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
Cellular Senescence: Defining a Path Forward
Gorgoulis, V., Adams, P. D., Alimonti, A., Bennett, D. C., Bischof, O., Bishop, C., Campisi, J., Collado, M., Evangelou, K., Ferbeyre, G., et al. (2019) · Cell · doi:10.1016/j.cell.2019.10.005 · Cited by 3,225
The cell biology of mitochondrial membrane dynamics
Giacomello, M., Pyakurel, A., Glytsou, C., & Scorrano, L. (2020) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-020-0210-7 · Cited by 1,550
Molecular mechanisms and physiological functions of mitophagy
Onishi, M., Yamano, K., Sato, M., Matsuda, N., & Okamoto, K. (2021) · The EMBO Journal · doi:10.15252/embj.2020104705 · Cited by 1,469
Mitochondrial dynamics in health and disease: mechanisms and potential targets
Chen, W., Zhao, H., & Li, Y. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01547-9 · Cited by 1,306
Mitochondrial signal transduction
Picard, M. A., & Shirihai, O. S. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.10.008 · Cited by 688
Self-citationMitochondria in health, disease, and aging
Harrington, J. S., Ryter, S. W., Plataki, M. E., Price, D. R., & Choi, A. M. K. (2023) · Physiological Reviews · doi:10.1152/physrev.00058.2021 · Cited by 641
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 632
Self-citationChaudhry, A., Shi, R., & Luciani, D. S. (2019) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00457.2019 · Cited by 446
Drp1-dependent mitochondrial fission in cardiovascular disease
Jin, J., Wei, X., Zhi, X., Wang, X., & Meng, D. (2020) · Acta Pharmacologica Sinica · doi:10.1038/s41401-020-00518-y · Cited by 400
Mitochondria as central hub of the immune system
Breda, C. N. D. S., Davanzo, G. G., Basso, P. J., Câmara, N. O. S., & Moraes‐Vieira, P. M. (2019) · Redox Biology · doi:10.1016/j.redox.2019.101255 · Cited by 289
Mitochondrial metabolism regulates macrophage biology
Wang, Y., Li, N., Zhang, X., & Horng, T. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100904 · Cited by 286
Mitochondria dysfunction and metabolic reprogramming as drivers of idiopathic pulmonary fibrosis
Bueno, M., Calyeca, J., Rojas, M. M., & Mora, A. L. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101509 · Cited by 280
Mitochondrial adaptation in cancer drug resistance: prevalence, mechanisms, and management
Jin, P., Jiang, J., Zhou, L., Huang, Z., Nice, E. C., Huang, C., & Fu, L. (2022) · Journal of Hematology & Oncology · doi:10.1186/s13045-022-01313-4 · Cited by 299
Pleiotropic effects of mitochondria in aging
de Lima, T. I., Li, T. Y., Mottis, A., & Auwerx, J. H. (2022) · Nature Aging · doi:10.1038/s43587-022-00191-2 · Cited by 254
Role of Mitochondria in Radiation Responses: Epigenetic, Metabolic, and Signaling Impacts
Averbeck, D., & Rodriguez‐Lafrasse, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222011047 · Cited by 262
Doblado, L., Lueck, C., Rey, C., Samhan-Arias, A. K., Priéto, I., Stacchiotti, A., & Monsalve, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22083903 · Cited by 238
Mitochondrial dynamics and their potential as a therapeutic target
Whitley, B. N., Engelhart, E. A., & Hoppins, S. C. (2019) · Mitochondrion · doi:10.1016/j.mito.2019.06.002 · Cited by 228
Mitochondrial dysfunction in fibrotic diseases
Li, X., Zhang, W. Y., Cao, Q., Wang, Z., Zhao, M., Xu, L., & Zhuang, Q. (2020) · Cell Death Discovery · doi:10.1038/s41420-020-00316-9 · Cited by 229
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 239
Malatesta, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222312789 · Cited by 248
Outstanding Questions in Mitophagy: What We Do and Do Not Know
Montava‐Garriga, L., & Ganley, I. G. (2019) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.06.032 · Cited by 218
Mitochondrial protein-induced stress triggers a global adaptive transcriptional programme
Boos, F., Krämer, L., Groh, C., Jung, F., Haberkant, P., Stein, F., Wollweber, F., Gackstatter, A., Zöller, E., van der Laan, M., et al. (2019) · Nature Cell Biology · doi:10.1038/s41556-019-0294-5 · Cited by 216
Richetin, K., Steullet, P., Pachoud, M., Perbet, R., Parietti, E., Maheswaran, M., Eddarkaoui, S., Bégard, S., Pythoud, C., Rey, M. J., et al. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-00728-x · Cited by 214
Iorio, R., Celenza, G., & Petricca, S. (2021) · Cells · doi:10.3390/cells11010030 · Cited by 222
Autophagy in cancer development, immune evasion, and drug resistance
Niu, X., You, Q., Hou, K., Tian, Y., Wei, P., Zhu, Y., Gao, B., Ashrafizadeh, M., Aref, A. R., Kalbasi, A., et al. (2024) · Drug Resistance Updates · doi:10.1016/j.drup.2024.101170 · Cited by 244
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
Self-citationMetabolic reprogramming in osteoclasts
Park‐Min, K. (2019) · Seminars in Immunopathology · doi:10.1007/s00281-019-00757-0 · Cited by 201
BNIP3L/NIX-mediated mitophagy protects against glucocorticoid-induced synapse defects
Choi, G. E., Lee, H. J., Chae, C. W., Cho, J. H., Jung, Y. H., Kim, J. S., Kim, S. Y., Lim, J. R., & Han, H. J. (2021) · Nature Communications · doi:10.1038/s41467-020-20679-y · Cited by 187
The Good and the Bad of Mitochondrial Breakups
Sprenger, H., & Langer, T. (2019) · Trends in Cell Biology · doi:10.1016/j.tcb.2019.08.003 · Cited by 179
Emerging role of mitophagy in cardiovascular physiology and pathology
Morales, P. E., Arias-Durán, C., Ávalos-Guajardo, Y., Aedo, G., Verdejo, H., Parra, V., & Lavandero, S. (2019) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2019.09.006 · Cited by 179
Mitochondrial morphology controls fatty acid utilization by changing CPT1 sensitivity to malonyl‐CoA
Ngo, J., Choi, D. W., Stanley, I. A., Stiles, L., Molina, A. J. A., Chen, P., Lako, A., Sung, I. C. H., Goswami, R., Kim, M., et al. (2023) · The EMBO Journal · doi:10.15252/embj.2022111901 · Cited by 180
Is Mitochondrial Dysfunction a Common Root of Noncommunicable Chronic Diseases?
Díaz‐Vegas, A., Sánchez-Aguilera, P., Krycer, J. R., Morales, P. E., Monsalves‐Álvarez, M., Cifuentes, M., Rothermel, B. A., & Lavandero, S. (2020) · Endocrine Reviews · doi:10.1210/endrev/bnaa005 · Cited by 179
Mitochondrial quality control: from molecule to organelle
Roca-Portoles, A., & Tait, S. W. G. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03775-0 · Cited by 178
Li, Y., Chen, H., Xie, X., Yang, B., Wang, X., Zhang, J., Qiao, T., Guan, J., Qiu, Y., Huang, Y., et al. (2022) · Cancer Research · doi:10.1158/0008-5472.can-22-2370 · Cited by 177
Yi, X., Guo, W., Shi, Q., Yang, Y., Zhang, W., Chen, X., Kang, P., Chen, J., Cui, T., Ma, J., et al. (2019) · Theranostics · doi:10.7150/thno.30398 · Cited by 167
Mitochondrial Dynamics: Fission and Fusion in Fate Determination of Mesenchymal Stem Cells
Ren, L., Chen, X., Chen, X., Li, J., Cheng, B., & Xia, J. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.580070 · Cited by 175
Mitochondrial Oxidative Stress and “Mito-Inflammation”: Actors in the Diseases
Patergnani, S., Bouhamida, E., Leo, S., Pinton, P., & Rimessi, A. (2021) · Biomedicines · doi:10.3390/biomedicines9020216 · Cited by 178
Mitochondrial dynamics and mitophagy in lung disorders
Sharma, A. K., Ahmad, S., Ahmad, T., Ali, S., & Syed, M. A. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119876 · Cited by 161
Yang, X., Xue, P., Chen, H., Yuan, M., Kang, Y., Duscher, D., Machens, H., & Chen, Z. (2020) · Theranostics · doi:10.7150/thno.40857 · Cited by 153
Ju, W., Perkins, G. A., Keun-young Kim, A., Bastola, T., Choi, W.-Y., & Choi, S. (2022) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2022.101136 · Cited by 152
Lin, K.-J., Lin, K.-L., Chen, S., Liou, C., Chuang, Y., Lin, H., & Lin, T. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20215312 · Cited by 141
Mechanisms and roles of mitochondrial localisation and dynamics in neuronal function
Seager, R., Lee, L. J., Henley, J. M., & Wilkinson, K. A. (2020) · Neuronal Signaling · doi:10.1042/ns20200008 · Cited by 152
A break in mitochondrial endosymbiosis as a basis for inflammatory diseases
Murphy, M. P., & O’Neill, L. A. J. (2024) · Nature · doi:10.1038/s41586-023-06866-z · Cited by 138
Structural mechanism of mitochondrial membrane remodelling by human OPA1
von der Malsburg, A., Sapp, G., Zuccaro, K. E., von Appen, A., Moss, F. R., Kalia, R., Bennett, J. A., Abriata, L. A., Peraro, M. D., van der Laan, M., et al. (2023) · Nature · doi:10.1038/s41586-023-06441-6 · Cited by 147
Yao, X., Zhang, J., Jing, X., Ye, Y., Guo, J., Sun, K., & Guo, F. (2018) · Pharmacological Research · doi:10.1016/j.phrs.2018.09.026 · Cited by 134
Nuclear-Mitochondrial Interactions
Walker, B. R., & Moraes, C. T. (2022) · Biomolecules · doi:10.3390/biom12030427 · Cited by 143
Motion of VAPB molecules reveals ER–mitochondria contact site subdomains
Obara, C. J., Nixon‐Abell, J., Moore, A. S., Riccio, F., Hoffman, D. P., Shtengel, G. E., Xu, C. S., Schaefer, K., Pasolli, H. A., Masson, J., et al. (2024) · Nature · doi:10.1038/s41586-023-06956-y · Cited by 147
Zhang, K., Zhou, X., Wang, J., Zhou, Y., Qi, W., Chen, H., Nie, S., & Xie, M. (2021) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2021.118018 · Cited by 128
Mitochondrial complex I as a therapeutic target for Alzheimer's disease
Trushina, E. V., Trushin, S., & Hasan, M. F. (2021) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.11.003 · Cited by 131
The roles of mitochondria in global and local intracellular calcium signalling
Cartes-Saavedra, B., Ghosh, A., & Hajnóczky, G. (2025) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-024-00820-1 · Cited by 126
Self-citationAltered mitochondrial dynamics and function in APOE4-expressing astrocytes
Schmukler, E., Solomon, S., Simonovitch, S., Goldshmit, Y., Wolfson, E., Michaelson, D. M., & Pinkas-Kramarski, R. (2020) · Cell Death & Disease · doi:10.1038/s41419-020-02776-4 · Cited by 125
Eynaudi, A., Díaz-Castro, F., Bórquez, J. C., Bravo-Sagua, R., Parra, V., & Troncoso, R. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.775382 · Cited by 125
Determinants, maintenance, and function of organellar pH
Freeman, S. A., Grinstein, S., & Orlowski, J. (2022) · Physiological Reviews · doi:10.1152/physrev.00009.2022 · Cited by 127
Aryaman, J., Johnston, I. G., & Jones, N. S. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2018.00718 · Cited by 123
The Balance of MFN2 and OPA1 in Mitochondrial Dynamics, Cellular Homeostasis, and Disease
Zanfardino, P., Amati, A., Perrone, M., & Petruzzella, V. (2025) · Biomolecules · doi:10.3390/biom15030433 · Cited by 129
Adaniya, S. M., O‐Uchi, J., Cypress, M. W., Kusakari, Y., & Jhun, B. S. (2019) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00523.2018 · Cited by 123
Paramos-de-Carvalho, D., Jacinto, A., & Saúde, L. (2021) · eLife · doi:10.7554/elife.72449 · Cited by 111
Physical Exercise: A Novel Tool to Protect Mitochondrial Health
Sorriento, D., Di Vaia, E., & Iaccarino, G. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.660068 · Cited by 118
da Silva Rosa, S. C., Martens, M. D., Field, J. T., Nguyen, L., Kereliuk, S. M., Hai, Y., Chapman, D., Diehl-Jones, W., Aliani, M., West, A. R., et al. (2021) · Autophagy · doi:10.1080/15548627.2020.1821548 · Cited by 117
Role of Mitochondria in Viral Infections
Elesela, S., & Lukacs, N. W. (2021) · Life · doi:10.3390/life11030232 · Cited by 113
Ahuja, P., Ng, C. F., Pang, B. P. S., Chan, W. S., Tse, M. C. L., Bi, X., Kwan, H.-L. R., Brobst, D., Herlea-Pana, O., Yang, X., et al. (2022) · Autophagy · doi:10.1080/15548627.2021.1985257 · Cited by 116
Succinyl-CoA Ligase Deficiency in Pro-inflammatory and Tissue-Invasive T Cells
Wu, B., Qiu, J., Zhao, T. V., Wang, Y., Maeda, T., Goronzy, I. N., Akiyama, M., Ohtsuki, S., Jin, K., Tian, L., et al. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.10.025 · Cited by 114
Yang, L., Li, X., Jiang, A., Li, X., Chang, W., Chen, J., & Ye, F. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101626 · Cited by 112
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
Mitochondria Signaling Pathways in Allergic Asthma
Qian, L., Nasab, E. M., Athari, S. M., & Athari, S. S. (2022) · Journal of Investigative Medicine · doi:10.1136/jim-2021-002098 · Cited by 117
Zhao, Y., Zhang, M., Zhang, W., Zhou, Y., Chen, L., Liu, Q., Wang, P., Chen, R., Duan, X., Chen, F., et al. (2022) · Nature Methods · doi:10.1038/s41592-022-01395-5 · Cited by 105
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 107
Self-citationNatural Compounds and Autophagy: Allies Against Neurodegeneration
Stacchiotti, A., & Corsetti, G. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.555409 · Cited by 106
Almeida, L. M., Pinho, B. R., Duchen, M. R., & Oliveira, J. M. A. (2022) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12860 · Cited by 103
Mitochondrial Fission and Fusion in Tumor Progression to Metastasis
Boulton, D. P., & Caino, M. C. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.849962 · Cited by 108
Gupta, P., Rai, N., Verma, A. K., & Gautam, V. (2023) · Medicinal Research Reviews · doi:10.1002/med.21981 · Cited by 105
Glucocorticoid impairs mitochondrial quality control in neurons
Choi, G. E., & Han, H. J. (2021) · Neurobiology of Disease · doi:10.1016/j.nbd.2021.105301 · Cited by 95
Wang, L., Wang, H., Luo, J., Xie, T., Mor, G., & Liao, A. (2022) · Theranostics · doi:10.7150/thno.78467 · Cited by 99
Nitric Oxide-cGMP Signaling in Hypertension
Ataabadi, E. A., Golshiri, K., Jüttner, A. A., Krenning, G., Danser, A. H. J., & Roks, A. J. M. (2020) · Hypertension · doi:10.1161/hypertensionaha.120.15856 · Cited by 94
ER-mitochondria interactions: Both strength and weakness within cancer cells
Doghman-Bouguerra, M., & Lalli, E. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2019.01.009 · Cited by 94
Mitophagy in the Pathogenesis of Liver Diseases
Ke, P. (2020) · Cells · doi:10.3390/cells9040831 · Cited by 91
The role of microbiota-mitochondria crosstalk in pathogenesis and therapy of intestinal diseases
Zhang, Y., Zhang, J., & Duan, L. (2022) · Pharmacological Research · doi:10.1016/j.phrs.2022.106530 · Cited by 94
The effect of extracellular vesicles on the regulation of mitochondria under hypoxia
Zhang, Y., Tan, J., Miao, Y., & Zhang, Q. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03640-9 · Cited by 92
Mitochondrial behaviour, morphology, and animal performance
Heine, K. B., & Hood, W. R. (2020) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12584 · Cited by 87
Galvan, D. L., Long, J., Green, N., Chang, B. H., Lin, J. S., Schumacker, P. T., Truong, L. D., Overbeek, P. A., & Danesh, F. R. (2019) · Journal of Clinical Investigation · doi:10.1172/jci127277 · Cited by 84
Casagrande, S., Stier, A., Monaghan, P., Loveland, J. L., Boner, W., Lupi, S., Trevisi, R., & Hau, M. (2020) · Journal of Experimental Biology · doi:10.1242/jeb.222513 · Cited by 89
Li, J., Agarwal, E., Bertolini, I., Seo, J. H., Caino, M. C., Ghosh, J. C., Kossenkov, A. V., Liu, Q., Tang, H., Goldman, A. R., et al. (2020) · Science Signaling · doi:10.1126/scisignal.aaz8240 · Cited by 83
Mitochondrial dynamics and metastasis
Altieri, D. C. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2961-2 · Cited by 88
Mancini, N. L., Goudie, L. J. L., Xu, W., Sabouny, R., Rajeev, S., Wang, A., Esquerre, N., Rajabi, A. A., Jayme, T. S., Bernardes, E. V. T., et al. (2020) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2020.04.004 · Cited by 83
Mitochondrial Dysfunction in the Pathogenesis of Preeclampsia
Hu, X., & Zhang, L. (2022) · Current Hypertension Reports · doi:10.1007/s11906-022-01184-7 · Cited by 86
Qi, Z., Huang, Z., Xie, F., & Chen, L. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27866 · Cited by 83
The Role of Autophagy for the Regeneration of the Aging Liver
Xu, F., Hua, C., Tautenhahn, H., Dirsch, O., & Dahmen, U. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103606 · Cited by 81
Chen, Y., Wu, Y., Si, H., Lu, Y., & Shen, B. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105497 · Cited by 77
CLUH granules coordinate translation of mitochondrial proteins with mTORC1 signaling and mitophagy
Pla‐Martín, D., Schatton, D., Wiederstein, J. L., Marx, M., Khiati, S., Krüger, M., & Rugarli, E. I. (2020) · The EMBO Journal · doi:10.15252/embj.2019102731 · Cited by 74
Strubbe, J. O., Schrad, J. R., Pavlov, E. V., Conway, J. F., Parent, K. N., & Bazil, J. N. (2021) · Scientific Reports · doi:10.1038/s41598-020-80398-8 · Cited by 75
Nicoletti, V., Palermo, G., Prete, E. D., Mancuso, M., & Ceravolo, R. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.636506 · Cited by 75
Smith, G. A., Lin, T.-H., Sheehan, A. E., van Naters, W. V. D. G., Neukomm, L. J., Graves, H. K., Bis‐Brewer, D. M., Zuchner, S. L., & Freeman, M. R. (2019) · Neuron · doi:10.1016/j.neuron.2019.04.017 · Cited by 71
The relationship of alpha-synuclein to mitochondrial dynamics and quality control
Thorne, N. J., & Tumbarello, D. A. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.947191 · Cited by 78
Yang, P., Luo, X., Li, J., Zhang, T., Gao, X., Hua, J., Li, Y., Ding, N., He, J., Zhang, Y., et al. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/5826932 · Cited by 76
Wang, Y., Mao, X., Chen, H., Feng, J., Yan, M., Wang, Y., & Yu, Y. (2019) · International Immunopharmacology · doi:10.1016/j.intimp.2019.05.027 · Cited by 71
Existence of Circulating Mitochondria in Human and Animal Peripheral Blood
Song, X. H., Hu, W., Yu, H., Wang, H., Zhao, Y., Korngold, R., & Zhao, Y. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21062122 · Cited by 71
Tran, H. C., & Aken, O. V. (2020) · Mitochondrion · doi:10.1016/j.mito.2020.05.009 · Cited by 70
Mitochondrial regulation of local supply of energy in neurons
López‐Doménech, G., & Kittler, J. T. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102747 · Cited by 78
Hu, B., Wang, P., Zhang, S., Liu, W., Lv, X., Shi, D., Zhao, L., Liu, H., Wang, B., Chen, S., et al. (2022) · Experimental & Molecular Medicine · doi:10.1038/s12276-022-00745-9 · Cited by 67
Swerdlow, N., & Wilkins, H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249661 · Cited by 66
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