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Journal Abstract Search

161 related items for PubMed ID: 8098723

  • 1. Genetic basis of human complement C8 beta deficiency.
    Kaufmann T, Hänsch G, Rittner C, Späth P, Tedesco F, Schneider PM.
    J Immunol; 1993 Jun 01; 150(11):4943-7. PubMed ID: 8098723
    [Abstract] [Full Text] [Related]

  • 2. [Further study on heterogeneic basis of complement C8 beta deficiency].
    Rao L, Li YB, Chen GD, Zhou B, Schneider PM, Zhang L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb 01; 21(1):10-3. PubMed ID: 14767900
    [Abstract] [Full Text] [Related]

  • 3. Detection of heterozygous C8 beta deficiency by PCR in a healthy Italian population.
    Bellavia D, Schneider PM, Rittner C, Malfitano G, Kaufmann TJ, Brai M.
    Exp Clin Immunogenet; 1996 Feb 01; 13(3-4):173-80. PubMed ID: 9165271
    [Abstract] [Full Text] [Related]

  • 4. Genetic basis of human complement C8 alpha-gamma deficiency.
    Kojima T, Horiuchi T, Nishizaka H, Fukumori Y, Amano T, Nagasawa K, Niho Y, Hayashi K.
    J Immunol; 1998 Oct 01; 161(7):3762-6. PubMed ID: 9759902
    [Abstract] [Full Text] [Related]

  • 5. Delineation of additional genetic bases for C8 beta deficiency. Prevalence of null alleles and predominance of C-->T transition in their genesis.
    Saucedo L, Ackermann L, Platonov AE, Gewurz A, Rakita RM, Densen P.
    J Immunol; 1995 Nov 15; 155(10):5022-8. PubMed ID: 7594510
    [Abstract] [Full Text] [Related]

  • 6. The human complement component C8B gene: structure and phylogenetic relationship.
    Kaufmann T, Rittner C, Schneider PM.
    Hum Genet; 1993 Aug 15; 92(1):69-75. PubMed ID: 8365729
    [Abstract] [Full Text] [Related]

  • 7. Polymorphism of the complement C8A and -B genes in two families with C8 beta deficiency and neisserial infections.
    Barba GM, Kaufmann TJ, Schneider PM, Rittner C, Brai M.
    Clin Immunol Immunopathol; 1994 Jul 15; 72(1):83-9. PubMed ID: 8020197
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Expression of the complement C8 genes during interleukin-6-mediated in vitro induction of the acute-phase response.
    Späth GF, Ramadori G, Rittner C, Schneider PM.
    Exp Clin Immunogenet; 1995 May 15; 12(1):53-60. PubMed ID: 7710765
    [Abstract] [Full Text] [Related]

  • 10. Decreased C5b67-inhibitor activity in two families with hereditary functional deficiency of the eighth component of complement.
    Zeitz HJ, Zeff RA, Gewurz H, Lint TF.
    J Immunol; 1983 Jun 15; 130(6):2809-13. PubMed ID: 6854017
    [Abstract] [Full Text] [Related]

  • 11. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 15; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 12. Reduced C8 beta messenger RNA expression in families with hereditary C8 beta deficiency.
    Warnick PR, Densen P.
    J Immunol; 1991 Feb 01; 146(3):1052-6. PubMed ID: 1988493
    [Abstract] [Full Text] [Related]

  • 13. Genetic basis of human complement C4A deficiency. Detection of a point mutation leading to nonexpression.
    Barba G, Rittner C, Schneider PM.
    J Clin Invest; 1993 Apr 01; 91(4):1681-6. PubMed ID: 8473511
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. C8 beta subunit deficiency in a patient with recurrent neisserial infections.
    Fontana L, Tedesco F, De Carolis C, Roncelli L, Teggi A, Paffetti A, Perricone R.
    Ric Clin Lab; 1987 May 15; 17(1):19-25. PubMed ID: 3109005
    [Abstract] [Full Text] [Related]

  • 16. Differential functional expression of the C8 subunits. Primary role of C8 beta in assembly of intact C8.
    Densen P, McRill CM.
    J Immunol; 1988 Oct 15; 141(8):2674-9. PubMed ID: 3171181
    [Abstract] [Full Text] [Related]

  • 17. The human complement C8G gene, a member of the lipocalin gene family: polymorphisms and mapping to chromosome 9q34.3.
    Dewald G, Cichon S, Bryant SP, Hemmer S, Nöthen MM, Spurr NK.
    Ann Hum Genet; 1996 Jul 15; 60(4):281-91. PubMed ID: 8865989
    [Abstract] [Full Text] [Related]

  • 18. [Detecting the DNA polymorphism of human complement component C8A by PCR-SSCP analysis].
    Yang ZH, Zhang L, Zhou B, Wang C, Jia J.
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2006 May 15; 37(3):471-3. PubMed ID: 16761437
    [Abstract] [Full Text] [Related]

  • 19. Genetic aspects of complement component C8 in Norwegian meningococcal disease patients.
    Rogde S, Høiby EA, Teisberg P, Olaisen B.
    Scand J Infect Dis; 1990 May 15; 22(6):673-9. PubMed ID: 2284574
    [Abstract] [Full Text] [Related]

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