Doug D Chung
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Explore the profile of Doug D Chung including associated specialties, affiliations and a list of published articles.
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Recent Articles
11.
Zhang W, Frausto R, Chung D, Griffis C, Kao L, Chen A, et al.
Invest Ophthalmol Vis Sci
. 2020 Jul;
61(8):39.
PMID: 32721020
Purpose: To elucidate the molecular events in solute carrier family 4 member 11 (SLC4A11)-deficient corneal endothelium that lead to the endothelial dysfunction that characterizes the dystrophies associated with SLC4A11 mutations,...
12.
Frausto R, Swamy V, Peh G, Boere P, Hanser E, Chung D, et al.
Sci Rep
. 2020 May;
10(1):7402.
PMID: 32366916
The advent of cell culture-based methods for the establishment and expansion of human corneal endothelial cells (CEnC) has provided a source of transplantable corneal endothelium, with a significant potential to...
13.
Dong P, Cung L, Sam T, Hang D, Chung D, Alkadi T, et al.
Case Rep Ophthalmol
. 2020 Apr;
11(1):120-126.
PMID: 32308613
Meesmann epithelial corneal dystrophy (MECD) is a rare dominantly inherited disorder that is characterized by corneal epithelial microcysts and is associated with mutations in the keratin 3 and keratin 12...
14.
Alio Del Barrio J, Chung D, Al-Shymali O, Barrington A, Jatavallabhula K, Swamy V, et al.
Am J Ophthalmol
. 2019 Nov;
212:88-97.
PMID: 31782998
Purpose: This study reports the clinical features and genetic bases of 3 previously unreported families with punctiform and polychromatic pre-Descemet corneal dystrophy (PPPCD). Design: Observational case series. Methods: Full ophthalmic...
15.
Chung D, Zhang W, Jatavallabhula K, Barrington A, Jung J, Aldave A
Exp Eye Res
. 2019 Jun;
188:107696.
PMID: 31233731
Mutations associated with posterior polymorphous corneal dystrophy (PPCD) have been identified in three genes: ZEB1 (zinc-finger E-box binding homeobox 1) associated with sub-type PPCD3; OVOL2 (ovol-like zinc finger 2) associated...
16.
Frausto R, Chung D, Boere P, Swamy V, Duong H, Kao L, et al.
PLoS One
. 2019 Jun;
14(6):e0218279.
PMID: 31194824
The zinc finger e-box binding homeobox 1 (ZEB1) transcription factor is a master regulator of the epithelial to mesenchymal transition (EMT), and of the reverse mesenchymal to epithelial transition (MET)...
17.
Modabber M, Darvish-Zargar M, Breton L, Chung D, Duong H, Aldave A, et al.
Cornea
. 2018 Dec;
38(5):635-638.
PMID: 30575622
Purpose: To report an unusual case of bilateral crystalline keratopathy presenting several years after a laser in situ keratomileusis (LASIK) procedure. Methods: Case report and review of the literature. Results:...
18.
Epithelial Recurrent Erosion Dystrophy Secondary to COL17A1 c.3156C>T Mutation in a Non-white Family
Vahedi F, Chung D, Gee K, Chuephanich P, Aldave A
Cornea
. 2018 May;
37(7):909-911.
PMID: 29708937
Purpose: To report the identification of the collagen, type XVII, alpha 1 (COL17A1) c.3156C>T mutation associated with epithelial recurrent erosion dystrophy (ERED) in a Thai family. Methods: Slit-lamp examination was...
19.
Zakharevich M, Kattan J, Chen J, Lin B, Cervantes A, Chung D, et al.
Mol Vis
. 2017 Oct;
23:740-752.
PMID: 29046608
Purpose: To investigate the functional role that the () gene, which underlies the genetic basis of posterior polymorphous corneal dystrophy 3 (PPCD3), plays in corneal endothelial cell proliferation, apoptosis, migration,...
20.
Chung D, Frausto R, Lin B, Hanser E, Cohen Z, Aldave A
Invest Ophthalmol Vis Sci
. 2017 Jun;
58(7):3202-3214.
PMID: 28654985
Purpose: To investigate the molecular basis of posterior polymorphous corneal dystrophy (PPCD) by examining the PPCD transcriptome and the effect of decreased ZEB1 expression on corneal endothelial cell (CEnC) gene...