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Journal Abstract Search

106 related items for PubMed ID: 9218625

  • 1. 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]

  • 2. 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]

  • 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
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Characterization of a large genomic deletion in four Irish families with C7 deficiency.
    Thomas AD, Orren A, Connaughton J, Feighery C, Morgan BP, Roberts AG.
    Mol Immunol; 2012 Feb 15; 50(1-2):57-9. PubMed ID: 22206826
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 114(3):355-61. PubMed ID: 9844043
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Hereditary complement deficiency in survivors of meningococcal disease: high prevalence of C7/C8 deficiency in Sephardic (Moroccan) Jews.
    Zimran A, Rudensky B, Kramer MR, Tedesco F, Ehrenfeld M, Raz R, Greif Z, Gelber M, Lishner M, Golan E.
    Q J Med; 1987 Apr 13; 63(240):349-58. PubMed ID: 3685247
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Complement component C7 deficiency in two Spanish families.
    Barroso S, Sánchez B, Alvarez AJ, López-Trascasa M, Lanuza A, Luque R, Wichmann I, Núñez-Roldán A.
    Immunology; 2004 Dec 15; 113(4):518-23. PubMed ID: 15554930
    [Abstract] [Full Text] [Related]

  • 12. C7 complement deficiency in an Israeli Arab village.
    Behar D, Schlesinger M, Halle D, Ben-Ami H, Edoute Y, Shahar E, Kasis I, Shihab S, Elstein D, Zimran A, Mandel H.
    Am J Med Genet; 2002 Jun 01; 110(1):25-9. PubMed ID: 12116267
    [Abstract] [Full Text] [Related]

  • 13. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 01; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Molecular defects of the C7 gene in two patients with complement C7 deficiency.
    Barroso S, Rieubland C, José álvarez A, López-Trascasa M, Bart PA, Núñez-Roldán A, Sánchez B.
    Immunology; 2006 Jun 01; 118(2):257-60. PubMed ID: 16771861
    [Abstract] [Full Text] [Related]

  • 16. Complement component C6 and C7 haplotypes associated with deficiencies of C6.
    Fernie BA, Orren A, Würzner R, Jones AM, Potter PC, Lachmann PJ, Hobart MJ.
    Ann Hum Genet; 1995 Apr 01; 59(2):183-95. PubMed ID: 7625765
    [Abstract] [Full Text] [Related]

  • 17. Combined genetic deficiency of C6 and C7 in man.
    Lachmann PJ, Hobart MJ, Woo P.
    Clin Exp Immunol; 1978 Aug 01; 33(2):193-203. PubMed ID: 102474
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 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 May 01; 10(1):38-44. PubMed ID: 7691111
    [Abstract] [Full Text] [Related]

  • 20. 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 May 01; 13(2):92-103. PubMed ID: 9063701
    [Abstract] [Full Text] [Related]

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