Mitochondria

Displaying 1 - 26 of 26CSV
Brestoff, J. R., Singh, K. K., Aquilano, K., Becker, L. B., Berridge, M. V., Boilard, E., Caicedo, A., Crewe, C., Enríquez, J. A., Gao, J., Gustafsson, Å. B., Hayakawa, K., Khoury, M., Lee, Y.-S., Lettieri-Barbato, D., Luz-Crawford, P., McBride, H. M., McCully, J. D., Nakai, R., … Zheng, M. (2025). Recommendations for mitochondria transfer and transplantation nomenclature and characterization. Nature Metabolism, 7(1), 53–67. https://doi.org/10.1038/s42255-024-01200-x
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Larrea, D., Tamucci, K. A., Kabra, K., Velasco, K. R., Yun, T. D., Pera, M., Montesinos, J., Agrawal, R. R., Paradas, C., Smerdon, J. W., Lowry, E. R., Stepanova, A., Yoval-Sanchez, B., Galkin, A., Wichterle, H., & Area-Gomez, E. (2025). Altered mitochondria-associated ER membrane (MAM) function shifts mitochondrial metabolism in amyotrophic lateral sclerosis (ALS). Nature Communications, 16(1). https://doi.org/10.1038/s41467-024-51578-1
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Guillen-Parra, M., Lin, J., Prather, A. A., Wolkowitz, O. M., Picard, M., & Epel, E. S. (2024). The relationship between mitochondrial health, telomerase activity and longitudinal telomere attrition, considering the role of chronic stress. Scientific Reports, 14(1). https://doi.org/10.1038/s41598-024-77279-9
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Zohar, H., Lindenboim, L., Gozlan, O., Gundersen, G. G., Worman, H. J., & Stein, R. (2024). Apoptosis-induced translocation of nesprin-2 from the nuclear envelope to mitochondria is associated with mitochondrial dysfunction. Nucleus, 15(1). https://doi.org/10.1080/19491034.2024.2413501
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Kelly, C., Trumpff, C., Acosta, C., Assuras, S., Baker, J., Basarrate, S., Behnke, A., Bo, K., Bobba-Alves, N., Champagne, F. A., Conklin, Q., Cross, M., De Jager, P., Engelstad, K., Epel, E., Franklin, S. G., Hirano, M., Huang, Q., Junker, A., … Picard, M. (2024). A platform to map the mind–mitochondria connection and the hallmarks of psychobiology: the MiSBIE study. Trends in Endocrinology & Metabolism, 35(10), 884–901. https://doi.org/10.1016/j.tem.2024.08.006
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Chung, Y.-M., Hu, C.-S., Sun, E., & Tseng, H. C. (2024). Morphological multiparameter filtration and persistent homology in mitochondrial image analysis. PLOS ONE, 19(9), e0310157. https://doi.org/10.1371/journal.pone.0310157
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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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Tung, P. W., Thaker, V. V., Gallagher, D., & Kupsco, A. (2024). Mitochondrial Health Markers and Obesity-Related Health in Human Population Studies: A Narrative Review of Recent Literature. Current Obesity Reports, 13(4), 724–738. https://doi.org/10.1007/s13679-024-00588-7
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Guo, L. (2024). F-ATP synthase inhibitory factor 1 and mitochondria-organelle interactions: New insight and implications. Pharmacological Research, 208, 107393. https://doi.org/10.1016/j.phrs.2024.107393
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Tomasello, D. L., Barrasa, M. I., Mankus, D., Alarcon, K. I., Lytton-Jean, A. K. R., Liu, X. S., & Jaenisch, R. (2024). Mitochondrial dysfunction and increased reactive oxygen species production in MECP2 mutant astrocytes and their impact on neurons. Scientific Reports, 14(1). https://doi.org/10.1038/s41598-024-71040-y
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Yang, T.-H., Kang, E. Y.-C., Lin, P.-H., Yu, B. B.-C., Wang, J. H.-H., Chen, V., & Wang, N.-K. (2024). Mitochondria in Retinal Ganglion Cells: Unraveling the Metabolic Nexus and Oxidative Stress. International Journal of Molecular Sciences, 25(16), 8626. https://doi.org/10.3390/ijms25168626
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Trumpff, C., Monzel, A. S., Sandi, C., Menon, V., Klein, H.-U., Fujita, M., Lee, A., Petyuk, V. A., Hurst, C., Duong, D. M., Seyfried, N. T., Wingo, A. P., Wingo, T. S., Wang, Y., Thambisetty, M., Ferrucci, L., Bennett, D. A., De Jager, P. L., & Picard, M. (2024). Psychosocial experiences are associated with human brain mitochondrial biology. Proceedings of the National Academy of Sciences, 121(27). https://doi.org/10.1073/pnas.2317673121
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Morcillo, P., Kabra, K., Velasco, K., Cordero, H., Jennings, S., Yun, T. D., Larrea, D., Akman, H. O., & Schon, E. A. (2024). Aberrant ER-mitochondria communication is a common pathomechanism in mitochondrial disease. Cell Death & Disease, 15(6). https://doi.org/10.1038/s41419-024-06781-9
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Caicedo, A., Benavides-Almeida, A., Haro-Vinueza, A., Peña-Cisneros, J., Pérez-Meza, Á. A., Michelson, J., Peñaherrera, S., & Picard, M. (2024). Decoding the nature and complexity of extracellular mtDNA: Types and implications for health and disease. Mitochondrion, 75, 101848. https://doi.org/10.1016/j.mito.2024.101848
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Monzel, A. S., Enríquez, J. A., & Picard, M. (2023). Multifaceted mitochondria: moving mitochondrial science beyond function and dysfunction. Nature Metabolism, 5(4), 546–562. https://doi.org/10.1038/s42255-023-00783-1
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Hewitt, V. L., Miller-Fleming, L., Twyning, M. J., Andreazza, S., Mattedi, F., Prudent, J., Polleux, F., Vagnoni, A., & Whitworth, A. J. (2022). Decreasing pdzd8-mediated mito–ER contacts improves organismal fitness and mitigates Aβ42toxicity. Life Science Alliance, 5(11), e202201531. https://doi.org/10.26508/lsa.202201531
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Coon, B. G., Timalsina, S., Astone, M., Zhuang, Z. W., Fang, J., Han, J., Themen, J., Chung, M., Yang-Klingler, Y. J., Jain, M., Hirschi, K. K., Yamamato, A., Trudeau, L.-E., Santoro, M., & Schwartz, M. A. (2022). A mitochondrial contribution to anti-inflammatory shear stress signaling in vascular endothelial cells. Journal of Cell Biology, 221(7). https://doi.org/10.1083/jcb.202109144
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Çoku, J., Booth, D. M., Skoda, J., Pedrotty, M. C., Vogel, J., Liu, K., Vu, A., Carpenter, E. L., Ye, J. C., Chen, M. A., Dunbar, P., Scadden, E., Yun, T. D., Nakamaru‐Ogiso, E., Area‐Gomez, E., Li, Y., Goldsmith, K. C., Reynolds, C. P., Hajnoczky, G., & Hogarty, M. D. (2022). Reduced ER–mitochondria connectivity promotes neuroblastoma multidrug resistance. The EMBO Journal, 41(8). Portico. https://doi.org/10.15252/embj.2021108272
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Junker, A., Wang, J., Gouspillou, G., Ehinger, J. K., Elmér, E., Sjövall, F., Fisher‐Wellman, K. H., Neufer, P. D., Molina, A. J. A., Ferrucci, L., & Picard, M. (2022). Human studies of mitochondrial biology demonstrate an overall lack of binary sex differences: A multivariate meta‐analysis. The FASEB Journal, 36(2). Portico. https://doi.org/10.1096/fj.202101628r
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Longchamps, R. J., Yang, S. Y., Castellani, C. A., Shi, W., Lane, J., Grove, M. L., Bartz, T. M., Sarnowski, C., Liu, C., Burrows, K., Guyatt, A. L., Gaunt, T. R., Kacprowski, T., Yang, J., De Jager, P. L., Yu, L., Bergman, A., Xia, R., Fornage, M., … Arking, D. E. (2021). Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation. Human Genetics, 141(1), 127–146. https://doi.org/10.1007/s00439-021-02394-w
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Zanou, N., Dridi, H., Reiken, S., Imamura de Lima, T., Donnelly, C., De Marchi, U., Ferrini, M., Vidal, J., Sittenfeld, L., Feige, J. N., Garcia-Roves, P. M., Lopez-Mejia, I. C., Marks, A. R., Auwerx, J., Kayser, B., & Place, N. (2021). Acute RyR1 Ca2+ leak enhances NADH-linked mitochondrial respiratory capacity. Nature Communications, 12(1). https://doi.org/10.1038/s41467-021-27422-1
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