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Phenotypic and functional characterization of corneal endothelial cells during in vitro expansion

Scientific reports, 2020-05, Vol.10 (1), p.7402-7402, Article 7402

2020

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Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells

PloS one, 2024-01, Vol.19 (1), p.e0296928-e0296928

2024

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Alterations in GRHL2-OVOL2-ZEB1 axis and aberrant activation of Wnt signaling lead to altered gene transcription in posterior polymorphous corneal dystrophy

Experimental eye research, 2019-11, Vol.188, p.107696-107696, Article 107696

2019

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Confirmation of the OVOL2 Promoter Mutation c.-307T>C in Posterior Polymorphous Corneal Dystrophy 1

PloS one, 2017-01, Vol.12 (1), p.e0169215-e0169215

2017

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ZEB1 insufficiency causes corneal endothelial cell state transition and altered cellular processing

PloS one, 2019-06, Vol.14 (6), p.e0218279-e0218279

2019

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Transcriptomic Profiling of Posterior Polymorphous Corneal Dystrophy

Investigative ophthalmology & visual science, 2017-06, Vol.58 (7), p.3202-3214

2017

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Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously Mapped to Chromosome 10q23-q24

PloS one, 2016-06, Vol.11 (6), p.e0157418-e0157418

2016

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Identification of a Novel Missense KRT12 Mutation in a Vietnamese Family with Meesmann Corneal Dystrophy

Case reports in ophthalmology, 2020-01, Vol.11 (1), p.120-126

2020

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Keratitis Fugax Hereditaria Associated With a Novel NLRP3 Mutation in a Non-Finnish Patient

Cornea, 2024-02, Vol.43 (2), p.253-256

2024

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Novel DCN Mutation in Armenian Family With Congenital Stromal Corneal Dystrophy

Cornea, 2023-04, Vol.42 (4), p.464-469

2023

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Energy Shortage in Human and Mouse Models of SLC4A11-Associated Corneal Endothelial Dystrophies

Investigative ophthalmology & visual science, 2020-07, Vol.61 (8), p.39-39

2020

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Confirmation of PRDX3 c.568G>C as the Genetic Basis of Punctiform and Polychromatic Pre-Descemet Corneal Dystrophy

Cornea, 2022-06, Vol.41 (6), p.779-781

2022

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Identification of a novel partial deletion of STS associated with pre-Descemet corneal dystrophy and X-linked ichthyosis

Molecular vision, 2023, Vol.29, p.25-30

2023

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Lisch Epithelial Corneal Dystrophy Is Caused by Heterozygous Loss-of-Function Variants in MCOLN1

American journal of ophthalmology, 2024-02, Vol.258, p.183-195

2024

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Crystalline Keratopathy in Post-LASIK Ectasia: A Case Report

Cornea, 2019-05, Vol.38 (5), p.635-638

2019

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Epithelial Recurrent Erosion Dystrophy Secondary to COL17A1 c.3156C>T Mutation in a Non-white Family

Cornea, 2018-07, Vol.37 (7), p.909-911

2018

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Punctiform and Polychromatic Pre-Descemet Corneal Dystrophy: Clinical Evaluation and Identification of the Genetic Basis

American journal of ophthalmology, 2020-04, Vol.212, p.88-97

2020

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Confirmation of association of TGFBI p.Ser591Phe mutation with variant lattice corneal dystrophy

Ophthalmic genetics, 2022-08, Vol.43 (4), p.530-533

2022

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Identification of A Novel TGFBI Gene Mutation (p.Serine524Cystine) Associated with Late Onset Recurrent Epithelial Erosions and Bowman Layer Opacities

Ophthalmic genetics, 2020-12, Vol.41 (6), p.639-644

2020

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Corneal ectasia associated with posterior lamellar opacification

Ophthalmic genetics, 2021-08, Vol.42 (4), p.486-492

2021

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Elucidating the molecular basis of PPCD: Effects of decreased ZEB1 expression on corneal endothelial cell function

Molecular vision, 2017-10, Vol.23, p.740-752

2017

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Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells

PloS one, 2024-01, Vol.19 (1), p.e0296928

2024

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Confirmation of the OVOL2 Promoter Mutation c.-307TC in Posterior Polymorphous Corneal Dystrophy 1

PloS one, 2017-01, Vol.12 (1), p.e0169215

2017

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The Effect of SkQ1 on the Oxidative Stress and Inflammatory Responses in Corneal Endothelial Cells During Ex Vivo Expansion

Eye Banking and Corneal Transplantation, 2023-12, Vol.2 (4), p.e0017

2023

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Genome-Wide Analysis of Gene Expression

Encyclopedia of Biological Chemistry, 2013, Vol.2, p.369-374

Second Edition, 2013

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Phenotypic and functional characterization of corneal endothelial cells during in vitro expansion

Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells

Alterations in GRHL2-OVOL2-ZEB1 axis and aberrant activation of Wnt signaling lead to altered gene transcription in posterior polymorphous corneal dystrophy

Confirmation of the OVOL2 Promoter Mutation c.-307T>C in Posterior Polymorphous Corneal Dystrophy 1

ZEB1 insufficiency causes corneal endothelial cell state transition and altered cellular processing

Transcriptomic Profiling of Posterior Polymorphous Corneal Dystrophy

Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously Mapped to Chromosome 10q23-q24

Identification of a Novel Missense KRT12 Mutation in a Vietnamese Family with Meesmann Corneal Dystrophy

Keratitis Fugax Hereditaria Associated With a Novel NLRP3 Mutation in a Non-Finnish Patient

Novel DCN Mutation in Armenian Family With Congenital Stromal Corneal Dystrophy

Energy Shortage in Human and Mouse Models of SLC4A11-Associated Corneal Endothelial Dystrophies

Confirmation of PRDX3 c.568G>C as the Genetic Basis of Punctiform and Polychromatic Pre-Descemet Corneal Dystrophy

Identification of a novel partial deletion of STS associated with pre-Descemet corneal dystrophy and X-linked ichthyosis

Lisch Epithelial Corneal Dystrophy Is Caused by Heterozygous Loss-of-Function Variants in MCOLN1

Crystalline Keratopathy in Post-LASIK Ectasia: A Case Report

Epithelial Recurrent Erosion Dystrophy Secondary to COL17A1 c.3156C>T Mutation in a Non-white Family

Punctiform and Polychromatic Pre-Descemet Corneal Dystrophy: Clinical Evaluation and Identification of the Genetic Basis

Confirmation of association of TGFBI p.Ser591Phe mutation with variant lattice corneal dystrophy

Identification of A Novel TGFBI Gene Mutation (p.Serine524Cystine) Associated with Late Onset Recurrent Epithelial Erosions and Bowman Layer Opacities

Corneal ectasia associated with posterior lamellar opacification

Elucidating the molecular basis of PPCD: Effects of decreased ZEB1 expression on corneal endothelial cell function

Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells

Confirmation of the OVOL2 Promoter Mutation c.-307TC in Posterior Polymorphous Corneal Dystrophy 1

The Effect of SkQ1 on the Oxidative Stress and Inflammatory Responses in Corneal Endothelial Cells During Ex Vivo Expansion

Genome-Wide Analysis of Gene Expression

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