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ARVO Annual Meeting Abstract June 2023

Novel oral drug treatment rescues progressive optic neuropathy in a phenotypic mouse model of familial dysautonomia

Anil Kumar Chekuri; Elisabetta Morini; Emily Logan; Jessica Bolduc; Emily Kirchner; Monica Salani; Aram Krauson; Jana Narasimhan; Vijayalakshmi Gabbeta; Amal Dakka; Jean Hedrick; Xin Zhao; Nikolai Naryshkin; Marla Weetal; Susan Salugenhaupt

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):3767.

ARVO Annual Meeting Abstract June 2022

Single-nucleus multi-modal analysis of MFRP associated retinal degeneration

Shikha Pachauri; Kelsey Dang; Pooja Biswas; Anil Kumar Chekuri; Manisha Dagar; Anne Marie Berry; Berzhan Kurmanov; Ryan Lancione; Donita Garland; Sebastian Preissl; Allen Wang; Radha Ayyagari

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

ARVO Annual Meeting Abstract June 2022

The role of the Complement pathway in L-ORD pathology caused by mutations in CTRP5.

Manisha Dagar; Anil Kumar Chekuri; Pooja Biswas; Shikha Pachauri; Donita Garland; Radha Ayyagari

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):1949 – F0367.

ARVO Annual Meeting Abstract June 2022

Proteome analysis of choroidal aging in wild type and L-ORD mouse models

Donita Garland; Manisha Dagar; Anil Kumar Chekuri; Pooja Biswas; Radha Ayyagari

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):1912 – A0058.

ARVO Annual Meeting Abstract June 2022

AAV mediated delivery of Exon-specific U1 snRNA corrects ELP1 splicing and prevents retinal degeneration in familial dysautonomia

Anil Kumar Chekuri; Elisabetta Morini; Emily Kirchner; Jessica Bolduc; Franco Pagani; Luk H. Vandenberghe; Susan Slaugenhaupt

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):3848.

ARVO Annual Meeting Abstract June 2021

A novel exon-specific U1snRNA therapeutic strategy to prevent retinal degeneration in familial dysautonomia

Anil Kumar Chekuri; Elisabetta Morini; Emily Logan; Aram Krauson; Monica Salani; Giulia Romano; Federico Riccardi; Franco Pagani; Luk H Vandenberghe; Susan Slaugenhaupt

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):1207.

ARVO Annual Meeting Abstract June 2020

Potential role of mast cells in the pathology of L-ORD

Donita Garland; Anil Kumar Chekuri; Venkata R M Chavali; John Suk; Shyamanga Borooah; Radha Ayyagari

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):4427.

ARVO Annual Meeting Abstract June 2020

Single cell genomic analysis to study the retinal cell type specific regulatory landscape of Mfrp-K O mice.

Pooja Biswas; Olivier Poirion; Anil Kumar Chekuri; Xiaomeng Hou; Qian Yang; Sebastian Preissl; Bing Ren; Radha Ayyagari

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2746.

ARVO Annual Meeting Abstract June 2020

Characterization of the retinal phenotype in a humanized FD mouse model with defective ELP1 splicing.

Anil Kumar Chekuri; Elisabetta Morini; Xia Wang; Emily Logan; Aram Krauson; Monica Salani; Paula Dietrich; Ioannis Dragatsis; Luk H Vandenberghe; Susan Slaugenhaupt

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):191.

ARVO Annual Meeting Abstract July 2019

Regulation of HTRA1 activity by CTRP5 may underlie the pathology of Late Onset Retinal Degeneration (L-ORD).

Anil Kumar Chekuri; Katarzyna Zientara-Rytter; Shyamanga Borooah; Marina voronchikhina; Angel Soto-Hermida; Chloe Stanton; Hiroko Matsui; Matteo D'Antonio; Peter Shaw; David S Goodsell; Kelly Frazer; Caroline Hayward; Suresh Subramani; Radha Ayyagari

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4896.

ARVO Annual Meeting Abstract July 2019

HTRA1 is increased in Bruch's membrane/choroid in a mouse model of L-ORD

Donita Garland; Anil Kumar Chekuri; Venkata Ramana Murthy Chavali; John Suk; Shyamanga Borooah; Radha Ayyagari

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4897.

ARVO Annual Meeting Abstract July 2019

Characterizing two novel mouse models of Ctrp5/C1qtnf5 to understand disease mechanism in late-onset retinal degeneration.

Shyamanga Borooah; Marina voronchikhina; Anil Kumar Chekuri; Venkata Ramana Murthy Chavali; John Suk; Akhila Alapati; Dirk-Uwe G Bartsch; Naheed W Khan; Monica M Jablonski; Radha Ayyagari

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):5030.

ARVO Annual Meeting Abstract July 2018

Mutations in the novel gene IFT88 are involved in causing non-syndromic inherited retinal degeneration (IRD)

Anil Kumar Chekuri; Aditya Ayyagari Guru; Pooja Biswas; Kari Branham; Hiroko Matsui; Angel Soto Hermida; Michael Hicks; Akhila Alapati; Amalio Talenti; John Heckenlively; Kelly A. Frazer; Paul Sieving; Radha Ayyagari

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):4466.

ARVO Annual Meeting Abstract July 2018

A homozygous mutation in the novel gene ARFGAP2 is associated with non-syndromic recessive inherited retinal degeneration (IRD).

Pooja Biswas; Anil Kumar Chekuri; Jason Ear; Shyamanga Borooah; Hiroko Matsui; Matteo D'Antonio; Kelly A. Frazer; Sindhura Devalaraja; Shahid Yar Khan; Muhammad Asif Naeem; Sheikh Riazuddin; Javed Akram; J. Fielding Hejtmancik; Pradipta Ghosh; S Amer Riazuddin; Radha Ayyagari

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5383.

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