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Journal Abstract Search
96 related items for PubMed ID: 7594539
1. Mouse VH7183 recombination signal sequences mediate recombination more frequently than those of VHJ558. Connor AM, Fanning LJ, Celler JW, Hicks LK, Ramsden DA, Wu GE. J Immunol; 1995 Dec 01; 155(11):5268-72. PubMed ID: 7594539 [Abstract] [Full Text] [Related]
10. Frequency of VH81x usage during B cell development: initial decline in usage is independent of Ig heavy chain cell surface expression. Marshall AJ, Wu GE, Paige GJ. J Immunol; 1996 Mar 15; 156(6):2077-84. PubMed ID: 8690895 [Abstract] [Full Text] [Related]
12. The utilization of individual VH exons in the primary repertoire of adult BALB/c mice. Sheehan KM, Mainville CA, Willert S, Brodeur PH. J Immunol; 1993 Nov 15; 151(10):5364-75. PubMed ID: 8228231 [Abstract] [Full Text] [Related]
13. 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]
14. Molecular characterization of anti-DNA antibodies induced in normal mice by immunization with bacterial DNA. Differences from spontaneous anti-DNA in the content and location of VH CDR3 arginines. Gilkeson GS, Bloom DD, Pisetsky DS, Clarke SH. J Immunol; 1993 Aug 01; 151(3):1353-64. PubMed ID: 8335932 [Abstract] [Full Text] [Related]
16. VH gene segments in the mouse and human genomes. de Bono B, Madera M, Chothia C. J Mol Biol; 2004 Sep 03; 342(1):131-43. PubMed ID: 15313612 [Abstract] [Full Text] [Related]
17. B cell deletion, anergy, and receptor editing in "knock in" mice targeted with a germline-encoded or somatically mutated anti-DNA heavy chain. Pewzner-Jung Y, Friedmann D, Sonoda E, Jung S, Rajewsky K, Eilat D. J Immunol; 1998 Nov 01; 161(9):4634-45. PubMed ID: 9794392 [Abstract] [Full Text] [Related]