VSV-G-Enveloped Vesicles for Traceless Delivery of CRISPR-Cas9.

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VSV-G-Enveloped Vesicles for Traceless Delivery of CRISPR-Cas9.

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http://www.wikidata.org/entity/Q55546604

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2018 nî lūn-bûn

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2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

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2018年學術文章

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name

VSV-G-Enveloped Vesicles for Traceless Delivery of CRISPR-Cas9.

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VSV-G-Enveloped Vesicles for Traceless Delivery of CRISPR-Cas9.

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Item

label

VSV-G-Enveloped Vesicles for Traceless Delivery of CRISPR-Cas9.

@en

VSV-G-Enveloped Vesicles for Traceless Delivery of CRISPR-Cas9.

@nl

altLabel

VSV-G-Enveloped Vesicles for Traceless Delivery of CRISPR-Cas9

@en

prefLabel

VSV-G-Enveloped Vesicles for Traceless Delivery of CRISPR-Cas9.

@en

VSV-G-Enveloped Vesicles for Traceless Delivery of CRISPR-Cas9.

@nl

P1476

VSV-G-Enveloped Vesicles for Traceless Delivery of CRISPR-Cas9

@en

P2093

Anna Cereseto

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

Antonio Casini

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

Claudia Montagna

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

Francesca Arnoldi

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

Giulia Maule

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

Ilaria Zanella

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

Lorena Zentilin

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

Mauro Giacca

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

Oscar R Burrone

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

P2860

Efficient mutagenesis by Cas9 protein-mediated oligonucleotide insertion and large-scale assessment of single-guide RNAs

Multiplex genome engineering using CRISPR/Cas systems

Adeno-associated virus vector integration

RIG-I-mediated antiviral responses to single-stranded RNA bearing 5'-phosphates

RNA-programmed genome editing in human cells

Adeno-associated virus vectors as therapeutic and investigational tools in the cardiovascular system

Gene editing in human stem cells using zinc finger nucleases and integrase-defective lentiviral vector delivery

Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity

High-frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells

High-throughput gene targeting and phenotyping in zebrafish using CRISPR/Cas9.

P304

453-462

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P31

scholarly article

P356

10.1016/J.OMTN.2018.05.010

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P407

English

P478

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

P50

Luciano Conti

Gianluca Petris

Serena Zacchigna

Gian Marco Franceschini

P577

2018-07-11T00:00:00Z

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

P698

30195783

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P921

drug discovery

molecular medicine

CRISPR

P932

6041463

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