(Q45867698)

17 December 2017

title

Efficiency of adenovirus-mediated gene transfer into hepatocytes by liver asanguineous perfusion method (English)

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17 December 2017

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Futagawa Y

1

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17 December 2017

Okamoto T

series ordinal

2

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17 December 2017

Ohashi T

series ordinal

3

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17 December 2017

Eto Y

series ordinal

4

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17 December 2017

publication date

1 April 2000

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17 December 2017

Research in Experimental Medicine

published in

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17 December 2017

volume

199

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17 December 2017

issue

5

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17 December 2017

page(s)

263-274

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17 December 2017

Asanguineous isolated hyperthermic in vivo perfusion of the liver in the rat

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

In vitro and in vivo hepatoma cell-specific expression of a gene transferred with an adenoviral vector

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

In situ retrovirus-mediated gene transfer into dog liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

Hepatic function is preserved following liver-directed, adenovirus-mediated gene transfer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

Efficient gene activation in mammalian cells by using recombinant adenovirus expressing site-specific Cre recombinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

In vivo hepatic gene therapy: complete albeit transient correction of factor IX deficiency in hemophilia B dogs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

Highly efficient retrovirus-mediated gene transfer into rat hepatocytes in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

Assessment of recombinant adenoviral vectors for hepatic gene therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

Direct intramuscular injection with recombinant AAV vectors results in sustained expression in a dog model of hemophilia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

Efficient selection for high-expression transfectants with a novel eukaryotic vector

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

Isolated-organ perfusion for local gene delivery: efficient adenovirus-mediated gene transfer into the liver.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

Adenovirus mediated expression of therapeutic plasma levels of human factor IX in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

MHC class I-restricted cytotoxic T lymphocytes to viral antigens destroy hepatocytes in mice infected with E1-deleted recombinant adenoviruses.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

A simple and efficient method for purification of infectious recombinant adenovirus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

A model for directed foreign gene delivery to rat liver cells in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004330050124

21 January 2018

Identifiers

DOI

10.1007/S004330050124

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17 December 2017

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17 December 2017