These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 26749309)

  • 1. Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2.
    Davidson AE; Liskova P; Evans CJ; Dudakova L; Nosková L; Pontikos N; Hartmannová H; Hodaňová K; Stránecký V; Kozmík Z; Levis HJ; Idigo N; Sasai N; Maher GJ; Bellingham J; Veli N; Ebenezer ND; Cheetham ME; Daniels JT; Thaung CM; Jirsova K; Plagnol V; Filipec M; Kmoch S; Tuft SJ; Hardcastle AJ
    Am J Hum Genet; 2016 Jan; 98(1):75-89. PubMed ID: 26749309
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4.
    Liskova P; Dudakova L; Evans CJ; Rojas Lopez KE; Pontikos N; Athanasiou D; Jama H; Sach J; Skalicka P; Stranecky V; Kmoch S; Thaung C; Filipec M; Cheetham ME; Davidson AE; Tuft SJ; Hardcastle AJ
    Am J Hum Genet; 2018 Mar; 102(3):447-459. PubMed ID: 29499165
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ovol2 promoter mutations in mice and human illuminate species-specific phenotypic divergence.
    Sunny SS; Lachova J; Kasparek P; Palkova M; Spoutil F; Prochazka J; Sedlacek R; Liskova P; Kozmik Z
    Hum Mol Genet; 2024 Feb; 33(6):491-500. PubMed ID: 37971355
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval.
    Aldave AJ; Yellore VS; Vo RC; Kamal KM; Rayner SA; Plaisier CL; Chen MC; Damani MR; Pham MN; Gorin MB; Sobel E; Papp J
    Cornea; 2009 Aug; 28(7):801-7. PubMed ID: 19574904
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Identification of Potentially Pathogenic Variants in the Posterior Polymorphous Corneal Dystrophy 1 Locus.
    Le DJ; Chung DW; Frausto RF; Kim MJ; Aldave AJ
    PLoS One; 2016; 11(6):e0158467. PubMed ID: 27355326
    [TBL] [Abstract][Full Text] [Related]  

  • 10. c.-61G>A in OVOL2 is a Pathogenic 5' Untranslated Region Variant Causing Posterior Polymorphous Corneal Dystrophy 1.
    Janeschitz-Kriegl L; Kamdar D; Quinodoz M; Kaminska K; Folcher M; György B; Meyer P; Wild A; Escher P; Scholl HPN; Rivolta C; Goldblum D
    Cornea; 2022 Jan; 41(1):89-94. PubMed ID: 34469340
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Genetics of the corneal endothelial dystrophies: an evidence-based review.
    Aldave AJ; Han J; Frausto RF
    Clin Genet; 2013 Aug; 84(2):109-19. PubMed ID: 23662738
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Update on the genetics of corneal endothelial dystrophies.
    Kannabiran C; Chaurasia S; Ramappa M; Mootha VV
    Indian J Ophthalmol; 2022 Jul; 70(7):2239-2248. PubMed ID: 35791103
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. CUGC for posterior polymorphous corneal dystrophy (PPCD).
    Davidson AE; Hafford-Tear NJ; Dudakova L; Sadan AN; Pontikos N; Hardcastle AJ; Tuft SJ; Liskova P
    Eur J Hum Genet; 2020 Jan; 28(1):126-131. PubMed ID: 31201376
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association of a Chromosomal Rearrangement Event with Mouse Posterior Polymorphous Corneal Dystrophy and Alterations in Csrp2bp, Dzank1, and Ovol2 Gene Expression.
    Shen AL; Moran SA; Glover EA; Drinkwater NR; Swearingen RE; Teixeira LB; Bradfield CA
    PLoS One; 2016; 11(6):e0157577. PubMed ID: 27310661
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.