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110 related items for PubMed ID: 1719084
21. Inhibition by chloroquine of the class II major histocompatibility complex-restricted presentation of endogenous antigens varies according to the cellular origin of the antigen-presenting cells, the nature of the T-cell epitope, and the responding T cell. Lombard-Platlet S, Bertolino P, Deng H, Gerlier D, Rabourdin-Combe C. Immunology; 1993 Dec; 80(4):566-73. PubMed ID: 7508420 [Abstract] [Full Text] [Related]
22. Constraints in antigen processing result in unresponsiveness to a T cell epitope of hen egg lysozyme in C57BL/6 mice. Kim BS, Jang YS. Eur J Immunol; 1992 Mar; 22(3):775-82. PubMed ID: 1372259 [Abstract] [Full Text] [Related]
23. Structural features of an antigen required for cellular interactions and for T cell activation in a MHC-restricted response. Langton BC, Mackewicz CE, Wan AM, Andria ML, Benjamini E. J Immunol; 1988 Jul 15; 141(2):447-56. PubMed ID: 3260252 [Abstract] [Full Text] [Related]
24. Processing of endogenously synthesized hen egg-white lysozyme retained in the endoplasmic reticulum or in secretory form gives rise to a similar but not identical set of epitopes recognized by class II-restricted T cells. Adorini L, Guéry JC, Fuchs S, Ortiz-Navarrete V, Hämmerling GJ, Momburg F. J Immunol; 1993 Oct 01; 151(7):3576-86. PubMed ID: 7690807 [Abstract] [Full Text] [Related]
25. The T cell response to allelic determinants on Igh-1-encoded IgG2a antibodies: dual recognition examined by using antigenic antibodies with binding affinity for Ia molecules. Hedrick SM, Schwartz RH. J Immunol; 1983 Apr 01; 130(4):1958-66. PubMed ID: 6187829 [Abstract] [Full Text] [Related]
26. Bacterial antigen delivery systems: phagocytic processing of bacterial antigens for MHC-I and MHC-II presentation to T cells. Svensson M, Pfeifer J, Stockinger B, Wick MJ. Behring Inst Mitt; 1997 Feb 01; (98):197-211. PubMed ID: 9382741 [Abstract] [Full Text] [Related]
27. Binding of malaria T cell epitopes to DR and DQ molecules in vitro correlates with immunogenicity in vivo: identification of a universal T cell epitope in the Plasmodium falciparum circumsporozoite protein. Calvo-Calle JM, Hammer J, Sinigaglia F, Clavijo P, Moya-Castro ZR, Nardin EH. J Immunol; 1997 Aug 01; 159(3):1362-73. PubMed ID: 9233633 [Abstract] [Full Text] [Related]
28. Determination of amino acids on agretopes of pigeon cytochrome c-related peptides specifically bound to I-A allelic products. Itoh Y, Ogasawara K, Takami K, Gotohda T, Naruse H, Good RA, Onoé K. Eur J Immunol; 1994 Jan 01; 24(1):76-83. PubMed ID: 7517365 [Abstract] [Full Text] [Related]
29. A peptide binding motif for I-Eg7, the MHC class II molecule that protects E alpha-transgenic nonobese diabetic mice from autoimmune diabetes. Gregori S, Trembleau S, Penna G, Gallazzi F, Hammer J, Papadopoulos GK, Adorini L. J Immunol; 1999 Jun 01; 162(11):6630-40. PubMed ID: 10352280 [Abstract] [Full Text] [Related]
30. Fine specificity of murine class II-restricted T cell clones for synthetic peptides of influenza virus hemagglutinin. Heterogeneity of antigen interaction with the T cell and the Ia molecule. Mills KH, Burt DS, Skehel JJ, Thomas DB. J Immunol; 1988 Jun 15; 140(12):4083-90. PubMed ID: 2453566 [Abstract] [Full Text] [Related]
31. [Promiscuous T cell hybridoma derived from NOD mouse]. Katoh M. Hokkaido Igaku Zasshi; 1995 Mar 15; 70(2):275-88. PubMed ID: 7774880 [Abstract] [Full Text] [Related]
32. Glycopeptides bind MHC molecules and elicit specific T cell responses. Harding CV, Kihlberg J, Elofsson M, Magnusson G, Unanue ER. J Immunol; 1993 Sep 01; 151(5):2419-25. PubMed ID: 8360471 [Abstract] [Full Text] [Related]
33. In vivo treatment with monoclonal anti-I-A antibodies: disappearance of splenic antigen-presenting cell function concomitant with modulation of splenic cell surface I-A and I-E antigens. Kruisbeek AM, Titus JA, Stephany DA, Gause BL, Longo DL. J Immunol; 1985 Jun 01; 134(6):3605-14. PubMed ID: 2580891 [Abstract] [Full Text] [Related]
34. Alteration of a non-polymorphic residue in a class II E beta gene eliminates an antibody-defined epitope without affecting T cell recognition. Griffith IJ, Carland FM, Glimcher LH. J Immunol; 1987 Jun 15; 138(12):4480-3. PubMed ID: 2438346 [Abstract] [Full Text] [Related]
35. 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 01; 146(9):2952-9. PubMed ID: 1849939 [Abstract] [Full Text] [Related]
36. Epitopes associated with major histocompatibility complex (MHC) restriction site of T cells. IV. I-J epitopes on MHC-restricted cloned T cells. Nakayama T, Kubo RT, Kubo M, Fujisawa I, Kishimoto H, Asano Y, Tada T. Eur J Immunol; 1988 May 01; 18(5):761-5. PubMed ID: 2454195 [Abstract] [Full Text] [Related]
37. H-2-associated effects of flanking residues on the recognition of a permissive mycobacterial T-cell epitope. Román E, Harris DP, Jurcevic S, Ivanyi J, Moreno C. Immunology; 1995 Oct 01; 86(2):183-9. PubMed ID: 7490116 [Abstract] [Full Text] [Related]
38. Functional effects of N-linked oligosaccharides located on the external domain of murine class II molecules. Wei BY, Buerstedde JM, Bell M, Chase C, Nilson A, Browne A, Pease L, McKean DJ. J Immunol; 1991 Apr 01; 146(7):2358-66. PubMed ID: 1706396 [Abstract] [Full Text] [Related]
39. The signal sequence of lymphocytic choriomeningitis virus contains an immunodominant cytotoxic T cell epitope that is restricted by both H-2D(b) and H-2K(b) molecules. Hudrisier D, Oldstone MB, Gairin JE. Virology; 1997 Jul 21; 234(1):62-73. PubMed ID: 9234947 [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 21; 87(1):42-8. PubMed ID: 8666434 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]