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Meeting Abstract (11)
Journal Articles (4)

Journal

Investigative Ophthalmology & Visual Science (15)

Article Type

ARVO Annual Meeting Abstract (11)
Cornea (2)
Biochemistry and Molecular Biology (1)
Glaucoma (1)

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Genetics (4)
Cornea (3)
Eye Anatomy and Disorders (3)
Biochemistry and Molecular Biology (1)
Glaucoma (1)
Immunology and Microbiology (1)
Pharmacology (1)

Tags

mutation (3)
hereditary corneal dystrophy (2)
proteins (2)
anti-inflammatory agents, non-steroidal (1)
biotinylation (1)
carbonic anhydrase iv (1)
cornea (1)
diclofenac (1)
dimethyl sulfoxide (1)
eye (1)

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Cornea August 2018

Ophthalmic Nonsteroidal Anti-Inflammatory Drugs as a Therapy for Corneal Dystrophies Caused by SLC4A11 Mutation

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Kumari Alka; Joseph R. Casey
TAGS: anti-inflammatory agents, non-steroidal, diclofenac, eye, hereditary corneal dystrophy, mutation, water, nepafenac
Invest. Ophthalmol. Vis. Sci.. 2018; 59(10):4258-4267. doi: https://doi.org/10.1167/iovs.18-24301

Includes: Supplemental Content

ARVO Annual Meeting Abstract July 2018

Corneal phenotype of a Slc4a11 knockout murine model for congenital hereditary endothelial dystrophy

Antoine Sylvestre-Bouchard; Sergiu Vlad; Hasitha De Alwis; Khampoun Sayasith; Marylise Piché; Joseph Roman Casey; Isabelle Brunette

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1350. doi:

ARVO Annual Meeting Abstract July 2018

SLC4A11 extracellular Loop 3 in corneal endothelial cell adhesion, FECD pathology and therapeutics

Darpan Malhotra; Martin Jung; Sergei Noskov; Richard Zimmermann; Joseph Roman Casey

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):4433. doi:

ARVO Annual Meeting Abstract July 2018

Targeted Gene Therapy of the Corneal Endothelium using Functionalized Nanoparticle Assisted Femtosecond Laser Technology

Rami Darwich; Hasitha de Alwis Weerasekera; Sergiy Patskovsky; Marilyse Piche; Joseph Roman Casey; Ariel Wilson; Santiago Costantino; Przemyslaw Mike Sapieha; Michel Meunier; Isabelle Brunette

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):4553. doi:

ARVO Annual Meeting Abstract June 2017

Hereditary Corneal Endothelial Dystrophy Protein, SLC4A11, has a role in Endothelial Cell Adhesion

Darpan Malhotra; Martin Jung; Richard Zimmermann; Joseph R Casey

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):1472. doi:

ARVO Annual Meeting Abstract June 2017

Rescue of Corneal Dystrophy-Causing SLC4A11 Mutants by Ophthalmological Non-Steroidal Anti-inflammatory Drugs

Kumari Alka; Joseph R Casey

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):5654. doi:

ARVO Annual Meeting Abstract September 2016

Identification of Protein-Protein Interactors of The Corneal Dystrophy-Causing Protein, SLC4A11

Nada Ahmed Alshumaimeri; Joseph R Casey

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):4802. doi:

ARVO Annual Meeting Abstract September 2016

SLC4A11 Three-Dimensional Model Explains Structural Basis for Endothelial Corneal Dystrophy-Causing Mutations

Kumari Alka; Katherine E Badior; Joseph R Casey

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):4820. doi:

Cornea December 2015

High Throughput Assay Identifies Glafenine as a Corrector for the Folding Defect in Corneal Dystrophy–Causing Mutants of SLC4A11

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Anthony M. Chiu; Jake J. Mandziuk; Sampath K. Loganathan; Kumari Alka; Joseph R. Casey
TAGS: glafenine, hereditary corneal dystrophy, proteins, biotinylation, dimethyl sulfoxide
Invest. Ophthalmol. Vis. Sci.. 2015; 56(13):7739-7753. doi: https://doi.org/10.1167/iovs.15-17802

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2015

A Personalized Medicine Approach to Corneal Dystrophy: Assessment of All Reported Missense SLC4A11 Mutants as Candidates for Folding Correction

Kumari Alka; Joseph R Casey

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):4660. doi:

ARVO Annual Meeting Abstract April 2014

Identifying Chemical Correctors for the Folding Defect in Corneal Dystrophy-Causing Mutants of SLC4a11

Anthony Michael Chiu; Jake Mandziuk; Joseph R Casey

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):496. doi:

Biochemistry and Molecular Biology August 2007

Identification and Characterization of a Novel Mutation in the Carbonic Anhydrase IV Gene that Causes Retinitis Pigmentosa

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Bernardo V. Alvarez; Eranga N. Vithana; Zhenglin Yang; Adrian H. Koh; Kit Yeung; Victor Yong; Haley J. Shandro; Yali Chen; Prasanna Kolatkar; Paaventhan Palasingam; Kang Zhang; Tin Aung; Joseph R. Casey
TAGS: carbonic anhydrase iv, genes, mutation, proteins, retinitis pigmentosa
Invest. Ophthalmol. Vis. Sci.. 2007; 48(8):3459-3468. doi: https://doi.org/10.1167/iovs.06-1515

ARVO Annual Meeting Abstract May 2007

Identification and Characterization of SLC4A11 Mutations in Fuchs Endothelial Corneal Dystrophy (FECD)

E. N. Vithana; V. H. K. Yong; P. Morgan; V. Ramprasad; S. Nagasamy; G. Kumaramanickevel; J. R. Casey; D. T. H. Tan; C. P. Pang; T. Aung

Invest. Ophthalmol. Vis. Sci.. 2007; 48(13):1329. doi:

ARVO Annual Meeting Abstract May 2007

Characterization of Novel SLC4A11 Mutations Identified in Recessive Congenital Hereditary Endothelial Dystrophy (CHED2)

P. E. Morgan; M. Saincher; E. N. Vithana; V. Ramprasad; G. Kumaramanickevel; T. Aung; J. R. Casey

Invest. Ophthalmol. Vis. Sci.. 2007; 48(13):5863. doi:

Glaucoma November 2006

Reduced Human and Murine Corneal Thickness in an Axenfeld-Rieger Syndrome Subtype

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Mika Asai-Coakwell; Christopher Backhouse; Ronald J. Casey; Philip J. Gage; Ordan J. Lehmann
TAGS: cornea, syndrome, mutation, glaucoma
Invest. Ophthalmol. Vis. Sci.. 2006; 47(11):4905-4909. doi: https://doi.org/10.1167/iovs.06-0457

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Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

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Copyright © 2015 Association for Research in Vision and Ophthalmology.

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