(Q40404509)

20 September 2017

title

Successful gene therapy of the Gunn rat by in vivo neonatal hepatic gene transfer using murine oncoretroviral vectors (English)

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20 September 2017

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Marta Bellodi-Privato

1

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20 September 2017

Dominique Aubert

2

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20 September 2017

Virginie Pichard

3

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20 September 2017

Anne Myara

4

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20 September 2017

François Trivin

5

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20 September 2017

Nicolas Ferry

6

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20 September 2017

language of work or name

English

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publication date

1 August 2005

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20 September 2017

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20 September 2017

volume

42

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20 September 2017

issue

2

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20 September 2017

page(s)

431-438

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UDP-Glucuronosyltransferases

20 September 2017

cites work

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7 January 2021

A replication-deficient rSV40 mediates liver-directed gene transfer and a long-term amelioration of jaundice in gunn rats

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7 January 2021

Long-term reduction of serum bilirubin levels in Gunn rats by retroviral gene transfer in vivo

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7 January 2021

Complementation of the genetic defect in Gunn rat hepatocytes in vitro by highly efficient gene transfer with cationic liposomes

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7 January 2021

Cytotoxic immune response blunts long-term transgene expression after efficient retroviral-mediated hepatic gene transfer in rat

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7 January 2021

Long-term correction of bilirubin UDPglucuronyltransferase deficiency in rats by in utero lentiviral gene transfer

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7 January 2021

A non-immunogenic adenoviral vector, coexpressing CTLA4Ig and bilirubin-uridine-diphosphoglucuronateglucuronosyltransferase permits long-term, repeatable transgene expression in the Gunn rat model of Crigler-Najjar syndrome

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7 January 2021

Induction of central tolerance by intrathymic inoculation of adenoviral antigens into the host thymus permits long-term gene therapy in Gunn rats

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7 January 2021

Transient immunosuppression with FK506 permits long-term expression of therapeutic genes introduced into the liver using recombinant adenoviruses in the rat.

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7 January 2021

Oral tolerization to adenoviral antigens permits long-term gene expression using recombinant adenoviral vectors

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7 January 2021

Lifelong elimination of hyperbilirubinemia in the Gunn rat with a single injection of helper-dependent adenoviral vector

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7 January 2021

Therapeutic neonatal hepatic gene therapy in mucopolysaccharidosis VII dogs

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7 January 2021

Neonatal or hepatocyte growth factor-potentiated adult gene therapy with a retroviral vector results in therapeutic levels of canine factor IX for hemophilia B.

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7 January 2021

Discrimination between Crigler-Najjar type I and II by expression of mutant bilirubin uridine diphosphate-glucuronosyltransferase

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7 January 2021

A stable human-derived packaging cell line for production of high titer retrovirus/vesicular stomatitis virus G pseudotypes

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7 January 2021

Characterization and tissue specificity of a monoclonal antibody against human uridine 5'-diphosphate-glucuronosyltransferase

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7 January 2021

AAV gene transfer to the retina does not protect retrovirally transduced hepatocytes from the immune response

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7 January 2021

Massive repopulation of rat liver by transplantation of hepatocytes into specific lobes of the liver and ligation of portal vein branches to other lobes

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7 January 2021

Effects of uridine diphosphate glucuronosyltransferase activity on the maximal secretion rate of bilirubin conjugates in the rat

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7 January 2021

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

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7 January 2021

The liver sieve and gene therapy

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7 January 2021

Treatment of the Crigler-Najjar syndrome type I with hepatocyte transplantation

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7 January 2021

Lack of expression from a retroviral vector after transduction of murine hematopoietic stem cells is associated with methylation in vivo

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7 January 2021

LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1

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7 January 2021

Identifiers

DOI

10.1002/HEP.20794

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20 September 2017

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