BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

719 related articles for article (PubMed ID: 11160315)

  • 1. Deletion of the DQ52 element within the Ig heavy chain locus leads to a selective reduction in VDJ recombination and altered D gene usage.
    Nitschke L; Kestler J; Tallone T; Pelkonen S; Pelkonen J
    J Immunol; 2001 Feb; 166(4):2540-52. PubMed ID: 11160315
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Preferential usage of JH2 in D-J joinings with DQ52 is determined by the primary DNA sequence and is largely dependent on recombination signal sequences.
    Suzuki H; Shiku H
    Eur J Immunol; 1992 Sep; 22(9):2225-30. PubMed ID: 1516615
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Most marginal zone B cells in rat express germline encoded Ig VH genes and are ligand selected.
    Dammers PM; Visser A; Popa ER; Nieuwenhuis P; Kroese FG
    J Immunol; 2000 Dec; 165(11):6156-69. PubMed ID: 11086049
    [TBL] [Abstract][Full Text] [Related]  

  • 4. B cell development arrest upon insertion of a neo gene between JH and Emu: promoter competition results in transcriptional silencing of germline JH and complete VDJ rearrangements.
    Delpy L; Decourt C; Le Bert M; Cogné M
    J Immunol; 2002 Dec; 169(12):6875-82. PubMed ID: 12471120
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Differential usage of VH gene segments is mediated by cis elements.
    Yu CC; Larijani M; Miljanic IN; Wu GE
    J Immunol; 1998 Oct; 161(7):3444-54. PubMed ID: 9759863
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rearrangement of upstream DH and VH genes to a rearranged immunoglobulin variable region gene inserted into the DQ52-JH region of the immunoglobulin heavy chain locus.
    Taki S; Schwenk F; Rajewsky K
    Eur J Immunol; 1995 Jul; 25(7):1888-96. PubMed ID: 7621865
    [TBL] [Abstract][Full Text] [Related]  

  • 7. B cell progenitors are arrested in maturation but have intact VDJ recombination in the absence of Ig-alpha and Ig-beta.
    Pelanda R; Braun U; Hobeika E; Nussenzweig MC; Reth M
    J Immunol; 2002 Jul; 169(2):865-72. PubMed ID: 12097390
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mice triallelic for the Ig heavy chain locus: implications for VHDJH recombination.
    Barreto V; Meo T; Cumano A
    J Immunol; 2001 May; 166(9):5638-45. PubMed ID: 11313404
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Selection of Ig mu heavy chains by complementarity-determining region 3 length and amino acid composition.
    Martin DA; Bradl H; Collins TJ; Roth E; Jäck HM; Wu GE
    J Immunol; 2003 Nov; 171(9):4663-71. PubMed ID: 14568941
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partitioning of rearranged Ig genes by mutation analysis demonstrates D-D fusion and V gene replacement in the expressed human repertoire.
    Collins AM; Ikutani M; Puiu D; Buck GA; Nadkarni A; Gaeta B
    J Immunol; 2004 Jan; 172(1):340-8. PubMed ID: 14688342
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rabbit DQ52 and DH gene expression in early B-cell development.
    Chen HT; Alexander CB; Chen FF; Mage RG
    Mol Immunol; 1996 Dec; 33(17-18):1313-21. PubMed ID: 9171891
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 26(1):63-9. PubMed ID: 8566085
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Preferential utilization of specific immunoglobulin heavy chain diversity and joining segments in adult human peripheral blood B lymphocytes.
    Yamada M; Wasserman R; Reichard BA; Shane S; Caton AJ; Rovera G
    J Exp Med; 1991 Feb; 173(2):395-407. PubMed ID: 1899102
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Preferential usage of JH2 in D-J joinings with DQ52 in murine lymphocytes.
    Suzuki H; Abe M; Nishikawa S; Nakayama E; Shiku H
    Int Immunol; 1989; 1(6):643-6. PubMed ID: 2489050
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Development of the expressed Ig CDR-H3 repertoire is marked by focusing of constraints in length, amino acid use, and charge that are first established in early B cell progenitors.
    Ivanov II; Schelonka RL; Zhuang Y; Gartland GL; Zemlin M; Schroeder HW
    J Immunol; 2005 Jun; 174(12):7773-80. PubMed ID: 15944280
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 22(1):247-51. PubMed ID: 1730252
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic dissection of lupus pathogenesis: Sle3/5 impacts IgH CDR3 sequences, somatic mutations, and receptor editing.
    Wakui M; Kim J; Butfiloski EJ; Morel L; Sobel ES
    J Immunol; 2004 Dec; 173(12):7368-76. PubMed ID: 15585861
    [TBL] [Abstract][Full Text] [Related]  

  • 18. VH replacement rescues progenitor B cells with two nonproductive VDJ alleles.
    Lutz J; Müller W; Jäck HM
    J Immunol; 2006 Nov; 177(10):7007-14. PubMed ID: 17082616
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Shark Ig light chain junctions are as diverse as in heavy chains.
    Fleurant M; Changchien L; Chen CT; Flajnik MF; Hsu E
    J Immunol; 2004 Nov; 173(9):5574-82. PubMed ID: 15494507
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ongoing hypermutation in the Ig V(D)J gene segments and c-myc proto-oncogene of an AIDS lymphoma segregates with neoplastic B cells at different sites: implications for clonal evolution.
    Ikematsu H; Cerutti A; Zan H; Knowles DM; Ikematsu W; Casali P
    Hum Immunol; 2000 Dec; 61(12):1242-53. PubMed ID: 11163079
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 36.