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Articles August 2020

Validating Fluorescent Chrnb4.EGFP Mouse Models for the Study of Cone Photoreceptor Degeneration

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Alicia A. Brunet; Paula I. Fuller-Carter; Annie L. Miller; Valentina Voigt; Sophia Vasiliou; Rabab Rashwan; David M. Hunt; Livia S. Carvalho
TAGS: mice, retinal cone, tissue degeneration
Trans. Vis. Sci. Tech.. 2020; 9(9):28. https://doi.org/10.1167/tvst.9.9.28

Includes: Supplemental Content

ARVO Annual Meeting Abstract July 2019

Pathophysiology of voltage-gated potassium channels in a mouse model of cone-rod dystrophy

Xiaotian Jiang; David M Hunt; Livia S Carvalho

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):457.

ARVO Annual Meeting Abstract July 2018

Validation and comparison of Achromatopsia mouse lines expressing a fluorescent marker in cone photoreceptors

Livia S Carvalho; Valentina Voigt; Iona Schuster; Paula Fuller-Carter; Juan Pablo Quesada; Sophia Vasiliou; David M Hunt

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):970.

ARVO Annual Meeting Abstract July 2018

Role of the voltage-gated potassium channel subunit Kv8.2 in inherited retinal disease and interaction with other channel proteins

David M Hunt; Nathan Hart; Jessica K Mountford; Melanie Barth; Paula Fuller-Carter; Livia S Carvalho

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):2328.

ARVO Annual Meeting Abstract April 2014

Variation in the L and M cone opsin genes as a causative factor in myopia

Jessica Kate Mountford; Wayne I Davies; John N De Roach; Terri L McLaren; Tina M Lamey; David A Mackey; David M Hunt

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):1350.

Biochemistry and Molecular Biology February 2013

Variations in Opsin Coding Sequences Cause X-Linked Cone Dysfunction Syndrome with Myopia and Dichromacy

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Michelle McClements; Wayne I. L. Davies; Michel Michaelides; Terri Young; Maureen Neitz; Robert E. MacLaren; Anthony T. Moore; David M. Hunt
TAGS: exons, family, genes, myopia, opsin, retinal cone, syndrome, pathophysiology, x-linked inheritance, pigment
Invest. Ophthalmol. Vis. Sci.. 2013; 54(2):1361-1369. https://doi.org/10.1167/iovs.12-11156

Multidisciplinary Ophthalmic Imaging December 2012

The Effect of Cone Opsin Mutations on Retinal Structure and the Integrity of the Photoreceptor Mosaic

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Joseph Carroll; Alfredo Dubra; Jessica C. Gardner; Liliana Mizrahi-Meissonnier; Robert F. Cooper; Adam M. Dubis; Rick Nordgren; Mohamed Genead; Thomas B. Connor, Jr; Kimberly E. Stepien; Dror Sharon; David M. Hunt; Eyal Banin; Alison J. Hardcastle; Anthony T. Moore; David R. Williams; Gerald Fishman; Jay Neitz; Maureen Neitz; Michel Michaelides
TAGS: mosaicism, mutation, opsin, phenotype, photoreceptors, retinal cone, retina, personal integrity
Invest. Ophthalmol. Vis. Sci.. 2012; 53(13):8006-8015. https://doi.org/10.1167/iovs.12-11087

Includes: Supplemental Content

Retina September 2010

The PROM1 Mutation p.R373C Causes an Autosomal Dominant Bull's Eye Maculopathy Associated with Rod, Rod–Cone, and Macular Dystrophy

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Michel Michaelides; Marie-Claire Gaillard; Pascal Escher; Leila Tiab; Matthew Bedell; François-Xavier Borruat; Daniel Barthelmes; Ruben Carmona; Kang Zhang; Edward White; Michelle McClements; Anthony G. Robson; Graham E. Holder; Keith Bradshaw; David M. Hunt; Andrew R. Webster; Anthony T. Moore; Daniel F. Schorderet; Francis L. Munier
TAGS: eye, family, macular disorders, macular dystrophy, mutation, retinal cone, rod photoreceptors, atrophy, phenotype
Invest. Ophthalmol. Vis. Sci.. 2010; 51(9):4771-4780. https://doi.org/10.1167/iovs.09-4561

ARVO Annual Meeting Abstract April 2010

Cone Dystrophy With Supernormal Electroretinogram (CDSE): Functional Analysis of Mutations in KCNV2 Encoding the Voltage-Gated Potassium Channel Subunit, Kv8.2

K. E. Smith; S. E. Wilkie; M. Stocker; D. M. Hunt

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):2586.

ARVO Annual Meeting Abstract April 2010

Bornholm Eye Disease Arises From a Specific Combination of Amino Acid Changes Encoded by Exon 3 of the L/M Cone Opsin Gene

M. E. McClements; M. Neitz; A. T. Moore; D. M. Hunt

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):2609.

ARVO Annual Meeting Abstract April 2010

Evaluating the Photoreceptor Mosaic in Blue Cone Monochromacy (BCM)

J. Carroll; E. Banin; D. M. Hunt; R. Martin; M. Michaelides; L. Mizrahi-Meissonnier; A. T. Moore; D. Sharon; D. R. Williams; A. Dubra

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):2935.

ARVO Annual Meeting Abstract April 2010

Improved Cone Function Following Gene Therapy in a Mouse Model of Leber Congenital Amaurosis (LCA) Caused by RetGC Deficiency

M. Mihelec; P. K. Buch; S. J. Robbie; A. J. Smith; D. M. Hunt; J. W. B. Bainbridge; R. R. Ali

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):3128.

Lens December 2009

A Mutant Connexin50 with Enhanced Hemichannel Function Leads to Cell Death

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Peter J. Minogue; Jun-Jie Tong; Anita Arora; Isabelle Russell-Eggitt; David M. Hunt; Anthony T. Moore; Lisa Ebihara; Eric C. Beyer; Viviana M. Berthoud
TAGS: cell death, complementary rna, gap junction protein, hela cells, oocytes, proteins, xenopus, apoptosis, cataract, dna
Invest. Ophthalmol. Vis. Sci.. 2009; 50(12):5837-5845. https://doi.org/10.1167/iovs.09-3759

Retinal Cell Biology December 2009

Differential Effects of TGFβ and Vitreous on the Transformation of Retinal Pigment Epithelial Cells

PDF

Sunil K. Parapuram; Binyue Chang; Lei Li; Ren A. Hartung; Kakarla V. Chalam; Joyce U. Nair-Menon; D. Margaret Hunt; Richard C. Hunt
TAGS: retinal pigment cell, vitreous body, signal transduction
Invest. Ophthalmol. Vis. Sci.. 2009; 50(12):5965-5974. https://doi.org/10.1167/iovs.09-3621

ARVO Annual Meeting Abstract April 2009

Gene Therapy in the RetGC Mouse Model of Dominant Cone-Rod Dystrophy

M. Mihelec; P. K. Buch; A. J. Smith; J. W. B. Bainbridge; D. M. Hunt; R. R. Ali

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):1739.

Biochemistry and Molecular Biology April 2009

Evaluation of the X-Linked High-Grade Myopia Locus (MYP1) with Cone Dysfunction and Color Vision Deficiencies

PDF

Ravikanth Metlapally; Michel Michaelides; Anuradha Bulusu; Yi-Ju Li; Marianne Schwartz; Thomas Rosenberg; David M. Hunt; Anthony T. Moore; Stephan Züchner; Catherine Bowes Rickman; Terri L. Young
TAGS: color vision defect, copy number polymorphism, dna, genetic pedigree, myopia, pathophysiology, polymerase chain reaction, retinal cone, screening, x-linked inheritance
Invest. Ophthalmol. Vis. Sci.. 2009; 50(4):1552-1558. https://doi.org/10.1167/iovs.08-2455

Includes: Supplemental Content

ARVO Annual Meeting Abstract May 2008

Proteome Network of Oxidative Stress in the RPE

H. Arnouk; H. Lee; R. Zhang; D. M. Hunt; R. C. Hunt; W. Jahng

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):5922.

ARVO Annual Meeting Abstract May 2008

A New Retinoid Signaling Molecule in the Retinal Pigment Epithelium: RPE45

W. Jahng; H. Arnouk; R. Zhang; F. Lamoke; R. C. Hunt; D. M. Hunt; W. J. M. Hrushesky; P. A. Wood; R. R. Rando; H. Lee

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):4531.

ARVO Annual Meeting Abstract May 2008

Fundus Autofluorescence and Intensity-Response Functions in "Cone Dystrophy With Supernormal Rod Electroretinogram" Consequent Upon Mutation in KCNV2

A. G. Robson; M. Michaelides; H. Wu; J. A. Cowing; D. M. Hunt; A. T. Moore; G. E. Holder; A. R. Webster

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):2167.

ARVO Annual Meeting Abstract May 2008

Origin of the Blue-Sensitive Visual Pigment in Primates: Site 86 Revisited

L. S. Carvalho; W. L. Davies; P. R. Robinson; J. K. Bowmaker; D. M. Hunt

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):3247.

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Validating Fluorescent Chrnb4.EGFP Mouse Models for the Study of Cone Photoreceptor Degeneration

Pathophysiology of voltage-gated potassium channels in a mouse model of cone-rod dystrophy

Validation and comparison of Achromatopsia mouse lines expressing a fluorescent marker in cone photoreceptors

Role of the voltage-gated potassium channel subunit Kv8.2 in inherited retinal disease and interaction with other channel proteins

Variation in the L and M cone opsin genes as a causative factor in myopia

Variations in Opsin Coding Sequences Cause X-Linked Cone Dysfunction Syndrome with Myopia and Dichromacy

The Effect of Cone Opsin Mutations on Retinal Structure and the Integrity of the Photoreceptor Mosaic

The PROM1 Mutation p.R373C Causes an Autosomal Dominant Bull's Eye Maculopathy Associated with Rod, Rod–Cone, and Macular Dystrophy

Cone Dystrophy With Supernormal Electroretinogram (CDSE): Functional Analysis of Mutations in KCNV2 Encoding the Voltage-Gated Potassium Channel Subunit, Kv8.2

Bornholm Eye Disease Arises From a Specific Combination of Amino Acid Changes Encoded by Exon 3 of the L/M Cone Opsin Gene

Evaluating the Photoreceptor Mosaic in Blue Cone Monochromacy (BCM)

Improved Cone Function Following Gene Therapy in a Mouse Model of Leber Congenital Amaurosis (LCA) Caused by RetGC Deficiency

A Mutant Connexin50 with Enhanced Hemichannel Function Leads to Cell Death

Differential Effects of TGFβ and Vitreous on the Transformation of Retinal Pigment Epithelial Cells

Gene Therapy in the RetGC Mouse Model of Dominant Cone-Rod Dystrophy

Evaluation of the X-Linked High-Grade Myopia Locus (MYP1) with Cone Dysfunction and Color Vision Deficiencies

Proteome Network of Oxidative Stress in the RPE

A New Retinoid Signaling Molecule in the Retinal Pigment Epithelium: RPE45

Fundus Autofluorescence and Intensity-Response Functions in "Cone Dystrophy With Supernormal Rod Electroretinogram" Consequent Upon Mutation in KCNV2

Origin of the Blue-Sensitive Visual Pigment in Primates: Site 86 Revisited

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