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Journal Abstract Search


130 related items for PubMed ID: 19553609

  • 1. Contribution of copy number variation in the regulation of complement activation locus to development of age-related macular degeneration.
    Schmid-Kubista KE, Tosakulwong N, Wu Y, Ryu E, Hecker LA, Baratz KH, Brown WL, Edwards AO.
    Invest Ophthalmol Vis Sci; 2009 Nov; 50(11):5070-9. PubMed ID: 19553609
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  • 3. Deletion of CFHR3 and CFHR1 genes in age-related macular degeneration.
    Spencer KL, Hauser MA, Olson LM, Schmidt S, Scott WK, Gallins P, Agarwal A, Postel EA, Pericak-Vance MA, Haines JL.
    Hum Mol Genet; 2008 Apr 01; 17(7):971-7. PubMed ID: 18084039
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  • 4. Copy number variation in the complement factor H-related genes and age-related macular degeneration.
    Kubista KE, Tosakulwong N, Wu Y, Ryu E, Roeder JL, Hecker LA, Baratz KH, Brown WL, Edwards AO.
    Mol Vis; 2011 Apr 01; 17():2080-92. PubMed ID: 21850184
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  • 5. A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration.
    Hughes AE, Orr N, Esfandiary H, Diaz-Torres M, Goodship T, Chakravarthy U.
    Nat Genet; 2006 Oct 01; 38(10):1173-7. PubMed ID: 16998489
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  • 6. Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration.
    Ansari M, McKeigue PM, Skerka C, Hayward C, Rudan I, Vitart V, Polasek O, Armbrecht AM, Yates JR, Vatavuk Z, Bencic G, Kolcic I, Oostra BA, Van Duijn CM, Campbell S, Stanton CM, Huffman J, Shu X, Khan JC, Shahid H, Harding SP, Bishop PN, Deary IJ, Moore AT, Dhillon B, Rudan P, Zipfel PF, Sim RB, Hastie ND, Campbell H, Wright AF.
    Hum Mol Genet; 2013 Dec 01; 22(23):4857-69. PubMed ID: 23873044
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  • 9. Analysis of the Y402H variant of the complement factor H gene in age-related macular degeneration.
    Baird PN, Islam FM, Richardson AJ, Cain M, Hunt N, Guymer R.
    Invest Ophthalmol Vis Sci; 2006 Oct 01; 47(10):4194-8. PubMed ID: 17003406
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  • 11. Atypical hemolytic uremic syndrome associated with complement factor H autoantibodies and CFHR1/CFHR3 deficiency.
    Lee BH, Kwak SH, Shin JI, Lee SH, Choi HJ, Kang HG, Ha IS, Lee JS, Dragon-Durey MA, Choi Y, Cheong HI.
    Pediatr Res; 2009 Sep 01; 66(3):336-40. PubMed ID: 19531976
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  • 13. Association study of complement factor H, C2, CFB, and C3 and age-related macular degeneration in a Han Chinese population.
    Liu X, Zhao P, Tang S, Lu F, Hu J, Lei C, Yang X, Lin Y, Ma S, Yang J, Zhang D, Shi Y, Li T, Chen Y, Fan Y, Yang Z.
    Retina; 2010 Sep 01; 30(8):1177-84. PubMed ID: 20523265
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  • 14. Associations of CFHR1-CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent.
    Raychaudhuri S, Ripke S, Li M, Neale BM, Fagerness J, Reynolds R, Sobrin L, Swaroop A, Abecasis G, Seddon JM, Daly MJ.
    Nat Genet; 2010 Jul 01; 42(7):553-5; author reply 555-6. PubMed ID: 20581873
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  • 16. Genetic deficiency of complement factor H in a patient with age-related macular degeneration and membranoproliferative glomerulonephritis.
    Montes T, Goicoechea de Jorge E, Ramos R, Gomà M, Pujol O, Sánchez-Corral P, Rodríguez de Córdoba S.
    Mol Immunol; 2008 May 01; 45(10):2897-904. PubMed ID: 18336910
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  • 17. Extended haplotypes in the complement factor H (CFH) and CFH-related (CFHR) family of genes protect against age-related macular degeneration: characterization, ethnic distribution and evolutionary implications.
    Hageman GS, Hancox LS, Taiber AJ, Gehrs KM, Anderson DH, Johnson LV, Radeke MJ, Kavanagh D, Richards A, Atkinson J, Meri S, Bergeron J, Zernant J, Merriam J, Gold B, Allikmets R, Dean M, AMD Clinical Study Group.
    Ann Med; 2006 May 01; 38(8):592-604. PubMed ID: 17438673
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  • 18. Complement factor H, FHR-3 and FHR-1 variants associate in an extended haplotype conferring increased risk of atypical hemolytic uremic syndrome.
    Bernabéu-Herrero ME, Jiménez-Alcázar M, Anter J, Pinto S, Sánchez Chinchilla D, Garrido S, López-Trascasa M, Rodríguez de Córdoba S, Sánchez-Corral P.
    Mol Immunol; 2015 Oct 01; 67(2 Pt B):276-86. PubMed ID: 26163426
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