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Modulation of in utero total body irradiation induced newborn mouse growth retardation by maternal manganese superoxide dismutase-plasmid liposome ( ) gene therapy

Gene therapy, 2011-06, Vol.18 (6), p.579-583

2011

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Local delivery of VEGF adenovirus to the uterine artery increases vasorelaxation and uterine blood flow in the pregnant sheep

Gene therapy, 2008-10, Vol.15 (19), p.1344-1350

2008

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Gene Therapy Progress and Prospects: Fetal gene therapy - first proofs of concept - some adverse effects

Gene therapy, 2005-11, Vol.12 (22), p.1601-1607

2005

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In utero administration of Ad5 and AAV pseudotypes to the fetal brain leads to efficient, widespread and long-term gene expression

Gene therapy, 2012-09, Vol.19 (9), p.936-946

2012

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Improvement of the mdx mouse dystrophic phenotype by systemic in utero AAV8 delivery of a minidystrophin gene

Gene therapy, 2010-11, Vol.17 (11), p.1355-1362

2010

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MMP-2 mediates mesenchymal stem cell tropism towards medulloblastoma tumors

Gene therapy, 2011-07, Vol.18 (7), p.692-701

2011

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The developmental stage determines the distribution and duration of gene expression after early intra-amniotic gene transfer using lentiviral vectors

Gene therapy, 2010-01, Vol.17 (1), p.61-71

2010

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Early gestational gene transfer of IL-10 by systemic administration of lentiviral vector can prevent arthritis in a murine model

Gene therapy, 2011-07, Vol.18 (7), p.719-726

2011

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Full-length dystrophin gene transfer to the mdx mouse in utero

Gene therapy, 2008-04, Vol.15 (7), p.531-536

2008

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HIV-1-derived lentiviral vectors and fetal route of administration on transgene biodistribution and expression in rhesus monkeys

Gene therapy, 2005-05, Vol.12 (10), p.821-830

2005

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Immunoresponse against the transgene limits hematopoietic engraftment of mice transplanted in utero with virally transduced fetal liver

Gene therapy, 2011-05, Vol.18 (5), p.469-478

2011

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Pulmonary inflammation associated with repeated, prenatal exposure to an E1, E3-deleted adenoviral vector in sheep

Gene therapy, 1999, Vol.6 (1), p.98-106

1999

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Integration of functional bacterial artificial chromosomes into human cord blood-derived multipotent stem cells

Gene therapy, 2009-03, Vol.16 (3), p.404-414

2009

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On the scientific and ethical issues of fetal somatic gene therapy

Gene therapy, 2002-06, Vol.9 (11), p.670-673

2002

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Comparison of high-capacity and first-generation adenoviral vector gene delivery to murine muscle in utero

Gene therapy, 2005-01, Vol.12 (1), p.39-47

2005

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High-titer lentiviral vectors stimulate fetal calf serum-specific human CD4 T-cell responses: implications in human gene therapy

Gene therapy, 2009-06, Vol.16 (6), p.788-795

2009

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Reduced toxicity of F-deficient Sendai virus vector in the mouse fetus

Gene therapy, 2004-04, Vol.11 (7), p.599-608

2004

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Use of the hereditary persistence of fetal hemoglobin 2 enhancer to increase the expression of oncoretrovirus vectors for human gamma-globin

Gene therapy, 2005-11, Vol.12 (21), p.1591-1600

2005

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Fetal muscle gene transfer is not enhanced by an RGD capsid modification to high-capacity adenoviral vectors

Gene therapy, 2003-10, Vol.10 (21), p.1821-1829

2003

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Efficient engraftment of in utero transplanted mice with retrovirally transduced hematopoietic stem cells

Gene therapy, 2005-02, Vol.12 (4), p.358-363

2005

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Successful expression of β-galactosidase and factor IX transgenes in fetal and neonatal sheep after ultrasound-guided percutaneous adenovirus vector administration into the umbilical vein

Gene therapy, 1999-07, Vol.6 (7), p.1239-1248

1999

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Nonviral transfection of distinct types of human dendritic cells : High-efficiency gene transfer by electroporation into hematopoietic progenitor- but not monocyte-derived dendritic cells

Gene therapy, 1998-05, Vol.5 (5), p.700-707

1998

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Possible mechanism of gene transfer into early to mid-gestational mouse fetuses by tail vein injection

Gene therapy, 2002-11, Vol.9 (22), p.1529-1541

2002

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Efficient gene transfer into human cord blood CD34+ cells and the CD34+CD38- subset using highly purified recombinant adeno-associated viral vector preparations that are free of helper virus and wild-type AAV

Gene therapy, 2000-02, Vol.7 (3), p.183-195

2000

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Temporally regulated expression patterns following in utero adenovirus-mediated gene transfer

Gene therapy, 1999-07, Vol.6 (7), p.1249-1257

1999

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Modulation of in utero total body irradiation induced newborn mouse growth retardation by maternal manganese superoxide dismutase-plasmid liposome ( ) gene therapy

Local delivery of VEGF adenovirus to the uterine artery increases vasorelaxation and uterine blood flow in the pregnant sheep

Gene Therapy Progress and Prospects: Fetal gene therapy - first proofs of concept - some adverse effects

In utero administration of Ad5 and AAV pseudotypes to the fetal brain leads to efficient, widespread and long-term gene expression

Improvement of the mdx mouse dystrophic phenotype by systemic in utero AAV8 delivery of a minidystrophin gene

MMP-2 mediates mesenchymal stem cell tropism towards medulloblastoma tumors

The developmental stage determines the distribution and duration of gene expression after early intra-amniotic gene transfer using lentiviral vectors

Early gestational gene transfer of IL-10 by systemic administration of lentiviral vector can prevent arthritis in a murine model

Full-length dystrophin gene transfer to the mdx mouse in utero

HIV-1-derived lentiviral vectors and fetal route of administration on transgene biodistribution and expression in rhesus monkeys

Immunoresponse against the transgene limits hematopoietic engraftment of mice transplanted in utero with virally transduced fetal liver

Pulmonary inflammation associated with repeated, prenatal exposure to an E1, E3-deleted adenoviral vector in sheep

Integration of functional bacterial artificial chromosomes into human cord blood-derived multipotent stem cells

On the scientific and ethical issues of fetal somatic gene therapy

Comparison of high-capacity and first-generation adenoviral vector gene delivery to murine muscle in utero

High-titer lentiviral vectors stimulate fetal calf serum-specific human CD4 T-cell responses: implications in human gene therapy

Reduced toxicity of F-deficient Sendai virus vector in the mouse fetus

Use of the hereditary persistence of fetal hemoglobin 2 enhancer to increase the expression of oncoretrovirus vectors for human gamma-globin

Fetal muscle gene transfer is not enhanced by an RGD capsid modification to high-capacity adenoviral vectors

Efficient engraftment of in utero transplanted mice with retrovirally transduced hematopoietic stem cells

Successful expression of β-galactosidase and factor IX transgenes in fetal and neonatal sheep after ultrasound-guided percutaneous adenovirus vector administration into the umbilical vein

Nonviral transfection of distinct types of human dendritic cells : High-efficiency gene transfer by electroporation into hematopoietic progenitor- but not monocyte-derived dendritic cells

Possible mechanism of gene transfer into early to mid-gestational mouse fetuses by tail vein injection

Efficient gene transfer into human cord blood CD34+ cells and the CD34+CD38- subset using highly purified recombinant adeno-associated viral vector preparations that are free of helper virus and wild-type AAV

Temporally regulated expression patterns following in utero adenovirus-mediated gene transfer

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