Search Results - "BAINBRIDGE, J. W. B"
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Gene therapy progress and prospects: the eye
Published in Gene therapy (01-08-2006)“…The eye has unique advantages as a target organ for gene therapy of both inherited and acquired ocular disorders and offers a valuable model system for gene…”
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In situ regeneration of retinal pigment epithelium by gene transfer of E2F2: a potential strategy for treatment of macular degenerations
Published in Gene therapy (01-12-2017)“…The retinal pigment epithelium (RPE) interacts closely with photoreceptors to maintain visual function. In degenerative diseases such as Stargardt disease and…”
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3
Correction: Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65
Published in Gene therapy (01-09-2024)Get full text
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4
Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65
Published in Gene therapy (01-12-2016)“…Leber congenital amaurosis is a group of inherited retinal dystrophies that cause severe sight impairment in childhood; RPE65-deficiency causes impaired rod…”
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5
Gene supplementation therapy for recessive forms of inherited retinal dystrophies
Published in Gene therapy (01-02-2012)“…Over the last decade, gene supplementation therapy for inherited retinal degeneration has come of age. Early proof-of-concept studies in animal models of…”
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6
RPE65 gene therapy slows cone loss in Rpe65-deficient dogs
Published in Gene therapy (01-05-2013)“…Recent clinical trials of retinal pigment epithelium gene ( RPE65 ) supplementation therapy in Leber congenital amaurosis type 2 patients have demonstrated…”
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7
AAV-mediated knockdown of Peripherin-2 in vivo using miRNA-based hairpins
Published in Gene therapy (01-04-2010)“…Gene therapy for inherited retinal degeneration in which expression of a mutant allele has a gain-of-function effect on photoreceptor cells is likely to depend…”
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8
Long-term preservation of retinal function in the RCS rat model of retinitis pigmentosa following lentivirus-mediated gene therapy
Published in Gene therapy (01-04-2005)“…The Royal College of Surgeons (RCS) rat is a well-characterized model of autosomal recessive retinitis pigmentosa (RP) due to a defect in the retinal pigment…”
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Absence of ocular malignant transformation after sub-retinal delivery of rAAV2/2 or integrating lentiviral vectors in p53-deficient mice
Published in Gene therapy (01-02-2012)“…Insertional mutagenesis following gene therapy with gammaretroviral vectors can cause the development of lymphoproliferation in children with X-linked severe…”
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10
EIAV vector-mediated delivery of endostatin or angiostatin inhibits angiogenesis and vascular hyperpermeability in experimental CNV
Published in Gene therapy (01-08-2006)“…We evaluated the efficacy of equine infectious anaemia virus (EIAV)-based lentiviral vectors encoding endostatin (EIAV.endostatin) or angiostatin…”
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11
Lentiviral-vector-mediated expression of murine IL-1 receptor antagonist or IL-10 reduces the severity of endotoxin-induced uveitis
Published in Gene therapy (01-11-2008)“…Uveitis is a sight threatening inflammatory disorder that remains a significant cause of visual loss. We investigated lentiviral gene delivery of interleukin 1…”
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12
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
Published in Gene therapy (02-03-2003)“…Intraocular delivery of a variety of neurotrophic factors has been widely investigated as a potential treatment for retinal dystrophy (RD). The most commonly…”
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13
Stable rAAV-mediated transduction of rod and cone photoreceptors in the canine retina
Published in Gene therapy (01-08-2003)“…Recombinant adeno-associated virus (rAAV) vectors are attractive candidates for the treatment of inherited and acquired retinal disease. Although rAAV vectors…”
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14
Hypoxia-regulated transgene expression in experimental retinal and choroidal neovascularization
Published in Gene therapy (01-06-2003)“…Recombinant AAV vectors mediate efficient and sustained transgene expression in retinal tissues and offer a powerful approach to the local, sustained delivery…”
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15
Correction: Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65
Published in Gene therapy (01-09-2018)“…The authors originally published this article under the incorrect license type; this has now been corrected and is published under the CC-BY license…”
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16
Inhibition of retinal neovascularisation by gene transfer of soluble VEGF receptor sFlt-1
Published in Gene therapy (01-03-2002)“…Retinal angiogenesis is a central feature of the leading causes of blindness. Current treatments for these conditions are of limited efficacy and cause…”
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17
Stable and efficient intraocular gene transfer using pseudotyped EIAV lentiviral vectors
Published in The journal of gene medicine (01-03-2006)“…Background We have developed minimal non‐primate lentiviral vectors based on the equine infectious anaemia virus (EIAV). We evaluated the in vivo expression…”
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18
Prospects for gene therapy of inherited retinal disease
Published in Eye (London) (01-10-2009)“…Gene-based therapies offer the means to address gene defects responsible for inherited retinal disorders. A number of studies in experimental and preclinical…”
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Long-Term Effect of Gene Therapy on Leber’s Congenital Amaurosis
Published in The New England journal of medicine (14-05-2015)“…Long-term follow-up of 12 persons with Leber's congenital amaurosis treated with gene therapy showed that about half of them had improvements in retinal…”
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20
Intraocular lens implants and risk of endophthalmitis
Published in British journal of ophthalmology (01-11-1998)“…AIM To investigate the possible association between the use of three piece foldable silicone polypropylene (SPP) intraocular lenses (IOLs) and an increased…”
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