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164 related items for PubMed ID: 9521084
21. Engagement of T-cell antigen receptor and CD4/CD8 co-receptors induces prolonged STAT activation through autocrine/paracrine stimulation in human primary T cells. Chueh FY, Yu CL. Biochem Biophys Res Commun; 2012 Sep 21; 426(2):242-6. PubMed ID: 22935418 [Abstract] [Full Text] [Related]
22. The cytoplasmic domain of CD8 beta regulates Lck kinase activation and CD8 T cell development. Irie HY, Mong MS, Itano A, Crooks ME, Littman DR, Burakoff SJ, Robey E. J Immunol; 1998 Jul 01; 161(1):183-91. PubMed ID: 9647223 [Abstract] [Full Text] [Related]
23. Expression of functional CD8alpha Beta heterodimer on rat gamma delta T cells does not correlate with the CDR3 length of the TCR delta chain predicted for MHC class I-restricted antigen recognition. Straube F, Herrmann T. Eur J Immunol; 2000 Dec 01; 30(12):3562-8. PubMed ID: 11169397 [Abstract] [Full Text] [Related]
24. Role of CD8beta domains in CD8 coreceptor function: importance for MHC I binding, signaling, and positive selection of CD8+ T cells in the thymus. Bosselut R, Kubo S, Guinter T, Kopacz JL, Altman JD, Feigenbaum L, Singer A. Immunity; 2000 Apr 01; 12(4):409-18. PubMed ID: 10795739 [Abstract] [Full Text] [Related]
25. Zinc is essential for binding of p56(lck) to CD4 and CD8alpha. Lin RS, Rodriguez C, Veillette A, Lodish HF. J Biol Chem; 1998 Dec 04; 273(49):32878-82. PubMed ID: 9830036 [Abstract] [Full Text] [Related]
27. PD-1 suppresses TCR-CD8 cooperativity during T-cell antigen recognition. Li K, Yuan Z, Lyu J, Ahn E, Davis SJ, Ahmed R, Zhu C. Nat Commun; 2021 May 12; 12(1):2746. PubMed ID: 33980853 [Abstract] [Full Text] [Related]
28. Functional evidence for TCR-intrinsic specificity for MHCII. Parrish HL, Deshpande NR, Vasic J, Kuhns MS. Proc Natl Acad Sci U S A; 2016 Mar 15; 113(11):3000-5. PubMed ID: 26831112 [Abstract] [Full Text] [Related]
29. S-acylation of LCK protein tyrosine kinase is essential for its signalling function in T lymphocytes. Kabouridis PS, Magee AI, Ley SC. EMBO J; 1997 Aug 15; 16(16):4983-98. PubMed ID: 9305640 [Abstract] [Full Text] [Related]
31. Inactivation of lck and loss of TCR-mediated signaling upon persistent engagement with complexes of peptide:MHC molecules. Lee JE, Cossoy MB, Chau LA, Singh B, Madrenas J. J Immunol; 1997 Jul 01; 159(1):61-9. PubMed ID: 9200439 [Abstract] [Full Text] [Related]
34. Trafficking of an acylated cytosolic protein: newly synthesized p56(lck) travels to the plasma membrane via the exocytic pathway. Bijlmakers MJ, Marsh M. J Cell Biol; 1999 May 03; 145(3):457-68. PubMed ID: 10225948 [Abstract] [Full Text] [Related]
36. The MHC class II ligand lymphocyte activation gene-3 is co-distributed with CD8 and CD3-TCR molecules after their engagement by mAb or peptide-MHC class I complexes. Hannier S, Triebel F. Int Immunol; 1999 Nov 03; 11(11):1745-52. PubMed ID: 10545478 [Abstract] [Full Text] [Related]
38. Two receptors, two kinases, and T cell lineage determination. Alarcón B, van Santen HM. Sci Signal; 2010 Mar 23; 3(114):pe11. PubMed ID: 20332426 [Abstract] [Full Text] [Related]
39. Association of the adaptor molecule LAT with CD4 and CD8 coreceptors identifies a new coreceptor function in T cell receptor signal transduction. Bosselut R, Zhang W, Ashe JM, Kopacz JL, Samelson LE, Singer A. J Exp Med; 1999 Nov 15; 190(10):1517-26. PubMed ID: 10562325 [Abstract] [Full Text] [Related]