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Progress and prospects: immune responses to viral vectors

Gene therapy, 2010-03, Vol.17 (3), p.295-304

2010

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Neutralizing antibodies against adeno-associated virus examined prospectively in pediatric patients with hemophilia

Gene therapy, 2012-03, Vol.19 (3), p.288-294

2012

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Human mesenchymal stem cells: from basic biology to clinical applications

Gene therapy, 2008-01, Vol.15 (2), p.109-116

2008

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AAV serotype 2 1-mediated gene delivery of anti-inflammatory interleukin-10 enhances neurogenesis and cognitive function in APP+PS1 mice

Gene therapy, 2012-07, Vol.19 (7), p.724-733

2012

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Gene therapy progress and prospects: synthetic polymer-based systems

Gene therapy, 2008-08, Vol.15 (16), p.1131-1138

2008

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Robust spinal motor neuron transduction following intrathecal delivery of AAV9 in pigs

Gene therapy, 2012-08, Vol.19 (8), p.852-859

2012

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Robust cardiomyocyte-specific gene expression following systemic injection of AAV: in vivo gene delivery follows a Poisson distribution

Gene therapy, 2011-01, Vol.18 (1), p.43-52

2011

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Phosphorothioate cap analogs increase stability and translational efficiency of RNA vaccines in immature dendritic cells and induce superior immune responses in vivo

Gene therapy, 2010-08, Vol.17 (8), p.961-971

2010

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Gene therapy progress and prospects: Ultrasound for gene transfer

Gene therapy, 2007-03, Vol.14 (6), p.465-475

2007

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Selective uptake of naked vaccine RNA by dendritic cells is driven by macropinocytosis and abrogated upon DC maturation

Gene therapy, 2011-07, Vol.18 (7), p.702-708

2011

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Progress and prospects: nuclear import of nonviral vectors

Gene therapy, 2010-04, Vol.17 (4), p.439-447

2010

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Randomized, double-blind, placebo-controlled clinical trial of hepatocyte growth factor plasmid for critical limb ischemia

Gene therapy, 2010-09, Vol.17 (9), p.1152-1161

2010

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Gene therapy progress and prospects: magnetic nanoparticle-based gene delivery

Gene therapy, 2006-02, Vol.13 (4), p.283-287

DOBSON, T

2006

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RNAi-mediated gene-targeting through systemic application of polyethylenimine (PEI)-complexed siRNA in vivo

Gene therapy, 2005-03, Vol.12 (5), p.461-466

2005

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Targeted cancer immunotherapy with oncolytic adenovirus coding for a fully human monoclonal antibody specific for CTLA-4

Gene therapy, 2012-10, Vol.19 (10), p.988-998

2012

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The size of endothelial fenestrae in human liver sinusoids: implications for hepatocyte-directed gene transfer

Gene therapy, 2008-09, Vol.15 (17), p.1193-1199

2008

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The effects of mesenchymal stem cells injected via different routes on modified IL-12-mediated antitumor activity

Gene therapy, 2011-05, Vol.18 (5), p.488-495

2011

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Progress and prospects: Zinc-finger nucleases as gene therapy agents

Gene therapy, 2008-11, Vol.15 (22), p.1463-1468

CARROLL, D

2008

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Gene therapy progress and prospects: non-viral gene therapy by systemic delivery

Gene therapy, 2006-09, Vol.13 (18), p.1313-1319

2006

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Novel random peptide libraries displayed on AAV serotype 9 for selection of endothelial cell-directed gene transfer vectors

Gene therapy, 2012-08, Vol.19 (8), p.800-809

2012

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Characterization of the distinct orthotopic bone-forming activity of 14 BMPs using recombinant adenovirus-mediated gene delivery

Gene therapy, 2004-09, Vol.11 (17), p.1312-1320

2004

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Development of a novel systemic gene delivery system for cancer therapy with a tumor-specific cleavable PEG-lipid

Gene therapy, 2007-01, Vol.14 (1), p.68-77

2007

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Liver-specific microRNA-122 target sequences incorporated in AAV vectors efficiently inhibits transgene expression in the liver

Gene therapy, 2011-04, Vol.18 (4), p.403-410

2011

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Antitumor effect of genetically engineered mesenchymal stem cells in a rat glioma model

Gene therapy, 2004-07, Vol.11 (14), p.1155-1164

2004

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Cancer gene therapy using mesenchymal stem cells expressing interferon-β in a mouse prostate cancer lung metastasis model

Gene therapy, 2008-11, Vol.15 (21), p.1446-1453

2008

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Progress and prospects: immune responses to viral vectors

Neutralizing antibodies against adeno-associated virus examined prospectively in pediatric patients with hemophilia

Human mesenchymal stem cells: from basic biology to clinical applications

AAV serotype 2 1-mediated gene delivery of anti-inflammatory interleukin-10 enhances neurogenesis and cognitive function in APP+PS1 mice

Gene therapy progress and prospects: synthetic polymer-based systems

Robust spinal motor neuron transduction following intrathecal delivery of AAV9 in pigs

Robust cardiomyocyte-specific gene expression following systemic injection of AAV: in vivo gene delivery follows a Poisson distribution

Phosphorothioate cap analogs increase stability and translational efficiency of RNA vaccines in immature dendritic cells and induce superior immune responses in vivo

Gene therapy progress and prospects: Ultrasound for gene transfer

Selective uptake of naked vaccine RNA by dendritic cells is driven by macropinocytosis and abrogated upon DC maturation

Progress and prospects: nuclear import of nonviral vectors

Randomized, double-blind, placebo-controlled clinical trial of hepatocyte growth factor plasmid for critical limb ischemia

Gene therapy progress and prospects: magnetic nanoparticle-based gene delivery

RNAi-mediated gene-targeting through systemic application of polyethylenimine (PEI)-complexed siRNA in vivo

Targeted cancer immunotherapy with oncolytic adenovirus coding for a fully human monoclonal antibody specific for CTLA-4

The size of endothelial fenestrae in human liver sinusoids: implications for hepatocyte-directed gene transfer

The effects of mesenchymal stem cells injected via different routes on modified IL-12-mediated antitumor activity

Progress and prospects: Zinc-finger nucleases as gene therapy agents

Gene therapy progress and prospects: non-viral gene therapy by systemic delivery

Novel random peptide libraries displayed on AAV serotype 9 for selection of endothelial cell-directed gene transfer vectors

Characterization of the distinct orthotopic bone-forming activity of 14 BMPs using recombinant adenovirus-mediated gene delivery

Development of a novel systemic gene delivery system for cancer therapy with a tumor-specific cleavable PEG-lipid

Liver-specific microRNA-122 target sequences incorporated in AAV vectors efficiently inhibits transgene expression in the liver

Antitumor effect of genetically engineered mesenchymal stem cells in a rat glioma model

Cancer gene therapy using mesenchymal stem cells expressing interferon-β in a mouse prostate cancer lung metastasis model

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