The DOI matches its Crossref record; 180 of the 180 references it cites were found in a registry or an index.
Mitochondrial dynamics in adaptive and maladaptive cellular stress responses
Open accessOverview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“During mitochondrial fission, cytosolic Drp1 is recruited to mitochondrial receptors (e.g., Fis1)3,4, allowing mitochondrial partitioning, turnover and reduction of network size under low energetic demand4,7.”
From Altered mitochondrial dynamics and function in APOE4-expressing astrocytes (2020) · cites this paper as [3]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Because mitochondrial dysfunction characterizes other cellular processes (Eisner et al., 2018), it is not a consistent biomarker of senescence.”
From Cellular Senescence: Defining a Path Forward (2019) · cites this paper as Eisner et al., 2018
The cited source says what the claim attributes to it.
In the citing paper
“Several proteins are required for mitochondrial fusion, including the mitofusins (Mfn1/Mfn2)3,4.”
From Altered mitochondrial dynamics and function in APOE4-expressing astrocytes (2020) · cites this paper as [3]
The cited source says what the claim attributes to it.
In the citing paper
“Mitochondrial dynamics include fusion, fission, and degradation events, linked to mitochondrial function3,4.”
From Altered mitochondrial dynamics and function in APOE4-expressing astrocytes (2020) · cites this paper as [3]
The cited source says what the claim attributes to it.
In the citing paper
“Mitochondrial fusion is mediated by mitofusins, which are regulated by transcription and protein modification, including ubiquitination3.”
From Altered mitochondrial dynamics and function in APOE4-expressing astrocytes (2020) · cites this paper as [3]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Mitochondrial Fission, Fusion, and Stress
Youle, R. J., & van der Bliek, A. M. (2012) · Science · doi:10.1126/science.1219855 · Cited by 3,674
Youle, R. J., & Narendra, D. P. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3028 · Cited by 3,273
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
Chen, H., Detmer, S. A., Ewald, A. J., Griffin, E. E., Fraser, S. E., & Chan, D. C. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200211046 · Cited by 2,601
Cellular mechanisms and physiological consequences of redox-dependent signalling
Holmström, K. M., & Finkel, T. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3801 · Cited by 2,093
Mitochondria as sensors and regulators of calcium signalling
Rizzuto, R., De Stefani, D., Raffaello, A., & Mammucari, C. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3412 · Cited by 1,781
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
OPA1 Controls Apoptotic Cristae Remodeling Independently from Mitochondrial Fusion
Frezza, C., Cipolat, S., Martins de Brito, O., Micaroni, M., Beznoussenko, G. V., Rudka, T., Bartoli, D., Polishuck, R. S., Danial, N. N., De Strooper, B., et al. (2006) · Cell · doi:10.1016/j.cell.2006.06.025 · Cited by 1,673
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
Mitochondrial Dynamics Controls T Cell Fate through Metabolic Programming
Buck, M. D., O’Sullivan, D., Geltink, R. I. K., Curtis, J. D., Chang, C., Sanin, D. E., Qiu, J., Kretz, O., Braas, D., van der Windt, G. J. W., et al. (2016) · Cell · doi:10.1016/j.cell.2016.05.035 · Cited by 1,491
Research works printed but not linked: 1
- Nicholls, D., G. Bioenergetics 4th ed. (Academic Press, Cambridge, MA, 2013).
Cited by
Sorted by citations
Items 101–200 of 622
Mitochondrial psychobiology: foundations and applications
Picard, M. A., Trumpff, C., & Burelle, Y. (2019) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2019.04.015 · Cited by 66
Self-citationLiu, M., Mu, J., Wang, M., Hu, C., Ji, J., Wen, C., & Zhang, D. (2023) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2023.131918 · Cited by 66
Chen, W., Guo, C., Feng, H., & Chen, Y. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.615451 · Cited by 64
Nutrients, Mitochondrial Function, and Perinatal Health
Rodríguez-Cano, A. M., Calzada‐Mendoza, C. C., Estrada‐Gutiérrez, G., Mendoza-Ortega, J. A., & Perichart‐Perera, O. (2020) · Nutrients · doi:10.3390/nu12072166 · Cited by 62
Spurlock, B., Tullet, J. M. A., Hartman, J. L., & Mitra, K. (2020) · Experimental Gerontology · doi:10.1016/j.exger.2020.110919 · Cited by 60
MFF Regulation of Mitochondrial Cell Death Is a Therapeutic Target in Cancer
Seo, J. H., Chae, Y. C., Kossenkov, A. V., Lee, Y. G., Tang, H., Agarwal, E., Gabrilovich, D. I., Languino, L. R., Speicher, D. W., Shastrula, P. K., et al. (2019) · Cancer Research · doi:10.1158/0008-5472.can-19-1982 · Cited by 61
Mitochondrial Mechanisms of Apoptosis and Necroptosis in Liver Diseases
Chu, Q., Gu, X., Zheng, Q., Wang, J., & Zhu, H. (2021) · Analytical Cellular Pathology · doi:10.1155/2021/8900122 · Cited by 62
Ophiopogonin D alleviates diabetic myocardial injuries by regulating mitochondrial dynamics
Li, W., Ji, L., Tian, J., Tang, W., Shan, X., Zhao, P., Chen, H., Zhang, C., Xu, M. G., Lü, R., et al. (2021) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2021.113853 · Cited by 60
Lin, K.-J., Wang, T., Chen, S., Lin, K.-L., Liou, C., Lan, M., Chuang, Y., Chuang, J., Wang, P., Lee, J., et al. (2021) · Antioxidants · doi:10.3390/antiox10121935 · Cited by 63
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 56
Wang, Q., Zhao, D., Xian, M., Wang, Z., Bi, E., Su, P., Qian, J., Ma, X., Yang, M., Liu, L., et al. (2020) · Blood · doi:10.1182/blood.2020005795 · Cited by 57
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 58
Neuronal Mitochondrial Dysfunction and Bioenergetic Failure in Inflammation-Associated Depression
Casaril, A. M., Dantzer, R., & Orth, C. B. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.725547 · Cited by 62
Glial mitochondrial function and dysfunction in health and neurodegeneration
McAvoy, K., & Kawamata, H. (2019) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2019.103417 · Cited by 59
Multi-omics analysis identifies mitochondrial pathways associated with anxiety-related behavior
Misiewicz, Z., Iurato, S., Kulesskaya, N., Salminen, L., Rodrigues, L., Maccarrone, G., Martins, J., Czamara, D., Laine, M. A., Sokolowska, E., et al. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008358 · Cited by 59
Lan, B., He, Y., Sun, H., Zheng, X., Gao, Y., & Li, N. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.116587 · Cited by 58
Identification of DRP1 as a prognostic factor correlated with immune infiltration in breast cancer
Liu, B., Fan, Y., Song, Z., Han, B., Meng, Y., Cao, P., & Tan, K. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.107078 · Cited by 55
Impaired flickering of the permeability transition pore causes SPG7 spastic paraplegia
Sambri, I., Massa, F., Gullo, F., Meneghini, S., Cassina, L., Carraro, M., Dina, G., Quattrini, A., Patanella, L., Carissimo, A., et al. (2020) · EBioMedicine · doi:10.1016/j.ebiom.2020.103050 · Cited by 55
Stressed mitochondria: A target to intrude alzheimer’s disease
Sharma, V., Singh, T. G., & Mehta, V. (2021) · Mitochondrion · doi:10.1016/j.mito.2021.04.004 · Cited by 53
Liu, Q., Weng, J., Li, C., Feng, Y., Xie, M., Wang, X., Chang, Q., Li, M., Chung, K. F., Adcock, I. M., et al. (2023) · Particle and Fibre Toxicology · doi:10.1186/s12989-023-00534-w · Cited by 57
Hinton, A. O., Jr., Katti, P., Christensen, T. A., Mungai, M., Shao, J., Zhang, L., Trushin, S., Alghanem, A. F., Jaspersen, A. L., Geroux, R. E., et al. (2023) · Advanced Biology · doi:10.1002/adbi.202200202 · Cited by 62
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia
Wiessner, M., Maroofian, R., Ni, M.-Y., Pedroni, A., Müller, J. S., Stucka, R., Beetz, C., Efthymiou, S., Santorelli, F. M., Alfares, A. A., et al. (2021) · Brain · doi:10.1093/brain/awab041 · Cited by 52
Mitochondrial Dysfunction and Diabetic Nephropathy: Nontraditional Therapeutic Opportunities
Zhang, P., Zhou, M., Guo, J., Zheng, H., Tang, J., Zhang, C., Liu, Y., Liu, W. J., & Wang, Y. (2021) · Journal of Diabetes Research · doi:10.1155/2021/1010268 · Cited by 57
Advances in pathogenesis of preeclampsia
Yang, M., Wang, M., & Li, N. (2024) · Archives of Gynecology and Obstetrics · doi:10.1007/s00404-024-07393-6 · Cited by 58
Reductive stress and mitochondrial dysfunction: The hidden link in chronic disease
Mercola, J. M. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.03.029 · Cited by 56
The emerging role of skeletal muscle mitochondrial dynamics in exercise and ageing
Casuso, R. A., & Huertas, J. R. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101025 · Cited by 56
Seo, J. H., Agarwal, E., Chae, Y. C., Lee, Y. G., Garlick, D. S., Storaci, A. M., Ferrero, S., Gaudioso, G., Gianelli, U., Vaira, V., et al. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2019.09.017 · Cited by 49
Role of Mitofusins and Mitophagy in Life or Death Decisions
Joaquim, M., & Escobar‐Henriques, M. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.572182 · Cited by 50
Harada, T., Sada, R., Osugi, Y., Matsumoto, S., Matsuda, T., Hayashi, M., Nagai, T., Harada, A., & Kikuchi, A. (2020) · Journal of Cell Science · doi:10.1242/jcs.249045 · Cited by 49
Baek, A., Son, S., Baek, Y. M., & Kim, D. (2021) · Autophagy · doi:10.1080/15548627.2021.1897962 · Cited by 48
Intracellular to Interorgan Mitochondrial Communication in Striated Muscle in Health and Disease
Boardman, N. T., Trani, G., Scalabrin, M., Romanello, V., & Wüst, R. C. I. (2023) · Endocrine Reviews · doi:10.1210/endrev/bnad004 · Cited by 51
Lin, L., Sun, B., Hu, Y., Yang, W., Li, J., Wang, D., Zhang, L., Lu, M., Li, Y., Li, Y., et al. (2025) · British Journal of Pharmacology · doi:10.1111/bph.70032 · Cited by 47
Ma, M., Lin, X., Liu, H., Zhang, R., & Chen, R. (2020) · Oncology Reports · doi:10.3892/or.2020.7476 · Cited by 48
Walker, O. S., Ragos, R., Gurm, H., Lapierre, M., May, L. L., & Raha, S. (2020) · Physiological Reports · doi:10.14814/phy2.14476 · Cited by 46
Wang, H., Yi, X., Guo, S., Wang, S., Ma, J., Zhao, T., Shi, Q., Tian, Y., Wang, H., Jia, L., et al. (2021) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2021.03.031 · Cited by 47
Watanabe, H., Dijkstra, J. M., & Nagatsu, T. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25042009 · Cited by 48
Xiong, X., Hou, J., Zheng, Y., Jiang, T., Zhao, X., Cai, J., Huang, J., He, H., Xu, J., Qian, S., et al. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-07062-1 · Cited by 54
Mitophagy in cardiovascular disease
Zhou, H., He, L., Xu, G., & Chen, L. (2020) · Clinica Chimica Acta · doi:10.1016/j.cca.2020.04.033 · Cited by 48
Ipponjima, S., Umino, Y., Nagayama, M., & Denda, M. (2020) · Scientific Reports · doi:10.1038/s41598-020-62240-3 · Cited by 46
Targeting P2RX1 alleviates renal ischemia/reperfusion injury by preserving mitochondrial dynamics
Zhuang, S., Xia, S., Huang, P.-Q., Wu, J., Qu, J., Chen, R., Sun, N., Li, D., Wu, H., Zhang, M., et al. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105712 · Cited by 45
Bacigalupa, Z. A., & Rathmell, W. K. (2020) · Cancer Letters · doi:10.1016/j.canlet.2020.05.034 · Cited by 47
Fan, C., Feng, J., Tang, C., Zhang, Z., Feng, Y., Duan, W., Zhai, M., Yan, Z., Zhu, L., Feng, L., et al. (2020) · Stem Cell Research & Therapy · doi:10.1186/s13287-020-01948-5 · Cited by 45
Sánchez‐Alvarez, R., Francesco, E. M. D., Fiorillo, M., Sotgia, F., & Lisanti, M. P. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.01776 · Cited by 50
Knocking Out Sigma-1 Receptors Reveals Diverse Health Problems
Couly, S., Goguadze, N., Yasui, Y., Kimura, Y., Wang, S., Sharikadze, N., Wu, H.-E., & Su, T. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00983-3 · Cited by 44
Regulation of neuronal bioenergetics as a therapeutic strategy in neurodegenerative diseases
Onyango, I. G., Bennett, J. P., & Stokin, G. B. (2021) · Neural Regeneration Research · doi:10.4103/1673-5374.303007 · Cited by 45
Zhu, H., Zhang, B., Zhu, N., Li, M., & Yu, Q. (2020) · Chinese Chemical Letters · doi:10.1016/j.cclet.2020.09.003 · Cited by 44
Peng, X., Wang, K., Zhang, C., Bao, J.-P., Cabral, V. L. F., Gao, J.-W., Zhou, Z.-M., & Wu, X. (2021) · Free Radical Research · doi:10.1080/10715762.2021.2018426 · 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
Sun, K., Wu, Y., Zeng, Y., Xu, J., Wu, L., Li, M., & Shen, B. (2022) · Arthritis Research & Therapy · doi:10.1186/s13075-022-02983-8 · Cited by 45
Palma, E., Riva, A., Moreno, C., Òdena, G., Mudan, S., Manyakin, N., Miquel, R., Degré, D., Trépo, E., Sancho‐Bru, P., et al. (2020) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.14299 · Cited by 45
Paul, S. C., Saha, D., & Binukumar, B. K. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02365-2 · Cited by 43
The fasting‐feeding metabolic transition regulates mitochondrial dynamics
Castro‐Sepúlveda, M., Morio, B., Tuñón‐Suárez, M., Jannas-Vela, S., Díaz‐Castro, F., Rieusset, J., & Zbinden‐Foncea, H. (2021) · The FASEB Journal · doi:10.1096/fj.202100929r · Cited by 43
Mitochondria: At the crossroads between mechanobiology and cell metabolism
Su, É., Villard, C., & Manneville, J. (2023) · Biology of the Cell · doi:10.1111/boc.202300010 · Cited by 44
Jiang, X., Jin, T., Zhang, H., Miao, J., Zhao, X., Su, Y., & Zhang, Y. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/4578462 · Cited by 43
Ďúranová, H., Válková, V., Kňažická, Z., Olexíková, L., & Vašíček, J. (2020) · Acta Histochemica · doi:10.1016/j.acthis.2020.151646 · Cited by 47
Mitochondrial Function and Reactive Oxygen/Nitrogen Species in Skeletal Muscle
Chen, M., Li, Y., Deng, S., Zhao, Y., Lian, Z., & Yu, K. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.826981 · Cited by 49
LONP1 downregulation with ageing contributes to osteoarthritis via mitochondrial dysfunction
He, Y., Ding, Q., Chen, W., Lin, C., Ge, L., Ying, C., Xu, K., Wu, Z., Xu, L., Ran, J., et al. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.08.038 · Cited by 43
Chan, W. S., Ng, C. F., Pang, B. P. S., Hang, M., Tse, M. C. L., Iu, E. C. Y., Ooi, X. C., Yang, X., Kim, J. K., Lee, C. W., et al. (2024) · Science Signaling · doi:10.1126/scisignal.adh2783 · Cited by 47
Xue, R., Zhao, M. F., Wu, Q., Yang, S., Cui, Y.-L., Yu, X., Liu, J., & Zang, W. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.09.025 · Cited by 40
Bertolini, I., Ghosh, J. C., Kossenkov, A. V., Mulugu, S., Krishn, S. R., Vaira, V., Qin, J., Plow, E. F., Languino, L. R., & Altieri, D. C. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.07.014 · Cited by 44
Steffen, J. B. M., Falfushynska, H., Piontkivska, H., & Sokolova, I. M. (2020) · Frontiers in Marine Science · doi:10.3389/fmars.2020.604411 · Cited by 46
Adrenergic Regulation of Drp1-Driven Mitochondrial Fission in Cardiac Physio-Pathology
Jhun, B. S., O‐Uchi, J., Adaniya, S. M., Cypress, M. W., & Yoon, Y. (2018) · Antioxidants · doi:10.3390/antiox7120195 · Cited by 43
Liu, A., Kage, F., & Higgs, H. N. (2021) · Molecular Biology of the Cell · doi:10.1091/mbc.e21-04-0224 · Cited by 42
Chen, Y., Yang, F., Chu, Y., Yun, Z., Yan, Y., & Jin, J. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03693-0 · Cited by 41
Mitochondrial stress and GDF15 in the pathophysiology of sepsis
Fujita, Y., Ito, M., & Ohsawa, I. (2020) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2020.108668 · Cited by 42
OPA1 Modulates Mitochondrial Ca2+ Uptake Through ER-Mitochondria Coupling
Cartes-Saavedra, B., Macuada, J., Lagos, D., Arancibia, D., Andrés, M. E., Yu‐Wai‐Man, P., Hajnóczky, G., & Eisner, V. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.774108 · Cited by 40
Self-citationMitochondria and their potential role in acute lung injury (Review)
Zhan, B., & Shen, J. (2022) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2022.11406 · Cited by 40
Mitochondrial fragmentation and network architecture in degenerative diseases
Shah, S. I., Paine, J. G., Perez, C., & Ullah, G. (2019) · PLoS ONE · doi:10.1371/journal.pone.0223014 · Cited by 40
Cellular Organelles Reorganization During Zika Virus Infection of Human Cells
García, C. C., Vázquez, C., Giovannoni, F., Russo, C., Cordo, S. M., Alaimo, A., & Damonte, E. B. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01558 · Cited by 40
Levada, K. V., Pshenichnikov, S. E., Omelyanchik, A. S., Rodionova, V. V., Nikitin, A. A., Савченко, А. Г., Щетинин, И. В., Zhukov, D., Abakumov, M. A., Majouga, A. G., et al. (2020) · Nano Convergence · doi:10.1186/s40580-020-00228-5 · Cited by 38
Battaglia, C. R., Cursano, S., Calzia, E., Catanese, A., & Boeckers, T. M. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-03204-3 · Cited by 38
Singh, G., George, G., Raja, S. O., Kandaswamy, P., Kumar, M., Thutupalli, S., Laxman, S., & Gulyani, A. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2213241120 · Cited by 38
Lefebvre, A. E. Y. T., Sturm, G., Lin, T., Stoops, E. H., López, M. P., Kaufmann-Malaga, B., & Hake, K. (2025) · Nature Methods · doi:10.1038/s41592-025-02612-7 · Cited by 43
Louis, F., Rocher, B., Barjhoux, I., Bultelle, F., Dedourge-Geffard, O., Gaillet, V., Bonnard, I., Delahaut, L., Pain-Devin, S., Geffard, A., et al. (2020) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2020.138450 · Cited by 37
Galectin-3 modulates epithelial cell adaptation to stress at the ER-mitochondria interface
Coppin, L., Jannin, A., Ait‐Yahya, E., Thuillier, C., Villenet, C., Tardivel, M., Bongiovanni, A., Gaston, C., de Beco, S., Barois, N., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2556-3 · Cited by 36
Pandya, S. R., Singh, H., Desimone, M. F., Singh, J., George, N., & Jasani, S. (2023) · Materials Advances · doi:10.1039/d3ma00629h · Cited by 37
Mitochondrial mechanisms in the pathogenesis of chronic inflammatory musculoskeletal disorders
Wu, K., Shieh, J.-S., Qin, L., & Guo, J. J. (2024) · Cell & Bioscience · doi:10.1186/s13578-024-01259-9 · Cited by 39
Mitochondrial dynamics and psychiatric disorders: The missing link
Papageorgiou, M. P., & Filiou, M. D. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105837 · Cited by 39
Zhang, X., Fan, Y., & Tan, K. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-07049-y · Cited by 36
Brain energetics, mitochondria, and traumatic brain injury
Benaroya, H. (2020) · Reviews in the Neurosciences · doi:10.1515/revneuro-2019-0086 · Cited by 37
Mitochondrial disease, mitophagy, and cellular distress in methylmalonic acidemia
Luciani, A., Denley, M. C. S., Govers, L. P., Sorrentino, V., & Froese, D. S. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03934-3 · Cited by 41
AMPK/MFF Activation: Role in Mitochondrial Fission and Mitophagy in Dry Eye
Peng, F., Jiang, D., Xu, W. X., Sun, Y., Zha, Z., Tan, X., Yu, J., Pan, C., Zheng, Q., & Chen, W. (2022) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.63.12.18 · Cited by 36
circ-CBFB upregulates p66Shc to perturb mitochondrial dynamics in APAP-induced liver injury
Wang, Z., Zhao, Y., Sun, R., Sun, Y., Liu, D., Lin, M., Chen, Z., Zhou, J., Lv, L., Tian, X., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-03160-y · Cited by 35
Trewin, A. J., Silver, J. L., Dillon, H. T., Gatta, P. A. D., Parker, L., Hiam, D., Lee, Y. P., Richardson, M. F., Wadley, G. D., & Lamon, S. (2022) · BMC Biology · doi:10.1186/s12915-022-01366-4 · Cited by 36
Disrupting metformin adaptation of liver cancer cells by targeting the TOMM34/ATP5B axis
Jin, P., Jiang, J., Zhou, L., Huang, Z., Qin, S., Chen, H., Peng, L., Zhang, Z., Li, B., Luo, M., et al. (2022) · EMBO Molecular Medicine · doi:10.15252/emmm.202216082 · Cited by 36
Wu, Q., Zhao, M. F., He, X., Xue, R., Li, D., Yu, X., Wang, S., & Zang, W. (2021) · Cell Cycle · doi:10.1080/15384101.2021.1965734 · Cited by 34
OPA1 disease-causing mutants have domain-specific effects on mitochondrial ultrastructure and fusion
Cartes-Saavedra, B., Lagos, D., Macuada, J., Arancibia, D., Burté, F., Sjöberg-Herrera, M. K., Andrés, M. E., Horváth, R., Yu‐Wai‐Man, P., Hajnóczky, G., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2207471120 · Cited by 37
Self-citationEmerging mechanistic insights of selective autophagy in hepatic diseases
Al‐Bari, M. A. A., Ito, Y., Thomes, P. G., Menon, M. B., Macia, M. G., Fadel, R. A., Stadlin, A., Peake, N., Faris, M. E., Eid, N. A. S., et al. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1149809 · Cited by 39
Castro‐Sepúlveda, M., Fernández‐Verdejo, R., Zbinden‐Foncea, H., & Rieusset, J. (2023) · Metabolism · doi:10.1016/j.metabol.2023.155578 · Cited by 35
Zhu, X., Deng, Z., Cao, Y., Zhou, Z., Sun, W., Liu, C., Fan, S., & Yin, X. (2023) · Phytotherapy Research · doi:10.1002/ptr.8004 · Cited by 34
Beyond fission and fusion—Diving into the mysteries of mitochondrial shape
Preminger, N., & Schuldiner, M. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002671 · Cited by 41
Acín‐Pérez, R., Benincá, C., Shabane, B., Shirihai, O. S., & Stiles, L. (2021) · Life · doi:10.3390/life11090949 · Cited by 38
Mitochondrial dynamics dysfunction: Unraveling the hidden link to depression
Chen, H., Lu, M., Lyu, Q., Shi, L., Zhou, C., Li, M., Feng, S., Liang, X., Zhou, X., & Ren, L. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116656 · Cited by 34
Huang, S., Gong, S., Zhao, Y., Ye, M., Li, J., He, Q., Qiao, H., Tan, X.-R., Wang, J.-Y., Liang, Y., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-49675-2 · Cited by 37
Bezafibrate Improves Mitochondrial Fission and Function in DNM1L-Deficient Patient Cells
Douiev, L., Sheffer, R. N., Horvath, G. A., & Saada, A. (2020) · Cells · doi:10.3390/cells9020301 · Cited by 33
Daviu, N., Portilla, Y., de Cedrón, M. G., de Molina, A. R., & Barber, D. F. (2023) · Biomaterials · doi:10.1016/j.biomaterials.2023.122409 · Cited by 33
Mitochondria-Associated Endoplasmic Reticulum Membranes in Breast Cancer
Yu, H., Sun, C., Gong, Q., & Feng, D. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.629669 · Cited by 34
The 3D organisation of mitochondria in primate photoreceptors
Hayes, M. J., Tracey‐White, D., Kam, J. H., Powner, M. B., & Jeffery, G. (2021) · Scientific Reports · doi:10.1038/s41598-021-98409-7 · Cited by 32
Boosting mitochondrial health to counteract neurodegeneration
Burtscher, J., Romani, M., Bernardo, G., Popa, T., Ziviani, E., Hummel, F. C., Sorrentino, V., & Millet, G. P. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102289 · Cited by 36
Universal structures for adaptation in biochemical reaction networks
Araujo, R. P., & Liotta, L. A. (2023) · Nature Communications · doi:10.1038/s41467-023-38011-9 · Cited by 32
Metadata
- Authors
- Eisner, V., Picard, M., & Hajnóczky, G.
- Affiliations
- Pontificia Universidad Católica de Chile (CL)
- Columbia University Irving Medical Center (US)
- Thomas Jefferson University (US)
- Corresponding author
- Hajnóczky, György
- Venue
- Nature Cell Biology
- Published
- 2018-06-27
- Volume
- 20
- Issue
- 7
- Pages
- 755-765
- ISSN
- 1465-7392 (ISSN-L)
- 1476-4679
- PMC
- PMC6716149
- OpenAlex
- W2809177340
- Cited by
- 622
- References
- 180
- Citations by year
- 2026: 63 · 2025: 78 · 2024: 83 · 2023: 86 · 2022: 81 · 2021: 93 · 2020: 87 · 2019: 44 · 2018: 5
- FWCI
- 5.62
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Americanae (AECID Library) (submittedVersion, cc-by-nc-nd)
- LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) (submittedVersion, cc-by-nc-nd)
- Funders
- National Institute on Alcohol Abuse and Alcoholism (U01AA021122)
- National Institute of Mental Health (R21MH113011)
- National Institute of General Medical Sciences (R35GM119793)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK051526)
- National Institute of Environmental Health Sciences (R33ES025672)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Keywords
- mitochondrial dynamics, mitochondrial fusion, mitochondrial fission, mitochondrial motility, endoplasmic reticulum-mitochondria interaction, cellular stress response, adaptive stress response, maladaptive stress response, cell survival and death, energy production, mitochondrial signalling, mitochondrial disease
- MeSH terms
- Adaptation, Physiological, Animals, Cell Survival, Energy Metabolism, Humans, Mitochondria, Stress, Physiological, Signal Transduction, Cell Death, Mitochondrial Dynamics
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