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ARVO Annual Meeting Abstract June 2022

Multi-Allelic Interactions of Glaucoma and Anterior Segment Dysgenesis-Associated Genes in the Pathogenesis of Primary Congenital Glaucoma

Goutham Pyatla; Samir Bera; Alice Anthony; Ashish Mishra; Laura France Moreno-Leon; Anil Kumar Mandal; Sirisha Senthil; Inderjeet Kaur; Rohit C Khanna; Hemant Khanna; Subhabrata Chakrabarti

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):1131.

ARVO Annual Meeting Abstract June 2022

A MiniCEP290 gene replacement therapy to treat CEP290-Leber congenital amaurosis (LCA10)

Laura Moreno Leon; Wei Zhang; Bhubanananda Sahu; Guangping Gao; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):3843.

Retina September 2021

Oxidative Stress Resistance 1 Gene Therapy Retards Neurodegeneration in the rd1 Mutant Mouse Model of Retinopathy

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Bhubanananda Sahu; Laura Moreno Leon; Wei Zhang; Nikita Puranik; Ramesh Periasamy; Hemant Khanna; Michael Volkert
TAGS: gene therapy, injections, mice, nerve degeneration, oxidative stress, retinal degeneration, retinal diseases, photoreceptors, caspases, electroretinography
Invest. Ophthalmol. Vis. Sci.. 2021; 62(12):8. https://doi.org/10.1167/iovs.62.12.8

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2020

RPGR (Retinitis Pigmentosa GTPase Regulator) isoform expression is modulated by miRNAs involved in cilia regulation

NIkita Puranik; Laura Moreno Leon; Wei Zhang; Satyavani Ravipati; Ruhi Sikka; Linjin Li; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):1271.

ARVO Annual Meeting Abstract June 2020

Alterations in RPGR isoform levels play a critical role in X-Linked Retinitis Pigmentosa pathogenesis

Laura Moreno Leon; Linjin Li; Emma L West; Michelle O’Hara-Wright; Alexander J Smith; Robin R Ali; Samuel G Jacobson; Artur V Cideciyan; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):1955.

ARVO Annual Meeting Abstract June 2020

Complex Molecular Mechanisms Underlie Primary Congenital Glaucoma Due to the Involvement of Multiple Biochemical Pathways

Subhabrata Chakrabarti; Goutham Pyatla; Wei Zhang; Ritu Dixit; Laura Moreno Leon; Anil Kumar Mandal; Sirisha Senthil; Samir Bera; Sneha Kumari; Meha Kabra; Sonika Rathi; Syed Hameed; Rohit Chandramohan Khanna; Inderjeet Kaur; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3516.

ARVO Annual Meeting Abstract June 2020

The alternative RPGR isoform RPGR CONST , not implicated in X-linked RP, plays a crucial role in mammalian retina.

bhubanananda sahu; Laura Moreno Leon; Linjin Li; Wei Zhang; Manisha Anand; Michael Brodsky; Raju V S Rajala; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):4420.

ARVO Annual Meeting Abstract July 2019

OXR1 (oxidation resistance gene 1) Reduces Oxidative Stress and Prolongs Photoreceptor Survival in Retinal Degeneration

Ramesh Periasamy; Wei Zhang; Hemant Khanna; Michael Volkert

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):3386.

ARVO Annual Meeting Abstract July 2019

Regulation of RPGR (retinitis pigmentosa GTPase regulator) isoform expression by miRNAs: insights into retinitis pigmentosa pathogenesis.

Laura Moreno Leon; Ruhi Sikka; Wei Zhang; Linjing Li; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4925.

ARVO Annual Meeting Abstract July 2019

Influence of Loss of Retinitis Pigmentosa 2 ( RP2 ) and Retinitis Pigmentosa GTPase Regulator ( RPGR ) Genes on Inner Retina

Mahesh Shivanna; Alaina Short; Benjamin Wadas; Ramesh Periasamy; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):5984.

ARVO Annual Meeting Abstract July 2019

Isoform-specific Rpgr mutant mice depict distinct roles of the RPGR isoforms in photoreceptors

Wei Zhang; Lijing li; Ramesh Periasamy; Laura Moreno Leon; Manisha Anand; Michael Brodsky; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):462.

ARVO Annual Meeting Abstract July 2018

CRISPR-Cas9-induced mutations in the mouse Rpgr (retinitis pigmentosa GTPase regulator) gene provide new insights into the role of the distinct RPGR isoforms in photoreceptor cilia

Wei Zhang; Linjing Li; Manisha Anand; Michael Brodsky; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):981.

ARVO Annual Meeting Abstract July 2018

Genetic Interactions of Crystallins with Known Primary Congenital Glaucoma Genes

Subhabrata Chakrabarti; Meha Kabra; Goutham Pyatla; Sonika Rathi; Anil K Mandal; Sirisha Senthil; Inderjeet Kaur; Rohit C Khanna; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5148.

ARVO Annual Meeting Abstract June 2017

Mutations in zebrafish cep290 result in age-related cone degeneration

Emma M Lessieur; Wei Zhang; Linjing Li; Gabrielle C Nivar; Ellen Piccillo; Ping Song; Brian D Perkins; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):364.

ARVO Annual Meeting Abstract June 2017

Digenic Inheritance and Physical Interactions of CYP1B1 and TEK in Primary Congenital Glaucoma

Subhabrata Chakrabarti; meha kabra; Sonika Rathi; Wei Zhang; Anil K Mandal; Sirisha Senthil; Inderjeet Kaur; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):2122.

ARVO Annual Meeting Abstract June 2017

Interocular Symmetry of Rod and Cone Topography in Human ORF15-RPGR -XLRP Disease Despite Large Intraretinal, Intrafamilial and Interfamilial Variation

Artur V Cideciyan; Jason Charng; Samuel G Jacobson; Alexander Sumaroka; Sharon B. Schwartz; Malgorzata Swider; Alejandro J Roman; Rebecca Sheplock; Manisha Anand; Marc C. Peden; Hemant Khanna; Elise Heon; Alan F. Wright; Anand Swaroop

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):3232.

ARVO Annual Meeting Abstract September 2016

RPGR, a retinal ciliopathy protein, localizes to cilia in a prenylation dependent manner

Wei Zhang; Nageswara Rao Kollu; Linjing Li; Manisha Anand; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):3193.

ARVO Annual Meeting Abstract June 2015

Gene therapy rescues cone function and viability in Rp2 knockout mice over a broad vector dose range and a wide therapeutic time window

Suddhasil Mookherjee; Suja Hiriyanna; Kayleigh Kaneshiro; Haohua Qian; Tiansen Li; Hemant Khanna; Peter Colosi; Anand Swaroop; Zhijian Wu

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2063.

ARVO Annual Meeting Abstract June 2015

Dissecting the Role of X-Linked Retinitis Pigmentosa-Causing Protein RPGR (RP GTPase regulator) in Photoreceptor Protein Trafficking

Nageswara Rao Kollu; Linjing Li; Manisha Anand; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):4642.

ARVO Annual Meeting Abstract June 2015

Evaluation of Cone Photoreceptor Pathogenesis in mouse models of X-linked retinitis pigmentosa due to mutations in RPGR and RP2

Linjing Li; Nageswara Rao Kollu; Hemant Khanna

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):4652.

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Multi-Allelic Interactions of Glaucoma and Anterior Segment Dysgenesis-Associated Genes in the Pathogenesis of Primary Congenital Glaucoma

A MiniCEP290 gene replacement therapy to treat CEP290-Leber congenital amaurosis (LCA10)

Oxidative Stress Resistance 1 Gene Therapy Retards Neurodegeneration in the rd1 Mutant Mouse Model of Retinopathy

RPGR (Retinitis Pigmentosa GTPase Regulator) isoform expression is modulated by miRNAs involved in cilia regulation

Alterations in RPGR isoform levels play a critical role in X-Linked Retinitis Pigmentosa pathogenesis

Complex Molecular Mechanisms Underlie Primary Congenital Glaucoma Due to the Involvement of Multiple Biochemical Pathways

The alternative RPGR isoform RPGR CONST , not implicated in X-linked RP, plays a crucial role in mammalian retina.

OXR1 (oxidation resistance gene 1) Reduces Oxidative Stress and Prolongs Photoreceptor Survival in Retinal Degeneration

Regulation of RPGR (retinitis pigmentosa GTPase regulator) isoform expression by miRNAs: insights into retinitis pigmentosa pathogenesis.

Influence of Loss of Retinitis Pigmentosa 2 ( RP2 ) and Retinitis Pigmentosa GTPase Regulator ( RPGR ) Genes on Inner Retina

Isoform-specific Rpgr mutant mice depict distinct roles of the RPGR isoforms in photoreceptors

CRISPR-Cas9-induced mutations in the mouse Rpgr (retinitis pigmentosa GTPase regulator) gene provide new insights into the role of the distinct RPGR isoforms in photoreceptor cilia

Genetic Interactions of Crystallins with Known Primary Congenital Glaucoma Genes

Mutations in zebrafish cep290 result in age-related cone degeneration

Digenic Inheritance and Physical Interactions of CYP1B1 and TEK in Primary Congenital Glaucoma

Interocular Symmetry of Rod and Cone Topography in Human ORF15-RPGR -XLRP Disease Despite Large Intraretinal, Intrafamilial and Interfamilial Variation

RPGR, a retinal ciliopathy protein, localizes to cilia in a prenylation dependent manner

Gene therapy rescues cone function and viability in Rp2 knockout mice over a broad vector dose range and a wide therapeutic time window

Dissecting the Role of X-Linked Retinitis Pigmentosa-Causing Protein RPGR (RP GTPase regulator) in Photoreceptor Protein Trafficking

Evaluation of Cone Photoreceptor Pathogenesis in mouse models of X-linked retinitis pigmentosa due to mutations in RPGR and RP2

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