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Restoration of vision after transplantation of photoreceptors

Nature (London), 2012-05, Vol.485 (7396), p.99-103

2012

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Correction: Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65

Gene therapy, 2024-09, Vol.31 (9-10), p.524-524

2024

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Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65

Gene therapy, 2016-12, Vol.23 (12), p.857-862

2016

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Gene therapy progress and prospects: the eye

Gene therapy, 2006-08, Vol.13 (16), p.1191-1197

2006

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In situ regeneration of retinal pigment epithelium by gene transfer of E2F2: a potential strategy for treatment of macular degenerations

Gene therapy, 2017-12, Vol.24 (12), p.810-818

2017

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RPE65 gene therapy slows cone loss in Rpe65-deficient dogs

Gene therapy, 2013-05, Vol.20 (5), p.545-555

2013

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Gene supplementation therapy for recessive forms of inherited retinal dystrophies

Gene therapy, 2012-02, Vol.19 (2), p.154-161

2012

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Gene therapy in the second eye of RPE65-deficient dogs improves retinal function

Gene therapy, 2011-01, Vol.18 (1), p.53-61

2011

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Targeted Disruption of Outer Limiting Membrane Junctional Proteins (Crb1 and ZO-1) Increases Integration of Transplanted Photoreceptor Precursors into the Adult Wild-Type and Degenerating Retina

Cell transplantation, 2010-01, Vol.19 (4), p.487-503

2010

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AAV-mediated knockdown of Peripherin-2 in vivo using miRNA-based hairpins

Gene therapy, 2010-04, Vol.17 (4), p.486-493

2010

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Long-term preservation of retinal function in the RCS rat model of retinitis pigmentosa following lentivirus-mediated gene therapy

Gene therapy, 2005-04, Vol.12 (8), p.694-701

2005

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Pilot randomised controlled trial of face-down positioning following macular hole surgery

Eye (London), 2012-02, Vol.26 (2), p.272-277

2012

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Absence of ocular malignant transformation after sub-retinal delivery of rAAV2/2 or integrating lentiviral vectors in p53-deficient mice

Gene therapy, 2012-02, Vol.19 (2), p.182-188

2012

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Lentiviral-vector-mediated expression of murine IL-1 receptor antagonist or IL-10 reduces the severity of endotoxin-induced uveitis

Gene therapy, 2008-11, Vol.15 (22), p.1478-1488

2008

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EIAV vector-mediated delivery of endostatin or angiostatin inhibits angiogenesis and vascular hyperpermeability in experimental CNV

Gene therapy, 2006-08, Vol.13 (15), p.1153-1165

2006

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Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy

Human molecular genetics, 2011-08, Vol.20 (16), p.3161-3175

2011

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Author Correction: Restoration of vision after transplantation of photoreceptors

Nature (London), 2024-07, Vol.631 (8019), p.E1-E2

2024

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AAV-mediated gene therapy for retinal disorders: from mouse to man

Gene therapy, 2008-06, Vol.15 (11), p.849-857

2008

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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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Ranibizumab pretreatment in diabetic vitrectomy: a pilot randomised controlled trial (the RaDiVit study)

Eye (London), 2017-09, Vol.31 (9), p.1253-1258

2017

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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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Success in sight: The eyes have it! Ocular gene therapy trials for LCA look promising

Gene therapy, 2008-09, Vol.15 (17), p.1191-1192

2008

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Correction: Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65

Gene therapy, 2018-09, Vol.25 (6), p.450-450

2018

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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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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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Restoration of vision after transplantation of photoreceptors

Correction: Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65

Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65

Gene therapy progress and prospects: the eye

In situ regeneration of retinal pigment epithelium by gene transfer of E2F2: a potential strategy for treatment of macular degenerations

RPE65 gene therapy slows cone loss in Rpe65-deficient dogs

Gene supplementation therapy for recessive forms of inherited retinal dystrophies

Gene therapy in the second eye of RPE65-deficient dogs improves retinal function

Targeted Disruption of Outer Limiting Membrane Junctional Proteins (Crb1 and ZO-1) Increases Integration of Transplanted Photoreceptor Precursors into the Adult Wild-Type and Degenerating Retina

AAV-mediated knockdown of Peripherin-2 in vivo using miRNA-based hairpins

Long-term preservation of retinal function in the RCS rat model of retinitis pigmentosa following lentivirus-mediated gene therapy

Pilot randomised controlled trial of face-down positioning following macular hole surgery

Absence of ocular malignant transformation after sub-retinal delivery of rAAV2/2 or integrating lentiviral vectors in p53-deficient mice

Lentiviral-vector-mediated expression of murine IL-1 receptor antagonist or IL-10 reduces the severity of endotoxin-induced uveitis

EIAV vector-mediated delivery of endostatin or angiostatin inhibits angiogenesis and vascular hyperpermeability in experimental CNV

Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy

Author Correction: Restoration of vision after transplantation of photoreceptors

AAV-mediated gene therapy for retinal disorders: from mouse to man

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

Ranibizumab pretreatment in diabetic vitrectomy: a pilot randomised controlled trial (the RaDiVit study)

Hypoxia-regulated transgene expression in experimental retinal and choroidal neovascularization

Success in sight: The eyes have it! Ocular gene therapy trials for LCA look promising

Correction: Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65

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

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

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