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Doug D Chung

Showing results (1-10 of 21) with videos related to

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Ophthalmic Genetics|January 21, 2025
Antioxidant MitoQ increases viability of human corneal endothelial cells with congenital hereditary endothelial dystrophy-associated <i>SLC4A11</i> mutationsSaloni Peshkar-Kulkarni, Doug D Chung, Anthony J Aldave
Ophthalmic Genetics|September 4, 2020
Identification of A Novel <i>TGFBI</i> Gene Mutation (p.Serine524Cystine) Associated with Late Onset Recurrent Epithelial Erosions and Bowman Layer OpacitiesAngela C Chen, Duangratn Niruthisard, Doug D Chung, et al.
Cornea|May 1, 2018
Epithelial Recurrent Erosion Dystrophy Secondary to COL17A1 c.3156C>T Mutation in a Non-white FamilyFarnoosh Vahedi, Doug D Chung, Katherine M Gee, et al.
Experimental Eye Research|June 25, 2019
Alterations in GRHL2-OVOL2-ZEB1 axis and aberrant activation of Wnt signaling lead to altered gene transcription in posterior polymorphous corneal dystrophyDoug D Chung, Wenlin Zhang, Kavya Jatavallabhula, et al.
Cornea|August 9, 2021
Confirmation of PRDX3 c.568G>C as the Genetic Basis of Punctiform and Polychromatic Pre-Descemet Corneal DystrophyCharlene H Choo, Ana Boto de Los Bueis, Doug D Chung, et al.
Cornea|October 12, 2023
Keratitis Fugax Hereditaria Associated With a Novel NLRP3 Mutation in a Non-Finnish PatientKavya Jatavallabhula, Onyinye Onyia, Doug D Chung, et al.
Cornea|December 19, 2022
Novel DCN Mutation in Armenian Family With Congenital Stromal Corneal DystrophyDominic Williams, Doug D Chung, Anna Hovakimyan, et al.
Ophthalmic Genetics|March 22, 2022
Confirmation of association of <i>TGFBI</i> p.Ser591Phe mutation with variant lattice corneal dystrophyCharlene H Choo, Doug D Chung, Kaitlyn V Ledwitch, et al.
Cornea|December 22, 2018
Crystalline Keratopathy in Post-LASIK Ectasia: A Case ReportMilad Modabber, Mahshad Darvish-Zargar, Léo Breton, et al.
Investigative Ophthalmology & Visual Science|June 28, 2017
Transcriptomic Profiling of Posterior Polymorphous Corneal DystrophyDoug D Chung, Ricardo F Frausto, Benjamin R Lin, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Ophthalmic Genetics|January 21, 2025
Antioxidant MitoQ increases viability of human corneal endothelial cells with congenital hereditary endothelial dystrophy-associated <i>SLC4A11</i> mutationsSaloni Peshkar-Kulkarni, Doug D Chung, Anthony J Aldave
Ophthalmic Genetics|September 4, 2020
Identification of A Novel <i>TGFBI</i> Gene Mutation (p.Serine524Cystine) Associated with Late Onset Recurrent Epithelial Erosions and Bowman Layer OpacitiesAngela C Chen, Duangratn Niruthisard, Doug D Chung, et al.
Cornea|May 1, 2018
Epithelial Recurrent Erosion Dystrophy Secondary to COL17A1 c.3156C>T Mutation in a Non-white FamilyFarnoosh Vahedi, Doug D Chung, Katherine M Gee, et al.
Experimental Eye Research|June 25, 2019
Alterations in GRHL2-OVOL2-ZEB1 axis and aberrant activation of Wnt signaling lead to altered gene transcription in posterior polymorphous corneal dystrophyDoug D Chung, Wenlin Zhang, Kavya Jatavallabhula, et al.
Cornea|August 9, 2021
Confirmation of PRDX3 c.568G>C as the Genetic Basis of Punctiform and Polychromatic Pre-Descemet Corneal DystrophyCharlene H Choo, Ana Boto de Los Bueis, Doug D Chung, et al.
Cornea|October 12, 2023
Keratitis Fugax Hereditaria Associated With a Novel NLRP3 Mutation in a Non-Finnish PatientKavya Jatavallabhula, Onyinye Onyia, Doug D Chung, et al.
Cornea|December 19, 2022
Novel DCN Mutation in Armenian Family With Congenital Stromal Corneal DystrophyDominic Williams, Doug D Chung, Anna Hovakimyan, et al.
Ophthalmic Genetics|March 22, 2022
Confirmation of association of <i>TGFBI</i> p.Ser591Phe mutation with variant lattice corneal dystrophyCharlene H Choo, Doug D Chung, Kaitlyn V Ledwitch, et al.
Cornea|December 22, 2018
Crystalline Keratopathy in Post-LASIK Ectasia: A Case ReportMilad Modabber, Mahshad Darvish-Zargar, Léo Breton, et al.
Investigative Ophthalmology & Visual Science|June 28, 2017
Transcriptomic Profiling of Posterior Polymorphous Corneal DystrophyDoug D Chung, Ricardo F Frausto, Benjamin R Lin, et al.
Pageof 3