Folding and Function.Gene editing technology as an approach to the treatment of liver diseases.Comprehensive Protocols for CRISPR/Cas9-based Gene Editing in Human Pluripotent Stem Cells Genome engineering through CRISPR/Cas9 technology in the human germline and pluripotent stem cells.CRISPR: taking the shortcut to a healthy genome editing enterprise.In vivo blunt-end cloning through CRISPR/Cas9-facilitated non-homologous end-joining CRISPR/Cas9 genome editing in human pluripotent stem cells: Harnessing human genetics in a dish.Rapid generation of endogenously driven transcriptional reporters in cells through CRISPR/Cas9.Vitreous Cryopreservation of Human Umbilical Vein Endothelial Cells with Low Concentration of Cryoprotective Agents for Vascular Tissue Engineering.Simplified CRISPR tools for efficient genome editing and streamlined protocols for their delivery into mammalian cells and mouse zygotes.Analysis of gene repair tracts from Cas9/gRNA double-stranded breaks in the human CFTR gene.The contribution of homology arms to nuclease-assisted genome engineering.A CRISPR/Cas-Mediated Selection-free Knockin Strategy in Human Embryonic Stem Cells.Modeling and correction of structural variations in patient-derived iPSCs using CRISPR/Cas9.Deletion of the GAA repeats from the human frataxin gene using the CRISPR-Cas9 system in YG8R-derived cells and mouse models of Friedreich ataxia.CRISPR/Cas-Mediated Knockin in Human Pluripotent Stem Cells.Beyond editing to writing large genomes.Targeted Gene Editing in Human Pluripotent Stem Cells Using Site-Specific Nucleases.Permanent inactivation of Huntington's disease mutation by personalized allele-specific CRISPR/Cas9.CRISPR/Cas9-Mediated Scanning for Regulatory Elements Required for HPRT1 Expression via Thousands of Large, Programmed Genomic Deletions.TALEN- and CRISPR/Cas9-Mediated Gene Editing in Human Pluripotent Stem Cells Using Lipid-Based Transfection.

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P2860

Multi-kilobase homozygous targeted gene replacement in human induced pluripotent stem cells.

http://www.wikidata.org/entity/Q35088938

description

2014 nî lūn-bûn

@nan

2014 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

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2014年論文

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2014年論文

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2014年論文

@zh-hk

2014年論文

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2014年論文

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2014年论文

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name

Multi-kilobase homozygous targ ...... nduced pluripotent stem cells.

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Multi-kilobase homozygous targ ...... nduced pluripotent stem cells.

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type

label

Multi-kilobase homozygous targ ...... nduced pluripotent stem cells.

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Multi-kilobase homozygous targ ...... nduced pluripotent stem cells.

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prefLabel

Multi-kilobase homozygous targ ...... nduced pluripotent stem cells.

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Multi-kilobase homozygous targ ...... nduced pluripotent stem cells.

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Nucleic Acids Research

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Multi-kilobase homozygous targ ...... nduced pluripotent stem cells.

@en

P2093

John Aach

http://www.w3.org/2001/XMLSchema#string

Luis Ortiz

http://www.w3.org/2001/XMLSchema#string

Prashant Mali

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Susan M Byrne

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P2860

RNA-guided human genome engineering via Cas9

Multiplex genome engineering using CRISPR/Cas systems

Targeted chromosomal deletions in human cells using zinc finger nucleases

Replacement of normal with mutant alleles in the genome of normal human cells unveils mutation-specific drug responses

A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity

A public resource facilitating clinical use of genomes

Enhancing gene targeting with designed zinc finger nucleases

High-throughput engineering of the mouse genome coupled with high-resolution expression analysis

Genome editing with engineered zinc finger nucleases

Genetic manipulation of genomes with rare-cutting endonucleases

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e21

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scholarly article

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10.1093/NAR/GKU1246

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3

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43

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George M. Church

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2014-11-20T00:00:00Z

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268790594

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25414332

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Human Induced Pluripotent Stem Cells

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4330342

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