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Journal Abstract Search
164 related items for PubMed ID: 9521084
41. Peptide modification or blocking of CD8, resulting in weak TCR signaling, can activate CTL for Fas- but not perforin-dependent cytotoxicity or cytokine production. Kessler B, Hudrisier D, Schroeter M, Tschopp J, Cerottini JC, Luescher IF. J Immunol; 1998 Dec 15; 161(12):6939-46. PubMed ID: 9862728 [Abstract] [Full Text] [Related]
42. The roles of CD4 and CD8 in T cell activation. Miceli MC, Parnes JR. Semin Immunol; 1991 May 15; 3(3):133-41. PubMed ID: 1909592 [Abstract] [Full Text] [Related]
44. [Coreceptor function of CD4 in response to MHC class I molecule]. Zvezdova ES, Grinenko TS, Pobezinskaia EL, Pobezinskiĭ LA, Kazanskiĭ DB. Mol Biol (Mosk); 2008 May 15; 42(4):662-72. PubMed ID: 18856067 [Abstract] [Full Text] [Related]
45. Lack of evidence for aggregation-dependent enhancement of p56lck in the signal transduction upon major histocompatibility complex recognition by mature T cells. Eshima K, Suzuki H, Shinohara N. Immunology; 2002 May 15; 106(1):46-52. PubMed ID: 11972631 [Abstract] [Full Text] [Related]
46. The coreceptor CD4 is expressed in distinct nanoclusters and does not colocalize with T-cell receptor and active protein tyrosine kinase p56lck. Roh KH, Lillemeier BF, Wang F, Davis MM. Proc Natl Acad Sci U S A; 2015 Mar 31; 112(13):E1604-13. PubMed ID: 25829544 [Abstract] [Full Text] [Related]
47. The Src tyrosine kinase Lck binds to CD2, CD4-1, and CD4-2 T cell co-receptors in channel catfish, Ictalurus punctatus. Taylor EB, Wilson M, Bengten E. Mol Immunol; 2015 Aug 31; 66(2):126-38. PubMed ID: 25771179 [Abstract] [Full Text] [Related]
49. Differential regulation of T cell receptor-mediated Th1 cell IFN-gamma production and proliferation by divergent cAMP-mediated redox pathways. Cochrane R, Clark RB, Huang CK, Cone RE. J Interferon Cytokine Res; 2001 Oct 31; 21(10):797-807. PubMed ID: 11710991 [Abstract] [Full Text] [Related]
50. Physical association of CD4 with the T cell receptor. Dianzani U, Shaw A, al-Ramadi BK, Kubo RT, Janeway CA. J Immunol; 1992 Feb 01; 148(3):678-88. PubMed ID: 1370513 [Abstract] [Full Text] [Related]
51. Noncanonical binding of Lck to CD3ε promotes TCR signaling and CAR function. Hartl FA, Beck-Garcìa E, Woessner NM, Flachsmann LJ, Cárdenas RMV, Brandl SM, Taromi S, Fiala GJ, Morath A, Mishra P, Yousefi OS, Zimmermann J, Hoefflin N, Köhn M, Wöhrl BM, Zeiser R, Schweimer K, Günther S, Schamel WW, Minguet S. Nat Immunol; 2020 Aug 01; 21(8):902-913. PubMed ID: 32690949 [Abstract] [Full Text] [Related]
52. Optimal colocalization of TCR and CD8 as a novel mechanism for the control of functional avidity. Cawthon AG, Alexander-Miller MA. J Immunol; 2002 Oct 01; 169(7):3492-8. PubMed ID: 12244138 [Abstract] [Full Text] [Related]
53. Lineage-specific control of superantigen-induced cell death by the protein tyrosine kinase p56(lck). Penninger JM, Wallace VA, Molina T, Mak TW. J Immunol; 1996 Dec 15; 157(12):5359-66. PubMed ID: 8955183 [Abstract] [Full Text] [Related]
55. Requirement for p56(lck) tyrosine kinase activation in Th subset differentiation. Yamashita M, Hashimoto K, Kimura M, Kubo M, Tada T, Nakayama T. Int Immunol; 1998 May 15; 10(5):577-91. PubMed ID: 9645606 [Abstract] [Full Text] [Related]
57. Galectin-1 specifically modulates TCR signals to enhance TCR apoptosis but inhibit IL-2 production and proliferation. Vespa GN, Lewis LA, Kozak KR, Moran M, Nguyen JT, Baum LG, Miceli MC. J Immunol; 1999 Jan 15; 162(2):799-806. PubMed ID: 9916701 [Abstract] [Full Text] [Related]
58. Lipid raft distribution of CD4 depends on its palmitoylation and association with Lck, and evidence for CD4-induced lipid raft aggregation as an additional mechanism to enhance CD3 signaling. Fragoso R, Ren D, Zhang X, Su MW, Burakoff SJ, Jin YJ. J Immunol; 2003 Jan 15; 170(2):913-21. PubMed ID: 12517957 [Abstract] [Full Text] [Related]