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Journal Abstract Search

176 related items for PubMed ID: 468996

  • 21. Deficiency of the eighth component of complement. Evidence for linkage of C8 alpha-gamma pattern with C8 beta deficiency in sera of twelve patients.
    Nürnberger W, Pietsch H, Willers R, Bufon T, Hänsch GM, Seger R, Rodriguez-Valverde V, Schroten H, Hershko C, Tedesco F.
    Scand J Immunol; 1989 Jul; 30(1):45-9. PubMed ID: 2667094
    [Abstract] [Full Text] [Related]

  • 22. Molecular, genetic, and functional analysis of homozygous C8 beta-chain deficiency in two siblings.
    Kotnik V, Luznik-Bufon T, Schneider PM, Kirschfink M.
    Immunopharmacology; 1997 Dec; 38(1-2):215-21. PubMed ID: 9476133
    [Abstract] [Full Text] [Related]

  • 23.
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  • 24. Hereditary C5 deficiency in man: genetic linkage studies.
    Rosenfeld SI, Weitkamp LR, Ward F.
    J Immunol; 1977 Aug; 119(2):604-8. PubMed ID: 886187
    [Abstract] [Full Text] [Related]

  • 25. DNA polymorphism of the human complement C8 beta gene: formal genetics and intragenic localization.
    Herrmann D, Sodetz JM, Rittner C, Schneider PM.
    Immunogenetics; 1989 Aug; 30(4):291-5. PubMed ID: 2571588
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  • 27. Genetic polymorphism of human factor I (C3b inactivator).
    Nakamura S, Abe K.
    Hum Genet; 1985 Aug; 71(1):45-8. PubMed ID: 3897024
    [Abstract] [Full Text] [Related]

  • 28. Complement component deficiencies and infection: C5, C8 and C3 deficiencies in three families.
    Sanal O, Loos M, Ersoy F, Kanra G, Seçmeer G, Tezcan I.
    Eur J Pediatr; 1992 Sep; 151(9):676-9. PubMed ID: 1396929
    [Abstract] [Full Text] [Related]

  • 29. 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; 130(6):2809-13. PubMed ID: 6854017
    [Abstract] [Full Text] [Related]

  • 30. The polymorphism of the C3b/C4b receptor in the normal population and in patients with systemic lupus erythematosus.
    Van Dyne S, Holers VM, Lublin DM, Atkinson JP.
    Clin Exp Immunol; 1987 Jun; 68(3):570-9. PubMed ID: 2958190
    [Abstract] [Full Text] [Related]

  • 31. 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; 60(4):281-91. PubMed ID: 8865989
    [Abstract] [Full Text] [Related]

  • 32. Genetic polymorphism of human complement component C81 in the Japanese population.
    Nakamura S, Ohue O, Abe K.
    Hum Genet; 1986 Apr; 72(4):344-7. PubMed ID: 3699824
    [Abstract] [Full Text] [Related]

  • 33. A BamHI RFLP of the C8A gene.
    Rogde S, Olaisen B, Teisberg P, Sodetz J.
    Nucleic Acids Res; 1991 Jul 11; 19(13):3762. PubMed ID: 1677187
    [No Abstract] [Full Text] [Related]

  • 34. 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 Jul 11; 12(1):53-60. PubMed ID: 7710765
    [Abstract] [Full Text] [Related]

  • 35. Genetic studies of low abundance human plasma proteins. III. Polymorphism of the C1R subcomponent of the first complement component.
    Kamboh MI, Ferrell RE.
    Am J Hum Genet; 1986 Dec 11; 39(6):826-31. PubMed ID: 3026176
    [Abstract] [Full Text] [Related]

  • 36. Genetic studies of human apolipoproteins. I. Polymorphism of apolipoprotein A-IV.
    Kamboh MI, Ferrell RE.
    Am J Hum Genet; 1987 Aug 11; 41(2):119-27. PubMed ID: 3618592
    [Abstract] [Full Text] [Related]

  • 37. 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]

  • 38. The genetics of the sixth and seventh components of complement in the dog: polymorphism, linkage, locus duplication, and silent alleles.
    Eldridge PR, Hobart MJ, Lachmann PJ.
    Biochem Genet; 1983 Feb 15; 21(1-2):81-91. PubMed ID: 6838492
    [Abstract] [Full Text] [Related]

  • 39. Linkage of total deficiency of the second component (C2) of the complement system and of genetic C2-polymorphism to the major histocompatibility complex of the guinea pig.
    Bitter-Suermann D, Hoffmann T, Burger R, Hadding U.
    J Immunol; 1981 Aug 15; 127(2):608-12. PubMed ID: 7252150
    [Abstract] [Full Text] [Related]

  • 40. Genetic polymorphism of human C1R subcomponent of the first complement component in the Japanese population.
    Nakamura S, Ohue O, Akiyama K, Abe K.
    Forensic Sci Int; 1988 Oct 15; 39(1):71-6. PubMed ID: 2850274
    [Abstract] [Full Text] [Related]

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