(Q45886566)

17 December 2017

title

Therapeutic lentivirus-mediated neonatal in vivo gene therapy in hyperbilirubinemic Gunn rats (English)

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17 December 2017

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Tuan Huy Nguyen

1

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17 December 2017

Marta Bellodi-Privato

2

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17 December 2017

Dominique Aubert

3

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17 December 2017

Virginie Pichard

4

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17 December 2017

Anne Myara

5

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17 December 2017

Didier Trono

6

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17 December 2017

Nicolas Ferry

7

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17 December 2017

publication date

2 September 2005

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17 December 2017

published in

Molecular Therapy

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17 December 2017

volume

12

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17 December 2017

issue

5

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17 December 2017

page(s)

852-859

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17 December 2017

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.06.482

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

7 January 2021

1 reference

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

7 January 2021

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Insertion of the adenoviral E3 region into a recombinant viral vector prevents antiviral humoral and cellular immune responses and permits long-term gene expression

7 January 2021

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

7 January 2021

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

7 January 2021

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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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.06.482

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.06.482

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.06.482

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.06.482

Gene therapy with bilirubin-UDP-glucuronosyltransferase in the Gunn rat model of Crigler-Najjar syndrome type 1.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.06.482

Long term correction of bilirubin-UDP-glucuronosyltransferase deficiency in Gunn rats by administration of a recombinant adenovirus during the neonatal period

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.06.482

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

7 January 2021

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

7 January 2021

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Liver gene therapy: advances and hurdles

7 January 2021

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Fatal systemic inflammatory response syndrome in a ornithine transcarbamylase deficient patient following adenoviral gene transfer

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.06.482

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.06.482

In vivo transduction of hematopoietic stem cells after neonatal intravenous injection of an amphotropic retroviral vector in mice

7 January 2021

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Efficient transduction of primary human B lymphocytes and nondividing myeloma B cells with HIV-1-derived lentiviral vectors

7 January 2021

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Site-directed mutagenesis of hepatocyte nuclear factor (HNF) binding sites in the mouse transthyretin (TTR) promoter reveal synergistic interactions with its enhancer region

7 January 2021

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A simple and highly effective method for the stable transduction of uncultured porcine hepatocytes using lentiviral vector

7 January 2021

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Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.06.482

HIV-1 genome nuclear import is mediated by a central DNA flap

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.06.482

Isolation and sequencing of rat liver bilirubin UDP-glucuronosyltransferase cDNA: possible alternate splicing of a common primary transcript

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.06.482

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.06.482

Woodchuck hepatitis virus posttranscriptional regulatory element enhances expression of transgenes delivered by retroviral vectors.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.06.482

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/J.YMTHE.2005.06.482

1 reference

17 December 2017

1 reference

17 December 2017