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Author Correction: Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott–Aldrich syndrome

Nature Medicine, 2022-10, Vol.28 (10), p.2217-2217

2022

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Efficient gene delivery to the adult and fetal CNS using pseudotyped non-integrating lentiviral vectors

Gene therapy, 2009-04, Vol.16 (4), p.509-520

2009

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Inhibition of retinal neovascularisation by gene transfer of soluble VEGF receptor sFlt-1

Gene therapy, 2002-03, Vol.9 (5), p.320-326

2002

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Lentiviral transduction of the murine lung provides efficient pseudotype and developmental stage-dependent cell-specific transgene expression

Gene therapy, 2008-08, Vol.15 (16), p.1167-1175

2008

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Ectopic retroviral expression of LMO2, but not IL2Rγ, blocks human T-cell development from CD34 + cells : implications for leukemogenesis in gene therapy

Leukemia, 2007-04, Vol.21 (4), p.754-763

2007

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In vivo gene transfer to the mouse eye using an HIV-based lentiviral vector; efficient long-term transduction of corneal endothelium and retinal pigment epithelium

Gene therapy, 2001-11, Vol.8 (21), p.1665-1668

2001

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Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy

Nature genetics, 2000-07, Vol.25 (3), p.306-310

2000

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Dendritic Cells: The Bare Bones of Immunity

Current biology, 2004-11, Vol.14 (22), p.R965-R967

2004

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Stable rAAV-mediated transduction of rod and cone photoreceptors in the canine retina

Gene therapy, 2003-08, Vol.10 (16), p.1336-1344

2003

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Hypoxia-regulated transgene expression in experimental retinal and choroidal neovascularization

Gene therapy, 2003-06, Vol.10 (12), p.1049-1054

2003

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Gene Transfer into the Mouse Retina Mediated by an Adeno-Associated Viral Vector

Human molecular genetics, 1996-05, Vol.5 (5), p.591-594

1996

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Molecular Evidence of Genome Editing in a Mouse Model of Immunodeficiency

Scientific reports, 2018-05, Vol.8 (1), p.8214-13, Article 8214

2018

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Kinetics of transgene expression in mouse retina following sub-retinal injection of recombinant adeno-associated virus

Vision research (Oxford), 2002-02, Vol.42 (4), p.541-549

2002

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WASP and WIP regulate podosomes in migrating leukocytes

Journal of microscopy (Oxford), 2008-09, Vol.231 (3), p.494-505

2008

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Inhibition of retinal neovascularisation by gene transfer of soluble VEGF receptor sFlt-1

Gene therapy, 2002-03, Vol.9 (5), p.320-326

2002

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An immune response after intraocular administration of an adenoviral vector containing a β galactosidase reporter gene slows retinal degeneration in the rd mouse

British journal of ophthalmology, 2001-03, Vol.85 (3), p.341-344

2001

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Intraocular gene delivery of ciliary neurotrophic factor results in significant loss of retinal function in normal mice and in the Prph2 model of retinal degeneration

Gene therapy, 2003-03, Vol.10 (6), p.523-527

2003

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Improvement of neuronal visual responses in the superior colliculus in Prph2(Rd2/Rd2) mice following gene therapy

Molecular and cellular neuroscience, 2004-01, Vol.25 (1), p.103-110

2004

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Immune responses limit adenovirally mediated gene expression in the adult mouse eye

Gene therapy, 1998, Vol.5 (8), p.1038-1046

1998

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High-titer recombinant adeno-associated virus production from replicating amplicons and herpes vectors deleted for glycoprotein H

Human gene therapy, 1999-10, Vol.10 (15), p.2527-2537

1999

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Intraocular gene delivery of ciliary neurotrophic factor results in significant loss of retinal function in normal mice and in the Prph2Rd2/Rd2 model of retinal degeneration

Gene therapy, 2003-03, Vol.10 (6), p.523-527

2003

Volltextzugriff (PDF)

Co-injection of adenovirus expressing CTLA4-Ig prolongs adenovirally mediated lacZ reporter gene expression in the mouse retina

Gene therapy, 1998-11, Vol.5 (11), p.1561-1565

1998

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Adeno-associated virus gene transfer to mouse retina

Human gene therapy, 1998-01, Vol.9 (1), p.81-86

1998

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Wiskott-Aldrich syndrome protein deficiency in B cells results in impaired peripheral homeostasis

Blood, 2008-11, Vol.112 (10), p.4158-4169

2008

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Immune responses limit adenovirally mediated gene expression in the adult mouse eye

Gene therapy, 1998-08, Vol.5 (8), p.1038-1046

1998

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Author Correction: Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott–Aldrich syndrome

Efficient gene delivery to the adult and fetal CNS using pseudotyped non-integrating lentiviral vectors

Inhibition of retinal neovascularisation by gene transfer of soluble VEGF receptor sFlt-1

Lentiviral transduction of the murine lung provides efficient pseudotype and developmental stage-dependent cell-specific transgene expression

Ectopic retroviral expression of LMO2, but not IL2Rγ, blocks human T-cell development from CD34 + cells : implications for leukemogenesis in gene therapy

In vivo gene transfer to the mouse eye using an HIV-based lentiviral vector; efficient long-term transduction of corneal endothelium and retinal pigment epithelium

Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy

Dendritic Cells: The Bare Bones of Immunity

Stable rAAV-mediated transduction of rod and cone photoreceptors in the canine retina

Hypoxia-regulated transgene expression in experimental retinal and choroidal neovascularization

Gene Transfer into the Mouse Retina Mediated by an Adeno-Associated Viral Vector

Molecular Evidence of Genome Editing in a Mouse Model of Immunodeficiency

Kinetics of transgene expression in mouse retina following sub-retinal injection of recombinant adeno-associated virus

WASP and WIP regulate podosomes in migrating leukocytes

Inhibition of retinal neovascularisation by gene transfer of soluble VEGF receptor sFlt-1

An immune response after intraocular administration of an adenoviral vector containing a β galactosidase reporter gene slows retinal degeneration in the rd mouse

Intraocular gene delivery of ciliary neurotrophic factor results in significant loss of retinal function in normal mice and in the Prph2 model of retinal degeneration

Improvement of neuronal visual responses in the superior colliculus in Prph2(Rd2/Rd2) mice following gene therapy

Immune responses limit adenovirally mediated gene expression in the adult mouse eye

High-titer recombinant adeno-associated virus production from replicating amplicons and herpes vectors deleted for glycoprotein H

Intraocular gene delivery of ciliary neurotrophic factor results in significant loss of retinal function in normal mice and in the Prph2Rd2/Rd2 model of retinal degeneration

Co-injection of adenovirus expressing CTLA4-Ig prolongs adenovirally mediated lacZ reporter gene expression in the mouse retina

Adeno-associated virus gene transfer to mouse retina

Wiskott-Aldrich syndrome protein deficiency in B cells results in impaired peripheral homeostasis

Immune responses limit adenovirally mediated gene expression in the adult mouse eye

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