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161 related items for PubMed ID: 8871666

  • 1. Molecular bases of combined subtotal deficiencies of C6 and C7: their effects in combination with other C6 and C7 deficiencies.
    Fernie BA, Würzner R, Orren A, Morgan BP, Potter PC, Platonov AE, Vershinina IV, Shipulin GA, Lachmann PJ, Hobart MJ.
    J Immunol; 1996 Oct 15; 157(8):3648-57. PubMed ID: 8871666
    [Abstract] [Full Text] [Related]

  • 2. Molecular bases of C7 deficiency: three different defects.
    Fernie BA, Orren A, Sheehan G, Schlesinger M, Hobart MJ.
    J Immunol; 1997 Jul 15; 159(2):1019-26. PubMed ID: 9218625
    [Abstract] [Full Text] [Related]

  • 3. DNA haplotypes of the complement C6 and C7 genes associated with deficiencies of the seventh component; and a new DNA polymorphism in C7 exon 13.
    Fernie BA, Orren A, Schlesinger M, Würzner R, Platonov AE, Cooper RC, Williams YE, Hobart MJ.
    Ann Hum Genet; 1997 Jul 15; 61(Pt 4):287-98. PubMed ID: 9365782
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  • 5. Genetic detection of the silent allele (*Q0) in hereditary deficiencies of the human complement C6, C7, and C9 components.
    Alvarez V, Coto E, Setién F, Spath PJ, López-Larrea C.
    Am J Med Genet; 1995 Feb 13; 55(4):408-13. PubMed ID: 7762578
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  • 6. Combined genetic deficiency of C6 and C7 in man.
    Lachmann PJ, Hobart MJ, Woo P.
    Clin Exp Immunol; 1978 Aug 13; 33(2):193-203. PubMed ID: 102474
    [Abstract] [Full Text] [Related]

  • 7. The human complement C9 gene: identification of two mutations causing deficiency and revision of the gene structure.
    Witzel-Schlömp K, Späth PJ, Hobart MJ, Fernie BA, Rittner C, Kaufmann T, Schneider PM.
    J Immunol; 1997 May 15; 158(10):5043-9. PubMed ID: 9144525
    [Abstract] [Full Text] [Related]

  • 8. Structure of the human C7 gene and comparison with the C6, C8A, C8B, and C9 genes.
    Hobart MJ, Fernie BA, DiScipio RG.
    J Immunol; 1995 May 15; 154(10):5188-94. PubMed ID: 7730625
    [Abstract] [Full Text] [Related]

  • 9. Genetic bases of human complement C7 deficiency.
    Nishizaka H, Horiuchi T, Zhu ZB, Fukumori Y, Volanakis JE.
    J Immunol; 1996 Nov 01; 157(9):4239-43. PubMed ID: 8892662
    [Abstract] [Full Text] [Related]

  • 10. Molecular basis of subtotal complement C6 deficiency. A carboxy-terminally truncated but functionally active C6.
    Würzner R, Hobart MJ, Fernie BA, Mewar D, Potter PC, Orren A, Lachmann PJ.
    J Clin Invest; 1995 Apr 01; 95(4):1877-83. PubMed ID: 7535801
    [Abstract] [Full Text] [Related]

  • 11. Complement C6 and C7 DNA polymorphisms analysed by PCR in seven ethnic groups and characterisation of the C6 MspI RFLP.
    Fernie BA, Finlay A, Price D, Chan E, Orren A, Joysey VC, Joysey KA, Hobart MJ.
    Exp Clin Immunogenet; 1996 Apr 01; 13(2):92-103. PubMed ID: 9063701
    [Abstract] [Full Text] [Related]

  • 12. Hereditary complement C7 deficiency in nine families: subtotal C7 deficiency revisited.
    Rameix-Welti MA, Régnier CH, Bienaimé F, Blouin J, Schifferli J, Fridman WH, Sautès-Fridman C, Frémeaux-Bacchi V.
    Eur J Immunol; 2007 May 01; 37(5):1377-85. PubMed ID: 17407100
    [Abstract] [Full Text] [Related]

  • 13. [Genetic polymorphism of the sixth (C6) and seventh (C7) components of complement in Russian rural inhabitants of the Tomsk region].
    Kucher AN, Puzyrev VP, Ivanova OF, Khu TsIu, Siuĭ TsTs, Du ZhF.
    Genetika; 1993 Nov 01; 29(11):1889-94. PubMed ID: 8307376
    [Abstract] [Full Text] [Related]

  • 14. Three Japanese families with members carrying C7 silent allele (C7*Q0). Possibility for an association between C7*Q0 and C6*B.
    Nishimukai H, Kitamura H, Takeuchi Y, Shinomiya T, Tamaki Y.
    Hum Hered; 1988 Nov 01; 38(4):246-50. PubMed ID: 3169800
    [Abstract] [Full Text] [Related]

  • 15. C7 M/N protein polymorphism typing applied to inherited deficiencies of human complement proteins C6 and C7.
    Würzner R, Rance N, Potter PC, Hendricks ML, Lachmann PJ, Orren A.
    Clin Exp Immunol; 1992 Sep 01; 89(3):485-9. PubMed ID: 1516263
    [Abstract] [Full Text] [Related]

  • 16. DNA polymorphisms of the complement C6 and C7 genes.
    Fernie BA, Würzner R, Unsworth DJ, Tuxworth RI, Hobart MJ.
    Ann Hum Genet; 1995 Apr 01; 59(2):163-81. PubMed ID: 7625764
    [Abstract] [Full Text] [Related]

  • 17. C7 deficiency in an Irish family: a deletion defect which is predominant in the Irish.
    O'Hara AM, Fernie BA, Moran AP, Williams YE, Connaughton JJ, Orren A, Hobart MJ.
    Clin Exp Immunol; 1998 Dec 01; 114(3):355-61. PubMed ID: 9844043
    [Abstract] [Full Text] [Related]

  • 18. A case of hereditary combined deficiency of complement components C6 and C7 in man.
    Morgan BP, Vora JP, Bennett AJ, Thomas JP, Matthews N.
    Clin Exp Immunol; 1989 Mar 01; 75(3):396-401. PubMed ID: 2702782
    [Abstract] [Full Text] [Related]

  • 19. Association of a 12.5-kilobase allele of the MspI restriction fragment length polymorphism of the C6 gene in patients with total deficiency of the sixth component of complement.
    Potter PC, Warburton C, Würzner R, Orren A, Di Scipio R.
    Exp Clin Immunogenet; 1993 Mar 01; 10(1):38-44. PubMed ID: 7691111
    [Abstract] [Full Text] [Related]

  • 20. C7 deficiency and meningococcal infection susceptibility in two spanish families.
    Barroso S, López-Trascasa M, Merino D, Alvarez AJ, Núñez-Roldán A, Sánchez B.
    Scand J Immunol; 2010 Jul 01; 72(1):38-43. PubMed ID: 20591074
    [Abstract] [Full Text] [Related]

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