209 related articles for article (PubMed ID: 1709141)
1. Bovine T cells recognize antigen in association with MHC class II haplotypes defined by one-dimensional isoelectric focusing.
Glass EJ; Oliver RA; Spooner RL
Immunology; 1991 Mar; 72(3):380-5. PubMed ID: 1709141
[TBL] [Abstract][Full Text] [Related]
2. MHC class II restricted recognition of FMDV peptides by bovine T cells.
Glass EJ; Oliver RA; Collen T; Doel TR; Dimarchi R; Spooner RL
Immunology; 1991 Dec; 74(4):594-9. PubMed ID: 1664415
[TBL] [Abstract][Full Text] [Related]
3. Alloreactive T-cell recognition of bovine major histocompatibility complex class II products defined by one-dimensional isoelectric focusing.
Glass EJ; Oliver RA; Williams JL; Millar P
Anim Genet; 1992; 23(2):97-111. PubMed ID: 1443783
[TBL] [Abstract][Full Text] [Related]
4. Induction of effective cross-reactive immunity by FMDV peptides is critically dependent upon specific MHC-peptide-T cell interactions.
Glass EJ; Millar P
Immunology; 1994 May; 82(1):1-8. PubMed ID: 8045586
[TBL] [Abstract][Full Text] [Related]
5. Parasite-accessory cell interactions in theileriosis. Antigen presentation by Theileria annulata-infected macrophages and production of continuously growing antigen-presenting cell lines.
Glass EJ; Spooner RL
Eur J Immunol; 1990 Nov; 20(11):2491-7. PubMed ID: 2253687
[TBL] [Abstract][Full Text] [Related]
6. Regulation of the in vitro presentation of minor lymphocyte stimulating determinants by major histocompatibility complex-encoded immune response genes.
Ryan JJ; Miner DW; Mond JJ; Finkelman FD; Woody JN
J Immunol; 1987 Apr; 138(8):2392-401. PubMed ID: 2435797
[TBL] [Abstract][Full Text] [Related]
7. Peptide vaccines incorporating a 'promiscuous' T-cell epitope bypass certain haplotype restricted immune responses and provide broad spectrum immunogenicity.
Kaumaya PT; Kobs-Conrad S; Seo YH; Lee H; VanBuskirk AM; Feng N; Sheridan JF; Stevens V
J Mol Recognit; 1993 Jun; 6(2):81-94. PubMed ID: 7508238
[TBL] [Abstract][Full Text] [Related]
8. Two distinct class II molecules encoded by the genes within HLA-DR subregion of HLA-Dw2 and Dw12 can act as stimulating and restriction molecules.
Sone T; Tsukamoto K; Hirayama K; Nishimura Y; Takenouchi T; Aizawa M; Sasazuki T
J Immunol; 1985 Aug; 135(2):1288-98. PubMed ID: 3159789
[TBL] [Abstract][Full Text] [Related]
9. Mechanisms involved in the Ir-gene control of T suppressor cell response to lactate dehydrogenase B.
Baxevanis CN; Ikezawa Z; Klein J; Nagy ZA
J Mol Cell Immunol; 1984; 1(4):201-10. PubMed ID: 6242858
[TBL] [Abstract][Full Text] [Related]
10. Human anti-porcine xenogeneic T cell response. Evidence for allelic specificity of mixed leukocyte reaction and for both direct and indirect pathways of recognition.
Yamada K; Sachs DH; DerSimonian H
J Immunol; 1995 Dec; 155(11):5249-56. PubMed ID: 7594537
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The influence of MHC polymorphism on the selection of T-cell determinants of FMDV in cattle.
Van Lierop MJ; Nilsson PR; Wagenaar JP; Van Noort JM; Campbell JD; Glass EJ; Joosten I; Hensen EJ
Immunology; 1995 Jan; 84(1):79-85. PubMed ID: 7534267
[TBL] [Abstract][Full Text] [Related]
13. Genetic regulation of the immune response to hepatitis B surface antigen (HBsAg). V. T cell proliferative response and cellular interactions.
Milich DR; Louie RE; Chisari FV
J Immunol; 1985 Jun; 134(6):4194-202. PubMed ID: 3921619
[TBL] [Abstract][Full Text] [Related]
14. Immune selection in murine tumors. Ph.d thesis.
Svane IM; Engel AM
APMIS Suppl; 2003; (106):1-46. PubMed ID: 12739251
[TBL] [Abstract][Full Text] [Related]
15. Requirement for MHC class II positive accessory cells in an antigen specific bovine T cell response.
Glass EJ; Spooner RL
Res Vet Sci; 1989 Mar; 46(2):196-201. PubMed ID: 2523083
[TBL] [Abstract][Full Text] [Related]
16. Antigen presentation by cells that are not of bone marrow origin.
Geppert TD; Lipsky PE
Reg Immunol; 1989; 2(1):60-71. PubMed ID: 2518360
[TBL] [Abstract][Full Text] [Related]
17. Modified MHC restriction of donor-origin T cells in humans with severe combined immunodeficiency transplanted with haploidentical bone marrow stem cells.
Roberts JL; Volkman DJ; Buckley RH
J Immunol; 1989 Sep; 143(5):1575-9. PubMed ID: 2474604
[TBL] [Abstract][Full Text] [Related]
18. Relationship among function, phenotype, and specificity in primary allospecific T cell populations: identification of phenotypically identical but functionally distinct primary T cell subsets that differ in their recognition of MHC class I and class II allodeterminants.
Golding H; Mizuochi T; McCarthy SA; Cleveland CA; Singer A
J Immunol; 1987 Jan; 138(1):10-7. PubMed ID: 2946773
[TBL] [Abstract][Full Text] [Related]
19. Comparison of antigen specificity, class II major histocompatibility complex restriction, and in vivo behavior of myelin basic protein-specific T cell lines and clones derived from (BALB/c x SJL/J) mice.
Trotter J; Zamvil SS; Steinman L
J Immunol; 1987 Sep; 139(6):1834-9. PubMed ID: 2442257
[TBL] [Abstract][Full Text] [Related]
20. Bacterial proteins that mediate the association of a defined subset of T cell receptor:CD4 complexes with class II MHC.
Yagi J; Baron J; Buxser S; Janeway CA
J Immunol; 1990 Feb; 144(3):892-901. PubMed ID: 2136903
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
