173 related articles for article (PubMed ID: 17437275)
1. Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy.
Liskova P; Tuft SJ; Gwilliam R; Ebenezer ND; Jirsova K; Prescott Q; Martincova R; Pretorius M; Sinclair N; Boase DL; Jeffrey MJ; Deloukas P; Hardcastle AJ; Filipec M; Bhattacharya SS
Hum Mutat; 2007 Jun; 28(6):638. PubMed ID: 17437275
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. Identification of six novel mutations in ZEB1 and description of the associated phenotypes in patients with posterior polymorphous corneal dystrophy 3.
Evans CJ; Liskova P; Dudakova L; Hrabcikova P; Horinek A; Jirsova K; Filipec M; Hardcastle AJ; Davidson AE; Tuft SJ
Ann Hum Genet; 2015 Jan; 79(1):1-9. PubMed ID: 25441224
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Posterior polymorphous corneal dystrophy in Czech families maps to chromosome 20 and excludes the VSX1 gene.
Gwilliam R; Liskova P; Filipec M; Kmoch S; Jirsova K; Huckle EJ; Stables CL; Bhattacharya SS; Hardcastle AJ; Deloukas P; Ebenezer ND
Invest Ophthalmol Vis Sci; 2005 Dec; 46(12):4480-4. PubMed ID: 16303937
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal hernia.
Aldave AJ; Yellore VS; Yu F; Bourla N; Sonmez B; Salem AK; Rayner SA; Sampat KM; Krafchak CM; Richards JE
Am J Med Genet A; 2007 Nov; 143A(21):2549-56. PubMed ID: 17935237
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Analysis of SLC4A11, ZEB1, LOXHD1, COL8A2 and TCF4 gene sequences in a multi-generational family with late-onset Fuchs corneal dystrophy.
Tang H; Zhang W; Yan XM; Wang LP; Dong H; Shou T; Lei H; Guo Q
Int J Mol Med; 2016 Jun; 37(6):1487-500. PubMed ID: 27121161
[TBL] [Abstract][Full Text] [Related]
17. High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutation.
Liskova P; Gwilliam R; Filipec M; Jirsova K; Reinstein Merjava S; Deloukas P; Webb TR; Bhattacharya SS; Ebenezer ND; Morris AG; Hardcastle AJ
PLoS One; 2012; 7(9):e45495. PubMed ID: 23049806
[TBL] [Abstract][Full Text] [Related]
18. Screening the visual system homeobox 1 gene in keratoconus and posterior polymorphous dystrophy cohorts identifies a novel variant.
Vincent AL; Jordan C; Sheck L; Niederer R; Patel DV; McGhee CN
Mol Vis; 2013; 19():852-60. PubMed ID: 23592923
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Genetic analysis of chromosome 20-related posterior polymorphous corneal dystrophy: genetic heterogeneity and exclusion of three candidate genes.
Hosseini SM; Herd S; Vincent AL; Héon E
Mol Vis; 2008 Jan; 14():71-80. PubMed ID: 18253095
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]