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616 related items for PubMed ID: 1676047

  • 21. Variable region genes of anti-HIV human monoclonal antibodies: non-restricted use of the V gene repertoire and extensive somatic mutation.
    Moran MJ, Andris JS, Matsumato Y, Capra JD, Hersh EM.
    Mol Immunol; 1993 Nov; 30(16):1543-51. PubMed ID: 8232339
    [Abstract] [Full Text] [Related]

  • 22. Structure of the VH and VL segments of monoreactive and polyreactive IgA autoantibodies to DNA in patients with systemic lupus erythematosus.
    Kasaian MT, Ikematsu H, Balow JE, Casali P.
    J Immunol; 1994 Mar 15; 152(6):3137-51. PubMed ID: 8144908
    [Abstract] [Full Text] [Related]

  • 23. Variable region sequences of murine IgM anti-IgG monoclonal autoantibodies (rheumatoid factors). A structural explanation for the high frequency of IgM anti-IgG B cells.
    Shlomchik MJ, Nemazee DA, Sato VL, Van Snick J, Carson DA, Weigert MG.
    J Exp Med; 1986 Aug 01; 164(2):407-27. PubMed ID: 3088205
    [Abstract] [Full Text] [Related]

  • 24. Variable region gene utilization and mutation in a group of neutralizing murine anti-human immunodeficiency virus type 1 principal neutralizing determinant antibodies.
    Pirofski LA, Thomas EK, Scharff MD.
    AIDS Res Hum Retroviruses; 1993 Jan 01; 9(1):41-9. PubMed ID: 7678971
    [Abstract] [Full Text] [Related]

  • 25. Variable region primary structures of a high affinity anti-fluorescein immunoglobulin M cryoglobulin exhibiting oxazolone cross-reactivity.
    Dombrink-Kurtzman MA, Johnson LS, Riordan GS, Bedzyk WD, Voss EW.
    J Biol Chem; 1989 Mar 15; 264(8):4513-22. PubMed ID: 2494173
    [Abstract] [Full Text] [Related]

  • 26. Two families of monoclonal antibodies to alpha(1----6)dextran, VH19.1.2 and VH9.14.7, show distinct patterns of J kappa and JH minigene usage and amino acid substitutions in CDR3.
    Wang DN, Chen HT, Liao J, Akolkar PN, Sikder SK, Gruezo F, Kabat EA.
    J Immunol; 1990 Nov 01; 145(9):3002-10. PubMed ID: 1698868
    [Abstract] [Full Text] [Related]

  • 27. Human rheumatoid B-1a (CD5+ B) cells make somatically hypermutated high affinity IgM rheumatoid factors.
    Mantovani L, Wilder RL, Casali P.
    J Immunol; 1993 Jul 01; 151(1):473-88. PubMed ID: 7686945
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  • 28. Molecular characterization of variable heavy and light chain regions of five HIV type 1-specific human monoclonal antibodies.
    van der Donk EM, Schutten M, Osterhaus AD, van der Heijden RW.
    AIDS Res Hum Retroviruses; 1994 Dec 01; 10(12):1639-49. PubMed ID: 7888223
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  • 29. Variable region sequences and idiotypic expression of a protective human immunoglobulin M antibody to capsular polysaccharides of Neisseria meningitidis group B and Escherichia coli K1.
    Azmi FH, Lucas AH, Raff HV, Granoff DM.
    Infect Immun; 1994 May 01; 62(5):1776-86. PubMed ID: 8168940
    [Abstract] [Full Text] [Related]

  • 30. Strain-dependent restricted VH and VL usage by anti-bacterial levan monoclonal antibodies.
    Boswell CM, Irwin DC, Goodnight J, Stein KE.
    J Immunol; 1992 Jun 15; 148(12):3864-72. PubMed ID: 1602134
    [Abstract] [Full Text] [Related]

  • 31. Molecular analysis of carbohydrate antigen-induced monoclonal IgM anti-IgG antibodies (rheumatoid factors).
    Stanley SL, Foster L, Phillips N.
    Mol Immunol; 1992 Apr 15; 29(4):453-61. PubMed ID: 1565097
    [Abstract] [Full Text] [Related]

  • 32. Protein-polysaccharide interactions. A monoclonal antibody specific for the capsular polysaccharide of Cryptococcus neoformans.
    Otteson EW, Welch WH, Kozel TR.
    J Biol Chem; 1994 Jan 21; 269(3):1858-64. PubMed ID: 8294434
    [Abstract] [Full Text] [Related]

  • 33. Complete sequence of the genes encoding the VH and VL regions of low- and high-affinity monoclonal IgM and IgA1 rheumatoid factors produced by CD5+ B cells from a rheumatoid arthritis patient.
    Harindranath N, Goldfarb IS, Ikematsu H, Burastero SE, Wilder RL, Notkins AL, Casali P.
    Int Immunol; 1991 Sep 21; 3(9):865-75. PubMed ID: 1718404
    [Abstract] [Full Text] [Related]

  • 34. Unexpected diversity in the fine specificity of monoclonal antibodies that use the same V region gene to glucuronoxylomannan of Cryptococcus neoformans.
    McFadden DC, Casadevall A.
    J Immunol; 2004 Mar 15; 172(6):3670-7. PubMed ID: 15004170
    [Abstract] [Full Text] [Related]

  • 35. The repertoire of human antibody to the Haemophilus influenzae type b capsular polysaccharide.
    Insel RA, Adderson EE, Carroll WL.
    Int Rev Immunol; 1992 Mar 15; 9(1):25-43. PubMed ID: 1484268
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  • 36. Molecular characterization of a human anti-Rh(D) antibody with a DH segment encoded by a germ-line sequence.
    Chouchane L, Van Spronsen A, Breyer J, Guglielmi P, Strosberg AD.
    Eur J Biochem; 1992 Aug 01; 207(3):1115-21. PubMed ID: 1499555
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  • 37. Germ-line origin of functional idiotypic interactions: identification of two idiotypically connected, natural antibodies that are encoded by germ-line gene elements.
    Carlsson L, Andersson A, Holmberg D.
    Eur J Immunol; 1991 Sep 01; 21(9):2285-8. PubMed ID: 1909648
    [Abstract] [Full Text] [Related]

  • 38. Human rheumatoid factors with restrictive specificity for rabbit immunoglobulin G: auto- and multi-reactivity, diverse VH gene segment usage and preferential usage of V lambda IIIb.
    Fang Q, Kannapell CC, Gaskin F, Solomon A, Koopman WJ, Fu SM.
    J Exp Med; 1994 May 01; 179(5):1445-56. PubMed ID: 7545920
    [Abstract] [Full Text] [Related]

  • 39. Variable region cDNA sequences and antigen binding specificity of mouse monoclonal antibodies to isomaltosyl oligosaccharides coupled to proteins. T-dependent analogues of alpha(1----6)dextran.
    Matsuda T, Kabat EA.
    J Immunol; 1989 Feb 01; 142(3):863-70. PubMed ID: 2464028
    [Abstract] [Full Text] [Related]

  • 40. Restricted CDR3 length of the heavy chain is characteristic of six randomly isolated disease-associated VH J558+ IgM autoantibodies in lupus prone motheaten mice.
    Lipsanen V, Walter B, Emara M, Siminovitch K, Lam J, Kaushik A.
    Int Immunol; 1997 May 01; 9(5):655-64. PubMed ID: 9184911
    [Abstract] [Full Text] [Related]


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