130 related articles for article (PubMed ID: 1688589)
21. Simultaneous involvement of all six predicted antigen binding loops of the T cell receptor in recognition of the MHC/antigenic peptide complex.
Kasibhatla S; Nalefski EA; Rao A
J Immunol; 1993 Sep; 151(6):3140-51. PubMed ID: 8376771
[TBL] [Abstract][Full Text] [Related]
22. Biased T cell receptor usage by Ld-restricted, tum- peptide-specific cytotoxic T lymphocyte clones.
Solheim JC; Alexander-Miller MA; Martinko JM; Connolly JM
J Immunol; 1993 Feb; 150(3):800-11. PubMed ID: 8380825
[TBL] [Abstract][Full Text] [Related]
23. Immunodominance correlates with T-cell receptor (alpha beta) gene usage in the class II-restricted response to influenza haemagglutinin.
Smith CA; Graham CM; Thomas DB
Immunology; 1994 Jul; 82(3):343-50. PubMed ID: 7959866
[TBL] [Abstract][Full Text] [Related]
24. Use of bispecific heteroconjugated antibodies (anti-T cell antigen receptor x anti-MHC class II) to study activation of T cells with a full length or truncated antigen receptor zeta-chain.
Wu S; Yang Y; Sadegh-Nasseri S; Ashwell JD
J Immunol; 1993 Mar; 150(6):2211-21. PubMed ID: 8450208
[TBL] [Abstract][Full Text] [Related]
25. Human TCR-gamma/delta alloreactive response to HLA-DR molecules. Comparison with response of TCR-alpha/beta.
Flament C; Benmerah A; Bonneville M; Triebel F; Mami-Chouaib F
J Immunol; 1994 Oct; 153(7):2890-904. PubMed ID: 8089476
[TBL] [Abstract][Full Text] [Related]
26. Two distinct mechanisms account for the immune response (Ir) gene control of the T cell response to pigeon cytochrome c.
McElligott DL; Sorger SB; Matis LA; Hedrick SM
J Immunol; 1988 Jun; 140(12):4123-31. PubMed ID: 2453567
[TBL] [Abstract][Full Text] [Related]
27. Experimental autoimmune encephalomyelitis-resistant mice have highly encephalitogenic myelin basic protein (MBP)-specific T cell clones that recognize a MBP peptide with high affinity for MHC class II.
Abromson-Leeman S; Alexander J; Bronson R; Carroll J; Southwood S; Dorf M
J Immunol; 1995 Jan; 154(1):388-98. PubMed ID: 7527816
[TBL] [Abstract][Full Text] [Related]
28. High frequency and nonrandom distribution of alloreactivity in T cell clones selected for recognition of foreign antigen in association with self class II molecules.
Ashwell JD; Chen C; Schwartz RH
J Immunol; 1986 Jan; 136(2):389-95. PubMed ID: 2416806
[TBL] [Abstract][Full Text] [Related]
29. Structural basis of specificity and degeneracy of T cell recognition: pluriallelic restriction of T cell responses to a peptide antigen involves both specific and promiscuous interactions between the T cell receptor, peptide, and HLA-DR.
Doherty DG; Penzotti JE; Koelle DM; Kwok WW; Lybrand TP; Masewicz S; Nepom GT
J Immunol; 1998 Oct; 161(7):3527-35. PubMed ID: 9759873
[TBL] [Abstract][Full Text] [Related]
30. Preferential usage of T cell antigen receptor V region gene segment V beta 5.1 by Borrelia burgdorferi antigen-reactive T cell clones isolated from a patient with Lyme disease.
Lahesmaa R; Shanafelt MC; Allsup A; Soderberg C; Anzola J; Freitas V; Turck C; Steinman L; Peltz G
J Immunol; 1993 May; 150(9):4125-35. PubMed ID: 7682589
[TBL] [Abstract][Full Text] [Related]
31. Unique T cell antagonist properties of the exact self-correlate of a peptide antigen revealed by self-substitution of non-self-positions in the peptide sequence.
Schountz T; Kasselman JP; Ford SR; Murray JS
Cell Immunol; 1996 Mar; 168(2):193-200. PubMed ID: 8640865
[TBL] [Abstract][Full Text] [Related]
32. [Promiscuous T cell hybridoma derived from NOD mouse].
Katoh M
Hokkaido Igaku Zasshi; 1995 Mar; 70(2):275-88. PubMed ID: 7774880
[TBL] [Abstract][Full Text] [Related]
33. I-Ak polymorphisms define a functionally dominant region for the presentation of hen egg lysozyme peptides.
Rosloniec EF; Vitez LJ; Beck BN; Buerstedde JM; McKean DJ; Landais D; Benoist C; Mathis D; Freed JH
J Immunol; 1989 Jul; 143(1):50-8. PubMed ID: 2786533
[TBL] [Abstract][Full Text] [Related]
34. Genetic restriction and fine specificity of human T cell clones reactive with rabies virus.
Celis E; Karr RW; Dietzschold B; Wunner WH; Koprowski H
J Immunol; 1988 Oct; 141(8):2721-8. PubMed ID: 2459225
[TBL] [Abstract][Full Text] [Related]
35. The relationship between immune interferon production and proliferation in antigen-specific, MHC-restricted T cell lines and clones.
Hecht TT; Longo DL; Matis LA
J Immunol; 1983 Sep; 131(3):1049-55. PubMed ID: 6193170
[TBL] [Abstract][Full Text] [Related]
36. A pentapeptide as minimal antigenic determinant for MHC class I-restricted T lymphocytes.
Reddehase MJ; Rothbard JB; Koszinowski UH
Nature; 1989 Feb; 337(6208):651-3. PubMed ID: 2465495
[TBL] [Abstract][Full Text] [Related]
37. Sequences outside a minimal immunodominant site exert negative effects on recognition by staphylococcal nuclease-specific T cell clones.
Vacchio MS; Berzofsky JA; Krzych U; Smith JA; Hodes RJ; Finnegan A
J Immunol; 1989 Nov; 143(9):2814-9. PubMed ID: 2478626
[TBL] [Abstract][Full Text] [Related]
38. Soluble MHC II-peptide complexes induce antigen-specific apoptosis in T cells.
Nag B; Kendrick T; Arimilli S; Yu SC; Sriram S
Cell Immunol; 1996 May; 170(1):25-33. PubMed ID: 8660796
[TBL] [Abstract][Full Text] [Related]
39. Analysis of peptide binding patterns in different major histocompatibility complex/T cell receptor complexes using pigeon cytochrome c-specific T cell hybridomas. Evidence that a single peptide binds major histocompatibility complex in different conformations.
Bhayani H; Paterson Y
J Exp Med; 1989 Nov; 170(5):1609-25. PubMed ID: 2553848
[TBL] [Abstract][Full Text] [Related]
40. Recognition of the influenza hemagglutinin by class II MHC-restricted T lymphocytes and antibodies. I. Site definition and implications for antigen presentation and T lymphocyte recognition.
Brown LR; Nygard NR; Graham MB; Bono C; Braciale VL; Gorka J; Schwartz BD; Braciale TJ
J Immunol; 1991 Oct; 147(8):2677-84. PubMed ID: 1717572
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]