The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.
Mitochondrial filaments and clusters as intracellular power-transmitting cables
Abstract
Mitochondria exist in two interconverting forms; as small isolated particles, and as extended filaments, networks or clusters connected with intermitochondrial junctions. Extended mitochondria can represent electrically united systems, which can facilitate energy delivery from the cell periphery to the cell core and organize antioxidant defence of the cell interior when O2 is consumed by mitochondrial clusters near the the outer cell membrane, and protonic potential is transmitted to the cell core mitochondria to form ATP. As to small mitochondria, they might represent a transportable form of these organelles.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“This operation is unique to myotubes, and previous reports on cardiac myocytes or on fibroblasts suggest there are several independent clusters of electrically connected mitochondria per cell (3”
From Mitofusin-2 Determines Mitochondrial Network Architecture and Mitochondrial Metabolism (2003) · cites this paper as [4]
In the citing paper
“This process enables the redistribution of energy in the form of mitochondrial potential, metabolites, proteins, and mtDNA, improving calcium handling, and ATP synthesis [24, 54–57].”
From The connection between the dynamic remodeling of the mitochondrial network and the regulation of muscle mass (2021) · cites this paper as [56]
In the citing paper
“In healthy cells, mitochondrial fusion provides a synchronized internal cable for translocating metabolites and intramitochondrial mixing during biogenesis, whereas mitochondrial division facilitates the equal distribution of mitochondria into daughter cells during mitosis and allows the selective degradation of damaged mitochondria through autophagy (Chen and Chan, 2009; Skulachev, 2001).”
From New insights into the role of mitochondria in aging: mitochondrial dynamics and more (2010) · cites this paper as Skulachev, 2001
Citations
Cites
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
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
Ichas, F., Jouaville, L. S., & Mazat, J. (1997) · Cell · doi:10.1016/s0092-8674(00)80301-3 · Cited by 748
Skulachev, V. P. (1996) · Quarterly Reviews of Biophysics · doi:10.1017/s0033583500005795 · Cited by 703
Self-citationMechanism 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
Self-citation
Research works printed but not linked: 2
- Walsh, 1979, Transport of serum components into structures similar to mitochondria, Cold Spring Harbor Conf. Proliferation, 6, 513
- Hüser, 1999, Subcellular coordination of mitochondrial metabolism in heart cells, Biophys. J., 76, A144
Cited by
Sorted by citations
Items 201–300 of 473
Pham, N., Richardson, T., Cameron, J. M., Chue, B., & Robinson, B. H. (2004) · Microscopy and Microanalysis · doi:10.1017/s143192760404005x · Cited by 47
Manteifel, V. M., & Кару, Т. Й. (2005) · Biology Bulletin · doi:10.1007/s10525-005-0143-x · Cited by 47
Jakobs, S., Schauss, A. C., & Hell, S. W. (2003) · FEBS Letters · doi:10.1016/s0014-5793(03)01170-0 · Cited by 47
Funk, R. H. W., & Scholkmann, F. (2022) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2022.12.002 · Cited by 46
Role of Mitochondrial Dysfunctions in Neurodegenerative Disorders: Advances in Mitochondrial Biology
Kathiresan, D. S., Balasubramani, R., Marudhachalam, K., Jaiswal, P., Ramesh, N., Suruthi, G. S., Moorthi, P. V., & Vijayan, M. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04469-x · Cited by 49
The quantum mitochondrion and optimal health
Nunn, A. V. W., Guy, G. W., & Bell, J. D. (2016) · Biochemical Society Transactions · doi:10.1042/bst20160096 · Cited by 45
Ďúranová, H., Válková, V., Kňažická, Z., Olexíková, L., & Vašíček, J. (2020) · Acta Histochemica · doi:10.1016/j.acthis.2020.151646 · Cited by 47
Implications of mitochondrial fusion and fission in skeletal muscle mass and health
Romanello, V., & Sandri, M. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.02.011 · Cited by 46
Lai, N., Kummitha, C. M., Rosca, M. G., Fujioka, H., Tandler, B., & Hoppel, C. L. (2018) · Acta Physiologica · doi:10.1111/apha.13182 · Cited by 48
Long range physical cell-to-cell signalling via mitochondria inside membrane nanotubes: a hypothesis
Scholkmann, F. (2016) · Theoretical Biology and Medical Modelling · doi:10.1186/s12976-016-0042-5 · Cited by 43
Grieco, J. P., Allen, M. E., Perry, J. B., Wang, Y., Song, Y., Rohani, A., Compton, S. L. E., Smyth, J. W., Swami, N. S., Brown, D. A., et al. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2020.600113 · Cited by 42
Baici, A., Müntener, K., Willimann, A., & Zwicky, R. (2006) · Biological Chemistry · doi:10.1515/bc.2006.125 · Cited by 42
Spontaneous and evoked neuronal activities regulate movements of single neuronal mitochondria
Mironov, S. L. (2006) · Synapse · doi:10.1002/syn.20256 · Cited by 42
Regulation of mitochondrial dynamics and neurodegenerative diseases.
Han, X.-J., Tomizawa, K., Fujimura, A., Ohmori, I., Nishiki, T., Matsushita, M., & Matsui, H. (2011) · PubMed · doi:10.18926/amo/43824 · Cited by 41
Ng, A. C.-H., Baird, S. D., & Screaton, R. A. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.01021-13 · Cited by 41
MacDougall, G., Anderton, R. S., Mastaglia, F. L., Knuckey, N. W., & Meloni, B. P. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.09.010 · Cited by 41
The enigma of an interconnected mitochondrial reticulum: new insights into mitochondrial fusion
Mattie, S., Krols, M., & McBride, H. M. (2019) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2019.05.004 · Cited by 42
Structural Dynamics of Myoglobin: FTIR-TDS Study of NO Migration and Binding†
Nienhaus, K., Palladino, P., & Nienhaus, G. U. (2007) · Biochemistry · doi:10.1021/bi701935v · Cited by 39
Mitochondrial remodeling in differentiating neuroblasts
Voccoli, V., & Colombaioni, L. (2008) · Brain Research · doi:10.1016/j.brainres.2008.11.026 · Cited by 41
Adaptations of Skeletal Muscle Mitochondria to Obesity, Exercise, and Polyunsaturated Fatty Acids
Chen, P. B., Yang, J. S., & Park, Y. (2018) · Lipids · doi:10.1002/lipd.12037 · Cited by 37
Glaser, V., Martins, R. D. P., Vieira, A. J. H., Oliveira, E. D. M., Straliotto, M. R., Mukdsi, J. H., Torres, A. I., Bem, A. F. D., Farina, M., da Rocha, J. B. T., et al. (2014) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-013-1870-9 · Cited by 37
Brain energetics, mitochondria, and traumatic brain injury
Benaroya, H. (2020) · Reviews in the Neurosciences · doi:10.1515/revneuro-2019-0086 · Cited by 37
Wildenberg, G. A., Sorokina, A. M., Koranda, J. L., Monical, A., Heer, C., Sheffield, M. E., Zhuang, X., McGehee, D., & Kasthuri, N. (2021) · eLife · doi:10.7554/elife.71981 · Cited by 39
Mitochondria: An overview of their origin, genome, architecture, and dynamics
Moura, J. P., Oliveira, P. J., & Urbano, A. M. (2025) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2025.167803 · Cited by 45
Human muscular mitochondrial fusion in athletes during exercise
Huertas, J. R., Ruiz‐Ojeda, F. J., Plaza‐Díaz, J., Nordsborg, N. B., Martín‐Albo, J., Rueda‐Robles, A., & Casuso, R. A. (2019) · The FASEB Journal · doi:10.1096/fj.201900365rr · Cited by 37
Lyamzaev, K. G., Pletjushkina, O. Y., Saprunova, V. B., Bakeeva, L. E., Chernyak, B. V., & Skulachev, V. P. (2004) · Biochemical Society Transactions · doi:10.1042/bst0321070 · Cited by 36
Self-citationMironov, S. L. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.04.009 · Cited by 36
Ahmed, M. E., Selvakumar, G. P., Kempuraj, D., Thangavel, R., Mentor, S., Dubova, I., Raikwar, S. P., Zaheer, S. A., Iyer, S. S., & Zaheer, A. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1544-z · Cited by 36
Osiewacz, H. D., Brust, D., Hamann, A., Kunstmann, B., Luce, K., Müller‐Ohldach, M., Scheckhuber, C. Q., Servos, J., & Strobel, I. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05190.x · Cited by 33
Autofluorescence microscopy: A non-destructive tool to monitor mitochondrial toxicity
Rodrigues, R. M., Macko, P., Palosaari, T., & Whelan, M. (2011) · Toxicology Letters · doi:10.1016/j.toxlet.2011.06.025 · Cited by 33
Zheng, F., Jia, B., Dong, F., Liu, L., Rasul, F., He, J., & Fu, C. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.010185 · Cited by 33
Mitochondrial Dynamics in Drug-Induced Liver Injury
Ramachandran, A., Umbaugh, D. S., & Jaeschke, H. (2021) · Livers · doi:10.3390/livers1030010 · Cited by 34
Zhou, J., Hao, J., Zhong, Z., Yang, J., Lv, T., Zhao, B., Lin, H., Chi, J., & Guo, H. (2023) · Antioxidants and Redox Signaling · doi:10.1089/ars.2023.0355 · Cited by 32
Cupp, J. D., & Nielsen, B. L. (2012) · Physiologia Plantarum · doi:10.1111/ppl.12009 · Cited by 36
Mitochondria in tumor cells studied by laser scanning confocal microscopy
VILLA, A. M., & Doglia, S. M. (2004) · Journal of Biomedical Optics · doi:10.1117/1.1646414 · Cited by 32
Mitochondrial “Movement” and Lens Optics following Oxidative Stress from UV‐B Irradiation
Bantseev, V., & Youn, H.-Y. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1378.051 · Cited by 32
Longitudinal metabolic profiling of cardiomyocytes derived from human-induced pluripotent stem cells
Bekhite, M. M., Delgado, A. G., Menz, F., Kretzschmar, T., Wu, J. M. F., Bekfani, T., Nietzsche, S., Wartenberg, M., Westermann, M., Greber, B., et al. (2020) · Basic Research in Cardiology · doi:10.1007/s00395-020-0796-0 · Cited by 31
Voltarelli, V. A., Coronado, M. J., Fernandes, L. G., Campos, J. C., Jannig, P. R., Ferreira, J. C. B., Fajardo, G., Brum, P. C., & Bernstein, D. (2021) · Cells · doi:10.3390/cells10010146 · Cited by 34
Picard, M. A., Wright, K. J., Ritchie, D., Thomas, M. M., & Hepple, R. T. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043003 · Cited by 31
Kif5 regulates mitochondrial movement, morphology, function and neuronal survival
Iworima, D. G., Pasqualotto, B. A., & Rintoul, G. L. (2016) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2015.12.014 · Cited by 32
Qin, W., Tong, X., Liang, R., Tang, K., Wu, X., Jia, Y., & Tan, N. (2021) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2021.113827 · Cited by 30
Koopman, W. J. H., Hink, M. A., Verkaart, S., Visch, H.-J., Smeitink, J. A. M., & Willems, P. H. G. M. (2007) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2007.03.013 · Cited by 30
Fusion, Fragmentation, and Fission of Mitochondria
Polyakov, V. Y., Soukhomlinova, M. Y., & Faĭs, D. (2003) · Biochemistry (Moscow) · doi:10.1023/a:1025738712958 · Cited by 30
Superoxide released into the mitochondrial matrix
Meany, D. L., Poe, B. G., Navratil, M., Moraes, C. T., & Arriaga, E. A. (2006) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2006.06.003 · Cited by 31
González Ibáñez, F., Halvorson, T., Sharma, K., McKee, C. G., Carrier, M., Picard, K., Vernoux, N., Bisht, K., Deslauriers, J., Lalowski, M., et al. (2023) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2023.09.006 · Cited by 28
Spatiotemporal dynamics of the proton motive force on single bacterial cells
Biquet‐Bisquert, A., Carrio, B., Meyer, N., Fernandes, T. F. D., Abkarian, M., Seduk, F., Magalon, A., Nord, A. L., & Pedaci, F. (2024) · Science Advances · doi:10.1126/sciadv.adl5849 · Cited by 28
Drp1 splice variants regulate ovarian cancer mitochondrial dynamics and tumor progression
Javed, Z., Shin, D. H., Pan, W., White, S. R., Elhaw, A. T., Kim, Y. S., Kamlapurkar, S., Cheng, Y.-Y., Benson, J. C., Abdelnaby, A. E., et al. (2024) · EMBO Reports · doi:10.1038/s44319-024-00232-4 · Cited by 31
Schizophrenia: Redox Regulation and Volume Neurotransmission
Bókkon, I., & Antal, I. (2011) · Current Neuropharmacology · doi:10.2174/157015911795596504 · Cited by 29
Kuznetsov, A. V., Janakiraman, M., Margreiter, R., & Troppmair, J. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.10.021 · Cited by 28
Malena, A., Pantic, B., Borgia, D., Sgarbi, G., Solaini, G., Holt, I. J., Spinazzola, A., Perissinotto, E., Sandri, M., Baracca, A., et al. (2016) · Autophagy · doi:10.1080/15548627.2016.1226734 · Cited by 31
Geniposide Alleviates Amyloid-Induced Synaptic Injury by Protecting Axonal Mitochondrial Trafficking
Zhang, H., Zhao, C., Lv, C., Liu, X., Du, S., Li, Z., Wang, Y., & Zhang, W. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00309 · Cited by 28
Wenchich, L., Drahota, Z., Honzík, T., Hansíková, H., Tesařová, M., Zeman, J., & Houštěk, J. (2003) · Physiological Research · doi:10.33549/physiolres.930391 · Cited by 28
Mitochondria Enter the Nucleus (One Further Problem in Chronic Alcoholism)
Bakeeva, L. E., Skulachev, V. P., Sudarikova, Y. V., & Tsyplenkova, V. G. (2001) · Biochemistry (Moscow) · doi:10.1023/a:1013374410540 · Cited by 27
Self-citationWildenberg, G. A., Sorokina, A., Koranda, J. L., Monical, A., Heer, C. M., Sheffield, M. E. J., Zhuang, X., McGehee, D. S., & Kasthuri, B. (2021) · University of Chicago · doi:10.6082/232sj-vk702 · Cited by 27
Teixeira, P., Galland, R., & Chevrollier, A. (2024) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2024.01.006 · Cited by 28
Photochemical Targeting of Mitochondria to Overcome Chemoresistance in Ovarian Cancer †
Rickard, B. P., Overchuk, M., Obaid, G., Ruhi, M. K., Demirci, U., Fenton, S. E., Santos, J. H., Kessel, D. H., & Rizvi, I. (2022) · Photochemistry and Photobiology · doi:10.1111/php.13723 · Cited by 26
Regulation of Mitochondrial Dynamics: Another Process Modulated by Ca 2+ Signals?
Yoon, Y. (2005) · Science s STKE · doi:10.1126/stke.2802005pe18 · Cited by 26
Sharpening the Scissors: Mitochondrial Fission With Aid
Yoon, Y. (2004) · Cell Biochemistry and Biophysics · doi:10.1385/cbb:41:2:193 · Cited by 27
Abdelwahid, E., Li, H., Wu, J., Irioda, A. C., de Carvalho, K. A. T., & Luo, X. (2016) · APOPTOSIS · doi:10.1007/s10495-016-1286-6 · Cited by 25
Qin, Z., Zhu, X., Shen, Y., Ling, H., Ruan, N., Ye, W., Xu, Y., & Gan, X. (2025) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-025-05802-w · Cited by 25
Zhang, B., Guo, X., Li, Y., Peng, Q., Gao, J., Liu, B., & Wang, M. (2017) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201600710 · Cited by 24
Mitochondria: A mirror into cellular dysfunction in heart disease
White, M. Y., Edwards, A. V. G., Cordwell, S. J., & Eyk, J. E. V. (2008) · PROTEOMICS - CLINICAL APPLICATIONS · doi:10.1002/prca.200780135 · Cited by 24
Dietary Macronutrient Management to Treat Mitochondrial Dysfunction in Parkinson’s Disease
Bajracharya, R., Youngson, N. A., & Ballard, J. W. O. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20081850 · Cited by 24
[Retracted] Involvement of Mitochondrial Dynamics and Mitophagy in Sevoflurane‐Induced Cell Toxicity
Li, M., Guo, J., Wang, H., & Li, Y. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/6685468 · Cited by 23
RetractedCollagen VI myopathies: From the animal model to the clinical trial
Maraldi, N. M., Sabatelli, P., Columbaro, M., Zamparelli, A., Manzoli, F. A., Bernardi, P., Bonaldo, P., & Merlini, L. (2009) · Advances in Enzyme Regulation · doi:10.1016/j.advenzreg.2008.12.009 · Cited by 23
Kuznetsov, A. V., Hermann, M., Troppmair, J., Margreiter, R., & Hengster, P. (2009) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2009.00750.x · Cited by 24
Choudhary, V., Kaddour‐Djebbar, I., Alaisami, R., Kumar, M. V., & Bollag, W. B. (2014) · International Journal of Oncology · doi:10.3892/ijo.2014.2343 · Cited by 23
Bókkon, I., Vas, J. P., Császár, N., & Lukács, T. (2014) · Reviews in the Neurosciences · doi:10.1515/revneuro-2013-0036 · Cited by 24
Nunn, A. V. W., Guy, G. W., & Bell, J. D. (2009) · Immunobiology · doi:10.1016/j.imbio.2009.03.005 · Cited by 22
Bevan, R. J., Williams, P. A., Waters, C. T., Thirgood, R. A., Mui, A., Seto, S., Good, M. A., Morgan, J. E., Votruba, M., & Erchova, I. A. (2020) · Brain Communications · doi:10.1093/braincomms/fcaa101 · Cited by 22
The Therapeutic Strategies Targeting Mitochondrial Metabolism in Cardiovascular Disease
Huang, X. J., Zeng, Z., Li, S., Xie, Y., & Tong, X. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14122760 · Cited by 25
Kras, K. A., Willis, W. T., Barker, N. K., Czyzyk, T. A., Langlais, P. R., & Katsanos, C. S. (2016) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2016.03.006 · Cited by 23
Role of mitochondria in serum withdrawal-induced apoptosis of immortalized neuronal precursors
Colombaioni, L., Colombini, L., & Garcia‐Gil, M. (2002) · Developmental Brain Research · doi:10.1016/s0165-3806(01)00326-1 · Cited by 22
Szczepanowska, J., Zabłocki, K., & Duszyński, J. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.11.022 · Cited by 21
Mitochondria: Starving to reach quorum?
Picard, M. A., & Burelle, Y. (2012) · BioEssays · doi:10.1002/bies.201100179 · Cited by 20
Wang, D., Jiang, D.-M., Yu, R.-R., Zhang, L., Liu, Y.-Z., Chen, J.-X., Chen, H., & Liu, Y. (2022) · Journal of Diabetes Research · doi:10.1155/2022/3780156 · Cited by 22
Flicker-assisted localization microscopy reveals altered mitochondrial architecture in hypertension
Chalmers, S., Saunter, C. D., Girkin, J. M., & McCarron, J. G. (2015) · Scientific Reports · doi:10.1038/srep16875 · Cited by 20
Mitochondrial dynamics and bioenergetics regulated by netrin‐1 in oligodendrocytes
Nakamura, D. S., Lin, Y. H., Khan, D., Gothié, J. M., de Faria, O., Dixon, J. A., McBride, H. M., Antel, J. P., & Kennedy, T. E. (2020) · Glia · doi:10.1002/glia.23905 · Cited by 20
Lally, J. S. V., Herbst, E. A. F., Matravadia, S., Maher, A. C., Perry, C. G. R., Ventura-Clapier, R., & Holloway, G. P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055660 · Cited by 19
Singh, G., & Kumar, A. (2023) · Neurochemical Research · doi:10.1007/s11064-023-03898-9 · Cited by 19
Rivera‐Ingraham, G. A., Rocchetta, I., Bickmeyer, U., Meyer, S., & Abele, D. (2016) · Frontiers in Zoology · doi:10.1186/s12983-016-0137-1 · Cited by 19
Diffusive search and trajectories on tubular networks: a propagator approach
Scott, Z. C., Brown, A. I., Mogre, S. S., Westrate, L. M., & Koslover, E. F. (2021) · The European Physical Journal E · doi:10.1140/epje/s10189-021-00083-0 · Cited by 19
Falchi, A. M., Isola, R., Diana, A., Putzolu, M., & Diaz, G. (2005) · FEBS Journal · doi:10.1111/j.1742-4658.2005.04586.x · Cited by 19
Coherent phase microscopy in cell biology: visualization of metabolic states
Tychinsky, V. P., Kretushev, A. V., Vyshenskaya, T. V., & Tikhonov, A. N. (2005) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2005.04.002 · Cited by 19
Vecchis, D. D., Brandner, A. F., Baaden, M., Cohen, M. M., & Taly, A. (2019) · The Journal of Membrane Biology · doi:10.1007/s00232-019-00089-y · Cited by 20
Iron insufficiency in floral buds impairs pollen development by disrupting tapetum function
Huang, T., & Suen, D. (2021) · The Plant Journal · doi:10.1111/tpj.15438 · Cited by 18
Katti, P., Rai, M., Srivastava, S., D’Silva, P., & Nongthomba, U. (2021) · Experimental Cell Research · doi:10.1016/j.yexcr.2021.112486 · Cited by 18
Bekhite, M. M., & Schulze, P. C. (2021) · Cells · doi:10.3390/cells10123483 · Cited by 21
Scheckhuber, C. Q., Mitterbauer, R., & Osiewacz, H. D. (2009) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-009-2205-3 · Cited by 18
Cardiac aging: Molecular mechanisms and therapeutic interventions
Li, X., Pang, X., Sun, H., Zhang, B., Wang, H., Wu, N., & Yang, L. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.107954 · Cited by 16
Chernyak, B. V., Pletjushkina, O. Y., Izyumov, D. S., Lyamzaev, K. G., & Avetisyan, A. V. (2005) · Biochemistry (Moscow) · doi:10.1007/s10541-005-0106-3 · Cited by 16
The intelligence paradox; will ET get the metabolic syndrome? Lessons from and for Earth
Nunn, A. V. W., Guy, G. W., & Bell, J. D. (2014) · Nutrition & Metabolism · doi:10.1186/1743-7075-11-34 · Cited by 16
Agrimi, G., Mena, M. C., Izumi, K., Pisano, I., Germinario, L., Fukuzaki, H., Palmieri, L., Blank, L. M., & Kitagaki, H. (2013) · FEMS Yeast Research · doi:10.1111/1567-1364.12120 · Cited by 16
All for one: changes in mitochondrial morphology and activity during syncytial oogenesis
Urbisz, A. Z., Chajec, Ł., Małota, K., Student, S., Sawadro, M. K., Śliwińska, M. A., & Świątek, P. (2022) · Biology of Reproduction · doi:10.1093/biolre/ioac035 · Cited by 15
Shiraishi, M., Sasaki, D., Hibino, M., Takeda, A., Harashima, H., & Yamada, Y. (2024) · Journal of Controlled Release · doi:10.1016/j.jconrel.2024.01.058 · Cited by 15
Pavlik, L. L., Mikheeva, I. B., Al’-Mugkhrabi, Y. M., Berest, V. P., Kirova, Y. I., Germanova, E. L., Lukyanova, L. D., & Mironova, G. D. (2018) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-018-3993-1 · Cited by 15
Running and Swimming Differently Adapt the BDNF/TrkB Pathway to a Slow Molecular Pattern at the NMJ
Just‐Borràs, L., Cilleros‐Mañé, V., Hurtado, E., Biondi, O., Charbonnier, F., Tomàs, M., García, N., Tomàs, J. M., & Lanuza, M. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094577 · Cited by 17
Non-conventional mitochondrial permeability transition: Its regulation by mitochondrial dynamics
Yoon, Y., Lee, H., Federico, M., & Sheu, S. (2022) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2022.148914 · Cited by 15
Energy flux modulation on the outer membrane of mitochondria by metabolically-derived potential
Lemeshko, S. V., & Lemeshko, V. V. (2003) · Molecular and Cellular Biochemistry · doi:10.1023/b:mcbi.0000009864.77216.00 · Cited by 15
Dimitrova, I., Toby, G. G., Tili, E., Strich, R., Kampranis, S. C., & Makris, A. M. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.04.012 · Cited by 15
Metadata
- Authors
- Skulachev, V. P.
- Affiliations
- Lomonosov Moscow State University (RU)
- Corresponding author
- Skulachev, Vladimir P.
- Venue
- Trends in Biochemical Sciences
- Publisher
- Elsevier BV
- Published
- 2001-01
- Volume
- 26
- Issue
- 1
- Pages
- 23-29
- ISSN
- 0968-0004 (ISSN-L)
- OpenAlex
- W2041061895
- Cited by
- 477
- References
- 40
- Citations by year
- 2026: 9 · 2025: 15 · 2024: 10 · 2023: 12 · 2022: 17 · 2021: 28 · 2020: 19 · 2019: 23 · 2018: 16 · 2017: 13 · 2016: 20 · 2015: 19 · 2014: 18 · 2013: 11 · 2012: 30
- FWCI
- 1.40
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Trends in Biochemical Sciences (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › ATP Synthase and ATPases Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Keywords
- mitochondrial network, antioxidant defense, proton potential, ATP production, mitochondrial transport, mitochondrial morphology
- MeSH terms
- Adenosine Triphosphate, Animals, Electrophysiology, Humans, Mitochondria, Neurons, Afferent
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review