Sustained FVIII expression and phenotypic correction of hemophilia A in neonatal mice using an endothelial-targeted sleeping beauty transposon (Q40319528)

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scientific article published on 7 February 2006

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English	Sustained FVIII expression and phenotypic correction of hemophilia A in neonatal mice using an endothelial-targeted sleeping beauty transposon	scientific article published on 7 February 2006

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Sustained FVIII expression and phenotypic correction of hemophilia A in neonatal mice using an endothelial-targeted sleeping beauty transposon (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

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Sleeping Beauty transposon system

1 reference

based on heuristic

inferred from title

author name string

Li Liu

1

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Europe PubMed Central

PubMed publication ID

19 September 2017

Cathryn Mah

2

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Bradley S Fletcher

3

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

publication date

7 February 2006

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Europe PubMed Central

PubMed publication ID

19 September 2017

Molecular Therapy

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Europe PubMed Central

PubMed publication ID

19 September 2017

13

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Europe PubMed Central

PubMed publication ID

19 September 2017

5

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Europe PubMed Central

PubMed publication ID

19 September 2017

1006-1015

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Europe PubMed Central

PubMed publication ID

19 September 2017

Prophylactic factor replacement in hemophilia

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7 January 2021

Gene therapy progress and prospects: gene therapy for the hemophilias

1 reference

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A review of gene therapy for haematological disorders

1 reference

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Nonviral gene therapy approaches to hemophilia

1 reference

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Immunity to adenovirus and adeno-associated viral vectors: implications for gene therapy

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Differential activation of innate immune responses by adenovirus and adeno-associated virus vectors

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AAV serotype 2 vectors preferentially integrate into active genes in mice

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The use of retroviral vectors for gene therapy-what are the risks? A review of retroviral pathogenesis and its relevance to retroviral vector-mediated gene delivery

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7 January 2021

High-Level Factor VIII Gene ExpressionIn VivoAchieved by Nonviral Liver-Specific Gene Therapy Vectors

1 reference

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7 January 2021

Increased maintenance and persistence of transgenes by excision of expression cassettes from plasmid sequences in vivo.

1 reference

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Molecular Reconstruction of Sleeping Beauty, a Tc1-like Transposon from Fish, and Its Transposition in Human Cells

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Sleeping beauty transposition: biology and applications for molecular therapy

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A phage integrase directs efficient site-specific integration in human cells

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Somatic integration and long-term transgene expression in normal and haemophilic mice using a DNA transposon system

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Site-specific genomic integration produces therapeutic Factor IX levels in mice

1 reference

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Phenotypic correction and long-term expression of factor VIII in hemophilic mice by immunotolerization and nonviral gene transfer using the Sleeping Beauty transposon system

1 reference

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7 January 2021

A direct comparison of two nonviral gene therapy vectors for somatic integration: in vivo evaluation of the bacteriophage integrase phiC31 and the Sleeping Beauty transposase

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Inhibitors in congenital coagulation disorders

1 reference

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7 January 2021

Systemic delivery of an adenoviral vector encoding canine factor VIII results in short-term phenotypic correction, inhibitor development, and biphasic liver toxicity in hemophilia A dogs.

1 reference

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7 January 2021

Efficient production of human FVIII in hemophilic mice using lentiviral vectors

1 reference

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7 January 2021

Immune implications of gene therapy for hemophilia

1 reference

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7 January 2021

Naked DNA transfer of Factor VIII induced transgene-specific, species-independent immune response in hemophilia A mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.11.021

7 January 2021

Induction of immunity to antigens expressed by recombinant adeno-associated virus depends on the route of administration

1 reference

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Dangerous liaisons: the role of "danger" signals in the immune response to gene therapy

1 reference

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7 January 2021

Humoral immune response in mice against a circulating antigen induced by adenoviral transfer is strictly dependent on expression in antigen-presenting cells

1 reference

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7 January 2021

Induction of immune tolerance by neonatal intravenous injection of human factor VIII in murine hemophilia A.

1 reference

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7 January 2021

In utero gene transfer of human factor IX to fetal mice can induce postnatal tolerance of the exogenous clotting factor

1 reference

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7 January 2021

Neonatal gene transfer with a retroviral vector results in tolerance to human factor IX in mice and dogs

1 reference

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7 January 2021

Absence of a desmopressin response after therapeutic expression of factor VIII in hemophilia A dogs with liver-directed neonatal gene therapy

1 reference

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7 January 2021

Endothelial targeting of the Sleeping Beauty transposon within lung

1 reference

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7 January 2021

Use of blood outgrowth endothelial cells for gene therapy for hemophilia A.

1 reference

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7 January 2021

Structure-function analysis of the inverted terminal repeats of the sleeping beauty transposon

1 reference

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7 January 2021

Hyperactive transposase mutants of the Sleeping Beauty transposon

1 reference

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7 January 2021

Polyethylenimine-based intravenous delivery of transgenes to mouse lung.

1 reference

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7 January 2021

Systemic linear polyethylenimine (L-PEI)-mediated gene delivery in the mouse

1 reference

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7 January 2021

Induction of immune tolerance to coagulation factor IX antigen by in vivo hepatic gene transfer

1 reference

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7 January 2021

Cancer gene discovery in solid tumours using transposon-based somatic mutagenesis in the mouse

1 reference

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7 January 2021

Mammalian mutagenesis using a highly mobile somatic Sleeping Beauty transposon system.

1 reference

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In vivo electrotransfer of the cardiotrophin-1 gene into skeletal muscle slows down progression of motor neuron degeneration in pmn mice

1 reference

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7 January 2021

Novel forms of B-domain-deleted recombinant factor VIII molecules. Construction and biochemical characterization

1 reference

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Functional cloning of SPIN-2, a nuclear anti-apoptotic protein with roles in cell cycle progression

1 reference

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Targeted disruption of the mouse factor VIII gene produces a model of haemophilia A

1 reference

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7 January 2021

Mammalian germ-line transgenesis by transposition.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.11.021

7 January 2021

Identifiers

10.1016/J.YMTHE.2005.11.021

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

ResearchGate publication ID

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