Precise in-frame integration of exogenous DNA mediated by CRISPR/Cas9 system in zebrafish - Wikidata - wikimedia - TriplyDB

Precise in-frame integration of exogenous DNA mediated by CRISPR/Cas9 system in zebrafish

Precise in-frame integration of exogenous DNA mediated by CRISPR/Cas9 system in zebrafish

http://www.wikidata.org/entity/Q41294499

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Defects of the Glycinergic Synapse in Zebrafish.Site-Specific Integration of Exogenous Genes Using Genome Editing Technologies in Zebrafish Advancements in zebrafish applications for 21st century toxicology.Functional visualization and disruption of targeted genes using CRISPR/Cas9-mediated eGFP reporter integration in zebrafish.The old and new face of craniofacial research: How animal models inform human craniofacial genetic and clinical data Dissection of zebrafish shha function using site-specific targeting with a Cre-dependent genetic switch Culture time of vitrified/warmed zygotes before microinjection affects the production efficiency of CRISPR-Cas9-mediated knock-in mice.CRISPR/Cas9 - Mediated Precise Targeted Integration In Vivo Using a Double Cut Donor with Short Homology Arms.Zebrafish Genome Engineering Using the CRISPR-Cas9 System.Gene cassette knock-in in mammalian cells and zygotes by enhanced MMEJ PCR artifact in testing for homologous recombination in genomic editing in zebrafish.CRISPR-STAT: an easy and reliable PCR-based method to evaluate target-specific sgRNA activity.CRISPRz: a database of zebrafish validated sgRNAs.CLARITY and PACT-based imaging of adult zebrafish and mouse for whole-animal analysis of infections.Precise Editing of the Zebrafish Genome Made Simple and Efficient.Knock-in of large reporter genes in human cells via CRISPR/Cas9-induced homology-dependent and independent DNA repair PiggyBac transposon-based polyadenylation-signal trap for genome-wide mutagenesis in mice.TALEN-mediated knock-in via non-homologous end joining in the crustacean Daphnia magna.Precise genome editing by homologous recombination.Efficient precise knockin with a double cut HDR donor after CRISPR/Cas9-mediated double-stranded DNA cleavage Intron-based genomic editing: a highly efficient method for generating knockin zebrafish.Recent Advances in CRISPR-Cas9 Genome Editing Technology for Biological and Biomedical Investigations.Homology-mediated end joining-based targeted integration using CRISPR/Cas9.Establishment of expanded and streamlined pipeline of PITCh knock-in - a web-based design tool for MMEJ-mediated gene knock-in, PITCh designer, and the variations of PITCh, PITCh-TG and PITCh-KIKO.Gene editing technology as an approach to the treatment of liver diseases.Targeted integration of genes in Xenopus tropicalis.A Powerful CRISPR/Cas9-Based Method for Targeted Transcriptional Activation.LITTLE FISH, BIG DATA: ZEBRAFISH AS A MODEL FOR CARDIOVASCULAR AND METABOLIC DISEASE.MMEJ-assisted gene knock-in using TALENs and CRISPR-Cas9 with the PITCh systems.Homology arms of targeting vectors for gene insertions and CRISPR/Cas9 technology: size does not matter; quality control of targeted clones does.Tissue-specific gene targeting using CRISPR/Cas9.Exogenous gene integration mediated by genome editing technologies in zebrafish.Molecular basis, applications and challenges of CRISPR/Cas9: a continuously evolving tool for genome editing.Targeted Genome Replacement via Homology-directed Repair in Non-dividing Cardiomyocytes.Homologous Recombination-Independent Large Gene Cassette Knock-in in CHO Cells Using TALEN and MMEJ-Directed Donor Plasmids.An efficient system for homology-dependent targeted gene integration in medaka (Oryzias latipes).Genetic targeting and anatomical registration of neuronal populations in the zebrafish brain with a new set of BAC transgenic tools.CRISPR/Cas9-induced Targeted Mutagenesis and Gene Replacement to Generate Long-shelf Life Tomato Lines.Internal epitope tagging informed by relative lack of sequence conservation.Polq-Mediated End Joining Is Essential for Surviving DNA Double-Strand Breaks during Early Zebrafish Development.

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Precise in-frame integration of exogenous DNA mediated by CRISPR/Cas9 system in zebrafish

http://www.wikidata.org/entity/Q41294499

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

Precise in-frame integration of exogenous DNA mediated by CRISPR/Cas9 system in zebrafish

@en

type

label

Precise in-frame integration of exogenous DNA mediated by CRISPR/Cas9 system in zebrafish

@en

prefLabel

Precise in-frame integration of exogenous DNA mediated by CRISPR/Cas9 system in zebrafish

@en

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Scientific Reports

P1476

Precise in-frame integration of exogenous DNA mediated by CRISPR/Cas9 system in zebrafish

@en

P2093

Atsuo Kawahara

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

Hitoshi Okamoto

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

Rie Ohga

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

Satoshi Ota

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

Shota Nakade

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

Yu Hisano

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

P2860

RNA-guided human genome engineering via Cas9

Multiplex genome engineering using CRISPR/Cas systems

Efficient genome editing in zebrafish using a CRISPR-Cas system

Heritable targeted gene disruption in zebrafish using designed zinc-finger nucleases

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

Development and applications of CRISPR-Cas9 for genome engineering.

Vap (Vascular Associated Protein): a novel factor involved in erythropoiesis and angiogenesis

Genome Engineering With Zinc-Finger Nucleases

One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering

MMEJ repair of double-strand breaks (director's cut): deleted sequences and alternative endings

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P304

8841

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10.1038/SREP08841

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P478

5

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Takashi Yamamoto

Tetsushi Sakuma

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2015-03-05T00:00:00Z

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273149535

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25740433

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P932

4350073

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