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.
625 related articles for article (PubMed ID: 2840479)
1. Enhanced T cell responses to antigenic peptides targeted to B cell surface Ig, Ia, or class I molecules. Casten LA; Kaumaya P; Pierce SK J Exp Med; 1988 Jul; 168(1):171-80. PubMed ID: 2840479 [TBL] [Abstract][Full Text] [Related]
2. Receptor-mediated B cell antigen processing. Increased antigenicity of a globular protein covalently coupled to antibodies specific for B cell surface structures. Casten LA; Pierce SK J Immunol; 1988 Jan; 140(2):404-10. PubMed ID: 2447176 [TBL] [Abstract][Full Text] [Related]
3. Time dependence of B cell processing and presentation of peptide and native protein antigens. Lakey EK; Casten LA; Niebling WL; Margoliash E; Pierce SK J Immunol; 1988 May; 140(10):3309-14. PubMed ID: 2834435 [TBL] [Abstract][Full Text] [Related]
4. T cell activation by processed antigen is equally blocked by I-E and I-A-restricted immunodominant peptides. Lakey EK; Casten LA; Anderson MS; Smolenski LA; Smith JA; Margoliash E; Pierce SK Eur J Immunol; 1987 Nov; 17(11):1605-9. PubMed ID: 3500065 [TBL] [Abstract][Full Text] [Related]
5. Isolation of a functional antigen-Ia complex. Srinivasan M; Pierce SK Proc Natl Acad Sci U S A; 1990 Feb; 87(3):919-22. PubMed ID: 2153978 [TBL] [Abstract][Full Text] [Related]
6. Role of L3T4 and Ia in the heteroclitic response of T cells to cytochrome c. Lakey EK; Margoliash E; Fitch FW; Pierce SK J Immunol; 1986 Jun; 136(11):3933-8. PubMed ID: 2422265 [TBL] [Abstract][Full Text] [Related]
7. Peptides related to the antigenic determinant block T cell recognition of the native protein as processed by antigen-presenting cells. Lakey EK; Margoliash E; Flouret G; Pierce SK Eur J Immunol; 1986 Jul; 16(7):721-7. PubMed ID: 2424770 [TBL] [Abstract][Full Text] [Related]
8. Antigen-presenting function of B lymphocytes. Pierce SK; Morris JF; Grusby MJ; Kaumaya P; van Buskirk A; Srinivasan M; Crump B; Smolenski LA Immunol Rev; 1988 Dec; 106():149-80. PubMed ID: 3075588 [TBL] [Abstract][Full Text] [Related]
9. Anti-immunoglobulin augments the B-cell antigen-presentation function independently of internalization of receptor-antigen complex. Casten LA; Lakey EK; Jelachich ML; Margoliash E; Pierce SK Proc Natl Acad Sci U S A; 1985 Sep; 82(17):5890-4. PubMed ID: 2994052 [TBL] [Abstract][Full Text] [Related]
10. Biochemical evidence for the rapid assembly and disassembly of processed antigen-major histocompatibility complex class II complexes in acidic vesicles of B cells. Marsh EW; Dalke DP; Pierce SK J Exp Med; 1992 Feb; 175(2):425-36. PubMed ID: 1310101 [TBL] [Abstract][Full Text] [Related]
11. Peptides of 23 residues or greater are required to stimulate a high affinity class II-restricted T cell response. Srinivasan M; Domanico SZ; Kaumaya PT; Pierce SK Eur J Immunol; 1993 May; 23(5):1011-6. PubMed ID: 8386663 [TBL] [Abstract][Full Text] [Related]
12. Identification of a peptide binding protein that plays a role in antigen presentation. Lakey EK; Margoliash E; Pierce SK Proc Natl Acad Sci U S A; 1987 Mar; 84(6):1659-63. PubMed ID: 3031645 [TBL] [Abstract][Full Text] [Related]
13. A monoclonal antibody specific for a cytochrome c T cell stimulatory peptide inhibits T cell responses and affects the way the peptide associates with antigen-presenting cells. Jemmerson R; Johnson JG; Burrell E; Taylor PS; Jenkins MK Eur J Immunol; 1991 Jan; 21(1):143-51. PubMed ID: 1846813 [TBL] [Abstract][Full Text] [Related]
14. Characteristics of peptides which compete for presented antigen-binding sites on antigen-presenting cells. Smolenski LA; Kaumaya P; Atassi MZ; Pierce SK Eur J Immunol; 1990 May; 20(5):953-60. PubMed ID: 2162778 [TBL] [Abstract][Full Text] [Related]
15. Processing of a minimal antigenic peptide alters its interaction with MHC molecules. Fox BS; Carbone FR; Germain RN; Paterson Y; Schwartz RH Nature; 1988 Feb; 331(6156):538-40. PubMed ID: 2448649 [TBL] [Abstract][Full Text] [Related]
16. The B10.A mouse B cell response to pigeon cytochrome c is directed against the same area of the protein that is recognized by B10.A T cells in association with the Ek beta:Ek alpha Ia molecule. Hannum CH; Matis LA; Schwartz RH; Margoliash E J Immunol; 1985 Nov; 135(5):3314-22. PubMed ID: 2995490 [TBL] [Abstract][Full Text] [Related]
17. Immune response gene function correlates with the expression of an Ia antigen. II. A quantitative deficiency in Ae:E alpha complex expression causes a corresponding defect in antigen-presenting cell function. Matis LA; Jones PP; Murphy DB; Hedrick SM; Lerner EA; Janeway CA; McNicholas JM; Schwartz RH J Exp Med; 1982 Feb; 155(2):508-23. PubMed ID: 6173457 [TBL] [Abstract][Full Text] [Related]
18. Functionally distinct agretopic and epitopic sites. Analysis of the dominant T cell determinant of moth and pigeon cytochromes c with the use of synthetic peptide antigens. Fox BS; Chen C; Fraga E; French CA; Singh B; Schwartz RH J Immunol; 1987 Sep; 139(5):1578-88. PubMed ID: 2442249 [TBL] [Abstract][Full Text] [Related]
19. Optimization of antigen presentation to T cell hybridomas by purified Ia molecules in planar membranes. Ia molecule polymorphism determines the antigenic fine specificity of the response to cytochrome c peptides. Quill H; Carlson L; Fox BS; Weinstein JN; Schwartz RH J Immunol Methods; 1987 Apr; 98(1):29-41. PubMed ID: 2435810 [TBL] [Abstract][Full Text] [Related]
20. The molecular basis of the requirement for antigen processing of pigeon cytochrome c prior to T cell activation. Kovac Z; Schwartz RH J Immunol; 1985 May; 134(5):3233-40. PubMed ID: 2580020 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]