Evaluation of transduction properties of an adenovirus vector in neonatal mice.

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Neonatal Gene Therapy for Hemophilia B by a Novel Adenovirus Vector Showing Reduced Leaky Expression of Viral Genes.

P2860

Q40075764-3F764185-09DF-4BD2-8C31-22F5355376ED

P2860

Evaluation of transduction properties of an adenovirus vector in neonatal mice.

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http://www.wikidata.org/entity/Q35649623

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

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2015年论文

@zh-cn

name

Evaluation of transduction properties of an adenovirus vector in neonatal mice.

@ast

Evaluation of transduction properties of an adenovirus vector in neonatal mice.

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type

Item

label

Evaluation of transduction properties of an adenovirus vector in neonatal mice.

@ast

Evaluation of transduction properties of an adenovirus vector in neonatal mice.

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prefLabel

Evaluation of transduction properties of an adenovirus vector in neonatal mice.

@ast

Evaluation of transduction properties of an adenovirus vector in neonatal mice.

@en

P1476

Evaluation of transduction properties of an adenovirus vector in neonatal mice

@en

P2093

Fuminori Sakurai

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Kazuo Ohashi

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Shin-Ichiro Nakamura

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Shunsuke Iizuka

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P2860

Therapeutic benefit of lentiviral-mediated neonatal intracerebral gene therapy in a mouse model of globoid cell leukodystrophy

Efficient gene transfer into human CD34(+) cells by a retargeted adenovirus vector

Development of the human coagulation system in the full-term infant.

Safety and feasibility of catheter-based local intracoronary vascular endothelial growth factor gene transfer in the prevention of postangioplasty and in-stent restenosis and in the treatment of chronic myocardial ischemia: phase II results of the K

Neonatal helper-dependent adenoviral vector gene therapy mediates correction of hemophilia A and tolerance to human factor VIII

Lysosomal disorders.

Suppression of leaky expression of adenovirus genes by insertion of microRNA-targeted sequences in the replication-incompetent adenovirus vector genome.

Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy

Long-term expression of human coagulation factor VIII and correction of hemophilia A after in vivo retroviral gene transfer in factor VIII-deficient mice.

The role of Kupffer cell activation and viral gene expression in early liver toxicity after infusion of recombinant adenovirus vectors.

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685374

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scholarly article

P356

10.1155/2015/685374

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P407

English

P478

2015

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P50

Masashi Tachibana

Kahori Shimizu

Hiroyuki Mizuguchi

P577

2015-05-13T00:00:00Z

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P5875

277352313

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26075257

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P921

Adenoviridae

P932

4444570

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Evaluation of transduction properties of an adenovirus vector in neonatal mice.

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P2860

P2860

Evaluation of transduction properties of an adenovirus vector in neonatal mice.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P478

P50

P577

P5875

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P478

P50

P577

P5875

P698

P921

P932