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. 2000 Mar 20;191(6):1017–1030. doi: 10.1084/jem.191.6.1017

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© 2000 The Rockefeller University Press

This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).

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p38 MAPK regulates FasL promoter activity. p38 (M) or pcDNA3 DO11.10 stable transfectants were transiently transfected with a FasL-511 luciferase construct, maintained in medium for 36 h at 37°C, and were then either left unstimulated or were stimulated with plate-bound anti-CD3 for 16 h. Luciferase activity in whole cell lysates was assayed and is shown as mean value ± SEM. Transfection efficiency was monitored by cotransfection of a pUC19 plasmid encoding β-galactosidase. Similar results were obtained in three independent and reproducible experiments.