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 301–400 of 622
The effect of vitrification on blastocyst mitochondrial DNA dynamics and gene expression profiles
Pérez-Sánchez, M., Pardiñas, M. L., Díez‐Juan, A., Quiñonero, A., Domı́nguez, F., Martín, Á., Vidal, C., Beltrán, D., Mifsud, A., Mercader, A., et al. (2023) · Journal of Assisted Reproduction and Genetics · doi:10.1007/s10815-023-02952-3 · Cited by 15
Belužić, R., Šimunić, E., Podgorski, I. I., Pinterić, M., Hadžija, M. P., Balog, T., & Sobočanec, S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25073868 · Cited by 17
Shi, Q., Song, Y., Cao, J., Na, J., Yang, Z., Chen, X., Wang, Z., Fan, Y., & Zheng, L. (2025) · Research · doi:10.34133/research.0602 · Cited by 20
The structure of the human LACTB filament reveals the mechanisms of assembly and membrane binding
Bennett, J. A., Steward, L. R., Rudolph, J., Voss, A. P., & Aydin, H. (2022) · PLOS Biology · doi:10.1371/journal.pbio.3001899 · Cited by 16
Kelley, D. P., Singleton, S. P., Venable, K. E., Sturm, G., Skovgaard, A., Francis, J., Neylan, T. C., Bradley, E., Woolley, J. D., Picard, M. A., et al. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106419 · Cited by 14
Self-citationGenetic mutations affecting mitochondrial function in cancer drug resistance
Lee, C., Park, S., & Yoon, S. K. (2023) · Genes & Genomics · doi:10.1007/s13258-022-01359-1 · Cited by 15
Li, A., Zhang, Y., Wang, J., Zhang, Y., Su, W., Gao, F., & Jiao, X. (2023) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0000000000001414 · Cited by 14
Liu, S. Y., Zhao, Y., Yao, H., Zhang, L., Chen, C., Zheng, Z., & Jin, S. (2023) · Experimental Cell Research · doi:10.1016/j.yexcr.2023.113688 · Cited by 13
The bridge between cell survival and cell death: reactive oxygen species-mediated cellular stress
Acar, N. V., & Özgül, R. K. (2023) · EXCLI journal · doi:10.17179/excli2023-6221 · Cited by 19
Sun, M., Zeng, Z., Xu, G., An, S. L., Deng, Z., Cheng, R., Yao, Y., Wu, J., Hu, H., Huang, Q., et al. (2023) · Shock · doi:10.1097/shk.0000000000002206 · Cited by 14
Shi, Y. X., Lin, J., Tao, X., Qu, J. T., Liao, S., Li, M., Deng, K., Du, P., Liu, K., Thissen, H. W., et al. (2021) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.1c02591 · Cited by 14
Wang, Y., Chen, F., Zhang, Y., Zheng, X., Liu, S., Tang, M., Wang, Z., Wang, P., Bao, Y., & Li, D. (2022) · Food & Function · doi:10.1039/d1fo04112f · Cited by 14
Molina-Riquelme, I., Barrientos, G., Breitsprecher, L. F., Gómez, W., Díaz‐Castro, F., Morris, S., Almarza, G., del Campo, A., Garrido‐Olivares, L., Verdejo, H., et al. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2508911123 · Cited by 13
Self-citationIron deficiency exacerbates aortic medial degeneration by inducing excessive mitochondrial fission
Zhong, X., Wu, Q., Wang, Z., Zhang, M., Zheng, S., Shi, F., Chen, Y., Che, Y., Yuan, S., & Xing, K. (2022) · Food & Function · doi:10.1039/d2fo01084d · Cited by 13
Mitohormesis and mitochondrial dynamics in the regulation of stem cell fate
Barzegari, A., Aboulhassanzadeh, S., Landon, R., Gueguen, V., Meddahi‐Pellé, A., Parvizpour, S., Anagnostou, F., & Pavon‐Djavid, G. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30820 · Cited by 14
Xie, Y., Zhang, Y., Sun, A., Peng, Y., Hou, W., Xiang, C., Zhang, G., Lai, B., Hou, X., Zheng, F., et al. (2022) · Redox Biology · doi:10.1016/j.redox.2022.102447 · Cited by 13
Li, X., Li, J., Shan, G., & Wang, X. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.1097571 · Cited by 13
Host Subcellular Organelles: Targets of Viral Manipulation
Song, M. S., Lee, D., Lee, C.-Y., Park, S., & Yang, J. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25031638 · Cited by 15
Cell life-or-death events in osteoporosis: All roads lead to mitochondrial dynamics
Li, Z., Liang, S., Ke, L., Wang, M., Gao, K., Li, D., Xu, Z., Li, N., Zhang, P., & Cheng, W. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107383 · Cited by 14
Long, M. J. C., Zhao, Y., & Aye, Y. (2020) · RSC Chemical Biology · doi:10.1039/d0cb00041h · Cited by 13
Pandey, A. K., Sarkar, S., Yadav, S. K., Yadav, S., Srikrishna, S., Siddiqui, M. H., Parmar, D., & Yadav, S. (2022) · Molecular Neurobiology · doi:10.1007/s12035-021-02667-5 · Cited by 13
Yang, K., Zhang, X., Yang, K., Liu, S., Zhang, J., Fu, Y., Liu, T., Wu, K., Li, J., Liu, C., et al. (2025) · Molecular Medicine · doi:10.1186/s10020-025-01263-w · Cited by 12
Liu, Z., Han, Z., Bao, W., Guo, Y., Yuan, Y., Cheng, J., Zhang, J., & Hu, Y. (2025) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70559 · Cited by 12
Romanova, N., Schmitz, J., Strakeljahn, M., Grünberger, A., Bahnemann, J., & Noll, T. (2022) · Cells · doi:10.3390/cells11111763 · Cited by 12
Exploring Single-Cell Exposomics by Mass Spectrometry
Gao, P. (2023) · Environmental Science & Technology · doi:10.1021/acs.est.3c04524 · Cited by 12
Silvagni, E., Missiroli, S., Patergnani, S., Boncompagni, C., d'Ugo, C., Garaffoni, C., Ciliento, M. S., Lanza, G., Bonora, M., Gafà, R., et al. (2023) · Journal of Autoimmunity · doi:10.1016/j.jaut.2023.103159 · Cited by 12
Dong, Z., Han, W., Jiang, P., Hao, L., & Fu, X. (2024) · Regenerative Biomaterials · doi:10.1093/rb/rbae052 · Cited by 12
Xu, H. G., Mao, X., Zhang, S., Ren, J., Jiang, S., Cai, L., Miao, X., Tao, Y., Peng, C., Lv, M., et al. (2024) · Toxicological Sciences · doi:10.1093/toxsci/kfae071 · Cited by 12
Zhang, J., Zhang, Z., Huang, Z., Guo, Q., Wu, Z., Ke, C., Lü, B., Wang, Z., & Ji, L. (2024) · Acta Pharmacologica Sinica · doi:10.1038/s41401-024-01335-3 · Cited by 12
Wang, Z., Wang, M., Wang, X.-C., Chen, L., Li, L.-F., Jiang, L., Xu, J.-H., & Dang, K. (2024) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2024.111705 · Cited by 12
Li, R., Ma, Y., He, A., Pu, Y., Wan, X., Sun, H., Wang, N., Luo, M., Wang, G., & Xia, Y. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.01.047 · Cited by 13
Das, H., Sarkar, S., Paidi, R. K., & Biswas, S. C. (2021) · The FASEB Journal · doi:10.1096/fj.202001676rr · Cited by 12
Serradell, A., Montero, D., Fernández-Montero, Á., Terova, G., Makol, A., Valdenegro, V., Acosta, F., Izquierdo, M. S., & Torrecillas, S. (2022) · Animals · doi:10.3390/ani12233332 · Cited by 12
Fang, J., Zhang, H., Pan, Y., Smith, Z. J., & Chu, K. (2023) · ACS Photonics · doi:10.1021/acsphotonics.2c01782 · Cited by 14
Yan, X., Qu, X., Tian, R., Xu, L., Jin, X., Yu, S., Zhao, Y., Ma, J., Liu, Y., Sun, L., et al. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.118171 · Cited by 13
Interpreting phospholipid and cardiolipin profiles in rare mitochondrial diseases
Keller, M. A. (2021) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2021.100383 · Cited by 12
Song, M., & Fan, X. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24098398 · Cited by 11
How are mitochondrial nucleoids trafficked?
Macuada, J., Molina-Riquelme, I., & Eisner, V. (2025) · Trends in Cell Biology · doi:10.1016/j.tcb.2024.12.007 · Cited by 11
Self-citationRHOA regulates mitochondria-ER contact sites through modulation of the VAPB/PTPIP51 tether
Yang, Z., Nakajima, S., Chen, H., Chakrabarty, Y., Feng, H., & Chan, D. C. (2025) · Nature Communications · doi:10.1038/s41467-025-66138-4 · Cited by 11
Mohiuddin, M., & Kasahara, K. (2021) · Cancer Genomics & Proteomics · doi:10.21873/cgp.20282 · Cited by 12
Charrasse, S., Racine, V., Saint-Omer, C., Poquillon, T., Lionnard, L., Ledru, M., Gonindard, C., Delaunois, S., Kissa, K., Frye, R. E., et al. (2024) · PLoS ONE · doi:10.1371/journal.pone.0301372 · Cited by 11
Deshmukh, V., & Martin, J. F. (2024) · Journal of Cell Science · doi:10.1242/jcs.261268 · Cited by 11
AI-recognized mitochondrial phenotype enables identification of drug targets
(2024) · Nature Computational Science · doi:10.1038/s43588-024-00682-9 · Cited by 11
OPA1 and disease-causing mutants perturb mitochondrial nucleoid distribution
Macuada, J., Molina-Riquelme, I., Vidal, G., Pérez-Bravo, N., Vásquez-Trincado, C., Aedo, G., Lagos, D., Yu‐Wai‐Man, P., Horváth, R., Rudge, T. J., et al. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-07165-9 · Cited by 12
Self-citationKaul, H., Isermann, L., Senft, K., Popović, M., Georgomanolis, T., Baumann, L. C., Sivanesan, P., Pouikli, A., Nolte, H., Lucic, B., et al. (2025) · Nature Metabolism · doi:10.1038/s42255-025-01332-8 · Cited by 10
Clusterin is involved in mediating the metabolic function of adipose SIRT1
Zhang, P., Konja, D., Zhang, Y., Xu, A., Lee, I., Jeon, J., Bashiri, G., MITRA, A. K., & Wang, Y. (2021) · iScience · doi:10.1016/j.isci.2021.103709 · Cited by 11
Zeng, Y., Xiong, C., Tang, N., Wang, S., Xiong, Z., Liang, T., Wang, Q., Li, M., & Li, J. (2023) · Journal of Cancer · doi:10.7150/jca.82949 · Cited by 11
IFN ‐γ and androgens disrupt mitochondrial function in murine myocytes
Fenimore, J. M., Springer, D., Romero, M. E., Edmondson, E. F., McVicar, D. W., Yanpallewar, S. U., Sanford, M. E., Spindel, T., Engle, E. M., Meyer, T. J., et al. (2023) · The Journal of Pathology · doi:10.1002/path.6081 · Cited by 11
You, Y., Chen, L., Wu, Y., Wang, M., Lu, H., Zhou, X., Liu, H., Fu, Z., He, Q., Ou, J., et al. (2020) · Cell Transplantation · doi:10.1177/0963689720950213 · Cited by 11
Jin, C., Zhong, Y., Han, J., Zhu, J., Liu, Q., Sun, D., Xia, X., & Peng, X. (2020) · Food and Chemical Toxicology · doi:10.1016/j.fct.2020.111740 · Cited by 11
Tsuboi, T., Leff, J., & Zid, B. M. (2020) · Biochemical Society Transactions · doi:10.1042/bst20200250 · Cited by 11
Liu, P., Chang, K., Requejo, G., & Bai, H. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.866210 · Cited by 9
Sloat, S. R., & Hoppins, S. C. (2022) · Life Science Alliance · doi:10.26508/lsa.202101305 · Cited by 10
Mitochondrial networks through the lens of mathematics
Lewis, G. R., & Marshall, W. F. (2023) · Physical Biology · doi:10.1088/1478-3975/acdcdb · Cited by 11
Convergent and divergent mechanisms of peroxisomal and mitochondrial division
Subramani, S. E., Shukla, N., & Farré, J. (2023) · The Journal of Cell Biology · doi:10.1083/jcb.202304076 · Cited by 10
Cao, Y., Cui, L., Tuo, S., Liu, H., & Cui, S. (2024) · European Journal of Histochemistry · doi:10.4081/ejh.2024.4004 · Cited by 10
SFXN1 promotes bladder cancer metastasis by restraining PINK1-dependent mitophagy
Zhang, B., Dong, G., Guo, X., Li, H., Chen, W., Diao, W., Lu, Q., Xu, G., Zhang, Q., Ding, M., et al. (2025) · Oncogene · doi:10.1038/s41388-025-03460-7 · Cited by 10
Emerging Promise of Therapeutic Approaches Targeting Mitochondria in Neurodegenerative Disorders
Rahman, M. M., Tumpa, M. A. A., Rahaman, M. S., Islam, F., Sutradhar, P. R., Ahmed, M., Alghamdi, B. S. A., Hafeez, A., Alexiou, A. T., Perveen, A., et al. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230316150559 · Cited by 11
Mularoni, V., Donati, B., Tameni, A., Manicardi, V., Reggiani, F., Sauta, E., Zanelli, M., Tigano, M., Vitale, E., Torricelli, F., et al. (2023) · Haematologica · doi:10.3324/haematol.2022.282552 · Cited by 10
Gurhan, H., Bajtoš, M., & Barnes, F. S. (2023) · Biomolecules · doi:10.3390/biom13071112 · Cited by 10
Milton assembles large mitochondrial clusters, mitoballs, to sustain spermatogenesis
Li, A. Y. Z., Di, Y., Rathore, S., Chiang, A. C.-Y., Ježek, J., & Ma, H. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2306073120 · Cited by 10
Karnan, S., Hanamura, I., Ota, A., Vu, L. Q., Uchino, K., Horio, T., Murakami, S., Mizuno, S., Rahman, M. L., Wahiduzzaman, M., et al. (2024) · Cell Death Discovery · doi:10.1038/s41420-024-01814-w · Cited by 10
Zhang, C., & Boppart, S. A. (2021) · Scientific Reports · doi:10.1038/s41598-021-85795-1 · Cited by 10
Content aware image restoration improves spatiotemporal resolution in luminescence imaging
Boothe, T., Ivanković, M., Grohme, M. A., Markus, M. A., Dullin, C., Xu, X., & Rink, J. C. (2023) · Communications Biology · doi:10.1038/s42003-023-04886-z · Cited by 9
Mitochondrial motility modulators coordinate quality control dynamics to promote neuronal health
Jenkins, J. E., Fazli, M., & Evans, C. S. (2024) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2024.102383 · Cited by 9
MMP8-mediated vascular remodeling in pulmonary hypertension
Deng, X., You, Y., Lv, S., & Liu, Y. (2024) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2024.167582 · Cited by 9
Wu, Y., Tang, K., Wang, C., Hao, S., Zhou, F., & Guo, Y. (2025) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2025.02.009 · Cited by 10
Qian, M., Zhu, Y., Lin, W.-L., Lian, H., Xia, Y. L., Papadimos, T. J., & Wang, J. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114685 · Cited by 9
Chu, Y., Chen, W., Lin, W.-R., Lai, M. W., & Yeh, C. (2025) · Cell & Bioscience · doi:10.1186/s13578-025-01456-0 · Cited by 11
Xiao, X., Zheng, M., Zhao, Y., Huang, K., Shi, Y., Ren, Y., Chen, L., Sun, J., Ye, R., Zheng, Z., et al. (2025) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2025.120736 · Cited by 9
ER stress induced mitochondrial dysfunction drives Treg instability in coronary artery disease
Parashar, S., Oliaeimotlagh, M., Roy, P., Lyu, Q., Bellapu, A., Fomin, M., Kumar, S., Wang, Y., McSkimming, C. C., McNamara, C. A., et al. (2025) · EMBO Molecular Medicine · doi:10.1038/s44321-025-00322-3 · Cited by 10
Talk to Me—Interplay between Mitochondria and Microbiota in Aging
Endres, K., & Friedland, K. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310818 · Cited by 9
Maes, M. E., Colombo, G., Uiterkamp, F. E. S., Sternberg, F., Venturino, A., Pohl, E. E., & Siegert, S. (2023) · iScience · doi:10.1016/j.isci.2023.107780 · Cited by 9
Mitochondrial morphology in the mouse adrenal cortex: Influence of chronic psychosocial stress
Vega-Vásquez, T., Langgartner, D., Wang, J. Y., Reber, S. O., Picard, M. A., & Basualto-Alarcón, C. (2023) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2023.106683 · Cited by 9
Self-citationTamoxifen modulates mitochondrial dynamics through AMPK and MAPK during nutrition deprivation
Gangipangi, V., Swetha, U. S., & Selvaraju, S. (2022) · Cell Biology International · doi:10.1002/cbin.11853 · Cited by 9
Zerihun, M., & Qvit, N. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1275370 · Cited by 9
Motion of single molecular tethers reveals dynamic subdomains at ER-mitochondria contact sitesPreprint
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. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.03.505525 · Cited by 10
Bhat, S. M., Massey, N., Shrestha, D., Karriker, L. A., Jelesijevic, T. P., Wang, C., & Charavaryamath, C. (2022) · Cell and Tissue Research · doi:10.1007/s00441-022-03602-3 · Cited by 8
Rapamycin alleviates mitochondrial dysfunction in anti-NMDAR encephalitis mice
Kong, L., Yang, X., Sun, A., Yang, X., Zhao, X., & Wang, S. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.111910 · Cited by 8
Arnhold, J. (2025) · Biomolecules · doi:10.3390/biom15040547 · Cited by 8
Tomatis, C., Charó, N. L., Ferrer, M. F., Aquila, S., Fuentes, F., Scalise, M. L., Aguiar, M. C. A. M., Valdivieso, G., Silva, E. A. C., & Gomez, R. M. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114699 · Cited by 8
Golovynska, I., Chen, Q., Stepanov, Y. V., Lin, D., & Qu, J. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1610204 · Cited by 8
Role of mitochondrial dysfunction in ocular surface diseases
Chen, X., Hong, J., & Le, Q. (2025) · Cell Stress · doi:10.15698/cst2025.08.309 · Cited by 8
Lounas, A., Breton, Y., Lebrun, A., Laflamme, I., Vernoux, N., Savage, J. C., Tremblay, M., Pelletier, M., Germain, M., & Richard, F. J. (2024) · Scientific Reports · doi:10.1038/s41598-023-50586-3 · Cited by 9
Zhao, J., Qiu, Y.-K., Xie, Y.-X., Li, X.-Y., Li, Y., Wu, B., Wang, Y., Tian, X.-Y., Lv, Y.-L., Zhang, L.-H., et al. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.174313 · Cited by 9
Giannopoulou, A. F., Velentzas, A. D., Anagnostopoulos, A. K., Agalou, A., Papandreou, N. C., Katarachia, S. A., Koumoundourou, D. G., Konstantakou, E. G., Pantazopoulou, V. I., Delis, A. D., et al. (2021) · Cancers · doi:10.3390/cancers13092024 · Cited by 8
The Many Roles Mitochondria Play in Mammalian Aging
Batalha, C. M. P. F., Vercesi, A. E., & de Souza-Pinto, N. C. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2021.0074 · Cited by 8
Mohammed, M. S., Adil, B. H., Obaid, A. S., & Al-Shammari, A. M. (2022) · Materials science forum · doi:10.4028/www.scientific.net/msf.1050.51 · Cited by 8
Mitochondria: Master Regulator of Metabolism, Homeostasis, Stress, Aging and Epigenetics
Meiliana, A., Dewi, N. M., & Wijaya, A. (2021) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v13i3.1616 · Cited by 7
BCR, not TCR, repertoire diversity is associated with favorable COVID-19 prognosis
Paran, F. J., Oyama, R., Khasawneh, A., Ai, T., Ismanto, H. S., Sherif, A., Saputri, D. S., Ono, C., Saita, M., Takei, S., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1405013 · Cited by 7
Osteosarcoma stem cells resist chemotherapy by maintaining mitochondrial dynamic stability via DRP1
Tian, B., Wu, Y., Du, X., & Zhang, Y. (2024) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2024.5451 · Cited by 7
Carriel‐Nesvara, A., Muñoz-Medina, C., Deldicque, L., & Castro‐Sepúlveda, M. (2025) · The Journal of Physiology · doi:10.1113/jp289019 · Cited by 8
Venkatesan, S., Comi, C., Marchi, F. D., Esposito, T., Gramaglia, C. M., Smirne, C., Pour, M. M. O., Pirisi, M., Vaschetto, R., Zeppegno, P., et al. (2026) · Biomolecules · doi:10.3390/biom16010117 · Cited by 10
Soluble Carrier Transporters and Mitochondria in the Immunometabolic Regulation of Macrophages
Silva, L. F. L., Lee, J., & Moraes‐Vieira, P. M. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2021.0181 · Cited by 7
Fu, J., He, S., Liu, J., Pang, J., Wang, K., & Chen, Y. (2024) · Journal of Materials Chemistry B · doi:10.1039/d4tb01486c · Cited by 7
Venable, K. E., Lee, C. C., & Francis, J. (2024) · Nutrients · doi:10.3390/nu16203539 · Cited by 6
Mitostasis in age-associated neurodegeneration
Panda, M., Markaki, M., & Tavernarakis, N. (2024) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2024.167547 · Cited by 7
Regulation of the mitochondrial permeability transition pore and its effects on aging
Pellegrino-Coppola, D. (2020) · Microbial Cell · doi:10.15698/mic2020.09.728 · Cited by 7
Organic dust exposure induces stress response and mitochondrial dysfunction in monocytic cells
Bhat, S. M., Shrestha, D., Massey, N., Karriker, L. A., Kanthasamy, A. G., & Charavaryamath, C. (2021) · Histochemistry and Cell Biology · doi:10.1007/s00418-021-01978-x · Cited by 10
Cavezzi, A., Colucci, R., & d’Errico, G. (2022) · Current Aging Science · doi:10.2174/1874609815666220606140754 · Cited by 10
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