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Journal Abstract Search

297 related items for PubMed ID: 16281287

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  • 3. A user's guide to the interactive Web database of factor H-associated hemolytic uremic syndrome.
    Saunders RE, Perkins SJ.
    Semin Thromb Hemost; 2006 Mar; 32(2):160-8. PubMed ID: 16575691
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  • 5. Hemolytic uremic syndrome: a factor H mutation (E1172Stop) causes defective complement control at the surface of endothelial cells.
    Heinen S, Józsi M, Hartmann A, Noris M, Remuzzi G, Skerka C, Zipfel PF.
    J Am Soc Nephrol; 2007 Feb; 18(2):506-14. PubMed ID: 17229916
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  • 7. De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome.
    Heinen S, Sanchez-Corral P, Jackson MS, Strain L, Goodship JA, Kemp EJ, Skerka C, Jokiranta TS, Meyers K, Wagner E, Robitaille P, Esparza-Gordillo J, Rodriguez de Cordoba S, Zipfel PF, Goodship TH.
    Hum Mutat; 2006 Mar; 27(3):292-3. PubMed ID: 16470555
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  • 8. Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome.
    Sellier-Leclerc AL, Fremeaux-Bacchi V, Dragon-Durey MA, Macher MA, Niaudet P, Guest G, Boudailliez B, Bouissou F, Deschenes G, Gie S, Tsimaratos M, Fischbach M, Morin D, Nivet H, Alberti C, Loirat C, French Society of Pediatric Nephrology.
    J Am Soc Nephrol; 2007 Aug; 18(8):2392-400. PubMed ID: 17599974
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  • 10. Comparison of surface recognition and C3b binding properties of mouse and human complement factor H.
    Cheng ZZ, Hellwage J, Seeberger H, Zipfel PF, Meri S, Jokiranta TS.
    Mol Immunol; 2006 Mar; 43(7):972-9. PubMed ID: 16023208
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  • 13. Structural analysis of eight novel and 112 previously reported missense mutations in the interactive FXI mutation database reveals new insight on FXI deficiency.
    Saunders RE, Shiltagh N, Gomez K, Mellars G, Cooper C, Perry DJ, Tuddenham EG, Perkins SJ.
    Thromb Haemost; 2009 Aug; 102(2):287-301. PubMed ID: 19652879
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  • 14. The effect of electrostatics on factor H function and related pathologies.
    Kieslich CA, Vazquez H, Goodman GN, López de Victoria A, Morikis D.
    J Mol Graph Model; 2011 Aug; 29(8):1047-55. PubMed ID: 21605993
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  • 15. The autoimmune disease DEAP-hemolytic uremic syndrome.
    Skerka C, Zipfel PF, Müller D, Micklisch S, Riedl M, Zimmerhackl LB, Hofer J.
    Semin Thromb Hemost; 2010 Sep; 36(6):625-32. PubMed ID: 20865639
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  • 18. Impact of compound heterozygous complement factor H mutations on development of atypical hemolytic uremic syndrome-A pedigree revisited.
    Johnson SA, Williams JM, Hakobyan S, Richards A, Perkins SJ, Marchbank KJ, Goodship TH, Morgan BP, Taylor CM, Savage CO.
    Mol Immunol; 2010 Apr; 47(7-8):1585-91. PubMed ID: 20304497
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  • 19. The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts.
    Fremeaux-Bacchi V, Kemp EJ, Goodship JA, Dragon-Durey MA, Strain L, Loirat C, Deng HW, Goodship TH.
    J Med Genet; 2005 Nov; 42(11):852-6. PubMed ID: 15784724
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  • 20. The spectrum of phenotypes caused by variants in the CFH gene.
    Boon CJ, van de Kar NC, Klevering BJ, Keunen JE, Cremers FP, Klaver CC, Hoyng CB, Daha MR, den Hollander AI.
    Mol Immunol; 2009 May; 46(8-9):1573-94. PubMed ID: 19297022
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