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Journal Abstract Search

332 related items for PubMed ID: 27121161

  • 1. 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
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  • 3. Genetic screen of African Americans with Fuchs endothelial corneal dystrophy.
    Minear MA, Li YJ, Rimmler J, Balajonda E, Watson S, Allingham RR, Hauser MA, Klintworth GK, Afshari NA, Gregory SG.
    Mol Vis; 2013 Jun; 19():2508-16. PubMed ID: 24348007
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  • 6. 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 03; 54(5):3215-23. PubMed ID: 23599324
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  • 7. [TGC Repeats in Intron 2 of the TCF4 Gene have a Good Predictive Power Regarding to Fuchs Endothelial Corneal Dystrophy].
    Luther M, Grünauer-Kloevekorn C, Weidle E, Passarge E, Rupprecht A, Hoffmann K, Foja S.
    Klin Monbl Augenheilkd; 2016 Feb 03; 233(2):187-94. PubMed ID: 26280645
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  • 13. Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophy.
    Riazuddin SA, Vithana EN, Seet LF, Liu Y, Al-Saif A, Koh LW, Heng YM, Aung T, Meadows DN, Eghrari AO, Gottsch JD, Katsanis N.
    Hum Mutat; 2010 Nov 03; 31(11):1261-8. PubMed ID: 20848555
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  • 14. Fuchs Endothelial Corneal Dystrophy in a Heterozygous Carrier of Congenital Hereditary Endothelial Dystrophy Type 2 with a Novel Mutation in SLC4A11.
    Kim JH, Ko JM, Tchah H.
    Ophthalmic Genet; 2015 Nov 03; 36(3):284-6. PubMed ID: 24502824
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  • 15. Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy.
    Riazuddin SA, Parker DS, McGlumphy EJ, Oh EC, Iliff BW, Schmedt T, Jurkunas U, Schleif R, Katsanis N, Gottsch JD.
    Am J Hum Genet; 2012 Mar 09; 90(3):533-9. PubMed ID: 22341973
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  • 17. CTG18.1 Expansion is the Best Classifier of Late-Onset Fuchs' Corneal Dystrophy Among 10 Biomarkers in a Cohort From the European Part of Russia.
    Skorodumova LO, Belodedova AV, Antonova OP, Sharova EI, Akopian TA, Selezneva OV, Kostryukova ES, Malyugin BE.
    Invest Ophthalmol Vis Sci; 2018 Sep 04; 59(11):4748-4754. PubMed ID: 30267097
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  • 20. Association of common variants in TCF4 and PTPRG with Fuchs' corneal dystrophy: a systematic review and meta-analysis.
    Lau LC, Ma L, Young AL, Rong SS, Jhanji V, Brelen ME, Pang CP, Chen LJ.
    PLoS One; 2014 Sep 04; 9(10):e109142. PubMed ID: 25299301
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