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Disease mechanisms of X‐linked cone dystrophy caused by missense mutations in the red and green cone opsins

The FASEB journal, 2021-10, Vol.35 (10), p.e21927-n/a

2021

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Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trial

Human genetics, 2016-03, Vol.135 (3), p.327-343

2016

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AAV-mediated cone rescue in a naturally occurring mouse model of CNGA3-achromatopsia

PloS one, 2012-04, Vol.7 (4), p.e35250-e35250

2012

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Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa

Proceedings of the National Academy of Sciences - PNAS, 2012-02, Vol.109 (6), p.2132-2137

2012

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Molecular characterization of the Arabidopsis 9‐cis epoxycarotenoid dioxygenase gene family

The Plant journal : for cell and molecular biology, 2003-07, Vol.35 (1), p.44-56

2003

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Successful arrest of photoreceptor and vision loss expands the therapeutic window of retinal gene therapy to later stages of disease

Proceedings of the National Academy of Sciences - PNAS, 2015-10, Vol.112 (43), p.E5844-E5853

2015

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Gene-based Therapy in a Mouse Model of Blue Cone Monochromacy

Scientific reports, 2017-07, Vol.7 (1), p.6690-8, Article 6690

2017

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Rescue of M-cone Function in Aged Opn1mw-/- Mice, a Model for Late-Stage Blue Cone Monochromacy

Investigative ophthalmology & visual science, 2019-08, Vol.60 (10), p.3644-3651

2019

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Prophylaxis Against Atrial Fibrillation After General Thoracic Surgery

Chest, 2017-01, Vol.151 (1), p.149-159

2017

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A clinically viable approach to restoring visual function using optogenetic gene therapy

Molecular therapy. Methods & clinical development, 2023-06, Vol.29, p.406-417

2023

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Stability and Safety of an AAV Vector for Treating RPGR-ORF15 X-Linked Retinitis Pigmentosa

Human gene therapy, 2015-09, Vol.26 (9), p.593-602

2015

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Incidence and risk factors of postoperative ileus after hysterectomy for benign indications

International journal of colorectal disease, 2020-11, Vol.35 (11), p.2105-2112

2020

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Expression of red/green-cone opsin mutants K82E, P187S, M273K result in unique pathobiological perturbations to cone structure and function

Frontiers in neuroscience, 2024-02, Vol.18, p.1368089-1368089

2024

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Risk factors for postoperative acute mesenteric ischemia among adult patients undergoing cardiac surgery: A systematic review and meta-analysis

Journal of critical care, 2017-12, Vol.42, p.294-303

2017

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Pathological Effects of Mutant C1QTNF5 (S163R) Expression in Murine Retinal Pigment Epithelium

Investigative ophthalmology & visual science, 2015-10, Vol.56 (11), p.6971-6980

2015

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AAV-Mediated Clarin-1 Expression in the Mouse Retina: Implications for USH3A Gene Therapy

PloS one, 2016-02, Vol.11 (2), p.e0148874-e0148874

2016

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Blue cone monochromacy and gene therapy

Vision research (Oxford), 2023-07, Vol.208, p.108221-108221, Article 108221

2023

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Comparative analysis of in vivo and in vitro AAV vector transduction in the neonatal mouse retina: Effects of serotype and site of administration

Vision research (Oxford), 2008-02, Vol.48 (3), p.377-385

2008

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Therapeutic potential of archaeal unfoldase PANet and the gateless T20S proteasome in P23H rhodopsin retinitis pigmentosa mice

PloS one, 2024-10, Vol.19 (10), p.e0308058

2024

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Mechanistic basis for the failure of cone transducin to translocate: why cones are never blinded by light

The Journal of neuroscience, 2010-05, Vol.30 (20), p.6815-6824

2010

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Cone Phosphodiesterase-6γ' Subunit Augments Cone PDE6 Holoenzyme Assembly and Stability in a Mouse Model Lacking Both Rod and Cone PDE6 Catalytic Subunits

Frontiers in molecular neuroscience, 2018-07, Vol.11, p.233-233

2018

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Prophylaxis Against Atrial Fibrillation After General Thoracic Surgery: Trial Sequential Analysis and Network Meta-Analysis

Chest, 2017-01, Vol.151 (1), p.149-159

2017

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Functional interchangeability of rod and cone transducin α-subunits

Proceedings of the National Academy of Sciences - PNAS, 2009-10, Vol.106 (42), p.17681-17686

2009

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Novel Properties of Tyrosine-mutant AAV2 Vectors in the Mouse Retina

Molecular therapy, 2011-02, Vol.19 (2), p.293-301

2011

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Correction: AAV-Mediated Cone Rescue in a Naturally Occurring Mouse Model of CNGA3-Achromatopsia

PloS one, 2014-01, Vol.9 (1)

2014

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Disease mechanisms of X‐linked cone dystrophy caused by missense mutations in the red and green cone opsins

Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trial

AAV-mediated cone rescue in a naturally occurring mouse model of CNGA3-achromatopsia

Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa

Molecular characterization of the Arabidopsis 9‐cis epoxycarotenoid dioxygenase gene family

Successful arrest of photoreceptor and vision loss expands the therapeutic window of retinal gene therapy to later stages of disease

Gene-based Therapy in a Mouse Model of Blue Cone Monochromacy

Rescue of M-cone Function in Aged Opn1mw-/- Mice, a Model for Late-Stage Blue Cone Monochromacy

Prophylaxis Against Atrial Fibrillation After General Thoracic Surgery

A clinically viable approach to restoring visual function using optogenetic gene therapy

Stability and Safety of an AAV Vector for Treating RPGR-ORF15 X-Linked Retinitis Pigmentosa

Incidence and risk factors of postoperative ileus after hysterectomy for benign indications

Expression of red/green-cone opsin mutants K82E, P187S, M273K result in unique pathobiological perturbations to cone structure and function

Risk factors for postoperative acute mesenteric ischemia among adult patients undergoing cardiac surgery: A systematic review and meta-analysis

Pathological Effects of Mutant C1QTNF5 (S163R) Expression in Murine Retinal Pigment Epithelium

AAV-Mediated Clarin-1 Expression in the Mouse Retina: Implications for USH3A Gene Therapy

Blue cone monochromacy and gene therapy

Comparative analysis of in vivo and in vitro AAV vector transduction in the neonatal mouse retina: Effects of serotype and site of administration

Therapeutic potential of archaeal unfoldase PANet and the gateless T20S proteasome in P23H rhodopsin retinitis pigmentosa mice

Mechanistic basis for the failure of cone transducin to translocate: why cones are never blinded by light

Cone Phosphodiesterase-6γ' Subunit Augments Cone PDE6 Holoenzyme Assembly and Stability in a Mouse Model Lacking Both Rod and Cone PDE6 Catalytic Subunits

Prophylaxis Against Atrial Fibrillation After General Thoracic Surgery: Trial Sequential Analysis and Network Meta-Analysis

Functional interchangeability of rod and cone transducin α-subunits

Novel Properties of Tyrosine-mutant AAV2 Vectors in the Mouse Retina

Correction: AAV-Mediated Cone Rescue in a Naturally Occurring Mouse Model of CNGA3-Achromatopsia

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