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. 2018 Jan 26;9(2):132. doi: 10.1038/s41419-017-0150-0

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — a and b Animals received a total of two IV injections of CD95Fc (30 mg/kg) at 12 h and again at 30 min before the induction of 45 min of warm ischemia of the median and left lateral liver lobe (68% of the liver). Control mice received the same volume of IgG (30 mg/kg) antibody. Mice were sacrificed after 3, 6, 12, 18 and 24 h following reperfusion and blood and tissue samples were harvested for serological and histological assessment of liver damage.