Genomic responses in mouse models poorly mimic human inflammatory diseases
By Junhee Seok, H. Warren, A. Cuenca, M. Mindrinos, H. Baker, Weihong Xu, Daniel R. Richards, G. McDonald-Smith, H. Gao, Laura V. Hennessy and 29 more. Proceedings of the National Academy of Sciences of the United States of America, 2013
3,053 citations recorded by the source corpus.
Subfields: Immunology, Oncology
View Paper: https://www.semanticscholar.org/paper/493dacfabcb17967f6f7a97e68e86e37a496f561
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Citations in the corpus
- Biology-inspired Microphysiological System Approaches to Solve the Prediction Dilemma of Substance Testing (2016, neutral): “Leist and Hartung, 2013; Matthews, 2008; Olson et al., 2000; Perel et al., 2007; Hartung and Leist, 2008; Schnerch et al., 2010; Sena et al., 2010; Seok et al., 2013; van der Worp et al., 2010; Hartung, 2013).”
- Immune Effector Mechanisms Implicated in Atherosclerosis: From Mice to Humans (2013, background): “Recent work suggests that the patterns of inflammatory gene responses in inflammation differ drastically between humans and mice, with concordance at random levels (Seok et al., 2013).”
- Lessons learned from the fate of AstraZeneca's drug pipeline: a five-dimensional framework (2014, background): “29 (13) Dose limited by compound characteristics or tissue exposure not established”
- The Role of Macrophage Phenotype in Vascularization of Tissue Engineering Scaffolds (2014, neutral): “In addition, the C57BL/6 strain is a commonly used animal model for biomaterial evaluation, but macrophage behavior is likely to be different in other strains of mice or animal models, and especially in humans [86].”