183 related articles for article (PubMed ID: 7819146)
1. Different types of in vivo induced cytolytic T lymphocytes are all LFA-Ihigh and lack CD45 exon 4 (CD45RA) but show distinct CD45RC profiles.
Hansson J; Ericsson PO; Widegren B; Dohlsten M; Sjögren HO; Hedlund G
Int Immunol; 1994 Sep; 6(9):1375-81. PubMed ID: 7819146
[TBL] [Abstract][Full Text] [Related]
2. Distinct splicing of CD45 mRNA in activated rat gamma delta cytotoxic T lymphocytes.
Hansson J; Dohlsten M; Sjögren HO; Hedlund G
Eur J Immunol; 1995 Jan; 25(1):75-9. PubMed ID: 7843256
[TBL] [Abstract][Full Text] [Related]
3. Expression of CD11a and CD45R isoforms defines distinct subsets of CD8+ TCR alpha beta and TCR gamma delta CTL in vivo.
Hedlund G; Hansson J; Ericsson PO; Sjögren HO; Dohlsten M
Immunol Rev; 1995 Aug; 146():82-94. PubMed ID: 7493762
[TBL] [Abstract][Full Text] [Related]
4. Locally superantigen-activated peritoneal cytolytic T lymphocytes belong to the CD8+ CD45RC- subset and lyse MHC class II+ tumor cells.
Hansson J; Ericsson PO; Dohlsten M; Sjögren HO; Kalland T; Hedlund G
Immunol Lett; 1992 Dec; 34(3):229-36. PubMed ID: 1487309
[TBL] [Abstract][Full Text] [Related]
5. Differential expression of three CD45 alternative structures on murine T cells: exon 6-dependent epitope as a marker for functional heterogeneity of CD4+ T cells.
Nishimura H; Hattori S; Abe M; Ueda G; Okamoto H; Tsurui H; Hirose S; Shirai T
Int Immunol; 1992 Aug; 4(8):923-30. PubMed ID: 1384687
[TBL] [Abstract][Full Text] [Related]
6. In vivo induction of gamma/delta T cells with highly potent and selective anti-tumor cytotoxicity.
Ericsson PO; Hansson J; Widegren B; Dohlsten M; Sjögren HO; Hedlund G
Eur J Immunol; 1991 Nov; 21(11):2797-802. PubMed ID: 1718760
[TBL] [Abstract][Full Text] [Related]
7. TCR alpha beta+ anti-tumor cytolytic T lymphocytes express NKR-P1 whilethe anti-tumor activity of TCR gamma delta+ T lymphocytes is not correlated to NKR-P1 expression.
Yrlid U; Petersson E; Dohlsten M; Hedlund G
Cell Immunol; 1996 Nov; 173(2):287-94. PubMed ID: 8912889
[TBL] [Abstract][Full Text] [Related]
8. Age-related accumulation of LFA-1high cells in a CD8+CD45RAhigh T cell population.
Okumura M; Fujii Y; Takeuchi Y; Inada K; Nakahara K; Matsuda H
Eur J Immunol; 1993 May; 23(5):1057-63. PubMed ID: 7682955
[TBL] [Abstract][Full Text] [Related]
9. Both CD45RA+ and CD45RA- subpopulations of CD8+ T cells contain cells with high levels of lymphocyte function-associated antigen-1 expression, a phenotype of primed T cells.
Okumura M; Fujii Y; Inada K; Nakahara K; Matsuda H
J Immunol; 1993 Jan; 150(2):429-37. PubMed ID: 7678274
[TBL] [Abstract][Full Text] [Related]
10. Identical expression of CD45R isoforms by CD45RC+ 'revertant' memory and CD45RC+ naive CD4 T cells.
Hargreaves M; Bell EB
Immunology; 1997 Jul; 91(3):323-30. PubMed ID: 9301519
[TBL] [Abstract][Full Text] [Related]
11. CD2/LFA-3 or LFA-1/ICAM-1 but not CD28/B7 interactions can augment cytotoxicity by virus-specific CD8+ cytotoxic T lymphocytes.
de Waal Malefyt R; Verma S; Bejarano MT; Ranes-Goldberg M; Hill M; Spits H
Eur J Immunol; 1993 Feb; 23(2):418-24. PubMed ID: 7679643
[TBL] [Abstract][Full Text] [Related]
12. Human CD45RC specificity. A novel marker for T cells at different maturation and activation stages.
Zapata JM; Pulido R; Acevedo A; Sánchez-Madrid F; de Landázuri MO
J Immunol; 1994 Apr; 152(8):3852-61. PubMed ID: 8144955
[TBL] [Abstract][Full Text] [Related]
13. Development of rat CD45+ 13-day-old fetal liver cells in SCID mouse fetal thymic organ cultures.
Alonso-C LM; Vicente A; Varas A; Zapata AG
Int Immunol; 1999 Jul; 11(7):1119-29. PubMed ID: 10383945
[TBL] [Abstract][Full Text] [Related]
14. Herpes simplex virus-specific human cytotoxic T-cell colonies expressing either gamma delta or alpha beta T-cell receptor: role of accessory molecules on HLA-unrestricted killing of virus-infected targets.
Maccario R; Comoli P; Percivalle E; Montagna D; Locatelli F; Gerna G
Immunology; 1995 May; 85(1):49-56. PubMed ID: 7635521
[TBL] [Abstract][Full Text] [Related]
15. Developmental expression of CD45 alternate exons in murine T cells. Evidence of additional alternate exon use.
Chang HL; Lefrancois L; Zaroukian MH; Esselman WJ
J Immunol; 1991 Sep; 147(5):1687-93. PubMed ID: 1831832
[TBL] [Abstract][Full Text] [Related]
16. Clonal expansions in acute EBV infection are detectable in the CD8 and not the CD4 subset and persist with a variable CD45 phenotype.
Maini MK; Gudgeon N; Wedderburn LR; Rickinson AB; Beverley PC
J Immunol; 2000 Nov; 165(10):5729-37. PubMed ID: 11067931
[TBL] [Abstract][Full Text] [Related]
17. Expression of CD45 isoforms lacking exons 7, 8 and 10.
Virts E; Barritt D; Raschke WC
Mol Immunol; 1998 Feb; 35(3):167-76. PubMed ID: 9694517
[TBL] [Abstract][Full Text] [Related]
18. Defective CD8+ T cell activation and cytolytic function in the absence of LFA-1 cannot be restored by increased TCR signaling.
Shier P; Ngo K; Fung-Leung WP
J Immunol; 1999 Nov; 163(9):4826-32. PubMed ID: 10528183
[TBL] [Abstract][Full Text] [Related]
19. A point mutation within CD45 exon A is the cause of variant CD45RA splicing in humans.
Zilch CF; Walker AM; Timón M; Goff LK; Wallace DL; Beverley PC
Eur J Immunol; 1998 Jan; 28(1):22-9. PubMed ID: 9485182
[TBL] [Abstract][Full Text] [Related]
20. Both LFA-1-positive and -deficient T cell clones require the CD2/LFA-3 interaction for specific cytolytic activation.
Van de Wiel-van Kemenade E; Te Velde AA; De Boer AJ; Weening RS; Fischer A; Borst J; Melief CJ; Figdor CG
Eur J Immunol; 1992 Jun; 22(6):1467-75. PubMed ID: 1376259
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
