Homeostasis

Displaying 1 - 11 of 11CSV
Pesini, A., Barriocanal-Casado, E., Compagnoni, G. M., Hidalgo-Gutierrez, A., Yanez, G., Bakkali, M., Chhonker, Y. S., Kleiner, G., Larrea, D., Tadesse, S., Lopez, L. C., Murry, D. J., Di Fonzo, A., Area-Gomez, E., & Quinzii, C. M. (2025). Coenzyme Q10 deficiency disrupts lipid metabolism by altering cholesterol homeostasis in neurons. Free Radical Biology and Medicine, 229, 441–457. https://doi.org/10.1016/j.freeradbiomed.2025.01.009
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Zhuang, X., Wang, Q., Joost, S., Ferrena, A., Humphreys, D. T., Li, Z., Blum, M., Krause, K., Ding, S., Landais, Y., Zhan, Y., Zhao, Y., Chaligne, R., Lee, J.-H., Carrasco, S. E., Bhanot, U. K., Koche, R. P., Bott, M. J., Katajisto, P., … Tammela, T. (2024). Ageing limits stemness and tumorigenesis by reprogramming iron homeostasis. Nature, 637(8044), 184–194. https://doi.org/10.1038/s41586-024-08285-0
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Kato, R., Yamamoto, T., Ogata, H., Miyata, K., Hayashi, S., Gershon, M. D., & Kadowaki, M. (2024). Indigenous gut microbiota constitutively drive release of ciliary neurotrophic factor from mucosal enteric glia to maintain the homeostasis of enteric neural circuits. Frontiers in Immunology, 15. https://doi.org/10.3389/fimmu.2024.1372670
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Ardanaz, C. G., de la Cruz, A., Minhas, P. S., Hernández-Martín, N., Pozo, M. Á., Valdecantos, M. P., Valverde, Á. M., Villa-Valverde, P., Elizalde-Horcada, M., Puerta, E., Ramírez, M. J., Ortega, J. E., Urbiola, A., Ederra, C., Ariz, M., Ortiz-de-Solórzano, C., Fernández-Irigoyen, J., Santamaría, E., Karsenty, G., … Solas, M. (2024). Astrocytic GLUT1 reduction paradoxically improves central and peripheral glucose homeostasis. Science Advances, 10(42). https://doi.org/10.1126/sciadv.adp1115
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Rodriguez, P., Kalia, V., Fenollar-Ferrer, C., Gibson, C. L., Gichi, Z., Rajoo, A., Matier, C. D., Pezacki, A. T., Xiao, T., Carvelli, L., Chang, C. J., Miller, G. W., Khamoui, A. V., Boerner, J., & Blakely, R. D. (2024). Glial swip-10 controls systemic mitochondrial function, oxidative stress, and neuronal viability via copper ion homeostasis. Proceedings of the National Academy of Sciences, 121(39). https://doi.org/10.1073/pnas.2320611121
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Shimonosono, M., Morimoto, M., Hirose, W., Tomita, Y., Matsuura, N., Flashner, S., Ebadi, M. S., Okayasu, E. H., Lee, C. Y., Britton, W. R., Martin, C., Wuertz, B. R., Parikh, A. S., Sachdeva, U. M., Ondrey, F. G., Atigadda, V. R., Elmets, C. A., Abrams, J. A., Muir, A. B., … Nakagawa, H. (2024). Modeling Epithelial Homeostasis and Perturbation in Three-Dimensional Human Esophageal Organoids. Biomolecules, 14(9), 1126. https://doi.org/10.3390/biom14091126
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Ahmed, A., Kato, N., & Gautier, J. (2024). Replication-Independent ICL Repair: From Chemotherapy to Cell Homeostasis. Journal of Molecular Biology, 436(13), 168618. https://doi.org/10.1016/j.jmb.2024.168618
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Malagola, E., Vasciaveo, A., Ochiai, Y., Kim, W., Zheng, B., Zanella, L., Wang, A. L. E., Middelhoff, M., Nienhüser, H., Deng, L., Wu, F., Waterbury, Q. T., Belin, B., LaBella, J., Zamechek, L. B., Wong, M. H., Li, L., Guha, C., Cheng, C.-W., … Wang, T. C. (2024). Isthmus progenitor cells contribute to homeostatic cellular turnover and support regeneration following intestinal injury. Cell, 187(12), 3056-3071.e17. https://doi.org/10.1016/j.cell.2024.05.004
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Ridha, M., Megjhani, M., Nametz, D., Kwon, S. B., Velazquez, A., Ghoshal, S., Agarwal, S., Claassen, J., Roh, D. J., Sander Connolly, E., & Park, S. (2023). Suboptimal Cerebral Perfusion is Associated with Ischemia After Intracerebral Hemorrhage. Neurocritical Care, 40(3), 996–1005. https://doi.org/10.1007/s12028-023-01863-6
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Park, S., Beqiri, E., Smielewski, P., Aries, M., Abecasis, F., Agrawal, S., Appavu, B., Balu, R., Brady, K., Brunsch, C., Budohoski, K., Czigler, A., Depreitere, B., Dias, C., Enblad, P., Ercole, A., Figaji, A., Foreman, B., … Frisvold, S. K. (2023). Inaugural State of the Union: Continuous Cerebral Autoregulation Monitoring in the Clinical Practice of Neurocritical Care and Anesthesia. Neurocritical Care, 40(3), 855–864. https://doi.org/10.1007/s12028-023-01860-9
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Park, J., Zuo, H., Frangaj, A., Fu, Z., Yen, L. Y., Zhang, Z., Mosyak, L., Slavkovich, V. N., Liu, J., Ray, K. M., Cao, B., Vallese, F., Geng, Y., Chen, S., Grassucci, R., Dandey, V. P., Tan, Y. Z., Eng, E., Lee, Y., … Fan, Q. R. (2021). Symmetric activation and modulation of the human calcium-sensing receptor. Proceedings of the National Academy of Sciences, 118(51). https://doi.org/10.1073/pnas.2115849118
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