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ARVO Annual Meeting Abstract June 2024

The role of protein binding domains of an LRR protein, LRIT3, in synaptic organization and retinal function

Nazarul Hasan; Ronald G Gregg

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):2192.

ARVO Annual Meeting Abstract June 2024

The Rho1-2 meganuclease targeted to the human P23H human rhodopsin allele in a transgenic pig model of Autosomal Dominant Retinitis Pigmentosa (adRP) generates wide variety of inactivating mutations.

Jacob Michael Young; Archana Jalligampala; Maureen A McCall; Ronald G Gregg

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):6073.

ARVO Annual Meeting Abstract June 2023

Restoration of low light vision in a mouse model of complete congenital stationary night blindness by intravitreal delivery of rAAV vectors targeting ON bipolar cells

Nazarul Hasan; Ronald G Gregg

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):1646.

ARVO Annual Meeting Abstract June 2022

The generation and characterization of a large animal model of USH3 disease

Astra Dinculescu; Maureen A McCall; Ronald G Gregg; Archana Jalligampala; Jennifer M. Noel; Rebecca Whiting; Kevin Donnelly; Kristin Whitworth; Randall S Prather; Kevin D Wells; Bethany Redel; J. Hugh McDowell

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):1926 – A0072.

ARVO Annual Meeting Abstract June 2022

Role of LRFN2 in synaptic function of cone photoreceptors in mouse retina

Nazarul Hasan; Ronald G Gregg

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):2696.

ARVO Annual Meeting Abstract June 2021

Restoration of cone ON bipolar cells siglanplex expression and function in a mouse model of cCSNB

Nazarul Hasan; Bart G Borghuis; Ronald G Gregg

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):2006.

ARVO Annual Meeting Abstract July 2019

Role of presynaptic LRIT3 expression in the restoration of dim light vision

Nazarul Hasan; gobinda Pangeni; Catherine Cobb; Emily R. Nettesheim; Daniel M. Lipinski; Maureen A McCall; Ronald G Gregg

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4788.

ARVO Annual Meeting Abstract June 2017

A dual function for LRIT3 – control of retinal photoreceptor synaptic morphology and depolarizing bipolar cell signaling

Nazarul Hasan; Jennifer Noel; Ian Scot Pyle; Gobinda Pangeni; Kathryn M Heath; Bart Gerard Borghuis; Maureen A McCall; Ronald G Gregg

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):1031.

ARVO Annual Meeting Abstract June 2017

Identification of mouse mutant lacking cone vision.

Catherine Cobb; Nazarul Hasan; Rui Ji; Timothy Hoffman; Ronald G Gregg

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):1025.

ARVO Annual Meeting Abstract June 2015

AAV-mediated rescue of a mouse model of X-linked Congenital Stationary Night Blindness

Miranda White; Sanford L Boye; Frank M Dyka; Kathryn MH Fransen; Charles N de Leeuw; Elizabeth M. Simpson; Ronald G Gregg; Maureen A McCall; Neal S Peachey; Shannon Elizabeth Boye

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2036.

ARVO Annual Meeting Abstract June 2015

LRIT3 and OPL Synaptic Structure and Function

Jennifer Michelle Noel; Patrick A Scott; Ian Scott Pyle; Kathryn MH Fransen; Nazarul Hasan; Thomas A Ray; Maureen A McCall; Ronald G Gregg

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2611.

Visual Neuroscience October 2013

Ultrastructural Localization of GPR179 and the Impact of Mutant Forms on Retinal Function in CSNB1 Patients and a Mouse Model

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Jan Klooster; Maria M. van Genderen; Minzhong Yu; Ralph J. Florijn; Frans C. C. Riemslag; Arthur A. B. Bergen; Ronald G. Gregg; Neal S. Peachey; Maarten Kamermans
TAGS: electroretinography, erg protein, human, mice, photopsia, mutation, biopharmaceutics classification system
Invest. Ophthalmol. Vis. Sci.. 2013; 54(10):6973-6981. https://doi.org/10.1167/iovs.13-12293

ARVO Annual Meeting Abstract June 2013

Presence of the Gpr179 nob5 mutation in C3H-derived transgenic mice

Jasmin Balmer; Rui Ji; Ronald Gregg; Neal Peachey; Volker Enzmann

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):6146.

ARVO Annual Meeting Abstract June 2013

CACNA1S expression, structure and function in retinal depolarizing bipolar cells

Thomas Ray; Nazarul Hasan; Maureen McCall; Ronald Gregg

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):6159.

ARVO Annual Meeting Abstract March 2012

GPR179, An Orphan G Protein-Coupled Receptor, Is Critical To Depolarizing Cell Function And Interacts With GRM6

Thomas A. Ray; Nazarul Hasan; Maureen A. McCall; Gianluca Tosini; Patsy M. Nishina; Neal S. Peachey; Ronald G. Gregg

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):3156.

ARVO Annual Meeting Abstract March 2012

Gpr179 Is Required For Depolarizing Bipolar Cell Function And Is Mutated In Autosomal Recessive Complete Congenital Stationary Night Blindness

Maarten Kamermans; Ralph Florijn; Trijntje Sjoerdsma; Jan Klooster; Thomas A. Ray; Robert K. Koenekoop; Neal S. Peachey; Ronald G. Gregg; Arthur Bergen

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):3157.

Retinal Cell Biology May 2011

The Loss of Vacuolar Protein Sorting 11 ( vps11 ) Causes Retinal Pathogenesis in a Vertebrate Model of Syndromic Albinism

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Jennifer L. Thomas; Thomas S. Vihtelic; Aaron D. denDekker; Gregory Willer; Xixia Luo; Taylor R. Murphy; Ronald G. Gregg; David R. Hyde; Ryan Thummel
TAGS: albinism, platinum, proteins, zebrafish, vacuole, pathogenesis, vertebrates
Invest. Ophthalmol. Vis. Sci.. 2011; 52(6):3119-3128. https://doi.org/10.1167/iovs.10-5957

Includes: Supplemental Content

ARVO Annual Meeting Abstract April 2011

Identification of a new mouse model of Complete Congenital Stationary Night Blindness

Thomas A. Ray; Jillian N. Pearring; Pasano Bojang, Jr.; Susana Contreras-Alcantara; Lucy Rowe; Gianluca Tosini; Patsy M. Nishina; Maureen A. McCall; Ronald G. Gregg; Neal S. Peachey

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):4122.

ARVO Annual Meeting Abstract April 2011

Trpm1 Point Mutation Underlies Retinal Dysfunction In The Mtvr27 Mouse Model Of Complete Congenital Stationary Night Blindness

Neal S. Peachey; Maureen A. McCall; Regina D. Nobles; Matthew A. Hirschtritt; Jillian N. Pearring; Pasano Bojang, Jr.; Yin Shen; Scott A. Nawy; Patsy M. Nishina; Ronald G. Gregg

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):4124.

ARVO Annual Meeting Abstract April 2011

The Loss of vacuolar protein sorting 11 (vps11) Causes Retinal Pathogenesis in a Vertebrate Model of Syndromic Albinism

Ryan Thummel; Jennifer L. Thomas; Thomas S. Vihtelic; Ronald G. Gregg; David R. Hyde

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):1825.

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The role of protein binding domains of an LRR protein, LRIT3, in synaptic organization and retinal function

The Rho1-2 meganuclease targeted to the human P23H human rhodopsin allele in a transgenic pig model of Autosomal Dominant Retinitis Pigmentosa (adRP) generates wide variety of inactivating mutations.

Restoration of low light vision in a mouse model of complete congenital stationary night blindness by intravitreal delivery of rAAV vectors targeting ON bipolar cells

The generation and characterization of a large animal model of USH3 disease

Role of LRFN2 in synaptic function of cone photoreceptors in mouse retina

Restoration of cone ON bipolar cells siglanplex expression and function in a mouse model of cCSNB

Role of presynaptic LRIT3 expression in the restoration of dim light vision

A dual function for LRIT3 – control of retinal photoreceptor synaptic morphology and depolarizing bipolar cell signaling

Identification of mouse mutant lacking cone vision.

AAV-mediated rescue of a mouse model of X-linked Congenital Stationary Night Blindness

LRIT3 and OPL Synaptic Structure and Function

Ultrastructural Localization of GPR179 and the Impact of Mutant Forms on Retinal Function in CSNB1 Patients and a Mouse Model

Presence of the Gpr179 nob5 mutation in C3H-derived transgenic mice

CACNA1S expression, structure and function in retinal depolarizing bipolar cells

GPR179, An Orphan G Protein-Coupled Receptor, Is Critical To Depolarizing Cell Function And Interacts With GRM6

Gpr179 Is Required For Depolarizing Bipolar Cell Function And Is Mutated In Autosomal Recessive Complete Congenital Stationary Night Blindness

The Loss of Vacuolar Protein Sorting 11 ( vps11 ) Causes Retinal Pathogenesis in a Vertebrate Model of Syndromic Albinism

Identification of a new mouse model of Complete Congenital Stationary Night Blindness

Trpm1 Point Mutation Underlies Retinal Dysfunction In The Mtvr27 Mouse Model Of Complete Congenital Stationary Night Blindness

The Loss of vacuolar protein sorting 11 (vps11) Causes Retinal Pathogenesis in a Vertebrate Model of Syndromic Albinism

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