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.
301 related articles for article (PubMed ID: 7963555)
1. Phagocytic processing of exogenous particulate antigens by macrophages for presentation by class I MHC molecules. Harding CV; Song R J Immunol; 1994 Dec; 153(11):4925-33. PubMed ID: 7963555 [TBL] [Abstract][Full Text] [Related]
2. 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; (98):197-211. PubMed ID: 9382741 [TBL] [Abstract][Full Text] [Related]
3. Bone marrow-derived dendritic cells can process bacteria for MHC-I and MHC-II presentation to T cells. Svensson M; Stockinger B; Wick MJ J Immunol; 1997 May; 158(9):4229-36. PubMed ID: 9126984 [TBL] [Abstract][Full Text] [Related]
4. Cloned dendritic cells can present exogenous antigens on both MHC class I and class II molecules. Shen Z; Reznikoff G; Dranoff G; Rock KL J Immunol; 1997 Mar; 158(6):2723-30. PubMed ID: 9058806 [TBL] [Abstract][Full Text] [Related]
5. Phagosomes are fully competent antigen-processing organelles that mediate the formation of peptide:class II MHC complexes. Ramachandra L; Song R; Harding CV J Immunol; 1999 Mar; 162(6):3263-72. PubMed ID: 10092778 [TBL] [Abstract][Full Text] [Related]
6. Sensitization of MHC class I-restricted T cells to exogenous proteins: evidence for an alternative class I-restricted antigen presentation pathway. Martinez-Kinader B; Lipford GB; Wagner H; Heeg K Immunology; 1995 Oct; 86(2):287-95. PubMed ID: 7490131 [TBL] [Abstract][Full Text] [Related]
7. Phagocytic processing of bacterial antigens for class I MHC presentation to T cells. Pfeifer JD; Wick MJ; Roberts RL; Findlay K; Normark SJ; Harding CV Nature; 1993 Jan; 361(6410):359-62. PubMed ID: 7678924 [TBL] [Abstract][Full Text] [Related]
8. Differences in antigen processing with haplotype-mismatched MHC class II heterodimers: Aalpha(d)Abeta(b) heterodimers participate in early endosomal processing. Askew D; Harding CV Eur J Immunol; 2002 Oct; 32(10):2726-36. PubMed ID: 12355424 [TBL] [Abstract][Full Text] [Related]
9. Primary in vivo responses to ovalbumin. Probing the predictive value of the Kb binding motif. Lipford GB; Hoffman M; Wagner H; Heeg K J Immunol; 1993 Feb; 150(4):1212-22. PubMed ID: 7679422 [TBL] [Abstract][Full Text] [Related]
10. Presentation of exogenous antigens by macrophages: analysis of major histocompatibility complex class I and II presentation and regulation by cytokines. Kovacsovics-Bankowski M; Rock KL Eur J Immunol; 1994 Oct; 24(10):2421-8. PubMed ID: 7925570 [TBL] [Abstract][Full Text] [Related]
11. Analysis of the role of MHC class II presentation in the stimulation of cytotoxic T lymphocytes by antigens targeted into the exogenous antigen-MHC class I presentation pathway. Rock KL; Clark K J Immunol; 1996 May; 156(10):3721-6. PubMed ID: 8621907 [TBL] [Abstract][Full Text] [Related]
12. Inhibition by brefeldin A of presentation of exogenous protein antigens to MHC class II-restricted T cells. Adorini L; Ullrich SJ; Appella E; Fuchs S Nature; 1990 Jul; 346(6279):63-6. PubMed ID: 2366863 [TBL] [Abstract][Full Text] [Related]
13. Class I-restricted presentation occurs without internalization or processing of exogenous antigenic peptides. Hosken NA; Bevan MJ; Carbone FR J Immunol; 1989 Feb; 142(4):1079-83. PubMed ID: 2492575 [TBL] [Abstract][Full Text] [Related]
14. Mouse Schwann cells activate MHC class I and II restricted T-cell responses, but require external peptide processing for MHC class II presentation. Meyer zu Hörste G; Heidenreich H; Mausberg AK; Lehmann HC; ten Asbroek AL; Saavedra JT; Baas F; Hartung HP; Wiendl H; Kieseier BC Neurobiol Dis; 2010 Feb; 37(2):483-90. PubMed ID: 19914379 [TBL] [Abstract][Full Text] [Related]
15. Antigen expressed by Salmonella typhimurium is processed for class I major histocompatibility complex presentation by macrophages but not infected epithelial cells. Harding CV; Pfeifer JD Immunology; 1994 Dec; 83(4):670-4. PubMed ID: 7875747 [TBL] [Abstract][Full Text] [Related]
16. Phagosomes are competent organelles for antigen cross-presentation. Houde M; Bertholet S; Gagnon E; Brunet S; Goyette G; Laplante A; Princiotta MF; Thibault P; Sacks D; Desjardins M Nature; 2003 Sep; 425(6956):402-6. PubMed ID: 14508490 [TBL] [Abstract][Full Text] [Related]
17. Viral and bacterial minigene products are presented by MHC class I molecules with similar efficiencies. Wolf BJ; Princiotta MF Mol Immunol; 2011 Jan; 48(4):463-71. PubMed ID: 21067810 [TBL] [Abstract][Full Text] [Related]
18. Alternative processing for MHC class I presentation by immature and CpG-activated dendritic cells. Chen L; Jondal M Eur J Immunol; 2004 Apr; 34(4):952-60. PubMed ID: 15048705 [TBL] [Abstract][Full Text] [Related]
19. Simultaneous presentation and cross-presentation of immune-stimulating complex-associated cognate antigen by antigen-specific B cells. Robson NC; Donachie AM; Mowat AM Eur J Immunol; 2008 May; 38(5):1238-46. PubMed ID: 18398931 [TBL] [Abstract][Full Text] [Related]
20. Identification of Salmonella typhimurium genes responsible for interference with peptide presentation on MHC class I molecules: Deltayej Salmonella mutants induce superior CD8+ T-cell responses. Qimron U; Madar N; Mittrücker HW; Zilka A; Yosef I; Bloushtain N; Kaufmann SH; Rosenshine I; Apte RN; Porgador A Cell Microbiol; 2004 Nov; 6(11):1057-70. PubMed ID: 15469434 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]