361 related articles for article (PubMed ID: 7515103)
1. Amino acid residues that flank core peptide epitopes and the extracellular domains of CD4 modulate differential signaling through the T cell receptor.
Vignali DA; Strominger JL
J Exp Med; 1994 Jun; 179(6):1945-56. PubMed ID: 7515103
[TBL] [Abstract][Full Text] [Related]
2. T cell receptor recognition of MHC class II-bound peptide flanking residues enhances immunogenicity and results in altered TCR V region usage.
Carson RT; Vignali KM; Woodland DL; Vignali DA
Immunity; 1997 Sep; 7(3):387-99. PubMed ID: 9324359
[TBL] [Abstract][Full Text] [Related]
3. The two membrane proximal domains of CD4 interact with the T cell receptor.
Vignali DA; Carson RT; Chang B; Mittler RS; Strominger JL
J Exp Med; 1996 May; 183(5):2097-107. PubMed ID: 8642320
[TBL] [Abstract][Full Text] [Related]
4. Recognition of core and flanking amino acids of MHC class II-bound peptides by the T cell receptor.
Sant'Angelo DB; Robinson E; Janeway CA; Denzin LK
Eur J Immunol; 2002 Sep; 32(9):2510-20. PubMed ID: 12207335
[TBL] [Abstract][Full Text] [Related]
5. Recombinant TCR ligand induces early TCR signaling and a unique pattern of downstream activation.
Wang C; Mooney JL; Meza-Romero R; Chou YK; Huan J; Vandenbark AA; Offner H; Burrows GG
J Immunol; 2003 Aug; 171(4):1934-40. PubMed ID: 12902496
[TBL] [Abstract][Full Text] [Related]
6. Does CD4 help to maintain the fidelity of T cell receptor specificity?
Vignali DA; Moreno J; Schiller D; Hämmerling GJ
Int Immunol; 1992 May; 4(5):621-6. PubMed ID: 1627497
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. The role of CD4-Lck in T-cell receptor antagonism: evidence for negative signaling.
Racioppi L; Matarese G; D'Oro U; De Pascale M; Masci AM; Fontana S; Zappacosta S
Proc Natl Acad Sci U S A; 1996 Sep; 93(19):10360-5. PubMed ID: 8816805
[TBL] [Abstract][Full Text] [Related]
9. The majority of immunogenic epitopes generate CD4+ T cells that are dependent on MHC class II-bound peptide-flanking residues.
Arnold PY; La Gruta NL; Miller T; Vignali KM; Adams PS; Woodland DL; Vignali DA
J Immunol; 2002 Jul; 169(2):739-49. PubMed ID: 12097376
[TBL] [Abstract][Full Text] [Related]
10. T cell epitope recognition involved in the low-responsiveness to a region of hen egg lysozyme (46-61) in C57BL/6 mice.
Jang YS; Mikszta JA; Kim BS
Mol Immunol; 1994 Aug; 31(11):803-12. PubMed ID: 7519304
[TBL] [Abstract][Full Text] [Related]
11. T cell recognition of major histocompatibility complex class II complexes with invariant chain processing intermediates.
Morkowski S; Goldrath AW; Eastman S; Ramachandra L; Freed DC; Whiteley P; Rudensky AYu
J Exp Med; 1995 Nov; 182(5):1403-13. PubMed ID: 7595211
[TBL] [Abstract][Full Text] [Related]
12. Profound enhancement of T cell activation mediated by the interaction between the TCR and the D3 domain of CD4.
Vignali DA; Vignali KM
J Immunol; 1999 Feb; 162(3):1431-9. PubMed ID: 9973399
[TBL] [Abstract][Full Text] [Related]
13. FK 506 and cyclosporin each block antigen-induced T cell receptor signalling that is dependent on CD4 co-receptor and operates in the absence of detectable cytoplasmic calcium fluxes.
Metcalfe S; Alexander D; Turner J
Transpl Int; 1994; 7 Suppl 1():S549-51. PubMed ID: 11271304
[TBL] [Abstract][Full Text] [Related]
14. Functional degeneracy of residues in a T cell peptide epitope contributes to its recognition by different T cell hybridomas.
Boyer M; Novak Z; Fraga E; Oikawa K; Kay CM; Fotedar A; Singh B
Int Immunol; 1990; 2(12):1221-33. PubMed ID: 1708677
[TBL] [Abstract][Full Text] [Related]
15. 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; 151(7):3576-86. PubMed ID: 7690807
[TBL] [Abstract][Full Text] [Related]
16. Minute quantities of a single immunodominant foreign epitope are presented as large nested sets by major histocompatibility complex class II molecules.
Vignali DA; Urban RG; Chicz RM; Strominger JL
Eur J Immunol; 1993 Jul; 23(7):1602-7. PubMed ID: 7686856
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Processing and reactivity of T cell epitopes containing two cysteine residues from hen egg-white lysozyme (HEL74-90).
Kang HK; Mikszta JA; Deng H; Sercarz EE; Jensen PE; Kim BS
J Immunol; 2000 Feb; 164(4):1775-82. PubMed ID: 10657624
[TBL] [Abstract][Full Text] [Related]
19. A synthetic peptide mimicking the HLA-DR beta 2-binding site for CD4 inhibits antigen-independent CD4+ T cell adhesion to B cells and CD4+ T cell activation.
Mazerolles F; Barbat C; Fischer A
Int Immunol; 1996 Feb; 8(2):267-74. PubMed ID: 8671612
[TBL] [Abstract][Full Text] [Related]
20. CD4 and CD8 accessory molecules function through interactions with major histocompatibility complex molecules which are not directly associated with the T cell receptor-antigen complex.
Lustgarten J; Waks T; Eshhar Z
Eur J Immunol; 1991 Oct; 21(10):2507-15. PubMed ID: 1915555
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]