Correction Correction: Durable Therapeutic Efficacy Utilizing Combinatorial Blockade against IDO, CTLA-4, and PD-L1 in Mice with Brain Tumors Clinical Cancer Research In this article (Clin Cancer Res 2014;20:5290–301), which was published in the October 15, 2014, issue of Clinical Cancer Research (1), the phrase ". . .whereas twotailed unpaired Student t tests were used for paired groups," within a sentence in the statistical analysis section, generated confusion among readers. The authors have provided clarification, and the new paragraph should read as follows: Data were analyzed using Prism 4.0 software (GraphPad Software). Experiments were repeated at least two times each. Data are represented as the mean SEM for all figure panels in which error bars are shown. The P values represent ANOVA for groups of 3 or more, whereas two-tailed unpaired Student t tests were used for comparisons between two groups. A P value of less than 0.05 was considered statistically significant. The authors regret this error. Reference 1. Wainwright DA, Chang AL, Dey M, Balyasnikova IV, Kim CK, Tobias A, et al. Durable therapeutic efficacy utilizing combinatorial blockade against IDO, CTLA-4, and PD-L1 in mice with brain tumors. Clin Cancer Res 2014;20:5290–301. Published online February 2, 2015. doi: 10.1158/1078-0432.CCR-14-3211 Ó2015 American Association for Cancer Research. 662 Clin Cancer Res; 21(3) February 1, 2015 Downloaded from clincancerres.aacrjournals.org on June 17, 2017. © 2015 American Association for Cancer Research. Correction: Durable Therapeutic Efficacy Utilizing Combinatorial Blockade against IDO, CTLA-4, and PD-L1 in Mice with Brain Tumors Clin Cancer Res 2015;21:662. Updated version Cited articles E-mail alerts Reprints and Subscriptions Permissions Access the most recent version of this article at: http://clincancerres.aacrjournals.org/content/21/3/662 This article cites 1 articles, 1 of which you can access for free at: http://clincancerres.aacrjournals.org/content/21/3/662.full.html#ref-list-1 Sign up to receive free email-alerts related to this article or journal. To order reprints of this article or to subscribe to the journal, contact the AACR Publications Department at [email protected]. To request permission to re-use all or part of this article, contact the AACR Publications Department at [email protected]. Downloaded from clincancerres.aacrjournals.org on June 17, 2017. © 2015 American Association for Cancer Research.
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