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Journal Abstract Search

437 related items for PubMed ID: 20843825

  • 1. An imbalance of human complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age-related macular degeneration (AMD).
    Fritsche LG, Lauer N, Hartmann A, Stippa S, Keilhauer CN, Oppermann M, Pandey MK, Köhl J, Zipfel PF, Weber BH, Skerka C.
    Hum Mol Genet; 2010 Dec 01; 19(23):4694-704. PubMed ID: 20843825
    [Abstract] [Full Text] [Related]

  • 2. 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 01; 50(11):5070-9. PubMed ID: 19553609
    [Abstract] [Full Text] [Related]

  • 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. 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
    [Abstract] [Full Text] [Related]

  • 5. 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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  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Relevance of complement factor H-related 1 (CFHR1) genotypes in age-related macular degeneration.
    Martínez-Barricarte R, Recalde S, Fernández-Robredo P, Millán I, Olavarrieta L, Viñuela A, Pérez-Pérez J, García-Layana A, Rodríguez de Córdoba S, Spanish Multicenter Group on AMD.
    Invest Ophthalmol Vis Sci; 2012 Mar 01; 53(3):1087-94. PubMed ID: 22247456
    [Abstract] [Full Text] [Related]

  • 9. 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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  • 10. 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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  • 12. 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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  • 13. A genome-wide association study identifies key modulators of complement factor H binding to malondialdehyde-epitopes.
    Alic L, Papac-Milicevic N, Czamara D, Rudnick RB, Ozsvar-Kozma M, Hartmann A, Gurbisz M, Hoermann G, Haslinger-Hutter S, Zipfel PF, Skerka C, Binder EB, Binder CJ.
    Proc Natl Acad Sci U S A; 2020 May 05; 117(18):9942-9951. PubMed ID: 32321835
    [Abstract] [Full Text] [Related]

  • 14. Variants in Complement Factor H and Complement Factor H-Related Protein Genes, CFHR3 and CFHR1, Affect Complement Activation in IgA Nephropathy.
    Zhu L, Zhai YL, Wang FM, Hou P, Lv JC, Xu DM, Shi SF, Liu LJ, Yu F, Zhao MH, Novak J, Gharavi AG, Zhang H.
    J Am Soc Nephrol; 2015 May 05; 26(5):1195-204. PubMed ID: 25205734
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  • 15. Complement factor H and hemicentin-1 in age-related macular degeneration and renal phenotypes.
    Thompson CL, Klein BE, Klein R, Xu Z, Capriotti J, Joshi T, Leontiev D, Lee KE, Elston RC, Iyengar SK.
    Hum Mol Genet; 2007 Sep 01; 16(17):2135-48. PubMed ID: 17591627
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  • 17. Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome.
    Zipfel PF, Edey M, Heinen S, Józsi M, Richter H, Misselwitz J, Hoppe B, Routledge D, Strain L, Hughes AE, Goodship JA, Licht C, Goodship TH, Skerka C.
    PLoS Genet; 2007 Mar 16; 3(3):e41. PubMed ID: 17367211
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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 16; 67(2 Pt B):276-86. PubMed ID: 26163426
    [Abstract] [Full Text] [Related]

  • 19. Associations of CFH polymorphisms and CFHR1-CFHR3 deletion with blood pressure and hypertension in Chinese population.
    Gan W, Wu J, Lu L, Xiao X, Huang H, Wang F, Zhu J, Sun L, Liu G, Pan Y, Li H, Lin X, Chen Y.
    PLoS One; 2012 Oct 16; 7(7):e42010. PubMed ID: 22848687
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  • 20. Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome.
    Abarrategui-Garrido C, Martínez-Barricarte R, López-Trascasa M, de Córdoba SR, Sánchez-Corral P.
    Blood; 2009 Nov 05; 114(19):4261-71. PubMed ID: 19745068
    [Abstract] [Full Text] [Related]

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