These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
704 related articles for article (PubMed ID: 1970351)
21. Polymorphic residues on the I-A beta chain modulate the stimulation of T cell clones specific for the N-terminal peptide of the autoantigen myelin basic protein. Davis CB; Mitchell DJ; Wraith DC; Todd JA; Zamvil SS; McDevitt HO; Steinman L; Jones PP J Immunol; 1989 Oct; 143(7):2083-93. PubMed ID: 2476496 [TBL] [Abstract][Full Text] [Related]
22. Functional mapping of MHC class II polymorphic residues. The alpha-chain controls the specificity for binding an Ad-versus an A k-restricted peptide and the beta-chain region 65-67 controls T cell recognition but not peptide binding. Lee JM; McKean DJ; Watts TH J Immunol; 1991 May; 146(9):2952-9. PubMed ID: 1849939 [TBL] [Abstract][Full Text] [Related]
23. Comparison of structural requirements for interaction of the same peptide with I-Ek and I-Ed molecules in the activation of MHC class II-restricted T cells. Leighton J; Sette A; Sidney J; Appella E; Ehrhardt C; Fuchs S; Adorini L J Immunol; 1991 Jul; 147(1):198-204. PubMed ID: 1711074 [TBL] [Abstract][Full Text] [Related]
24. Insulin-specific T cell hybridomas derived from (H-2b x H-2k)F1 mice preferably employ F1-unique restriction elements for antigen recognition. Reske-Kunz AB; Rüde E Eur J Immunol; 1985 Oct; 15(10):1048-54. PubMed ID: 2414111 [TBL] [Abstract][Full Text] [Related]
25. Permissive recognition of a mycobacterial T-cell epitope: localization of overlapping epitope core sequences recognized in association with multiple major histocompatibility complex class II I-A molecules. Harris DP; Vordermeier HM; Arya A; Moreno C; Ivanyi J Immunology; 1995 Apr; 84(4):555-61. PubMed ID: 7790029 [TBL] [Abstract][Full Text] [Related]
26. Epitope specificity and Ia restriction of T cell responses to insulin in a system of complementing Ir genes: analysis with primed lymph node T cells and a long-term cultured T cell line. Spaeth E; Rüde E Eur J Immunol; 1983 Sep; 13(9):756-61. PubMed ID: 6193966 [TBL] [Abstract][Full Text] [Related]
28. T cell recognition of Mlsc. I. Influence of MHC gene products in Mlsc-specific T cell recognition. Abe R; Hodes RJ J Immunol; 1988 Jun; 140(12):4132-8. PubMed ID: 2453568 [TBL] [Abstract][Full Text] [Related]
29. Identification of the T-cell and Ia contact residues of a T-cell antigenic epitope. Allen PM; Matsueda GR; Evans RJ; Dunbar JB; Marshall GR; Unanue ER Nature; 1987 Jun 25-Jul 1; 327(6124):713-5. PubMed ID: 2439915 [TBL] [Abstract][Full Text] [Related]
30. T cells that recognize peptide sequences of self MHC class II molecules exist in syngeneic mice. Agrawal B; Manickasundari M; Fraga E; Singh B J Immunol; 1991 Jul; 147(2):383-90. PubMed ID: 1649218 [TBL] [Abstract][Full Text] [Related]
31. T cell receptor gene segment usage in a panel of hen-egg white lysozyme specific, I-Ak-restricted T helper hybridomas. Johnson NA; Carland F; Allen PM; Glimcher LH J Immunol; 1989 May; 142(9):3298-304. PubMed ID: 2468715 [TBL] [Abstract][Full Text] [Related]
32. Broad recognition of cytotoxic T cell epitopes from the HIV-1 envelope protein with multiple class I histocompatibility molecules. Shirai M; Pendleton CD; Berzofsky JA J Immunol; 1992 Mar; 148(6):1657-67. PubMed ID: 1371784 [TBL] [Abstract][Full Text] [Related]
33. The expressed T cell repertoire is hierarchical: the precise focus of lysozyme-specific T cell clones is dependent upon the structure of the immunogen. Shastri N; Miller A; Sercarz EE J Mol Cell Immunol; 1984; 1(6):369-79. PubMed ID: 6086045 [TBL] [Abstract][Full Text] [Related]
34. The influence of self-MHC and non-MHC antigens on the selection of an antigen-specific T cell receptor repertoire. Fry AM; Cotterman MM; Matis LA J Immunol; 1989 Oct; 143(8):2723-9. PubMed ID: 2477456 [TBL] [Abstract][Full Text] [Related]
35. Cytotoxic T lymphocyte response to minor H-43a alloantigen in H-43b mice. Privileged H-2Kb restriction to the response is not due to immunodominance or epistatic effect but due to Ir gene function of H-2Kb itself. Hino T; Ishikawa H; Saito K J Immunol; 1988 Jan; 140(1):44-51. PubMed ID: 3121741 [TBL] [Abstract][Full Text] [Related]
36. Cross-reactive trinitrophenylated peptides as antigens for class II major histocompatibility complex-restricted T cells and inducers of contact sensitivity in mice. Limited T cell receptor repertoire. Kohler J; Martin S; Pflugfelder U; Ruh H; Vollmer J; Weltzien HU Eur J Immunol; 1995 Jan; 25(1):92-101. PubMed ID: 7843258 [TBL] [Abstract][Full Text] [Related]
37. Analysis of the interaction of peptide hen egg white lysozyme (34-45) with the I-Ak molecule. Lambert LE; Unanue ER J Immunol; 1989 Aug; 143(3):802-7. PubMed ID: 2787347 [TBL] [Abstract][Full Text] [Related]
38. Dominant suppressive effect of the silent Eb alpha allele on an in vivo T helper cell response under Ed beta Ed alpha region-linked immune response gene control. Bogen B Eur J Immunol; 1985 Oct; 15(10):1033-7. PubMed ID: 2932337 [TBL] [Abstract][Full Text] [Related]
39. Complexes generated by the binding of free peptides to class II MHC molecules are antigenically diverse compared with those generated by intracellular processing. Viner NJ; Nelson CA; Deck B; Unanue ER J Immunol; 1996 Apr; 156(7):2365-8. PubMed ID: 8786292 [TBL] [Abstract][Full Text] [Related]
40. Both H-2- and non-H-2-linked genes influence influenza nucleoprotein epitope recognition by CD4+ T cells. Brett SJ; Tite JP Immunology; 1996 Jan; 87(1):42-8. PubMed ID: 8666434 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]