194 related articles for article (PubMed ID: 6814767)
1. Antibody responses to trinitrophenyl (TNP)-L-glutamic acid60-L-alanine30-L-tyrosine10 (GAT) in microcultures: anti-hapten and anti-carrier responses appear to be under separable control.
Letvin NL; Rock KL; Nepom JT; Gramm CF; Benacerraf B
Cell Immunol; 1982 Jul; 71(1):89-98. PubMed ID: 6814767
[No Abstract] [Full Text] [Related]
2. Plaque-forming cell responses to trinitrophenyl (TNP)-L-glutamic acid60-L-alanine30-L-tyrosine10 (GAT) in microcultures are not under conventional Ir gene control.
Letvin NL; Benacerraf B; Germain RN
J Immunol; 1981 Oct; 127(4):1534-8. PubMed ID: 6792278
[TBL] [Abstract][Full Text] [Related]
3. L-glutamic acid60-L-alanine30-L-tyrosine10 (GAT): A probe for regulatory mechanisms in antibody responses.
Pierce CW; Kapp JA
Adv Exp Med Biol; 1978; 98():419-28. PubMed ID: 102128
[TBL] [Abstract][Full Text] [Related]
4. Stimulation of the in vivo dinitrophenyl antibody response to the DNP conjugate of L-glutamic acid60-L-alanine30-L-Tyrosine10 (GAT) polymer by a synthetic adjuvant, muramyl dipeptide (MDP): target cells for adjuvant activity and isotypic pattern of MDP-stimulated response.
Lowy I; Theze J; Chedid L
J Immunol; 1980 Jan; 124(1):100-4. PubMed ID: 6965289
[TBL] [Abstract][Full Text] [Related]
5. Cellular and genetic control of antibody responses. VI. Expression of Ir gene function by H-2a accessory cells, but not H-2a T or B cells in responses to TNP-(T,G)-A--L.
Hodes RJ; Hathcock KS; Singer A
J Immunol; 1979 Dec; 123(6):2823-9. PubMed ID: 115922
[No Abstract] [Full Text] [Related]
6. Use of particulate antigen to enhance primary in vitro antibody responses to trinitrophenyl-keyhole limpet hemocyanin.
Buttke TM; Pourbohloul S; Miller NW
J Immunol Methods; 1986 May; 89(2):233-8. PubMed ID: 3517178
[TBL] [Abstract][Full Text] [Related]
7. Regulation of human in vitro anti-hapten responses: demonstration of a carrier effect.
Dosch HM; Lam P; Gelfand EW
Cell Immunol; 1982 Jul; 71(1):110-7. PubMed ID: 6754097
[No Abstract] [Full Text] [Related]
8. Antigen-specific suppression in genetic responder mice to L-glutamic acid60-L-alanine30-L-tyrosine10 (GAT). Characterization of conventional and hybridoma-derived factors produced by suppressor T cells from mice injected as neonates with syngeneic GAT macrophages.
Sorensen CM; Pierce CW
J Exp Med; 1982 Dec; 156(6):1691-710. PubMed ID: 6184435
[TBL] [Abstract][Full Text] [Related]
9. Genetic restrictions in the development of antibody responses to L-glutamic acid60-L-alanine30-L-tyrosine10 by nude mice implanted with semiallogeneic thymus glands.
Lake JP; Kapp JA; Pierce CW
J Immunol; 1986 Feb; 136(3):805-12. PubMed ID: 2934479
[TBL] [Abstract][Full Text] [Related]
10. Immunosuppressive factors from lymphoid cells of nonresponder mice primed with L-glutamic acid60-L-alanine30-L-tyrosine10. IV. Lack of strain restrictions among allogeneic, nonresponder donors and recipients.
Kapp JA
J Exp Med; 1978 Apr; 147(4):997-1006. PubMed ID: 418136
[TBL] [Abstract][Full Text] [Related]
11. Carrier-independent hapten recognition and promiscuous MHC restriction by CD4 T cells induced by trinitrophenylated peptides.
Kohler J; Hartmann U; Grimm R; Pflugfelder U; Weltzien HU
J Immunol; 1997 Jan; 158(2):591-7. PubMed ID: 8992972
[TBL] [Abstract][Full Text] [Related]
12. Genetic control of antibody responses to TNP-nuclease in vitro.
Nadler PI; Miller GP; Sachs DH; Hodes RJ
J Immunol; 1981 May; 126(5):1706-12. PubMed ID: 6783697
[No Abstract] [Full Text] [Related]
13. The induction of cytolytic T lymphocytes with syngeneic trinitrophenyl-coupled membranes.
Sherman L; Mescher MF; Burakoff SJ
J Immunol; 1979 Jul; 123(1):501-2. PubMed ID: 312884
[TBL] [Abstract][Full Text] [Related]
14. Analysis of B cell activation requirements with TNP-conjugated polyacrylamide beads.
Mond JJ; Stein KE; Subbarao B; Paul WE
J Immunol; 1979 Jul; 123(1):239-45. PubMed ID: 376741
[No Abstract] [Full Text] [Related]
15. Hapten, carrier recognition and response by immunocytes of the primitive vertebrate, Notophthalmus viridescens.
Ruben LN
Immunol Lett; 1983 Jan; 6(1):25-7. PubMed ID: 6840813
[TBL] [Abstract][Full Text] [Related]
16. Role of self-carriers in the immune response and tolerance. I. B-cell unresponsiveness and cytotoxic T-cell immunity induced by haptenated syngeneic lymphoid cells.
Scott DW; Long CA
J Exp Med; 1976 Nov; 144(5):1369-74. PubMed ID: 1086885
[TBL] [Abstract][Full Text] [Related]
17. Immune response to the p-azobenzenearsonate-L-glutamic acid60-L-alanine30-L-tyrosine10 (GAT) conjugate. III. Mechanisms of Ir gene-controlled phenotype conversion.
Flores de Castaneda M; Regnier D; Hermier B; Dubert JM; Seman M
Eur J Immunol; 1984 Oct; 14(10):943-50. PubMed ID: 6237921
[TBL] [Abstract][Full Text] [Related]
18. Role of self carriers in the immune response and tolerance. IV. Active T cell suppression in the maintenance of B cell tolerance to a "T-independent" antigen.
Jandinski JJ; Scott DW
J Immunol; 1979 Dec; 123(6):2447-50. PubMed ID: 315422
[TBL] [Abstract][Full Text] [Related]
19. The involvement of suppressor T cells in Ir gene regulation of secondary antibody responses of primed (responder X nonresponder)F1 mice to macrophage-bound L-glutamic acid60-L-alanine30-L-tyrosine.
Germain RN; Benacerraf B
J Exp Med; 1978 Nov; 148(5):1324-37. PubMed ID: 102725
[TBL] [Abstract][Full Text] [Related]
20. Regulation of thymus-independent responses: unresponsiveness to a second challenge of TNP-Ficoll is mediated by hapten-specific antibodies.
Brodeur PH; Wortis HH
J Immunol; 1980 Oct; 125(4):1499-505. PubMed ID: 6967907
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
