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| Caputa, G., Matsushita, M., & Sanin, D. E. (2022). Intracellular infection and immune system cues rewire adipocytes to acquire immune function. Cell Metabolism, 34(8), 747–760. |
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| Folmes, C. D. L., Nelson, T. J., & Martinez-Fernandez, A. (2011). Somatic Oxidative Bioenergetics Transitions into Pluripotency-Dependent Glycolysis to Facilitate Nuclear Reprogramming. Cell Metabolism, 14(2), 264–271. |
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| Kim, K. H., Son, J. M., & Benayoun, B. A. (2018). The Mitochondrial-Encoded Peptide MOTS-c Translocates to the Nucleus to Regulate Nuclear Gene Expression in Response to Metabolic Stress. Cell Metabolism, 28(3), 516–524.e7. |
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| Lampropoulou, V., Sergushichev, A., Bambouskova, M., & others. (2016). Itaconate Links Inhibition of Succinate Dehydrogenase with Macrophage Metabolic Remodeling and Regulation of Inflammation. Cell Metabolism, 24(1), 158–166. |
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| Ly, H. C., Lynch, G. S., & Ryall, J. G. (2020). A Metabolic Roadmap for Somatic Stem Cell Fate. Cell Metabolism, 31(5), 1052–1067. |
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| Novak, J. S. S., Polak, L., & Baksh, S. C. (2025). The integrated stress response fine-tunes stem cell fate decisions upon serine deprivation and tissue injury. Cell Metabolism. |
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| Tang, X. (2023). Regenerating the heart by metabolically reprogramming the cardiomyocyte epigenome. Cell Metabolism, 35(11), 1849–1851. |
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| Willmann, K., & Moita, L. F. (2024). Physiologic disruption and metabolic reprogramming in infection and sepsis. Cell Metabolism, 36(5), 927–946. |
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| Yu, L., Wan, Q., & Liu, Q. (2024). IgG is an aging factor that drives adipose tissue fibrosis and metabolic decline. Cell Metabolism, 36(4), 793–507. |
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