151 related articles for article (PubMed ID: 36613650)
1. Posterior Polymorphous Corneal Dystrophy in a Patient with a Novel
Fernández-Gutiérrez E; Fernández-Pérez P; Boto-De-Los-Bueis A; García-Fernández L; Rodríguez-Solana P; Solís M; Vallespín E
Int J Mol Sci; 2022 Dec; 24(1):. PubMed ID: 36613650
[TBL] [Abstract][Full Text] [Related]
2. Alterations in GRHL2-OVOL2-ZEB1 axis and aberrant activation of Wnt signaling lead to altered gene transcription in posterior polymorphous corneal dystrophy.
Chung DD; Zhang W; Jatavallabhula K; Barrington A; Jung J; Aldave AJ
Exp Eye Res; 2019 Nov; 188():107696. PubMed ID: 31233731
[TBL] [Abstract][Full Text] [Related]
3. Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation.
Lechner J; Dash DP; Muszynska D; Hosseini M; Segev F; George S; Frazer DG; Moore JE; Kaye SB; Young T; Simpson DA; Churchill AJ; Héon E; Willoughby CE
Invest Ophthalmol Vis Sci; 2013 May; 54(5):3215-23. PubMed ID: 23599324
[TBL] [Abstract][Full Text] [Related]
4. Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells.
Krafchak CM; Pawar H; Moroi SE; Sugar A; Lichter PR; Mackey DA; Mian S; Nairus T; Elner V; Schteingart MT; Downs CA; Kijek TG; Johnson JM; Trager EH; Rozsa FW; Mandal MN; Epstein MP; Vollrath D; Ayyagari R; Boehnke M; Richards JE
Am J Hum Genet; 2005 Nov; 77(5):694-708. PubMed ID: 16252232
[TBL] [Abstract][Full Text] [Related]
5. Further genetic and clinical insights of posterior polymorphous corneal dystrophy 3.
Liskova P; Palos M; Hardcastle AJ; Vincent AL
JAMA Ophthalmol; 2013 Oct; 131(10):1296-303. PubMed ID: 23807282
[TBL] [Abstract][Full Text] [Related]
6. Unusual presentation of presumed posterior polymorphous dystrophy associated with iris heterochromia, band keratopathy, and keratoconus.
Lam HY; Wiggs JL; Jurkunas UV
Cornea; 2010 Oct; 29(10):1180-5. PubMed ID: 20567203
[TBL] [Abstract][Full Text] [Related]
7. Transcriptomic Profiling of Posterior Polymorphous Corneal Dystrophy.
Chung DD; Frausto RF; Lin BR; Hanser EM; Cohen Z; Aldave AJ
Invest Ophthalmol Vis Sci; 2017 Jun; 58(7):3202-3214. PubMed ID: 28654985
[TBL] [Abstract][Full Text] [Related]
8. Zeb1 mutant mice as a model of posterior corneal dystrophy.
Liu Y; Peng X; Tan J; Darling DS; Kaplan HJ; Dean DC
Invest Ophthalmol Vis Sci; 2008 May; 49(5):1843-9. PubMed ID: 18436818
[TBL] [Abstract][Full Text] [Related]
9. Variable ocular phenotypes of posterior polymorphous corneal dystrophy caused by mutations in the ZEB1 gene.
Liskova P; Filipec M; Merjava S; Jirsova K; Tuft SJ
Ophthalmic Genet; 2010 Dec; 31(4):230-4. PubMed ID: 21067486
[TBL] [Abstract][Full Text] [Related]
10. Classification of posterior polymorphous corneal dystrophy as a corneal ectatic disorder following confirmation of associated significant corneal steepening.
Aldave AJ; Ann LB; Frausto RF; Nguyen CK; Yu F; Raber IM
JAMA Ophthalmol; 2013 Dec; 131(12):1583-90. PubMed ID: 24113819
[TBL] [Abstract][Full Text] [Related]
11. Posterior polymorphous corneal dystrophy 3 is associated with agenesis and hypoplasia of the corpus callosum.
Jang MS; Roldan AN; Frausto RF; Aldave AJ
Vision Res; 2014 Jul; 100():88-92. PubMed ID: 24780443
[TBL] [Abstract][Full Text] [Related]
12. Clinical phenotype of posterior polymorphous corneal dystrophy in a family with a novel ZEB1 mutation.
Nguyen DQ; Hosseini M; Billingsley G; Héon E; Churchill AJ
Acta Ophthalmol; 2010 Sep; 88(6):695-9. PubMed ID: 19432861
[TBL] [Abstract][Full Text] [Related]
13. Phenotypic characterisation and ZEB1 mutational analysis in posterior polymorphous corneal dystrophy in a New Zealand population.
Vincent AL; Niederer RL; Richards A; Karolyi B; Patel DV; McGhee CN
Mol Vis; 2009 Dec; 15():2544-53. PubMed ID: 19997581
[TBL] [Abstract][Full Text] [Related]
14. Functional impact of ZEB1 mutations associated with posterior polymorphous and Fuchs' endothelial corneal dystrophies.
Chung DW; Frausto RF; Ann LB; Jang MS; Aldave AJ
Invest Ophthalmol Vis Sci; 2014 Sep; 55(10):6159-66. PubMed ID: 25190660
[TBL] [Abstract][Full Text] [Related]
15. Exclusion of pathogenic promoter region variants and identification of novel nonsense mutations in the zinc finger E-box binding homeobox 1 gene in posterior polymorphous corneal dystrophy.
Bakhtiari P; Frausto RF; Roldan AN; Wang C; Yu F; Aldave AJ
Mol Vis; 2013; 19():575-80. PubMed ID: 23559851
[TBL] [Abstract][Full Text] [Related]
16. ZEB1 insufficiency causes corneal endothelial cell state transition and altered cellular processing.
Frausto RF; Chung DD; Boere PM; Swamy VS; Duong HNV; Kao L; Azimov R; Zhang W; Carrigan L; Wong D; Morselli M; Zakharevich M; Hanser EM; Kassels AC; Kurtz I; Pellegrini M; Aldave AJ
PLoS One; 2019; 14(6):e0218279. PubMed ID: 31194824
[TBL] [Abstract][Full Text] [Related]
17. Analysis of the role of ZEB1 in the pathogenesis of posterior polymorphous corneal dystrophy.
Yellore VS; Rayner SA; Nguyen CK; Gangalum RK; Jing Z; Bhat SP; Aldave AJ
Invest Ophthalmol Vis Sci; 2012 Jan; 53(1):273-8. PubMed ID: 22199242
[TBL] [Abstract][Full Text] [Related]
18. Confirmation of the OVOL2 Promoter Mutation c.-307T>C in Posterior Polymorphous Corneal Dystrophy 1.
Chung DD; Frausto RF; Cervantes AE; Gee KM; Zakharevich M; Hanser EM; Stone EM; Heon E; Aldave AJ
PLoS One; 2017; 12(1):e0169215. PubMed ID: 28046031
[TBL] [Abstract][Full Text] [Related]
19. Heterozygous deletions at the ZEB1 locus verify haploinsufficiency as the mechanism of disease for posterior polymorphous corneal dystrophy type 3.
Liskova P; Evans CJ; Davidson AE; Zaliova M; Dudakova L; Trkova M; Stranecky V; Carnt N; Plagnol V; Vincent AL; Tuft SJ; Hardcastle AJ
Eur J Hum Genet; 2016 Jul; 24(7):985-91. PubMed ID: 26508574
[TBL] [Abstract][Full Text] [Related]
20. The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis.
Dudakova L; Evans CJ; Pontikos N; Hafford-Tear NJ; Malinka F; Skalicka P; Horinek A; Munier FL; Voide N; Studeny P; Vanikova L; Kubena T; Rojas Lopez KE; Davidson AE; Hardcastle AJ; Tuft SJ; Liskova P
Exp Eye Res; 2019 May; 182():160-166. PubMed ID: 30851240
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]