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ARVO Annual Meeting Abstract June 2024

Aberrant DNA cooperative binding underlies defective photoreceptor differentiation in mouse models of dominant CRX diseases

Yiqiao Zheng; Chi Sun; Gary D. Stormo; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):1293.

ARVO Annual Meeting Abstract June 2024

Indispensable role of potassium channel KCNJ13 in the functional maintenance of RPE and photoreceptors

Chi Sun; Xiaodong Zhang; Nandini Das; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):6720.

ARVO Annual Meeting Abstract June 2024

Genotype-Phenotype Associations for Cone-Rod Homeobox-linked Retinopathies

Isabella Gomes; Chi Sun; Xiaodong Zhang; Samuel J Huang; Austin David Igelman; Ryan Schmidt; Molly Marra; Mark E Pennesi; Rithwick Rajagopal; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):6703.

Retina June 2023

Cat LCA- CRX Model, Homozygous for an Antimorphic Mutation Has a Unique Phenotype

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Laurence M. Occelli; Nicholas M. Tran; Shiming Chen; Simon M. Petersen-Jones
TAGS: cats, eye, homozygote, mutation, phenotype, photoreceptors, retina, spectral domain-optical coherence tomography, transcription factor, tissue degeneration
Trans. Vis. Sci. Tech.. 2023; 12(6):15. https://doi.org/10.1167/tvst.12.6.15

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2023

Aberrant outer nuclear layer (ONL) phenotypes and vasculature in mouse models of dominant CRX homeodomain (HD) mutations

CHI SUN; Chas Pfeifer; Yiqiao Zheng; Rajendra S Apte; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):1248.

ARVO Annual Meeting Abstract June 2023

High-throughput identification of cis-regulatory elements for genes associated with inherited retinal diseases

Jiaxiong Lu; Jongsu Choi; Jun Wang; Yiqiao Zheng; Shiming Chen; Rui Chen

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):1857.

ARVO Annual Meeting Abstract June 2023

Phenotypic heterogeneity in a family with a late Cone-Rod Homeobox truncation mutation

Isabella Gomes; CHI SUN; Xiaodong Zhang; Rithwick Rajagopal; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):3671.

ARVO Annual Meeting Abstract June 2022

Phenotypic characterization of murine models with CRX homeodomain mutations

CHI SUN; Yiqiao Zheng; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):1962 – F0380.

ARVO Annual Meeting Abstract June 2022

Deciphering how missense mutations in CRX homeodomain produce distinct dominant retinopathies

Yiqiao Zheng; CHI SUN; Xiaodong Zhang; Philip A Ruzycki; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):3817.

ARVO Annual Meeting Abstract June 2021

Redundant functions of MLL1 and MLL2 in retinal development and cone cell maintenance

CHI SUN; Xiaodong Zhang; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):1659.

ARVO Annual Meeting Abstract June 2020

Evaluation of a gene augmentation strategy for treating CRX -linked retinopathies

CHI SUN; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2743.

ARVO Annual Meeting Abstract July 2019

Global RNA metabolic changes associated with a dominant-negative Crx mutation

Inez Oh; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):1003.

ARVO Annual Meeting Abstract July 2019

Rhodopsin enhancers mediate distinct temporal control of gene expression

Philip Ruzycki; Xiaodong Zhang; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):1735.

ARVO Annual Meeting Abstract July 2019

Generation of a transgenic mouse for inducible ectopic CRX expression

CHI SUN; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2374.

Biochemistry and Molecular Biology September 2017

Crx-L253X Mutation Produces Dominant Photoreceptor Defects in TVRM65 Mice

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Philip A. Ruzycki; Courtney D. Linne; Anne K. Hennig; Shiming Chen
TAGS: mice, mutation, photoreceptors, retina, proteins, rna, messenger
Invest. Ophthalmol. Vis. Sci.. 2017; 58(11):4644-4653. https://doi.org/10.1167/iovs.17-22075

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2017

Crx-L253X mutation produces dominant photoreceptor defects in TVRM65 mice

Courtney Danielle Linne; Philip Andrew Ruzycki; Anne Hennig; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):3588.

ARVO Annual Meeting Abstract June 2017

TFIIH-ERCC2 Is Essential For Photoreceptor Gene Expression and Development

Xiaodong Zhang; Philip Andrew Ruzycki; Anne Hennig; Mingyan Yang; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):3589.

ARVO Annual Meeting Abstract June 2017

Hyper-stability of mutant mRNA causes pathogenic overexpression of mutant CRX in autosomal dominant retinopathies

Inez Oh; Xiaodong Zhang; Nicholas Tran; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):3590.

ARVO Annual Meeting Abstract June 2017

Long Range Genomic Interactions Regulate Photoreceptor Gene Expression

Philip Andrew Ruzycki; Courtney Danielle Linne; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):4774.

ARVO Annual Meeting Abstract September 2016

ChIPseq profiling of histone modification changes reveals gene misregulation mechanisms in mouse models of photoreceptor disease.

Philip Andrew Ruzycki; Xiaodong Zhang; Shiming Chen

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):4816.

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Aberrant DNA cooperative binding underlies defective photoreceptor differentiation in mouse models of dominant CRX diseases

Indispensable role of potassium channel KCNJ13 in the functional maintenance of RPE and photoreceptors

Genotype-Phenotype Associations for Cone-Rod Homeobox-linked Retinopathies

Cat LCA- CRX Model, Homozygous for an Antimorphic Mutation Has a Unique Phenotype

Aberrant outer nuclear layer (ONL) phenotypes and vasculature in mouse models of dominant CRX homeodomain (HD) mutations

High-throughput identification of cis-regulatory elements for genes associated with inherited retinal diseases

Phenotypic heterogeneity in a family with a late Cone-Rod Homeobox truncation mutation

Phenotypic characterization of murine models with CRX homeodomain mutations

Deciphering how missense mutations in CRX homeodomain produce distinct dominant retinopathies

Redundant functions of MLL1 and MLL2 in retinal development and cone cell maintenance

Evaluation of a gene augmentation strategy for treating CRX -linked retinopathies

Global RNA metabolic changes associated with a dominant-negative Crx mutation

Rhodopsin enhancers mediate distinct temporal control of gene expression

Generation of a transgenic mouse for inducible ectopic CRX expression

Crx-L253X Mutation Produces Dominant Photoreceptor Defects in TVRM65 Mice

Crx-L253X mutation produces dominant photoreceptor defects in TVRM65 mice

TFIIH-ERCC2 Is Essential For Photoreceptor Gene Expression and Development

Hyper-stability of mutant mRNA causes pathogenic overexpression of mutant CRX in autosomal dominant retinopathies

Long Range Genomic Interactions Regulate Photoreceptor Gene Expression

ChIPseq profiling of histone modification changes reveals gene misregulation mechanisms in mouse models of photoreceptor disease.

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