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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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Gene therapy progress and prospects: the eye

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

2006

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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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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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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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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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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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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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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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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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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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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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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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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

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Long-Term Effect of Gene Therapy on Leber’s Congenital Amaurosis

The New England journal of medicine, 2015-05, Vol.372 (20), p.1887-1897

2015

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Stable and efficient intraocular gene transfer using pseudotyped EIAV lentiviral vectors

The journal of gene medicine, 2006-03, Vol.8 (3), p.275-285

2006

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Prospects for gene therapy of inherited retinal disease

Eye (London), 2009-10, Vol.23 (10), p.1898-1903

Bainbridge, J W B

2009

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Intraocular lens implants and risk of endophthalmitis

British journal of ophthalmology, 1998-11, Vol.82 (11), p.1312-1315

1998

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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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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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Ocular complications of intravenous cidofovir for cytomegalovirus retinitis in patients with AIDS

Eye (London), 1999-06, Vol.13 (3a), p.353-356

1999

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Decreased visual acuity in patients with cytomegalovirus retinitis and AIDS

Eye, 2000-02, Vol.14 (1), p.8-12

2000

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Is eye padding routinely necessary after uncomplicated phacoemulsification?

Eye (London), 1998, Vol.12 (4), p.637-640

1998

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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 progress and prospects: the eye

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

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

RPE65 gene therapy slows cone loss in Rpe65-deficient dogs

Gene supplementation therapy for recessive forms of inherited retinal dystrophies

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

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

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

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

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

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

Hypoxia-regulated transgene expression in experimental retinal and choroidal neovascularization

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

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

Long-Term Effect of Gene Therapy on Leber’s Congenital Amaurosis

Stable and efficient intraocular gene transfer using pseudotyped EIAV lentiviral vectors

Prospects for gene therapy of inherited retinal disease

Intraocular lens implants and risk of endophthalmitis

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

Ocular complications of intravenous cidofovir for cytomegalovirus retinitis in patients with AIDS

Decreased visual acuity in patients with cytomegalovirus retinitis and AIDS

Is eye padding routinely necessary after uncomplicated phacoemulsification?

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