Mitochondrial filaments and clusters as intracellular power-transmitting cables

Coupling of phosphorylation to electron and hydrogen transfer by a chemi-osmotic type of mechanism

MITCHELL, P. (1961) · Nature · doi:10.1038/191144a0 · Cited by 4,704

An endotoxin-induced serum factor that causes necrosis of tumors

Carswell, E. A., Old, L. J., Kassel, R. L., Green, S., Fiore, N., & Williamson, B. (1975) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.72.9.3666 · Cited by 4,532

Molecular characterization of mitochondrial apoptosis-inducing factor

Susin, S. A., Lorenzo, H. K., Zamzami, N., Marzo, I., Snow, B. E., Brothers, G. M., Mangion, J., Jacotot, E., Costantini, P., Loeffler, M., et al. (1999) · Nature · doi:10.1038/17135 · Cited by 4,060

The mitochondrial permeability transition pore and its role in cell death

CROMPTON, M. (1999) · Biochemical Journal · doi:10.1042/bj3410233 · Cited by 2,432

Close Contacts with the Endoplasmic Reticulum as Determinants of Mitochondrial Ca 2+ Responses

Rizzuto, R., Pinton, P., Carrington, W., Fay, F. S., Fogarty, K. E., Lifshitz, L. M., Tuft, R. A., & Pozzan, T. (1998) · Science · doi:10.1126/science.280.5370.1763 · Cited by 2,257

Intracellular heterogeneity in mitochondrial membrane potentials revealed by a J-aggregate-forming lipophilic cation JC-1.

Smiley, S. T., Reers, M., Mottola-Hartshorn, C., Lin, M., Chen, A. B., Smith, T. W., Steele, G., & Chen, L. B. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.9.3671 · Cited by 1,629

Localization of mitochondria in living cells with rhodamine 123.

Johnson, L. V., Walsh, M. L., & Chen, L. B. (1980) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.77.2.990 · Cited by 1,548

Mitochondria Are Excitable Organelles Capable of Generating and Conveying Electrical and Calcium Signals

Ichas, F., Jouaville, L. S., & Mazat, J. (1997) · Cell · doi:10.1016/s0092-8674(00)80301-3 · Cited by 748

Role of uncoupled and non-coupled oxidations in maintenance of safely low levels of oxygen and its one-electron reductants

Skulachev, V. P. (1996) · Quarterly Reviews of Biophysics · doi:10.1017/s0033583500005795 · Cited by 703

Mechanism of Coupling of Oxidative Phosphorylation and the Membrane Potential of Mitochondria

Liberman, E. A., Vp, T., Tsofina, L. M., JASAITIS, A. A., & Skulachev, V. P. (1969) · Nature · doi:10.1038/2221076a0 · Cited by 490

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

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

Mitochondrial fusion and fission in cell life and death

Westermann, B. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3013 · Cited by 2,002

Mitochondria: Dynamic Organelles in Disease, Aging, and Development

Chan, D. C. (2006) · Cell · doi:10.1016/j.cell.2006.06.010 · Cited by 1,987

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

Züchner, S., Mersiyanova, I. V., Muglia, M., Bissar-Tadmouri, N., Rochelle, J., Dadali, E. L., Zappia, M., Nelis, E., Patitucci, A., Senderek, J., et al. (2004) · Nature Genetics · doi:10.1038/ng1341 · Cited by 1,572

Disruption of Fusion Results in Mitochondrial Heterogeneity and Dysfunction

Chen, H., Chomyn, A., & Chan, D. C. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m503062200 · Cited by 1,376

Mitochondrial H2O2 emission and cellular redox state link excess fat intake to insulin resistance in both rodents and humans

Anderson, E. J., Lustig, M. E., Boyle, K. E., Woodlief, T. L., Kane, D. A., Lin, C.-T., Price, J. W., Kang, L., Rabinovitch, P. S., Szeto, H. H., et al. (2009) · Journal of Clinical Investigation · doi:10.1172/jci37048 · Cited by 1,253

Increased production of reactive oxygen species in hyperglycemic conditions requires dynamic change of mitochondrial morphology

Yu, T., Robotham, J. L., & Yoon, Y. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0511154103 · Cited by 1,246

Metabolic regulation of mitochondrial dynamics

Mishra, P., & Chan, D. C. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201511036 · Cited by 1,143

Coherent Anti-Stokes Raman Scattering Microscopy: Instrumentation, Theory, and Applications

Cheng, J., & Xie, X. S. (2003) · The Journal of Physical Chemistry B · doi:10.1021/jp035693v · Cited by 962

Mitochondrial Dynamics in Mammalian Health and Disease

Liesa, M., Palacín, M., & Zorzano, A. (2009) · Physiological Reviews · doi:10.1152/physrev.00030.2008 · Cited by 953

Mitochondria and neuronal activity

Kann, O., & Kovács, R. (2006) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00222.2006 · Cited by 871

Mitofusin-2 Determines Mitochondrial Network Architecture and Mitochondrial Metabolism

Bach, D., Pich, S., Soriano, F. X., Vega, N., Baumgartner, B., Oriola, J., Daugaard, J. R., Lloberas, J., Camps, M., Zierath, J. R., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m212754200 · Cited by 832

The Interplay Between Mitochondrial Dynamics and Mitophagy

Twig, G., & Shirihai, O. S. (2011) · Antioxidants & Redox Signaling · doi:10.1089/ars.2010.3779 · Cited by 778

SLP‐2 is required for stress‐induced mitochondrial hyperfusion

Tondera, D., Grandemange, S., Jourdain, A. A., Karbowski, M., Mattenberger, Y., Herzig, S., Cruz, S. D., Clerc, P., Lauria, I., Merkwirth, C., et al. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.89 · Cited by 796

Dynamics of mitochondrial morphology in healthy cells and during apoptosis

Karbowski, M., & Youle, R. J. (2003) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401260 · Cited by 780

Bioenergetic role of mitochondrial fusion and fission

Westermann, B. (2012) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2012.02.033 · Cited by 687

Mitochondria are morphologically and functionally heterogeneous within cells

Collins, T. J., Berridge, M. J., Lipp, P., & Bootman, M. D. (2002) · The EMBO Journal · doi:10.1093/emboj/21.7.1616 · Cited by 588

Repeated transient mRNA bursts precede increases in transcriptional and mitochondrial proteins during training in human skeletal muscle: Molecular responses during mitochondrial biogenesis

Perry, C. G. R., Lally, J., Holloway, G. P., Heigenhauser, G. J. F., Bonen, A., & Spriet, L. L. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2010.199448 · Cited by 559

New insights into the role of mitochondria in aging: mitochondrial dynamics and more

Seo, A. Y., Joseph, A.-M., Dutta, D., Hwang, J. C. Y., Aris, J. P., & Leeuwenburgh, C. (2010) · Journal of Cell Science · doi:10.1242/jcs.070490 · Cited by 522

Loss-of-Function of Human PINK1 Results in Mitochondrial Pathology and Can Be Rescued by Parkin

Exner, N., Treske, B., Paquet, D., Holmström, K. M., Schiesling, C., Gispert, S., Carballo‐Carbajal, I., Berg, D., Hoepken, H.-H., Gasser, T., et al. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0719-07.2007 · Cited by 523

The Charcot-Marie-Tooth type 2A gene product, Mfn2, up-regulates fuel oxidation through expression of OXPHOS system

Pich, S., Bach, D., Briones, P., Liesa, M., Camps, M., Testar, X., Palacín, M., & Zorzano, A. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi149 · Cited by 455

Mitofusin-1 protein is a generally expressed mediator of mitochondrial fusion in mammalian cells

Santel, A., Frank, S., Gaume, B. R., Herrler, M., Youle, R. J., & Fuller, M. T. (2003) · Journal of Cell Science · doi:10.1242/jcs.00479 · Cited by 445

Mitochondrial fission in apoptosis, neurodegeneration and aging

Bossy‐Wetzel, E., Barsoum, M. J., Godzik, A., Schwarzenbacher, R., & Lipton, S. A. (2003) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2003.10.015 · Cited by 438

Mitochondria as a Source of Reactive Oxygen and Nitrogen Species: From Molecular Mechanisms to Human Health

Figueira, T. R., de Barros, M. H., Camargo, A. A., Castilho, R. F., Ferreira, J. C. B., Kowaltowski, A. J., Sluse, F. E., de Souza-Pinto, N. C., & Vercesi, A. E. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2012.4729 · Cited by 430

Mitochondrial Trafficking to Synapses in Cultured Primary Cortical Neurons

Chang, D. T. W., Honick, A. S., & Reynolds, I. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1012-06.2006 · Cited by 391

Bioenergetic aspects of apoptosis, necrosis and mitoptosis

Skulachev, V. P. (2006) · APOPTOSIS · doi:10.1007/s10495-006-5881-9 · Cited by 391

Mitochondrial Networking Protects β-Cells From Nutrient-Induced Apoptosis

Molina, A. J. A., Wikstrom, J. D., Stiles, L., Las, G., Mohamed, H., Elorza, A., Walzer, G., Twig, G., Katz, S., Corkey, B. E., et al. (2009) · Diabetes · doi:10.2337/db07-1781 · Cited by 381

Interactions between ROS and AMP kinase activity in the regulation of PGC-1α transcription in skeletal muscle cells

Irrcher, I., Ljubicic, V., & Hood, D. A. (2009) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00267.2007 · Cited by 356

Reducing mitochondrial fission results in increased life span and fitness of two fungal ageing models

Scheckhuber, C. Q., Erjavec, N., Tinazli, A., Hamann, A., Nyström, T., & Osiewacz, H. D. (2007) · Nature Cell Biology · doi:10.1038/ncb1524 · Cited by 344

Individual cristae within the same mitochondrion display different membrane potentials and are functionally independent

Wolf, D. M., Segawa, M., Kondadi, A. K., Anand, R., Bailey, S. T., Reichert, A. S., van der Bliek, A. M., Shackelford, D. B., Liesa, M., & Shirihai, O. S. (2019) · The EMBO Journal · doi:10.15252/embj.2018101056 · Cited by 347

MITO-Porter: A liposome-based carrier system for delivery of macromolecules into mitochondria via membrane fusion

Yamada, Y., Akita, H., Kamiya, H., Kogure, K., Yamamoto, T., Shinohara, Y., Yamashita, K., Kobayashi, H., Kikuchi, H., & Harashima, H. (2007) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2007.11.002 · Cited by 324

Mitochondrial Membrane Permeabilization and Cell Death During Myocardial Infarction: Roles of Calcium and Reactive Oxygen Species

Webster, K. A. (2012) · Future Cardiology · doi:10.2217/fca.12.58 · Cited by 311

The Permeability Transition Pore Controls Cardiac Mitochondrial Maturation and Myocyte Differentiation

Hom, J., Quintanilla, R. A., Hoffman, D. L., Bentley, K. L. D. M., Molkentin, J. D., Sheu, S., & Porter, G. A. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.08.008 · Cited by 301

Far-Red Fluorescence Probe for Monitoring Singlet Oxygen during Photodynamic Therapy

Kim, S., Tachikawa, T., Fujitsuka, M., & Majima, T. (2014) · Journal of the American Chemical Society · doi:10.1021/ja504279r · Cited by 284

Muscle fiber type diversification during exercise and regeneration

Qaisar, R., Bhaskaran, S., & Van Remmen, H. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.03.025 · Cited by 283

Formation of elongated giant mitochondria in DFO‐induced cellular senescence: Involvement of enhanced fusion process through modulation of Fis1

Yoon, Y., Yoon, D., Lim, I. K., Yoon, S., Chung, H., Rojo, M., Malka, F., Jou, M., Martinou, J., & Yoon, G. (2006) · Journal of Cellular Physiology · doi:10.1002/jcp.20753 · Cited by 275

Molecular mechanisms for mitochondrial adaptation to exercise training in skeletal muscle

Drake, J. C., Wilson, R. J., & Yan, Z. (2016) · The FASEB Journal · doi:10.1096/fj.15-276337 · Cited by 263

Neural stem cells traffic functional mitochondria via extracellular vesicles

Peruzzotti-Jametti, L., Bernstock, J. D., Willis, C. M., Manferrari, G., Rogall, R., Fernandez-Vizarra, E., Williamson, J. C., Braga, A., van den Bosch, A., Leonardi, T., et al. (2021) · PLOS Biology · doi:10.1371/journal.pbio.3001166 · Cited by 263

Mitochondrial morphology, topology, and membrane interactions in skeletal muscle: a quantitative three-dimensional electron microscopy study

Picard, M. A., White, K., & Turnbull, D. M. (2012) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01096.2012 · Cited by 273

Creatine metabolism: energy homeostasis, immunity and cancer biology

Kazak, L., & Cohen, P. (2020) · Nature Reviews Endocrinology · doi:10.1038/s41574-020-0365-5 · Cited by 267

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 270

Mitochondrial intermembrane junctional complexes and their involvement in cell death

Crompton, M., Barksby, E., Johnson, N., & Capano, M. (2002) · Biochimie · doi:10.1016/s0300-9084(02)01368-8 · Cited by 256

Regulation of mitochondrial morphology by membrane potential, and DRP1-dependent division and FZO1-dependent fusion reaction in mammalian cells

Ishihara, N., Jofuku, A., Eura, Y., & Mihara, K. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(03)00050-0 · Cited by 255

Molecular Machinery of Mitochondrial Fusion and Fission

Westermann, B. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.r800011200 · Cited by 258

Mitochondrial quality control: An integrated network of pathways

Fischer, F., Hamann, A., & Osiewacz, H. D. (2012) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2012.02.004 · Cited by 248

The Association of Tau With Mitochondrial Dysfunction in Alzheimer’s Disease

Cheng, Y., & Bai, F. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00163 · Cited by 239

Mitochondrial dynamics in the adult cardiomyocytes: which roles for a highly specialized cell?

Piquereau, J., Caffin, F., Novotová, M., Lemaire, C., Veksler, V., Garnier, A., Ventura‐Clapier, R., & Joubert, F. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00102 · Cited by 251

Changes in mitochondrial dynamics during ceramide-induced cardiomyocyte early apoptosis

Parra, V., Eisner, V., Chiong, M., Criollo, A., Moraga, F., García, A., Härtel, S., Jaimovich, E., Zorzano, A., Hidalgo, C., et al. (2007) · Cardiovascular Research · doi:10.1093/cvr/cvm029 · Cited by 232

Mitochondrial trafficking and morphology in healthy and injured neurons

Chang, D. T. W., & Reynolds, I. J. (2006) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2006.09.003 · Cited by 235

Mitofusins 1 and 2 Are Essential for Postnatal Metabolic Remodeling in Heart

Papanicolaou, K. N., Kikuchi, R., Ngoh, G. A., Coughlan, K. A., Dominguez, I. M., Stanley, W. C., & Walsh, K. X. (2012) · Circulation Research · doi:10.1161/circresaha.112.274142 · Cited by 223

Role of mitochondrial dynamics proteins in the pathophysiology of obesity and type 2 diabetes

Zorzano, A., Liesa, M., & Palacín, M. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.02.004 · Cited by 209

Protons @ interfaces: Implications for biological energy conversion

Mulkidjanian, A. Y., Heberle, J., & Cherepanov, D. A. (2006) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2006.02.015 · Cited by 208

Cardiomyocyte deletion of mitofusin-1 leads to mitochondrial fragmentation and improves tolerance to ROS-induced mitochondrial dysfunction and cell death

Papanicolaou, K. N., Ngoh, G. A., Dabkowski, E. R., O’Connell, K. A., Júnior, R. F. R., Stanley, W. C., & Walsh, K. X. (2011) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00833.2011 · Cited by 208

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

Mitochondrial network complexity and pathological decrease in complex I activity are tightly correlated in isolated human complex I deficiency

Koopman, W. J. H., Visch, H.-J., Verkaart, S., van den Heuvel, L. P., Smeitink, J. A. M., & Willems, P. H. G. M. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00104.2005 · Cited by 192

Mechanisms of mitochondria and autophagy crosstalk

Rambold, A. S., & Lippincott‐Schwartz, J. (2011) · Cell Cycle · doi:10.4161/cc.10.23.18384 · Cited by 200

OPA1 (Kjer Type) Dominant Optic Atrophy: A Novel Mitochondrial Disease

Delettre, C., Lenaers, G., Pelloquin, L., Belenguer, P., & Hamel, C. (2002) · Molecular Genetics and Metabolism · doi:10.1006/mgme.2001.3278 · Cited by 191

HDAC6 inhibition effectively reverses chemotherapy-induced peripheral neuropathy

Krukowski, K., Ma, J., Golonzhka, O., Laumet, G. O., Gutti, T., van Duzer, J. H., Mazitschek, R., Jarpe, M. B., Heijnen, C. J., & Kavelaars, A. (2017) · Pain · doi:10.1097/j.pain.0000000000000893 · Cited by 189

Optical and pharmacological tools to investigate the role of mitochondria during oxidative stress and neurodegeneration

Foster, K. A., Galeffi, F., Gerich, F. J., Turner, D. A., & Müller, M. (2006) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2006.07.001 · Cited by 190

Mitochondrial Dynamics in Mammals

Chen, H., & Chan, D. C. (2004) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(04)59005-1 · Cited by 180

Morphological dynamics of mitochondria — A special emphasis on cardiac muscle cells

Hom, J., & Sheu, S. (2009) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2009.02.023 · Cited by 189

Regulation of Mitochondrial Morphology by USP30, a Deubiquitinating Enzyme Present in the Mitochondrial Outer Membrane

Nakamura, N., & Hirose, S. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-11-1103 · Cited by 181

Mitochondria form a filamentous reticular network in hippocampal dendrites but are present as discrete bodies in axons: A three-dimensional ultrastructural study

Popov, V. I., Medvedev, N. I., Davies, H. A., & Stewart, M. G. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20682 · Cited by 175

Cell cycle dependent morphology changes and associated mitochondrial DNA redistribution in mitochondria of human cell lines

Margineantu, D. H., Cox, W. G., Sundell, L., Sherwood, S. W., Beechem, J., & Capaldi, R. (2002) · Mitochondrion · doi:10.1016/s1567-7249(02)00006-5 · Cited by 173

Physiological and structural differences in spatially distinct subpopulations of cardiac mitochondria: influence of cardiac pathologies

Hollander, J. M., Thapa, D., & Shepherd, D. L. (2014) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00747.2013 · Cited by 171

Mitochondria-specific transgenic overexpression of phospholipid hydroperoxide glutathione peroxidase (GPx4) attenuates ischemia/reperfusion-associated cardiac dysfunction

Dabkowski, E. R., Williamson, C. L., & Hollander, J. M. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.06.021 · Cited by 171

Cristae Membrane Dynamics – A Paradigm Change

Kondadi, A. K., Anand, R., & Reichert, A. S. (2020) · Trends in Cell Biology · doi:10.1016/j.tcb.2020.08.008 · Cited by 170

A Wave of Reactive Oxygen Species (ROS)-Induced ROS Release in a Sea of Excitable Mitochondria

Brady, N. R., Hamacher‐Brady, A., Westerhoff, H. V., & Gottlieb, R. A. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2006.8.1651 · Cited by 172

The cell-type specificity of mitochondrial dynamics

Kuznetsov, A. V., Hermann, M., Saks, V. A., Hengster, P., & Margreiter, R. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.03.007 · Cited by 184

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

Mitochondrial respiratory chain dysfunction: Implications in neurodegeneration

Morán, M., Moreno-Lastres, D., Marín-Buera, L., Arenas, J., Martín, M. A., & Ugalde, C. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.05.009 · Cited by 168

A Small Molecule Promotes Mitochondrial Fusion in Mammalian Cells

Wang, D., Wang, J., Bonamy, G. M. C., Meeusen, S., Brusch, R. G., Turk, C. N., Yang, P., & Schultz, P. G. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201204589 · Cited by 165

Mitochondrial biogenesis in the axons of vertebrate peripheral neurons

Amiri, M., & Hollenbeck, P. J. (2008) · Developmental Neurobiology · doi:10.1002/dneu.20668 · Cited by 165

What is the function of mitochondrial networks? A theoretical assessment of hypotheses and proposal for future research

Hoitzing, H., Johnston, I. G., & Jones, N. S. (2015) · BioEssays · doi:10.1002/bies.201400188 · Cited by 159

Simultaneous quantitative measurement and automated analysis of mitochondrial morphology, mass, potential, and motility in living human skin fibroblasts

Koopman, W. J. H., Visch, H.-J., Smeitink, J. A. M., & Willems, P. H. G. M. (2005) · Cytometry Part A · doi:10.1002/cyto.a.20198 · Cited by 158

Age-Related Changes in Axonal and Mitochondrial Ultrastructure and Function in White Matter

Stahon, K. E., Bastian, C., Griffith, S., Kidd, G. J., Brunet, S., & Baltan, S. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1316-16.2016 · Cited by 157

Exercise training increases skeletal muscle mitochondrial volume density by enlargement of existing mitochondria and not de novo biogenesis

Lundby, A., Jacobs, R. A., Gehrig, S. M., de Leur, J., Hauser, M., Bonne, T. C., Flück, D., Dandanell, S., Kirk, N., Kaech, A., et al. (2017) · Acta Physiologica · doi:10.1111/apha.12905 · Cited by 158

Induction of Endogenous Uncoupling Protein 3 Suppresses Mitochondrial Oxidant Emission during Fatty Acid-supported Respiration

Anderson, E. J., Yamazaki, H., & Neufer, P. D. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m706129200 · Cited by 151

Thread-grain transition of mitochondrial reticulum as a step of mitoptosis and apoptosis

Skulachev, V. P., Bakeeva, L. E., Chernyak, B. V., Domnina, L. V., Minin, A. А., Pletjushkina, O. Y., Saprunova, V. B., Skulachev, I. V., Tsyplenkova, V. G., Vasiliev, J. M., et al. (2003) · Molecular and Cellular Biochemistry · doi:10.1023/b:mcbi.0000009880.94044.49 · Cited by 153

Response of mitochondrial fusion and fission protein gene expression to exercise in rat skeletal muscle

Ding, H., Jiang, N., Liu, H., Liu, X., Liu, D., Zhao, F., Wen, L., Liu, S., Ji, L. L., & Zhang, Y. (2009) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2009.08.007 · Cited by 149

Mitochondrial dysfunction and mitochondrial therapies in heart failure

Wu, C., Zhang, Z., Zhang, W., & Liu, X. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.106038 · Cited by 148

Acute exercise remodels mitochondrial membrane interactions in mouse skeletal muscle

Picard, M. A., Gentil, B. J., McManus, M. J., White, K., Louis, K. S., Gartside, S. E., Wallace, D. C., & Turnbull, D. M. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00819.2013 · Cited by 145

Mitochondrial Aberrations in Mucolipidosis Type IV

Jennings, J. J., Zhu, J.-H., Rbaibi, Y., Luo, X., Chu, C. T., & Kiselyov, K. I. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m607982200 · Cited by 144

Mitochondrial Function and Cell Size: An Allometric Relationship

Miettinen, T. P., & Björklund, M. (2017) · Trends in Cell Biology · doi:10.1016/j.tcb.2017.02.006 · Cited by 151

Merging mitochondria matters

Westermann, B. (2002) · EMBO Reports · doi:10.1093/embo-reports/kvf113 · Cited by 149

Mitochondrial fission is an upstream and required event for bax foci formation in response to nitric oxide in cortical neurons

Yuan, H., Gerencser, A. A., Liot, G., Lipton, S. A., Ellisman, M. H., Perkins, G. A., & Bossy‐Wetzel, E. (2006) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4402046 · Cited by 140

Mdm30 Is an F-Box Protein Required for Maintenance of Fusion-competent Mitochondria in Yeast

Fritz, S., Weinbach, N., & Westermann, B. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-12-0831 · Cited by 140

Analysis of Mitochondrial Dynamics and Functions Using Imaging Approaches

Mitra, K., & Lippincott‐Schwartz, J. (2010) · Current Protocols in Cell Biology · doi:10.1002/0471143030.cb0425s46 · Cited by 144

Biophotons as neural communication signals demonstrated by in situ biophoton autography

Sun, Y., Wang, C., & Dai, J. (2010) · Photochemical & Photobiological Sciences · doi:10.1039/b9pp00125e · Cited by 137

Genome-wide Analysis of the H3K4 Histone Demethylase RBP2 Reveals a Transcriptional Program Controlling Differentiation

López-Bigas, N., Kisiel, T. A., DeWaal, D. C., Holmes, K. B., Volkert, T. L., Gupta, S., Love, J. A., Murray, H. L., Young, R. A., & Benevolenskaya, E. V. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.08.004 · Cited by 134

The programmed death phenomena, aging, and the Samurai law of biology

Skulachev, V. P. (2001) · Experimental Gerontology · doi:10.1016/s0531-5565(01)00109-7 · Cited by 134

Mitochondrial Dynamics in Diabetic Cardiomyopathy

Galloway, C. A., & Yoon, Y. (2015) · Antioxidants and Redox Signaling · doi:10.1089/ars.2015.6293 · Cited by 135

High resolution imaging of live mitochondria

Jakobs, S. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.04.004 · Cited by 144

Human NADH:ubiquinone oxidoreductase deficiency: radical changes in mitochondrial morphology?

Koopman, W. J. H., Verkaart, S., Visch, H.-J., Vries, S. E. V. E., Nijtmans, L. G. J., Smeitink, J. A. M., & Willems, P. H. G. M. (2007) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00194.2006 · Cited by 134

Perturbation in Mitochondrial Network Dynamics and in Complex I Dependent Cellular Respiration in Schizophrenia

Rosenfeld, M., Brenner-Lavie, H., Gal-Ben-Ari, S., Kavushansky, A., & Ben‐Shachar, D. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.01.010 · Cited by 132

A fuzzy mitochondrial fusion apparatus comes into focus

Mozdy, A. D., & Shaw, J. M. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1125 · Cited by 130

EMISSION OF MITOCHONDRIAL BIOPHOTONS AND THEIR EFFECT ON ELECTRICAL ACTIVITY OF MEMBRANE VIA MICROTUBULES

Rahnama, M., Tuszyński, J. A., Bókkon, I., Cifra, M., Sardar, P., & Salari, V. (2011) · Journal of Integrative Neuroscience · doi:10.1142/s0219635211002622 · Cited by 135

ADP Regulates Movements of Mitochondria in Neurons

Mironov, S. L. (2007) · Biophysical Journal · doi:10.1529/biophysj.106.092981 · Cited by 129

Control of mitochondria dynamics and oxidative metabolism by cAMP, AKAPs and the proteasome

Carlucci, A., Lignitto, L., & Feliciello, A. (2008) · Trends in Cell Biology · doi:10.1016/j.tcb.2008.09.006 · Cited by 134

Mitochondrial network: electric cable and more

Abramicheva, P. A., Andrianova, N. V., Babenko, V. А., Zorova, L. D., Zorov, S. D., Pevzner, I. B., Popkov, V. A., Semenovich, D. S., & Yakupova, E. I. (2023) · Biochemistry (Moscow) · doi:10.31857/s0320972523100147 · Cited by 2

A model for intracellular energy transport

Mainwood, G. W., & Rakusan, K. (1982) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y82-016 · Cited by 91

Mitochondria and chloroplasts: localized and delocalized bioenergetic transduction

Williams, R. J. P. (2000) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(00)01675-3 · Cited by 10

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 270

The Functions, Methods, and Mobility of Mitochondrial Transfer Between Cells

Qin, Y., Jiang, X., Yang, Q., Zhao, J., Zhou, Q., & Zhou, Y. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.672781 · Cited by 120