Excision of Nucleopolyhedrovirus Form Transgenic Silkworm Using the CRISPR/Cas9 System.

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Efficient Genome Editing of AMB-1 by CRISPR-Cas9 System for Analyzing Magnetotactic Behavior

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Excision of Nucleopolyhedrovirus Form Transgenic Silkworm Using the CRISPR/Cas9 System.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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Excision of Nucleopolyhedrovirus Form Transgenic Silkworm Using the CRISPR/Cas9 System.

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Excision of Nucleopolyhedrovirus Form Transgenic Silkworm Using the CRISPR/Cas9 System.

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Excision of Nucleopolyhedrovirus Form Transgenic Silkworm Using the CRISPR/Cas9 System.

@en

Excision of Nucleopolyhedrovirus Form Transgenic Silkworm Using the CRISPR/Cas9 System.

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Excision of Nucleopolyhedrovirus Form Transgenic Silkworm Using the CRISPR/Cas9 System.

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Excision of Nucleopolyhedrovirus Form Transgenic Silkworm Using the CRISPR/Cas9 System.

@nl

P1476

Excision of Nucleopolyhedrovirus Form Transgenic Silkworm Using the CRISPR/Cas9 System.

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Cheng Lu

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

Feifan Dong

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

Liang Huang

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

Minhui Pan

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

Peng Chen

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

Xinbo Yu

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

Yaming Jiang

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

Zhanqi Dong

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

Zhigang Hu

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P2860

Application of CRISPR/Cas9 Technology to HBV

A CRISPR toolbox to study virus-host interactions

Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivo

A genome-wide CRISPR screen identifies a restricted set of HIV host dependency factors.

Bacteriophage genes that inactivate the CRISPR/Cas bacterial immune system.

[Application progress of CRISPR/Cas9 genome editing technology in the treatment of HIV-1 infection].

Differential susceptibilities to BmNPV infection of two cell lines derived from the same silkworm ovarian tissues.

Resistance to BmNPV via overexpression of an exogenous gene controlled by an inducible promoter and enhancer in transgenic silkworm, Bombyx mori

CRISPRdirect: software for designing CRISPR/Cas guide RNA with reduced off-target sites.

Precision engineering for PRRSV resistance in pigs: Macrophages from genome edited pigs lacking CD163 SRCR5 domain are fully resistant to both PRRSV genotypes while maintaining biological function.

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209

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scholarly article

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10.3389/FMICB.2018.00209

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P478

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

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2018-02-16T00:00:00Z

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

P698

29503634

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P921

CRISPR

P932

5820291

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

Excision of Nucleopolyhedrovirus Form Transgenic Silkworm Using the CRISPR/Cas9 System.

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P2860

P2860

Excision of Nucleopolyhedrovirus Form Transgenic Silkworm Using the CRISPR/Cas9 System.

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P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P698

P921

P932