205 related articles for article (PubMed ID: 2118933)
1. A set of closely related antibodies dominates the primary antibody response to the antigenic site CB of the A/PR/8/34 influenza virus hemagglutinin.
Kavaler J; Caton AJ; Staudt LM; Schwartz D; Gerhard W
J Immunol; 1990 Oct; 145(7):2312-21. PubMed ID: 2118933
[TBL] [Abstract][Full Text] [Related]
2. Many variable region genes are utilized in the antibody response of BALB/c mice to the influenza virus A/PR/8/34 hemagglutinin.
Caton AJ; Stark SE; Kavaler J; Staudt LM; Schwartz D; Gerhard W
J Immunol; 1991 Sep; 147(5):1675-86. PubMed ID: 1908881
[TBL] [Abstract][Full Text] [Related]
3. V region gene usage and somatic mutation in the primary and secondary responses to influenza virus hemagglutinin.
Clarke SH; Staudt LM; Kavaler J; Schwartz D; Gerhard WU; Weigert MG
J Immunol; 1990 Apr; 144(7):2795-801. PubMed ID: 2108213
[TBL] [Abstract][Full Text] [Related]
4. Influence of a V kappa 8 L chain transgene on endogenous rearrangements and the immune response to the HA(Sb) determinant on influenza virus.
Carmack CE; Camper SA; Mackle JJ; Gerhard WU; Weigert MG
J Immunol; 1991 Sep; 147(6):2024-33. PubMed ID: 1909739
[TBL] [Abstract][Full Text] [Related]
5. The BALB/c secondary response to the Sb site of influenza virus hemagglutinin. Nonrandom silent mutation and unequal numbers of VH and Vk mutations.
Clarke S; Rickert R; Wloch MK; Staudt L; Gerhard W; Weigert M
J Immunol; 1990 Oct; 145(7):2286-96. PubMed ID: 2398280
[TBL] [Abstract][Full Text] [Related]
6. Immunodominance with progenitor B cell diversity in the neutralizing antibody repertoire to influenza infection.
Patera AC; Graham CM; Thomas DB; Smith CA
Eur J Immunol; 1995 Jul; 25(7):1803-9. PubMed ID: 7621857
[TBL] [Abstract][Full Text] [Related]
7. Characterization of monoclonal antibodies specific for sequential influenza A/PR/8/34 virus variants.
Reale MA; Manheimer AJ; Moran TM; Norton G; Bona CA; Schulman JL
J Immunol; 1986 Aug; 137(4):1352-8. PubMed ID: 2426361
[TBL] [Abstract][Full Text] [Related]
8. A B cell population that dominates the primary response to influenza virus hemagglutinin does not participate in the memory response.
Kavaler J; Caton AJ; Staudt LM; Gerhard W
Eur J Immunol; 1991 Nov; 21(11):2687-95. PubMed ID: 1936117
[TBL] [Abstract][Full Text] [Related]
9. Fine specificity and sequence of antibodies directed against the ectodomain of matrix protein 2 of influenza A virus.
Zhang M; Zharikova D; Mozdzanowska K; Otvos L; Gerhard W
Mol Immunol; 2006 Jul; 43(14):2195-206. PubMed ID: 16472860
[TBL] [Abstract][Full Text] [Related]
10. Molecular analysis of heavy and light chains used by primary and secondary anti-(T,G)-A--L antibodies produced by normal and xid mice.
Busto P; Gerstein R; Dupre L; Giorgetti CA; Selsing E; Press JL
J Immunol; 1987 Jul; 139(2):608-18. PubMed ID: 3110274
[TBL] [Abstract][Full Text] [Related]
11. Amino acid sequence of a phosphocholine-binding antibody from an immune defective CBA/N mouse employing the T15 VH region associated with unusual DH, JH, and V kappa segments.
Clarke SH; Kenny JJ; Sieckmann DG; Rudikoff S
J Immunol; 1984 Mar; 132(3):1544-9. PubMed ID: 6420465
[TBL] [Abstract][Full Text] [Related]
12. Patterns of Ig V region expression among neonatal hemagglutinin-responsive B cells. Evidence for non-random VH gene representation during later stages of development.
Kienker LJ; Korostoff JM; Cancro MP
J Immunol; 1988 Nov; 141(10):3634-41. PubMed ID: 3141502
[TBL] [Abstract][Full Text] [Related]
13. 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; 144(2):583-92. PubMed ID: 2129539
[TBL] [Abstract][Full Text] [Related]
14. Germline V genes encode viable motheaten mouse autoantibodies against thymocytes and red blood cells.
Kasturi KN; Mayer R; Bona CA; Scott VE; Sidman CL
J Immunol; 1990 Oct; 145(7):2304-11. PubMed ID: 2118932
[TBL] [Abstract][Full Text] [Related]
15. Sequences of the VH and VL regions of murine monoclonal antibodies against 3-fucosyllactosamine.
Kimura H; Cook R; Meek K; Umeda M; Ball E; Capra JD; Marcus DM
J Immunol; 1988 Feb; 140(4):1212-7. PubMed ID: 2893825
[TBL] [Abstract][Full Text] [Related]
16. V genes of the primary antibody response of C57BL/10 mice to the hapten phenyloxazolone.
Kaartinen M; Pelkonen E; Even J; Mäkelä O
Eur J Immunol; 1988 Jul; 18(7):1095-100. PubMed ID: 3136024
[TBL] [Abstract][Full Text] [Related]
17. Antibodies that are specific for a single amino acid interchange in a protein epitope use structurally distinct variable regions.
Stark SE; Caton AJ
J Exp Med; 1991 Sep; 174(3):613-24. PubMed ID: 1908510
[TBL] [Abstract][Full Text] [Related]
18. VH and VL gene usage by murine IgG antibodies that bind autologous insulin.
Ewulonu UK; Nell LJ; Thomas JW
J Immunol; 1990 Apr; 144(8):3091-8. PubMed ID: 2109009
[TBL] [Abstract][Full Text] [Related]
19. Characteristics of two idiotypic subfamilies of murine anti-p-azobenzenearsonate antibodies.
Robbins PF; Nisonoff A
J Immunol; 1987 Dec; 139(11):3868-77. PubMed ID: 3119722
[TBL] [Abstract][Full Text] [Related]
20. Autoantibodies to thyroglobulin are encoded by diverse V-gene segments and recognize restricted epitopes.
Gleason SL; Gearhart P; Rose NR; Kuppers RC
J Immunol; 1990 Sep; 145(6):1768-75. PubMed ID: 1697309
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
