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Journal Abstract Search

126 related items for PubMed ID: 8419161

  • 1. Mechanisms that generate human immunoglobulin diversity operate from the 8th week of gestation in fetal liver.
    Cuisinier AM, Gauthier L, Boubli L, Fougereau M, Tonnelle C.
    Eur J Immunol; 1993 Jan; 23(1):110-8. PubMed ID: 8419161
    [Abstract] [Full Text] [Related]

  • 2. Antibody repertoire development in fetal and neonatal piglets. I. Four VH genes account for 80 percent of VH usage during 84 days of fetal life.
    Sun J, Hayward C, Shinde R, Christenson R, Ford SP, Butler JE.
    J Immunol; 1998 Nov 01; 161(9):5070-8. PubMed ID: 9794445
    [Abstract] [Full Text] [Related]

  • 3. Restricted utilization of germ-line VH3 genes and short diverse third complementarity-determining regions (CDR3) in human fetal B lymphocyte immunoglobulin heavy chain rearrangements.
    Raaphorst FM, Timmers E, Kenter MJ, Van Tol MJ, Vossen JM, Schuurman RK.
    Eur J Immunol; 1992 Jan 01; 22(1):247-51. PubMed ID: 1730252
    [Abstract] [Full Text] [Related]

  • 4. Use of the most JH-proximal human Ig H chain V region gene, VH6, in the expressed immune repertoire.
    Varade WS, Marin E, Kittelberger AM, Insel RA.
    J Immunol; 1993 Jun 01; 150(11):4985-95. PubMed ID: 8496600
    [Abstract] [Full Text] [Related]

  • 5. The human cord blood antibody repertoire. Frequent usage of the VH7 gene family.
    Mortari F, Newton JA, Wang JY, Schroeder HW.
    Eur J Immunol; 1992 Jan 01; 22(1):241-5. PubMed ID: 1730251
    [Abstract] [Full Text] [Related]

  • 6. A majority of Ig H chain cDNA of normal human adult blood lymphocytes resembles cDNA for fetal Ig and natural autoantibodies.
    Huang C, Stollar BD.
    J Immunol; 1993 Nov 15; 151(10):5290-300. PubMed ID: 8228225
    [Abstract] [Full Text] [Related]

  • 7. The VDJ repertoire expressed in human preB cells reflects the selection of bona fide heavy chains.
    Milili M, Schiff C, Fougereau M, Tonnelle C.
    Eur J Immunol; 1996 Jan 15; 26(1):63-9. PubMed ID: 8566085
    [Abstract] [Full Text] [Related]

  • 8. Restricted utilization of germ-line VH genes and diversity of D regions in rabbit splenic Ig mRNA.
    DiPietro LA, Knight KL.
    J Immunol; 1990 Mar 01; 144(5):1969-73. PubMed ID: 2106559
    [Abstract] [Full Text] [Related]

  • 9. Rapid expansion of human immunoglobulin repertoire (VH, V kappa, V lambda) expressed in early fetal bone marrow.
    Cuisinier AM, Fumoux F, Moinier D, Boubli L, Guigou V, Milili M, Schiff C, Fougereau M, Tonnelle C.
    New Biol; 1990 Aug 01; 2(8):689-99. PubMed ID: 2178002
    [Abstract] [Full Text] [Related]

  • 10. Analysis of Ig H chain gene segment utilization in human fetal liver. Revisiting the "proximal utilization hypothesis".
    Pascual V, Verkruyse L, Casey ML, Capra JD.
    J Immunol; 1993 Oct 15; 151(8):4164-72. PubMed ID: 8409393
    [Abstract] [Full Text] [Related]

  • 11. Developmental regulation of D beta reading frame and junctional diversity in T cell receptor-beta transcripts from human thymus.
    George JF, Schroeder HW.
    J Immunol; 1992 Feb 15; 148(4):1230-9. PubMed ID: 1310710
    [Abstract] [Full Text] [Related]

  • 12. V region diversity in human anti-insulin antibodies. Preferential use of a VHIII gene subset.
    Thomas JW.
    J Immunol; 1993 Feb 15; 150(4):1375-82. PubMed ID: 8432983
    [Abstract] [Full Text] [Related]

  • 13. B precursor acute lymphoblastic leukemia third complementarity-determining regions predominantly represent an unbiased recombination repertoire: leukemic transformation frequently occurs in fetal life.
    Steenbergen EJ, Verhagen OJ, van Leeuwen EF, Behrendt H, Merle PA, Wester MR, von dem Borne AE, van der Schoot CE.
    Eur J Immunol; 1994 Apr 15; 24(4):900-8. PubMed ID: 8149961
    [Abstract] [Full Text] [Related]

  • 14. VDJ genes in VHa2 allotype-suppressed rabbits. Limited germline VH gene usage and accumulation of somatic mutations in D regions.
    Short JA, Sethupathi P, Zhai SK, Knight KL.
    J Immunol; 1991 Dec 01; 147(11):4014-8. PubMed ID: 1940383
    [Abstract] [Full Text] [Related]

  • 15. Neonatal and adult primary B cells use the same germ-line VH and V kappa genes in their (T,G)-A-L-specific repertoire.
    Borriero L, Giorgetti C, Smith G, Landry D, Selsing E, Zhukovsky E, Press JL.
    J Immunol; 1990 Jan 15; 144(2):583-92. PubMed ID: 2129539
    [Abstract] [Full Text] [Related]

  • 16. Multiple mechanisms participate in the generation of diversity of human H chain CDR3 regions.
    Sanz I.
    J Immunol; 1991 Sep 01; 147(5):1720-9. PubMed ID: 1908883
    [Abstract] [Full Text] [Related]

  • 17. Diversity of immunoglobulin heavy chain gene segment rearrangement in B lymphoblastoid cell lines from X-linked agammaglobulinemia patients.
    Timmers E, Kenter M, Thompson A, Kraakman ME, Berman JE, Alt FW, Schuurman RK.
    Eur J Immunol; 1991 Oct 01; 21(10):2355-63. PubMed ID: 1915549
    [Abstract] [Full Text] [Related]

  • 18. Expression pattern of the most JH-proximal human VH gene segment (VH6) in the B cell and antibody repertoire suggests a role of VH6-encoded IgM antibodies in early ontogeny.
    Van Es JH, Raaphorst FM, van Tol MJ, Meyling FH, Logtenberg T.
    J Immunol; 1993 Jan 01; 150(1):161-8. PubMed ID: 8417121
    [Abstract] [Full Text] [Related]

  • 19. Immunoglobulin heavy chain variable region family usage is independent of tumor cell phenotype in human B lineage leukemias.
    Deane M, Norton JD.
    Eur J Immunol; 1990 Oct 01; 20(10):2209-17. PubMed ID: 1700749
    [Abstract] [Full Text] [Related]

  • 20. VH gene usage and CDR3 analysis of B cell receptor in the peripheral blood of patients with PBC.
    Foreman AL, Lemercier B, Lim A, Kourlisky P, Kenny T, Gershwin ME, Gougeon ML.
    Autoimmunity; 2008 Feb 01; 41(1):80-6. PubMed ID: 18176868
    [Abstract] [Full Text] [Related]

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