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Journal Abstract Search

389 related items for PubMed ID: 18081690

  • 1. Translational mini-review series on complement factor H: genetics and disease associations of human complement factor H.
    de Córdoba SR, de Jorge EG.
    Clin Exp Immunol; 2008 Jan; 151(1):1-13. PubMed ID: 18081690
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  • 3. Translational mini-review series on complement factor H: therapies of renal diseases associated with complement factor H abnormalities: atypical haemolytic uraemic syndrome and membranoproliferative glomerulonephritis.
    Noris M, Remuzzi G.
    Clin Exp Immunol; 2008 Feb; 151(2):199-209. PubMed ID: 18070148
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  • 6. The complement fitness factor H: role in human diseases and for immune escape of pathogens, like pneumococci.
    Zipfel PF, Hallström T, Hammerschmidt S, Skerka C.
    Vaccine; 2008 Dec 30; 26 Suppl 8():I67-74. PubMed ID: 19388168
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  • 8. Factor H family proteins and human diseases.
    Józsi M, Zipfel PF.
    Trends Immunol; 2008 Aug 30; 29(8):380-7. PubMed ID: 18602340
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  • 9. Membrano-proliferative glomerulonephritis, atypical hemolytic uremic syndrome, and a new complement factor H mutation: report of a case.
    Gnappi E, Allinovi M, Vaglio A, Bresin E, Sorosina A, Pilato FP, Allegri L, Manenti L.
    Pediatr Nephrol; 2012 Oct 30; 27(10):1995-9. PubMed ID: 22669321
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  • 12. The role of complement in AMD.
    Zipfel PF, Lauer N, Skerka C.
    Adv Exp Med Biol; 2010 Oct 30; 703():9-24. PubMed ID: 20711704
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  • 13. Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome.
    Servais A, Frémeaux-Bacchi V, Lequintrec M, Salomon R, Blouin J, Knebelmann B, Grünfeld JP, Lesavre P, Noël LH, Fakhouri F.
    J Med Genet; 2007 Mar 30; 44(3):193-9. PubMed ID: 17018561
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  • 14. Genotype-phenotype correlations of low-frequency variants in the complement system in renal disease and age-related macular degeneration.
    Geerlings MJ, Volokhina EB, de Jong EK, van de Kar N, Pauper M, Hoyng CB, van den Heuvel LP, den Hollander AI.
    Clin Genet; 2018 Oct 30; 94(3-4):330-338. PubMed ID: 29888403
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  • 15. Functional Characterization of Rare Genetic Variants in the N-Terminus of Complement Factor H in aHUS, C3G, and AMD.
    Wong EKS, Hallam TM, Brocklebank V, Walsh PR, Smith-Jackson K, Shuttleworth VG, Cox TE, Anderson HE, Barlow PN, Marchbank KJ, Harris CL, Kavanagh D.
    Front Immunol; 2020 Oct 30; 11():602284. PubMed ID: 33519811
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  • 16. The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models.
    Saunders RE, Abarrategui-Garrido C, Frémeaux-Bacchi V, Goicoechea de Jorge E, Goodship TH, López Trascasa M, Noris M, Ponce Castro IM, Remuzzi G, Rodríguez de Córdoba S, Sánchez-Corral P, Skerka C, Zipfel PF, Perkins SJ.
    Hum Mutat; 2007 Mar 30; 28(3):222-34. PubMed ID: 17089378
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  • 18. Complement factor H related proteins (CFHRs).
    Skerka C, Chen Q, Fremeaux-Bacchi V, Roumenina LT.
    Mol Immunol; 2013 Dec 15; 56(3):170-80. PubMed ID: 23830046
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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
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