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Journal Abstract Search

150 related items for PubMed ID: 7508079

  • 1. An apparently common mechanism of generating antibody diversity: length variation of the VL-JL junction.
    Victor KD, Capra JD.
    Mol Immunol; 1994 Jan; 31(1):39-46. PubMed ID: 7508079
    [Abstract] [Full Text] [Related]

  • 2. Frequent N addition and clonal relatedness among immunoglobulin lambda light chains expressed in rheumatoid arthritis synovia and PBL, and the influence of V lambda gene segment utilization on CDR3 length.
    Bridges SL.
    Mol Med; 1998 Aug; 4(8):525-53. PubMed ID: 9742508
    [Abstract] [Full Text] [Related]

  • 3.
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  • 4. An immunoglobulin heavy chain variable region gene is generated from three segments of DNA: VH, D and JH.
    Early P, Huang H, Davis M, Calame K, Hood L.
    Cell; 1980 Apr; 19(4):981-92. PubMed ID: 6769593
    [Abstract] [Full Text] [Related]

  • 5. Structure of a germline rabbit immunoglobulin V kappa-region gene: implications for rabbit V kappa-J kappa recombination.
    Lieberman R, Emorine L, Max EE.
    J Immunol; 1984 Nov; 133(5):2753-6. PubMed ID: 6434636
    [Abstract] [Full Text] [Related]

  • 6. Limited junctional diversity in kappa light chains. Junctional sequences from CD43+B220+ early B cell progenitors resemble those from peripheral B cells.
    Victor KD, Vu K, Feeney AJ.
    J Immunol; 1994 Apr 01; 152(7):3467-75. PubMed ID: 7511648
    [Abstract] [Full Text] [Related]

  • 7. The efficiency of B cell receptor (BCR) editing is dependent on BCR light chain rearrangement status.
    Yachimovich N, Mostoslavsky G, Yarkoni Y, Verbovetski I, Eilat D.
    Eur J Immunol; 2002 Apr 01; 32(4):1164-74. PubMed ID: 11932924
    [Abstract] [Full Text] [Related]

  • 8. Antibody repertoire development in fetal and neonatal piglets. II. Characterization of heavy chain complementarity-determining region 3 diversity in the developing fetus.
    Butler JE, Weber P, Sinkora M, Sun J, Ford SJ, Christenson RK.
    J Immunol; 2000 Dec 15; 165(12):6999-7010. PubMed ID: 11120827
    [Abstract] [Full Text] [Related]

  • 9. Generation of the primary antibody repertoire in rabbits: expression of a diverse set of Igk-V genes may compensate for limited combinatorial diversity at the heavy chain locus.
    Sehgal D, Johnson G, Wu TT, Mage RG.
    Immunogenetics; 1999 Oct 15; 50(1-2):31-42. PubMed ID: 10541804
    [Abstract] [Full Text] [Related]

  • 10. Antibody repertoire development in fetal and neonatal pigs. VII. Characterization of the preimmune kappa light chain repertoire.
    Butler JE, Wertz N, Sun J, Wang H, Chardon P, Piumi F, Wells K.
    J Immunol; 2004 Dec 01; 173(11):6794-805. PubMed ID: 15557173
    [Abstract] [Full Text] [Related]

  • 11. Evidence that the V kappa III gene usage is nonstochastic in both adult and newborn peripheral B cells and that peripheral CD5+ adult B cells are oligoclonal.
    Weber JC, Blaison G, Martin T, Knapp AM, Pasquali JL.
    J Clin Invest; 1994 May 01; 93(5):2093-105. PubMed ID: 7514192
    [Abstract] [Full Text] [Related]

  • 12. Abbreviated junctional sequences impoverish antibody diversity in urodele amphibians.
    Patel HM, Hsu E.
    J Immunol; 1997 Oct 01; 159(7):3391-9. PubMed ID: 9317138
    [Abstract] [Full Text] [Related]

  • 13. An unusual type of V-J joining diversifies the primary repertoire of mouse lambda 1 light chains.
    Karjalainen K, Coleclough C.
    Nature; 1997 Oct 01; 314(6011):544-6. PubMed ID: 3921849
    [Abstract] [Full Text] [Related]

  • 14. Clonal analysis of a human antibody response. III. Nucleotide sequences of monoclonal IgM, IgG, and IgA to rabies virus reveal restricted V kappa gene utilization, junctional V kappa J kappa and V lambda J lambda diversity, and somatic hypermutation.
    Ikematsu W, Kobarg J, Ikematsu H, Ichiyoshi Y, Casali P.
    J Immunol; 1998 Sep 15; 161(6):2895-905. PubMed ID: 9743351
    [Abstract] [Full Text] [Related]

  • 15. Molecular analysis of the V kappa III-J kappa junctional diversity of polyclonal rheumatoid factors during rheumatoid arthritis frequently reveals N addition.
    Martin T, Blaison G, Levallois H, Pasquali JL.
    Eur J Immunol; 1992 Jul 15; 22(7):1773-9. PubMed ID: 1339352
    [Abstract] [Full Text] [Related]

  • 16. Functional analogues of the VKOx1 gene in different strains of mice: evolutionary conservation but diversity based on V-J joining.
    Kaartinen M, Mäkelä O.
    J Immunol; 1987 Mar 01; 138(5):1613-7. PubMed ID: 3100644
    [Abstract] [Full Text] [Related]

  • 17. Extensive junctional diversity in Ig light chain genes from early B cell progenitors of mu MT mice.
    Bentolila LA, Olson S, Marshall A, Rougeon F, Paige CJ, Doyen N, Wu GE.
    J Immunol; 1999 Feb 15; 162(4):2123-8. PubMed ID: 9973486
    [Abstract] [Full Text] [Related]

  • 18. Structure of rearranged and germ-line rabbit V kappa genes indicated that the CDR3 is encoded by the V kappa gene.
    Ayadi H, Cazenave PA, Marche PN.
    Eur J Immunol; 1990 Feb 15; 20(2):259-64. PubMed ID: 2107083
    [Abstract] [Full Text] [Related]

  • 19. Age-related alterations of somatic hypermutation and CDR3 lengths in human Vkappa4-expressing B lymphocytes.
    Troutaud D, Drouet M, Decourt C, Le Morvan C, Cogné M.
    Immunology; 1999 Jun 15; 97(2):197-203. PubMed ID: 10447732
    [Abstract] [Full Text] [Related]

  • 20. Restricted kappa chain expression in early ontogeny: biased utilization of V kappa exons and preferential V kappa-J kappa recombinations.
    Medina CA, Teale JM.
    J Exp Med; 1993 May 01; 177(5):1317-30. PubMed ID: 8478611
    [Abstract] [Full Text] [Related]

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