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.
686 related articles for article (PubMed ID: 2420871)
1. Ia-specific mixed leukocyte reactive T cell hybridomas: analysis of their specificity by using purified class II MHC molecules in synthetic membrane system. Coeshott CM; Chesnut RW; Kubo RT; Grammer SF; Jenis DM; Grey HM J Immunol; 1986 Apr; 136(8):2832-8. PubMed ID: 2420871 [TBL] [Abstract][Full Text] [Related]
2. Specific lymphocyte-target cell conjugate formation between tumor-specific helper T-cell hybridomas and IA-bearing RCS tumors and IE-bearing allogeneic cells. I. Role of Ia and both L3T4 and LFA-1 antigens in recognition/binding. Ohnishi K; Bonavida B J Immunol; 1986 Dec; 137(11):3681-8. PubMed ID: 2946766 [TBL] [Abstract][Full Text] [Related]
3. Mapping of SJL/J reticulum cell sarcoma tumor-associated Ia antigens by T cell hybridomas: characterization of tumor-specific and shared epitopes detected on IE+ allogeneic cells. Ohnishi K; Bonavida B J Immunol; 1986 Jul; 137(2):733-40. PubMed ID: 2424977 [TBL] [Abstract][Full Text] [Related]
4. Studies on the capacity of intact cells and purified Ia from different B cell sources to function in antigen presentation to T cells. Krieger J; Jenis DM; Chesnut RW; Grey HM J Immunol; 1988 Jan; 140(2):388-94. PubMed ID: 2961812 [TBL] [Abstract][Full Text] [Related]
5. A rat anti-mouse T4 monoclonal antibody (H129.19) inhibits the proliferation of Ia-reactive T cell clones and delineates two phenotypically distinct (T4+, Lyt-2,3-, and T4-, Lyt-2,3+) subsets among anti-Ia cytolytic T cell clones. Pierres A; Naquet P; Van Agthoven A; Bekkhoucha F; Denizot F; Mishal Z; Schmitt-Verhulst AM; Pierres M J Immunol; 1984 Jun; 132(6):2775-82. PubMed ID: 6202760 [TBL] [Abstract][Full Text] [Related]
6. Two roles for Ia in antigen-specific T cell activation. II. Toward a Velcro model of antigen recognition. Kim KH; Thomas DW J Immunol; 1988 Apr; 140(8):2500-7. PubMed ID: 3258611 [TBL] [Abstract][Full Text] [Related]
7. Transfer of antigen-presenting capacity to Ia-negative cells upon fusion with Ia-bearing liposomes. Coeshott C; Grey HM J Immunol; 1985 Mar; 134(3):1343-8. PubMed ID: 2981915 [TBL] [Abstract][Full Text] [Related]
8. Search for class II major histocompatibility complex molecular involvement in the response of Lyt-2+ cytotoxic T lymphocyte precursors to alloantigen. Romani L; Mage MG Eur J Immunol; 1985 Nov; 15(11):1125-30. PubMed ID: 2933265 [TBL] [Abstract][Full Text] [Related]
9. Requirement for recognition of class II molecules and processed tumor antigen for optimal generation of syngeneic tumor-specific class I-restricted CTL. Kern DE; Klarnet JP; Jensen MC; Greenberg PD J Immunol; 1986 Jun; 136(11):4303-10. PubMed ID: 2422280 [TBL] [Abstract][Full Text] [Related]
10. Requirement of Ia-positive accessory cells in the MLR response against class II antigen on human B cell tumor line. Yamamoto M; Yano A J Immunol; 1985 Dec; 135(6):3887-96. PubMed ID: 2999233 [TBL] [Abstract][Full Text] [Related]
11. The major histocompatibility complex-restricted antigen receptor on T cells. IX. Role of accessory molecules in recognition of antigen plus isolated IA. Gay D; Coeshott C; Golde W; Kappler J; Marrack P J Immunol; 1986 Mar; 136(6):2026-32. PubMed ID: 3512708 [TBL] [Abstract][Full Text] [Related]
13. Studies on the mechanism of stimulation of T cells by the Mycoplasma arthritidis-derived mitogen. Role of class II IE molecules. Bekoff MC; Cole BC; Grey HM J Immunol; 1987 Nov; 139(10):3189-94. PubMed ID: 3500207 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Analysis of T hybridomas prepared from a T cell clone with three specificities. Recognition of self + X and allo-H-2 determinants segregates from recognition of Mlsa determinants. Webb SR; Okamoto A; Sprent J J Immunol; 1988 Sep; 141(6):1828-34. PubMed ID: 2459192 [TBL] [Abstract][Full Text] [Related]
16. T cell responses to Mls determinants are restricted by cross-reactive MHC determinants. Lynch DH; Gress RE; Needleman BW; Rosenberg SA; Hodes RJ J Immunol; 1985 Apr; 134(4):2071-8. PubMed ID: 2579127 [TBL] [Abstract][Full Text] [Related]
17. The role of class II MHC molecules in the activation of class I-reactive T cell hybridomas. Minami M; Nariuchi H; Kawasaki H; Dorf ME J Immunol; 1986 May; 136(9):3341-5. PubMed ID: 2420887 [TBL] [Abstract][Full Text] [Related]
18. Epidermal cells as accessory cells in the generation of allo-reactive and hapten-specific cytotoxic T lymphocyte (CTL) responses. Steiner G; Wolff K; Pehamberger H; Stingl G J Immunol; 1985 Feb; 134(2):736-41. PubMed ID: 2578162 [TBL] [Abstract][Full Text] [Related]
19. Production of T-T hybrids from T cell clones. Direct comparison between cloned T cells and T hybridoma cells derived from them. Ozaki S; Durum SK; Muegge K; York-Jolley J; Berzofsky JA J Immunol; 1988 Jul; 141(1):71-8. PubMed ID: 2454265 [TBL] [Abstract][Full Text] [Related]
20. Allo-Ia reactive murine T-cell lines. II. Mechanisms of clonal expansion of T cells explored by use of the allo-Ia reactive T cell clones. Narimatsu H; Saito K J Immunol; 1983 Jul; 131(1):37-44. PubMed ID: 6190916 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]