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The effects of PEGylation on LNP based mRNA delivery to the eye

PloS one, 2020-10, Vol.15 (10), p.e0241006

2020

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Targeting photoreceptors via intravitreal delivery using novel, capsid-mutated AAV vectors

PloS one, 2013-04, Vol.8 (4), p.e62097-e62097

2013

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Lipid nanoparticles with PEG-variant surface modifications mediate genome editing in the mouse retina

Nature communications, 2023-10, Vol.14 (1), p.6468-6468, Article 6468

2023

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The genome of self-complementary adeno-associated viral vectors increases Toll-like receptor 9–dependent innate immune responses in the liver

Blood, 2011-06, Vol.117 (24), p.6459-6468

2011

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Long-term Characterization of Retinal Degeneration in Royal College of Surgeons Rats Using Spectral-Domain Optical Coherence Tomography

Investigative ophthalmology & visual science, 2017-03, Vol.58 (3), p.1378-1386

2017

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Monomethyl Fumarate Protects the Retina From Light-Induced Retinopathy

Investigative ophthalmology & visual science, 2019-03, Vol.60 (4), p.1275-1285

2019

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Strategies for non-viral vectors targeting organs beyond the liver

Nature nanotechnology, 2024-04, Vol.19 (4), p.428-447

2024

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Lipid nanoparticles for delivery of messenger RNA to the back of the eye

Journal of controlled release, 2019-06, Vol.303, p.91-100

2019

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The Role of ERK1/2 Activation in Sarpogrelate-Mediated Neuroprotection

Investigative ophthalmology & visual science, 2018-01, Vol.59 (1), p.462-471

2018

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Retinal Neuroprotective Effects of Flibanserin, an FDA-Approved Dual Serotonin Receptor Agonist-Antagonist

PloS one, 2016-07, Vol.11 (7), p.e0159776-e0159776

2016

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An improved protocol for generation and characterization of human-induced pluripotent stem cell-derived retinal pigment epithelium cells

STAR protocols, 2022-12, Vol.3 (4), p.101803-101803, Article 101803

2022

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Natural history of cone disease in the murine model of Leber congenital amaurosis due to CEP290 mutation: determining the timing and expectation of therapy

PloS one, 2014-03, Vol.9 (3), p.e92928-e92928

2014

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The LCHADD Mouse Model Recapitulates Early-Stage Chorioretinopathy in LCHADD Patients

Investigative ophthalmology & visual science, 2024-06, Vol.65 (6), p.33

2024

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Thiophene-based lipids for mRNA delivery to pulmonary and retinal tissues

Proceedings of the National Academy of Sciences - PNAS, 2024-03, Vol.121 (11), p.e2307813120-e2307813120

2024

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Peptide-guided lipid nanoparticles deliver mRNA to the neural retina of rodents and nonhuman primates

Science advances, 2023-01, Vol.9 (2), p.eadd4623

2023

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Correction: Targeting Photoreceptors via Intravitreal Delivery Using Novel, Capsid-Mutated AAV Vectors

PloS one, 2013-09, Vol.8 (9)

2013

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Spontaneous allelic variant in deafness–blindness gene Ush1g resulting in an expanded phenotype

Genes, brain and behavior, 2023-08, Vol.22 (4), p.e12849-n/a

2023

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Sarpogrelate, a 5-HT2A Receptor Antagonist, Protects the Retina From Light-Induced Retinopathy

Investigative ophthalmology & visual science, 2015-07, Vol.56 (8), p.4560-4569

2015

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Gene therapy to rescue retinal degeneration caused by mutations in rhodopsin

Methods in molecular biology (Clifton, N.J.), 2015, Vol.1271, p.391

2015

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A Ketogenic & Low-Protein Diet Slows Retinal Degeneration in rd10 Mice

Translational vision science & technology, 2020-10, Vol.9 (11), p.18-18

2020

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Quantifying transduction efficiencies of unmodified and tyrosine capsid mutant AAV vectors in vitro using two ocular cell lines

Molecular vision, 2011-04, Vol.17, p.1090-1102

2011

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Cone specific promoter for use in gene therapy of retinal degenerative diseases

Advances in experimental medicine and biology, 2014, Vol.801, p.695

2014

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γ-Secretase inhibition of murine choroidal neovascularization is associated with reduction of superoxide and proinflammatory cytokines

Investigative ophthalmology & visual science, 2012-02, Vol.53 (2), p.574-585

2012

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Sarpogrelate, a 5-HT 2A Receptor Antagonist, Protects the Retina From Light-Induced Retinopathy

Investigative ophthalmology & visual science, 2015-07, Vol.56 (8), p.4560

2015

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Natural History of Cone Disease in the Murine Model of Leber Congenital Amaurosis Due to CEP290 Mutation: Determining the Timing and Expectation of Therapy: e92928

PloS one, 2014-03, Vol.9 (3)

2014

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The effects of PEGylation on LNP based mRNA delivery to the eye

Targeting photoreceptors via intravitreal delivery using novel, capsid-mutated AAV vectors

Lipid nanoparticles with PEG-variant surface modifications mediate genome editing in the mouse retina

The genome of self-complementary adeno-associated viral vectors increases Toll-like receptor 9–dependent innate immune responses in the liver

Long-term Characterization of Retinal Degeneration in Royal College of Surgeons Rats Using Spectral-Domain Optical Coherence Tomography

Monomethyl Fumarate Protects the Retina From Light-Induced Retinopathy

Strategies for non-viral vectors targeting organs beyond the liver

Lipid nanoparticles for delivery of messenger RNA to the back of the eye

The Role of ERK1/2 Activation in Sarpogrelate-Mediated Neuroprotection

Retinal Neuroprotective Effects of Flibanserin, an FDA-Approved Dual Serotonin Receptor Agonist-Antagonist

An improved protocol for generation and characterization of human-induced pluripotent stem cell-derived retinal pigment epithelium cells

Natural history of cone disease in the murine model of Leber congenital amaurosis due to CEP290 mutation: determining the timing and expectation of therapy

The LCHADD Mouse Model Recapitulates Early-Stage Chorioretinopathy in LCHADD Patients

Thiophene-based lipids for mRNA delivery to pulmonary and retinal tissues

Peptide-guided lipid nanoparticles deliver mRNA to the neural retina of rodents and nonhuman primates

Correction: Targeting Photoreceptors via Intravitreal Delivery Using Novel, Capsid-Mutated AAV Vectors

Spontaneous allelic variant in deafness–blindness gene Ush1g resulting in an expanded phenotype

Sarpogrelate, a 5-HT2A Receptor Antagonist, Protects the Retina From Light-Induced Retinopathy

Gene therapy to rescue retinal degeneration caused by mutations in rhodopsin

A Ketogenic & Low-Protein Diet Slows Retinal Degeneration in rd10 Mice

Quantifying transduction efficiencies of unmodified and tyrosine capsid mutant AAV vectors in vitro using two ocular cell lines

Cone specific promoter for use in gene therapy of retinal degenerative diseases

γ-Secretase inhibition of murine choroidal neovascularization is associated with reduction of superoxide and proinflammatory cytokines

Sarpogrelate, a 5-HT 2A Receptor Antagonist, Protects the Retina From Light-Induced Retinopathy

Natural History of Cone Disease in the Murine Model of Leber Congenital Amaurosis Due to CEP290 Mutation: Determining the Timing and Expectation of Therapy: e92928

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