Mitochondrial Nanotunnels

Network biology: understanding the cell's functional organization

Barabási, A.-L., & Oltvai, Z. N. (2004) · Nature Reviews Genetics · doi:10.1038/nrg1272 · Cited by 7,903 · see citing works

Mitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release

Zorov, D. B., Juhaszova, M., & Sollott, S. J. (2014) · Physiological Reviews · doi:10.1152/physrev.00026.2013 · Cited by 5,383 · see citing works

Fission and selective fusion govern mitochondrial segregation and elimination by autophagy

Twig, G., Elorza, A., Molina, A. J. A., Mohamed, H., Wikstrom, J. D., Walzer, G., Stiles, L., Haigh, S. E., Katz, S., Las, G., et al. (2008) · The EMBO Journal · doi:10.1038/sj.emboj.7601963 · Cited by 3,082 · see citing works

Mitochondrial form and function

Friedman, J. R., & Nunnari, J. (2014) · Nature · doi:10.1038/nature12985 · Cited by 1,803 · cited 1× · see citing works

During autophagy mitochondria elongate, are spared from degradation and sustain cell viability

Gomes, L. C., Benedetto, G. D., & Scorrano, L. (2011) · Nature Cell Biology · doi:10.1038/ncb2220 · Cited by 1,735 · see citing works

Serial Block-Face Scanning Electron Microscopy to Reconstruct Three-Dimensional Tissue Nanostructure

Denk, W., & Horstmann, H. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020329 · Cited by 1,644 · see citing works

Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations

Chen, H., Vermulst, M., Wang, Y. E., Chomyn, A., Prolla, T. A., McCaffery, J. M., & Chan, D. C. (2010) · Cell · doi:10.1016/j.cell.2010.02.026 · Cited by 1,211 · see citing works

Tubular network formation protects mitochondria from autophagosomal degradation during nutrient starvation

Rambold, A. S., Kostelecky, B., Elia, N., & Lippincott‐Schwartz, J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1107402108 · Cited by 1,144 · see citing works

Mitochondrial Dynamics — Mitochondrial Fission and Fusion in Human Diseases

Archer, S. L. (2013) · New England Journal of Medicine · doi:10.1056/nejmra1215233 · Cited by 1,103 · see citing works

Structure and function of ER membrane contact sites with other organelles

Phillips, M. J., & Voeltz, G. K. (2016) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2015.8 · Cited by 933 · see citing works

A new pathway for mitochondrial quality control: Mitochondrial-derived vesicles

Sugiura, A., McLelland, G., Fon, E. A., & McBride, H. M. (2014) · The EMBO Journal · doi:10.15252/embj.201488104 · Cited by 862 · see citing works

Mitonuclear communication in homeostasis and stress

Quirós, P. M., Mottis, A., & Auwerx, J. (2016) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2016.23 · Cited by 787 · see citing works

Transcellular degradation of axonal mitochondria

Davis, C.-H. O., Kim, K.-Y., Bushong, E. A., Mills, E. A., Boassa, D., Shih, T., Kinebuchi, M., Phan, S., Zhou, Y., Bihlmeyer, N. A., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1404651111 · Cited by 673 · see citing works

Role of Mitochondrial Ca2+ in the Regulation of Cellular Energetics

Glancy, B. C., & Balaban, R. S. (2012) · Biochemistry · doi:10.1021/bi2018909 · Cited by 649 · see citing works

Intercellular Nanotubes Mediate Bacterial Communication

Dubey, G. P., & Ben‐Yehuda, S. (2011) · Cell · doi:10.1016/j.cell.2011.01.015 · Cited by 567 · see citing works

Evolution of Mitochondria as Signaling Organelles

Chandel, N. S. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.05.013 · Cited by 555 · see citing works

Multiple dynamin family members collaborate to drive mitochondrial division

Lee, J. E., Westrate, L. M., Wu, H., Page, C., & Voeltz, G. K. (2016) · Nature · doi:10.1038/nature20555 · Cited by 512 · see citing works

Mitochondria Know No Boundaries: Mechanisms and Functions of Intercellular Mitochondrial Transfer

Torralba, D., Baixauli, F., & Sánchez-Madrid, F. (2016) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2016.00107 · Cited by 440 · see citing works

Conformational changes in Dnm1 support a contractile mechanism for mitochondrial fission

Mears, J. A., Lackner, L. L., Fang, S., Ingerman, E., Nunnari, J. M., & Hinshaw, J. E. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1949 · Cited by 418 · see citing works

Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing

Latorre-Pellicer, A., Moreno‐Loshuertos, R., Lechuga‐Vieco, A. V., Sánchez‐Cabo, F., Torroja, C., Acín‐Pérez, R., Calvo, E., Aix, E., González-Guerra, A., Logan, A., et al. (2016) · Nature · doi:10.1038/nature18618 · Cited by 396 · see citing works

Desmin Cytoskeleton Linked to Muscle Mitochondrial Distribution and Respiratory Function

Milner, D. J., Mavroidis, M., Weisleder, N. L., & Capetanaki, Y. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.150.6.1283 · Cited by 385 · see citing works

Cross-strand binding of TFAM to a single mtDNA molecule forms the mitochondrial nucleoid

Kukat, C., Davies, K. M., Wurm, C. A., Spåhr, H., Bonekamp, N. A., Kühl, I., Joos, F., Polosa, P. L., Park, C. B., Posse, V., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1512131112 · Cited by 378 · see citing works

Mitochondrial ‘kiss‐and‐run’: interplay between mitochondrial motility and fusion–fission dynamics

Liu, X., Weaver, D., Shirihai, O. S., & Hajnóczky, G. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.255 · Cited by 344 · see citing works

Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming

Picard, M. A., Zhang, J., Hancock, S. A., Derbeneva, O. A., Golhar, R., Golik, P., O’Hearn, S. F., Levy, S., Potluri, P., Lvova, M., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1414028111 · Cited by 311 · see citing works

Redox Nanodomains Are Induced by and Control Calcium Signaling at the ER-Mitochondrial Interface

Booth, D. M., Enyedi, B., Geiszt, M., Várnai, P., & Hajnóczky, G. (2016) · Molecular Cell · doi:10.1016/j.molcel.2016.05.040 · Cited by 310 · see citing works

Metabolic cross-feeding via intercellular nanotubes among bacteria

Pande, S., Shitut, S., Freund, L., Westermann, M., Bertels, F., Colesie, C., Bischofs, I. B., & Kost, C. (2015) · Nature Communications · doi:10.1038/ncomms7238 · Cited by 273 · see citing works

Super-resolution Microscopy Approaches for Live Cell Imaging

Godin, A. G., Lounis, B., & Cognet, L. (2014) · Biophysical Journal · doi:10.1016/j.bpj.2014.08.028 · Cited by 247 · see citing works

Propagation of the apoptotic signal by mitochondrial waves

Pacher, P., & Hajnóczky, G. (2001) · The EMBO Journal · doi:10.1093/emboj/20.15.4107 · Cited by 240 · see citing works

The Spectrum of Mitochondrial Ultrastructural Defects in Mitochondrial Myopathy

Vincent, A. E., Ng, Y. S., White, K., Davey, T., Mannella, C. A., Falkous, G., Feeney, C. L., Schaefer, A. M., McFarland, R., Gorman, G. S., et al. (2016) · Scientific Reports · doi:10.1038/srep30610 · Cited by 234 · see citing works

STED super-resolution microscopy reveals an array of MINOS clusters along human mitochondria

Jans, D. C., Wurm, C. A., Riedel, D., Wenzel, D., Stagge, F., Deckers, M., Rehling, P., & Jakobs, S. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1301820110 · Cited by 199 · see citing works

Altered brain energetics induces mitochondrial fission arrest in Alzheimer’s Disease

Zhang, L., Trushin, S., Christensen, T. A., Bachmeier, B. V., Gateno, B., Schroeder, A., Yao, J., Itoh, K., Sesaki, H., Poon, W. W., et al. (2016) · Scientific Reports · doi:10.1038/srep18725 · Cited by 198 · see citing works

Tissue-Specific Mitochondrial Decoding of Cytoplasmic Ca2+ Signals Is Controlled by the Stoichiometry of MICU1/2 and MCU

Paillard, M., Csordás, G., Szanda, G., Golenár, T., Debattisti, V., Bartók, Á., Wang, N., Moffat, C., Seifert, E. L., Spät, A., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.02.032 · Cited by 194 · see citing works

Nanotubes mediate niche–stem-cell signalling in the Drosophila testis

Inaba, M., Buszczak, M., & Yamashita, Y. M. (2015) · Nature · doi:10.1038/nature14602 · Cited by 191 · see citing works

Mitochondrial fusion is frequent in skeletal muscle and supports excitation–contraction coupling

Eisner, V., Lenaers, G., & Hajnóczky, G. (2014) · Journal of Cell Biology · doi:10.1083/jcb.201312066 · Cited by 177 · see citing works

Power Grid Protection of the Muscle Mitochondrial Reticulum

Glancy, B., Hartnell, L. M., Combs, C. A., Femnou, A., Sun, J., Murphy, E., Subramaniam, S., & Balaban, R. S. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.03.063 · Cited by 172 · see citing works

Trans-mitochondrial coordination of cristae at regulated membrane junctions

Picard, M., McManus, M. J., Csordás, G., Várnai, P., Dorn II, G. W., Williams, D., Hajnóczky, G., & Wallace, D. C. (2015) · Nature Communications · doi:10.1038/ncomms7259 · Cited by 166 · see citing works

Kissing and nanotunneling mediate intermitochondrial communication in the heart

Huang, X., Sun, L., Ji, S., Zhao, T. S., Zhang, W., Xu, J., Zhang, J., Wang, Y., Wang, X., Franzini‐Armstrong, C., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1300741110 · Cited by 164 · see citing works

Mitochondrial fusion dynamics is robust in the heart and depends on calcium oscillations and contractile activity

Eisner, V., Cupo, R. R., Gao, E., Csordás, G., Slovinsky, W. S., Paillard, M., Cheng, L., Ibetti, J., Chen, S. R. W., Chuprun, J. K., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1617288114 · Cited by 161 · see citing works

Staying cool in difficult times: Mitochondrial dynamics, quality control and the stress response

Shutt, T. E., & McBride, H. M. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.05.024 · Cited by 160 · see citing works

The Mechanism of DNA Transfer in the Mating System of an Archaebacterium

Rosenshine, I., Tchelet, R., & Mevarech, M. (1989) · Science · doi:10.1126/science.2818746 · Cited by 159 · see citing works

Communication in Neural Circuits: Tools, Opportunities, and Challenges

Lerner, T. N., Ye, L., & Deisseroth, K. (2016) · Cell · doi:10.1016/j.cell.2016.02.027 · Cited by 159 · see citing works

Control of bacterial metabolism by quorum sensing

Goo, E., An, J. H., Kang, Y., & Hwang, I. (2015) · Trends in Microbiology · doi:10.1016/j.tim.2015.05.007 · Cited by 155 · see citing works

The Mitochondrial Nucleoid: Integrating Mitochondrial DNA into Cellular HomeostasisPreprint

Gilkerson, R., Bravo, L., Garcia, I., Gaytan, N., Herrera, A., Maldonado, A., & Quintanilla, B. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a011080 · Cited by 136 · see citing works

Dynamic tubulation of mitochondria drives mitochondrial network formation

Wang, C., Du, W., Su, Q. P., Zhu, M., Feng, P., Li, Y., Zhou, Y., Mi, N., Zhu, Y., Jiang, D., et al. (2015) · Cell Research · doi:10.1038/cr.2015.89 · Cited by 133 · see citing works

Making connections: interorganelle contacts orchestrate mitochondrial behavior

Klecker, T., Böckler, S., & Westermann, B. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.04.004 · Cited by 129 · see citing works

Architecture and Characteristics of Bacterial Nanotubes

Dubey, G. P., Mohan, G. B. M., Dubrovsky-Gaupp, A., Amen, T., Tsipshtein, S., Rouvinski, A., Rosenberg, A., Kaganovich, D., Sherman, E., Medalia, O., et al. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.01.013 · Cited by 121 · see citing works

The Mechanoenzymatic Core of Dynamin-related Protein 1 Comprises the Minimal Machinery Required for Membrane Constriction

Francy, C. A., Alvarez, F. J. D., Zhou, L., Ramachandran, R., & Mears, J. A. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.610881 · Cited by 116 · see citing works

The Upsides and Downsides of Organelle Interconnectivity

Gottschling, D. E., & Nyström, T. (2017) · Cell · doi:10.1016/j.cell.2017.02.030 · Cited by 104 · see citing works

Mitochondrial fusion provides an ‘initial metabolic complementation’ controlled by mtDNA

Yang, L., Long, Q., Liu, J., Tang, H., Li, Y., Bao, F., Qin, D., Pei, D., & Liu, X. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1863-9 · Cited by 95 · see citing works

Increased mitochondrial nanotunneling activity, induced by calcium imbalance, affects intermitochondrial matrix exchanges

Lavorato, M., Iyer, V. R., Dewight, W., Cupo, R. R., Debattisti, V., Gomez, L., de la Fuente, S., Zhao, Y.-T., Valdivia, H. H., Hajnóczky, G., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1617788113 · Cited by 81 · see citing works

The Scale-Free Dynamics of Eukaryotic Cells

Aon, M. A., Roussel, M. R., Cortassa, S. C., O'Rourke, B. P., Murray, D. B., Beckmann, M., & Lloyd, D. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003624 · Cited by 76 · see citing works

Effects of arc3, arc5 and arc6 Mutations on Plastid Morphology and Stromule Formation in Green and Nongreen Tissues of Arabidopsis thaliana†

Holzinger, A., Kwok, E. Y., & Hanson, M. R. (2008) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.2008.00437.x · Cited by 74 · see citing works

Signaling by Cellular Protrusions: Keeping the Conversation Private

Buszczak, M., Inaba, M., & Yamashita, Y. M. (2016) · Trends in Cell Biology · doi:10.1016/j.tcb.2016.03.003 · Cited by 74 · see citing works

Novel mitochondrial extensions provide evidence for a link between microtubule-directed movement and mitochondrial fission

Bowes, T., & Gupta, R. S. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.08.120 · Cited by 33 · see citing works

Two modes of exocytosis in an artificial cell

Mellander, L. J., Kurczy, M. E., Najafinobar, N., Dunevall, J., Ewing, A. G., & Cans, A.-S. U. (2014) · Scientific Reports · doi:10.1038/srep03847 · Cited by 33 · see citing works

Mitochondria: Starving to reach quorum?

Picard, M. A., & Burelle, Y. (2012) · BioEssays · doi:10.1002/bies.201100179 · Cited by 20 · see citing works

Mitochondrial Dysfunction in Neurodegenerative Disorders

Turnbull, D. M., Duchen, M. R., Simcox, E. M., & Reeve, A. K. (2016) · Springer eBooks · doi:10.1007/978-3-319-28637-2 · Cited by 20 · see citing works

Mitochondrial Signaling and Neurodegeneration

Picard, M. A., & McManus, M. J. (2016) · Springer eBooks · doi:10.1007/978-3-319-28637-2_5 · Cited by 10 · see citing works

Focusing super resolution on the cytoskeleton

Shelden, E. A., Colburn, Z. T., & Jones, J. (2016) · F1000Research · doi:10.12688/f1000research.8233.1 · Cited by 8 · see citing works

Electron Tomography of Mitochondrial Nanotunnels in a CPVT Model with RyR2 Loss-of-Function Mutation

Lavorato, M., Iyer, V. R., Zhao, Y.-T., Valdivia, H. H., & Franzini‐Armstrong, C. (2016) · Biophysical Journal · doi:10.1016/j.bpj.2015.11.1978 · Cited by 2 · see citing works

Mitochondrial signal transduction

Picard, M. A., & Shirihai, O. S. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.10.008 · Cited by 666 · see citing works

Mitochondrial dynamics in adaptive and maladaptive cellular stress responses

Eisner, V., Picard, M., & Hajnóczky, G. (2018) · Nature Cell Biology · doi:10.1038/s41556-018-0133-0 · Cited by 622 · see citing works

Multifaceted mitochondria: moving mitochondrial science beyond function and dysfunction

Monzel, A. S., Enrı́quez, J. A., & Picard, M. A. (2023) · Nature Metabolism · doi:10.1038/s42255-023-00783-1 · Cited by 618 · see citing works

Mitochondrial Dysfunction, Oxidative Stress, and Neuroinflammation: Intertwined Roads to Neurodegeneration

Picca, A., Calvani, R., Coelho‐Júnior, H. J., Landi, F., Bernabei, R., & Marzetti, E. (2020) · Antioxidants · doi:10.3390/antiox9080647 · Cited by 456 · see citing works

Molecular mechanisms of mitochondrial dynamics

Tábara, L. C., Segawa, M., & Prudent, J. (2024) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-024-00785-1 · Cited by 431 · see citing works

Exercise and mitochondrial health

Memme, J. M., Erlich, A. T., Phukan, G., & Hood, D. A. (2021) · The Journal of Physiology · doi:10.1113/jp278853 · Cited by 343 · see citing works

Psychological Stress and Mitochondria: A Systematic Review

Picard, M. A., & McEwen, B. S. (2018) · Psychosomatic Medicine · doi:10.1097/psy.0000000000000545 · Cited by 339 · see citing works

Psychological Stress and Mitochondria: A Conceptual Framework

Picard, M. A., & McEwen, B. S. (2018) · Psychosomatic Medicine · doi:10.1097/psy.0000000000000544 · Cited by 318 · see citing works

The Functional Impact of Mitochondrial Structure Across Subcellular Scales

Glancy, B. C., Kim, Y., Katti, P., & Willingham, T. B. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.541040 · Cited by 259 · see citing works

Mitochondrial Structure and Function in Human Heart Failure

Hinton, A. O., Jr., Claypool, S. M., Neikirk, K., Senoo, N., Wanjalla, C. N., Kirabo, A., & Williams, C. R. (2024) · Circulation Research · doi:10.1161/circresaha.124.323800 · Cited by 226 · see citing works

Mitochondrial lactate metabolism: history and implications for exercise and disease

Glancy, B. C., Kane, D. A., Kavazis, A. N., Goodwin, M. L., Willis, W. T., & Gladden, L. B. (2020) · The Journal of Physiology · doi:10.1113/jp278930 · Cited by 203 · see citing works

Mitochondrial dynamics and transport in Alzheimer's disease

Flannery, P. J., & Trushina, E. V. (2019) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2019.06.009 · Cited by 198 · see citing works

Cell Death and Inflammation: The Role of Mitochondria in Health and Disease

Picca, A., Calvani, R., Coelho‐Júnior, H. J., & Marzetti, E. (2021) · Cells · doi:10.3390/cells10030537 · Cited by 203 · see citing works

The connection between the dynamic remodeling of the mitochondrial network and the regulation of muscle mass

Romanello, V., & Sandri, M. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03662-0 · Cited by 197 · see citing works

Quantitative 3D Mapping of the Human Skeletal Muscle Mitochondrial Network

Vincent, A. E., White, K., Davey, T., Philips, J., Ogden, R. T., Lawless, C., Warren, C., Hall, M. G., Ng, Y. S., Falkous, G., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.01.010 · Cited by 195 · see citing works

Mitochondrial function in development and disease

Rossmann, M. P., Dubois, S. M., Agarwal, S., & Zon, L. I. (2021) · Disease Models & Mechanisms · doi:10.1242/dmm.048912 · Cited by 191 · see citing works

Mitochondria in disease: changes in shapes and dynamics

Jenkins, B. C., Neikirk, K., Katti, P., Claypool, S. M., Kirabo, A., McReynolds, M. R., & Hinton, A. O., Jr. (2024) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2024.01.011 · Cited by 154 · see citing works

Exercise and mitochondrial dynamics: keeping in shape with ROS and AMPK

Trewin, A., Berry, B., & Wojtovich, A. (2018) · Antioxidants · doi:10.3390/antiox7010007 · Cited by 129 · see citing works

Mitochondrial Morphofunction in Mammalian Cells

Bulthuis, E. P., Adjobo-Hermans, M. J. W., Willems, P. H. G. M., & Koopman, W. J. H. (2018) · Antioxidants and Redox Signaling · doi:10.1089/ars.2018.7534 · Cited by 128 · see citing works

OPA1 regulation of mitochondrial dynamics in skeletal and cardiac muscle

Noone, J., O’Gorman, D. J., & Kenny, H. (2022) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2022.07.003 · Cited by 119 · see citing works

Instance segmentation of mitochondria in electron microscopy images with a generalist deep learning model trained on a diverse dataset

Conrad, R., & Narayan, K. (2023) · Cell Systems · doi:10.1016/j.cels.2022.12.006 · Cited by 116 · see citing works

Mitochondrial stress and mitokines in aging

Burtscher, J., Soltany, A., Visavadiya, N. P., Burtscher, M., Millet, G. P., Khoramipour, K., & Khamoui, A. V. (2023) · Aging Cell · doi:10.1111/acel.13770 · Cited by 116 · see citing works

Powerhouse of the mind: mitochondrial plasticity at the synapse

Rossi, M., & Pekkurnaz, G. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.02.001 · Cited by 110 · see citing works

ER-mitochondria contacts promote mtDNA nucleoids active transportation via mitochondrial dynamic tubulation

Qin, J., Guo, Y., Xue, B., Shi, P., Yang, C., Su, Q. P., Hao, H., Zhao, S., Wu, C., Yu, L., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-18202-4 · Cited by 110 · see citing works

Cyclooctatetraene-conjugated cyanine mitochondrial probes minimize phototoxicity in fluorescence and nanoscopic imaging

Yang, Z., Li, L., Ling, J., Liu, T., Huang, X., Ying, Y., Zhao, Y., Zhao, Y. T., Lei, K., Chen, L., et al. (2020) · Chemical Science · doi:10.1039/d0sc02837a · Cited by 105 · see citing works

The social nature of mitochondria: Implications for human health

Picard, M. A., & Sandi, C. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.017 · Cited by 102 · see citing works

Biomarkers of Physical Frailty and Sarcopenia: Coming up to the Place?

Picca, A., Calvani, R., Cesari, M., Landi, F., Bernabei, R., Coelho‐Júnior, H. J., & Marzetti, E. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21165635 · Cited by 101 · see citing works

Visualizing Mitochondrial Form and Function within the Cell

Glancy, B. C. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2019.09.009 · Cited by 96 · see citing works

Mitochondrial membrane potential and compartmentalized signaling: Calcium, ROS, and beyond

Selim, N. A., & Wojtovich, A. P. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103859 · Cited by 92 · see citing works

Energy metabolism design of the striated muscle cell

Glancy, B. C., & Balaban, R. S. (2021) · Physiological Reviews · doi:10.1152/physrev.00040.2020 · Cited by 83 · see citing works

Interaction of the Joining Region in Junctophilin-2 With the L-Type Ca 2+ Channel Is Pivotal for Cardiac Dyad Assembly and Intracellular Ca 2+ Dynamics

Gross, P., Johnson, J. P., Romero, C. M., Eaton, D., Poulet, C. E., Sanchez‐Alonso, J. L., Lucarelli, C., Ross, J., Gibb, A., Garbincius, J. F., et al. (2020) · Circulation Research · doi:10.1161/circresaha.119.315715 · Cited by 77 · see citing works

3D reconstruction of murine mitochondria reveals changes in structure during aging linked to the MICOS complex

Vue, Z., Lopez, E. G., Neikirk, K., Katti, P., Vang, L., Beasley, H. K., Shao, J., Marshall, A. G., Crabtree, A., Murphy, A. C., et al. (2023) · Aging Cell · doi:10.1111/acel.14009 · Cited by 66 · see citing works

Three-dimensional mitochondria reconstructions of murine cardiac muscle changes in size across aging

Vue, Z., Neikirk, K., Vang, L., Lopez, E. G., Christensen, T. A., Shao, J., Lam, J., Beasley, H. K., Marshall, A. G., Crabtree, A., et al. (2023) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00202.2023 · Cited by 55 · see citing works

Defective Mitochondrial Dynamics Underlie Manganese-Induced Neurotoxicity

Morcillo, P., Cordero, H., Ijomone, O. M., Ayodele, A. J., Bornhorst, J., Gunther-Cummins, L., Macaluso, F., Bowman, A. B., & Aschner, M. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02341-w · Cited by 55 · see citing works

Extracellular Vesicles and Damage-Associated Molecular Patterns: A Pandora’s Box in Health and Disease

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A Comprehensive Approach to Sample Preparation for Electron Microscopy and the Assessment of Mitochondrial Morphology in Tissue and Cultured Cells

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