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Journal Abstract Search

236 related items for PubMed ID: 24348007

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  • 3. Association of ZEB1 and TCF4 rs613872 changes with late onset Fuchs endothelial corneal dystrophy in patients from northern India.
    Gupta R, Kumawat BL, Paliwal P, Tandon R, Sharma N, Sen S, Kashyap S, Nag TC, Vajpayee RB, Sharma A.
    Mol Vis; 2015; 21():1252-60. PubMed ID: 26622166
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  • 4. Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India.
    Hemadevi B, Srinivasan M, Arunkumar J, Prajna NV, Sundaresan P.
    BMC Ophthalmol; 2010 Feb 10; 10():3. PubMed ID: 20144242
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  • 6. Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy.
    Igo RP, Kopplin LJ, Joseph P, Truitt B, Fondran J, Bardenstein D, Aldave AJ, Croasdale CR, Price MO, Rosenwasser M, Lass JH, Iyengar SK, FECD Genetics Multi-center Study Group.
    PLoS One; 2012 Feb 10; 7(10):e46742. PubMed ID: 23110055
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  • 7. Coexistence of Congenital Hereditary Endothelial Dystrophy and Fuchs Endothelial Corneal Dystrophy Associated With SLC4A11 Mutations in Affected Families.
    Chaurasia S, Ramappa M, Annapurna M, Kannabiran C.
    Cornea; 2020 Mar 10; 39(3):354-357. PubMed ID: 31714402
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  • 8. Q455V mutation in COL8A2 is associated with Fuchs' corneal dystrophy in Korean patients.
    Mok JW, Kim HS, Joo CK.
    Eye (Lond); 2009 Apr 10; 23(4):895-903. PubMed ID: 18464802
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  • 9. 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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  • 10. 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 May 03; 36(3):284-6. PubMed ID: 24502824
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  • 11. Analysis of COL8A2 gene mutation in Japanese patients with Fuchs' endothelial dystrophy and posterior polymorphous dystrophy.
    Kobayashi A, Fujiki K, Murakami A, Kato T, Chen LZ, Onoe H, Nakayasu K, Sakurai M, Takahashi M, Sugiyama K, Kanai A.
    Jpn J Ophthalmol; 2004 May 03; 48(3):195-8. PubMed ID: 15175909
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  • 12. Analysis of candidate genes ZEB1 and LOXHD1 in late-onset Fuchs' endothelial corneal dystrophy in an Indian cohort.
    Rao BS, Ansar S, Arokiasamy T, Sudhir RR, Umashankar V, Rajagopal R, Soumittra N.
    Ophthalmic Genet; 2018 Aug 03; 39(4):443-449. PubMed ID: 29799290
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  • 13. SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
    Vithana EN, Morgan PE, Ramprasad V, Tan DT, Yong VH, Venkataraman D, Venkatraman A, Yam GH, Nagasamy S, Law RW, Rajagopal R, Pang CP, Kumaramanickevel G, Casey JR, Aung T.
    Hum Mol Genet; 2008 Mar 01; 17(5):656-66. PubMed ID: 18024964
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  • 15. Loss of ion transporters and increased unfolded protein response in Fuchs' dystrophy.
    Jalimarada SS, Ogando DG, Bonanno JA.
    Mol Vis; 2014 Mar 01; 20():1668-79. PubMed ID: 25548511
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  • 16. Update on the genetics of corneal endothelial dystrophies.
    Kannabiran C, Chaurasia S, Ramappa M, Mootha VV.
    Indian J Ophthalmol; 2022 Jul 01; 70(7):2239-2248. PubMed ID: 35791103
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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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  • 18. 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 04; 55(10):6159-66. PubMed ID: 25190660
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  • 19. Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutations.
    Vilas GL, Loganathan SK, Quon A, Sundaresan P, Vithana EN, Casey J.
    Hum Mutat; 2012 Feb 04; 33(2):419-28. PubMed ID: 22072594
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  • 20. L450W and Q455K Col8a2 knock-in mouse models of Fuchs endothelial corneal dystrophy show distinct phenotypes and evidence for altered autophagy.
    Meng H, Matthaei M, Ramanan N, Grebe R, Chakravarti S, Speck CL, Kimos M, Vij N, Eberhart CG, Jun AS.
    Invest Ophthalmol Vis Sci; 2013 Mar 28; 54(3):1887-97. PubMed ID: 23422828
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