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 401–500 of 622
Miro1 regulates mitochondrial homeostasis and meiotic resumption of mouse oocyte
Xue, Y., Meng, T., Ouyang, Y., Liu, S., Guo, J., Wang, Z., Schatten, H., Song, C., Guo, X., & Sun, Q. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30890 · Cited by 7
Wang, X., Zhang, Y., Lin, Q., Zhao, K., Zhu, D., & Hu, Y. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102825 · Cited by 7
Belosludtseva, N. V., Serov, D. A., Starinets, V. S., Penkov, N. V., & Belosludtsev, K. N. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241512485 · Cited by 7
Jiang, L., Liu, Y., Tumbath, S., Boudreau, M. W., Chatkewitz, L. E., Wang, J., Su, X., Zahid, K. R., Li, K., Chen, Y., et al. (2023) · Antioxidants and Redox Signaling · doi:10.1089/ars.2022.0224 · Cited by 7
Rasheed, M., Wang, H., Wang, C., Sun, J., Chen, Z., & Deng, Y. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15766 · Cited by 7
Wen, H., Tu, X., Luo, F., Zeng, C., Xia, C., Zhao, Q., Xian, Z., Zhou, Z., Xu, J., & Wang, H. (2025) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2025.111405 · Cited by 6
Yang, M., Qin, X., & Liu, X. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106087 · Cited by 8
Soltero‐Rivera, M. M., Arzi, B., Bourebaba, L., & Marycz, K. (2025) · Stem Cells · doi:10.1093/stmcls/sxaf014 · Cited by 7
Cellular stress and macrophage activation
Yu, J., & Qian, B. (2025) · Seminars in Immunology · doi:10.1016/j.smim.2025.101953 · Cited by 6
Bai, J., He, S., Wang, X., Zhang, L., Ma, C., Gao, D., Yuan, H., Mei, J., Guan, X., Yu, H., et al. (2025) · The FASEB Journal · doi:10.1096/fj.202500389r · Cited by 6
Chattopadhyay, M., Jenkins, E. C., Janssen, W. F., Mashaka, T., & Germain, D. (2025) · Nature Communications · doi:10.1038/s41467-025-61666-5 · Cited by 6
Wang, Y., Zuo, Y.-B., Weng, J., & Peng, X. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.148001 · Cited by 9
付茹婷, Fang, L., Liu, J., Liu, Y., Wang, Y., Kong, D., & Guo, J. (2025) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.107248 · Cited by 8
Yang, Y., Fei, W., Liu, M., Zhang, Y.-C., Gao, R.-S., Hu, Y., Pang, E., & Hou, L. (2022) · Current Stem Cell Research & Therapy · doi:10.2174/1574888x17666220926115240 · Cited by 6
Tonner, H., Hunn, S., Auler, N., Schmelter, C., Pfeiffer, N., & Grus, F. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113618 · Cited by 5
Cheramangalam, R. N., Anand, T., Pandey, P., Balasubramanian, D., Varghese, R., Singhal, N., Nagarkar-Jaiswal, S., & Jaiswal, M. (2023) · PLoS Genetics · doi:10.1371/journal.pgen.1010493 · Cited by 6
Meng, F., Liu, T., Lv, Q., He, J., Niu, J., Gao, P., & Yu, X. (2023) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2023.134328 · Cited by 6
Scheepers, R., & Araujo, R. P. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1244297 · Cited by 6
Wang, L., Huang, X., Dai, T., Xie, J., Lv, Q., Hou, Y., Kong, L., Song, Y., & Liu, F. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.12.025 · Cited by 6
Effects of electromagnetic waves on oocyte maturation and embryonic development in pigs
Chen, J.-S., Tsai, L., Ting-Yu, Y. E. H., Li, T.-S., Li, C.-H., Wei, Z., Lo, N., & Ju, J.-C. (2021) · Journal of Reproduction and Development · doi:10.1262/jrd.2021-074 · Cited by 6
Mitochondrial changes in fish cells in vitro in response to serum deprivation
Fan, X., Yan, T., Hou, T., Xiong, X., Feng, L., Li, S., & Wang, Z. (2022) · Fish Physiology and Biochemistry · doi:10.1007/s10695-022-01088-y · Cited by 6
Mod3D: A low-cost, flexible modular system of live-cell microscopy chambers and holders
Goss, S., Bazan, C. B., Neuman, K., Peng, C. Y., Begeja, N., Suart, C., & Truant, R. (2022) · PLoS ONE · doi:10.1371/journal.pone.0269345 · Cited by 6
Vásquez-Trincado, C., Navarro-Márquez, M., Morales, P. E., Westermeier, F., Chiong, M., Parra, V., Espinosa, A., & Lavandero, S. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1072315 · Cited by 6
Lin, J., Li, X., Lu, K., Song, K., Wang, L., Dai, W., Mohamed, M., & Zhang, C. (2024) · Journal of Nutrition · doi:10.1016/j.tjnut.2024.10.044 · Cited by 6
Methods to detect mitophagy in neurons during disease
Carter, F. E., Moore, M. E., & Pickrell, A. M. (2019) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2019.108351 · Cited by 8
Frantsiyants, E. M., Neskubina, I. V., Surikova, E. I., Shikhlyarova, A. I., Kaplieva, I. V., Nemashkalova, L. A., & Trepitaki, L. K. (2021) · Research and Practical Medicine Journal · doi:10.17709/2409-2231-2021-8-1-1 · Cited by 6
Humanin, MOTS-c and physical exercise: A new perspective
Monteiro, A. R. B., Scarlato, G. C. G., Cavalini, D. F., & Shiguemoto, G. E. (2019) · Biomedical Research and Reviews · doi:10.15761/brr.1000129 · Cited by 6
Rebalancing Cardiac Structure and Function With Synthetic Mitochondria-Endoplasmic Reticulum Tethers
Katti, P., & Glancy, B. C. (2023) · Circulation Research · doi:10.1161/circresaha.123.322911 · Cited by 6
Ghai, U., Chachra, P., Mendon, S., Janakiraman, B., Fanibunda, S. E., Sarkar, A., Gohil, D., Jayaprasad, A. B., Kukkemane, K., Singh, V. K., et al. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.04.026 · Cited by 7
Sutharsan, R., Hontaas, M. B., Li, Y., Xiong, H., Preckel, H., Sue, C. M., & Wali, G. (2025) · Scientific Reports · doi:10.1038/s41598-025-99972-z · Cited by 5
Radulescu, E., Chen, Q., Pergola, G., Eagles, N. J., Stolz, J. M., Shin, J. H., Hyde, T. M., Kleinman, J. E., & Weinberger, D. R. (2023) · PLoS Genetics · doi:10.1371/journal.pgen.1010989 · Cited by 6
Mitochondrial deoxyguanosine kinase is required for female fertility in mice
Gao, Y., Dong, R., Yan, J., Chen, H., Sang, L., Yao, X., Fan, D., Wang, X., Zuo, X., Zhang, X., et al. (2024) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2024003 · Cited by 5
IL-1β-Mediated Immunometabolic Adaptation in Corneal Epithelial Cells
Sanches, J. M., Ramachandran, R. A., Mussi, N., Baniasadi, H. R., & Robertson, D. M. (2025) · Journal of Inflammation Research · doi:10.2147/jir.s495323 · Cited by 5
Factors affecting liver mitochondrial hydrogen peroxide emission
Okoye, C. N., Chinnappareddy, N., Stevens, D., & Kamunde, C. (2022) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2022.110713 · Cited by 5
Voituron, Y., Roussel, D., Galliard, J. L., Dupoué, A., Romestaing, C., & Meylan, S. (2022) · Journal of Comparative Physiology B · doi:10.1007/s00360-022-01454-5 · Cited by 5
Protein adsorption by nanomechanical mass spectrometry: Beyond the real-time molecular weighting
Stachiv, I., Kuo, C.-Y., & Li, W. (2023) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.1058441 · Cited by 5
Kelley, D. P., Albrechet‐Souza, L., Cruise, S. C., Maiya, R., Destouni, A., Sakamuri, S. S. V. P., Duplooy, A., Hibicke, M., Nichols, C. D., Katakam, P. V. G., et al. (2023) · Genes Brain & Behavior · doi:10.1111/gbb.12840 · Cited by 5
Σκώκου, Μ., Oikonomakis, V., Andreopoulou, O., Kypreos, K. E., Gourzis, P., & Halaris, A. E. (2023) · Journal of Affective Disorders Reports · doi:10.1016/j.jadr.2023.100634 · Cited by 6
Chen, C., Smith, Z. J., Fang, J., & Chu, K. (2023) · Biomedical Optics Express · doi:10.1364/boe.510243 · Cited by 6
Sherpa, R. T., Moshal, K. S., Agarwal, S. R., Ostrom, R. S., & Harvey, R. D. (2024) · British Journal of Pharmacology · doi:10.1111/bph.16357 · Cited by 5
Shimpi, G. G., Vargas, S., Bentlage, B., & Wörheide, G. (2024) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2024.152051 · Cited by 5
ANO7 expression in the prostate modulates mitochondrial function and lipid metabolism
Löf, C., Sultana, N., Goel, N., Heron, S., Wahlström, G., House, A. H., Holopainen, M., Käkelä, R., & Schleutker, J. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02081-7 · Cited by 5
Splitting up to heal: mitochondrial shape regulates signaling for focal membrane repair
Horn, A. J., & Jaiswal, J. K. (2020) · Biochemical Society Transactions · doi:10.1042/bst20200120 · Cited by 5
Mitochondrial Biogenesis and Dynamics in Health and Disease
Campos, J. C., Bozi, L. H. M., & Ferreira, J. C. B. (2021) · Springer eBooks · doi:10.1007/978-3-030-86684-6_3 · Cited by 4
Disruption of Mitochondrial Quality Control in Inherited Metabolic Disorders
Marcuzzo, M. B., Silveira, J. D. A., STRECK, E. L., Vockley, J., & Leipnitz, G. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04467-z · Cited by 4
Chivite, Í., Monelli, E., Munar-Gelabert, M., Gómez-Valadés, A. G., Alvarado-Diaz, A., Pozo, M., Varela, L. C., Ramírez, S., Haddad-Tóvolli, R., Toledo, M., et al. (2026) · Cell Metabolism · doi:10.1016/j.cmet.2026.01.012 · Cited by 6
Rasmussen, L. K., Moreira, D. G., Okarmus, J., Simonsen, A., & Meyer, M. (2026) · Autophagy · doi:10.1080/15548627.2026.2711596 · Cited by 4
Mitochondrial Activation and Therapeutics: Innovations in Cell- and Organelle-Specific Medicine
Sato, I., Shiraishi, M., Norota, K., Shiraki, K., & Yamada, Y. (2025) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b25-00218 · Cited by 5
Luo, Y., & Wang, W. (2023) · Environmental Science Nano · doi:10.1039/d3en00181d · Cited by 4
Darden, C., Donkor, J. E., Korolkova, O. Y., Barozai, M. Y. K., & Chaudhuri, M. (2024) · mSphere · doi:10.1128/msphere.00558-23 · Cited by 4
Yang, N., Li, S., Zhang, Y., Pan, F., Liu, G., Chen, X., Yu, C., Li, K., & Liu, Y. (2024) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-024-01450-9 · Cited by 4
Reid, D. M., Choe, J. Y., Bruce, M. A., Thorpe, R. J., Jones, H. P., & Phillips, N. (2024) · Methods in molecular biology · doi:10.1007/978-1-0716-4200-9_6 · Cited by 4
Cardiac effects of OPA1 protein promotion in a transgenic animal model
Bruszt, K., Horváth, O., Ördög, K., Toth, S., Juhász, K., Vámos, E., Fekete, K., Gallyas, F., Tóth, K., Halmosi, R., et al. (2024) · PLoS ONE · doi:10.1371/journal.pone.0310394 · Cited by 4
Mitochondrial encephalopathies and myopathies: Our tertiary center's experience
Özlü, C., Messahel, S., Minassian, B. A., & Kayani, S. N. (2024) · European Journal of Paediatric Neurology · doi:10.1016/j.ejpn.2024.03.005 · Cited by 4
Pasula, D. J., Shi, R., Vanderkruk, B., Shih, A. Z. L., Zou, Y., Chaudhry, A., Hoffman, B. G., & Luciani, D. S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.25.465491 · Cited by 4
Tau clearance reverses touch neuron dysfunction in both young and aged C. elegans
Carroll, T., Johnson, G. V. W., & Nehrke, K. W. (2025) · Journal of Alzheimer s Disease · doi:10.1177/13872877251392935 · Cited by 3
Molecular mechanisms of mitochondrial function in neurodegenerative diseases
Wilkins, H., & Patergnani, S. (2025) · Molecular Biology Reports · doi:10.1007/s11033-025-11303-7 · Cited by 3
Mitochondria in corneal physiology and pathology: A mechanistic perspective
Yang, L., Chen, S., Ge, J., Chen, Z., Chen, K., Li, J., Zhang, J., Li, Y., Qu, M., Neo, D. J. H., et al. (2025) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2025.101432 · Cited by 4
Yang, Z., Zhu, S., Lyu, C.-A., Fu, H., Chen, W., Qiu, X., Zhang, W., Yu, T., Yang, M., Zhang, Z. Y., et al. (2026) · Developmental Cell · doi:10.1016/j.devcel.2026.02.006 · Cited by 5
PI(3)P regulates mitochondrial dynamics through FGD-dependent actin organization
Zhao, S., Zhang, J., Ma, T., Li, J., Duan, M., Wang, X., Li, M., & Yang, C. (2026) · The Journal of Cell Biology · doi:10.1083/jcb.202508040 · Cited by 3
Peruch, M., Giacomello, E., Radaelli, D., Concato, M., Addobbati, R., Fluca, A. L., Aleksova, A., & D’Errico, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914517 · Cited by 6
Li, B., Wang, H., Zeng, X., Liu, S., & Zhuang, Z. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25031512 · Cited by 3
Fast axial resolution enhancement microscopy with structured illumination
Luo, S., Gong, R., Zhang, M., Xu, T., Ji, W., & Gu, L. (2024) · APL Photonics · doi:10.1063/5.0239482 · Cited by 3
Xu, K., Zhang, J., Ma, W., Huang, H., Yan, S., Wang, L., & Zhang, W. (2022) · Chinese Chemical Letters · doi:10.1016/j.cclet.2022.04.084 · Cited by 3
Schaeffer, C., Fusco, M. D., Pasqualetto, E., Scolari, C., Izzi, C., Scolari, F., & Rampoldi, L. (2023) · Disease Models & Mechanisms · doi:10.1242/dmm.049963 · Cited by 3
Regular exercise attenuates alcoholic myopathy in zebrafish by modulating mitochondrial homeostasis
Wen, W., Guo, C., Chen, Z., Yang, D. K., Zhu, D., Jing, Q., Zheng, L., Sun, C., & Tang, C. (2023) · PLoS ONE · doi:10.1371/journal.pone.0294700 · Cited by 3
A mito-centric view on muscle aging and function
Burtscher, J., Strasser, B., & Burtscher, M. (2024) · Frontiers in Public Health · doi:10.3389/fpubh.2023.1330131 · Cited by 3
Bastari, G., Fernandez, V. S., Muzzi, M., Moreno, S., Marino, M., & Fiocchetti, M. (2024) · Cell Stress · doi:10.15698/cst2024.11.300 · Cited by 3
Lan, X., Yang, M., Wang, J., Huang, C., Wu, A., Cui, L., Guo, Y., Zeng, L., Guo, X., Zhang, Y., et al. (2025) · Toxins · doi:10.3390/toxins17020072 · Cited by 3
Marquez, G., Jafari, M., Kesapragada, M., Zhu, K., Baniya, P., Sun, Y., Hsieh, H., Hernandez, C. O., Teodorescu, M., Rolandi, M., et al. (2025) · Bioengineering · doi:10.3390/bioengineering12070678 · Cited by 2
Aging impairs peroxisome biogenesis in human B cells
Correia, J., Roy, P. L., Holden, K. G., Kohut, M. L., & Bai, H. (2025) · The Journals of Gerontology Series A · doi:10.1093/gerona/glaf148 · Cited by 3
Fakhir, S. D., Arif, I. S., & Waheed, H. J. (2025) · Pharmacia · doi:10.3897/pharmacia.72.e175259 · Cited by 2
Spatiotemporal Ca2+ nanodomain remodeling at MERCS regulates mitochondrial proteostasis
Lv, Y., Zhao, X., Li, D., Hao, Z., Zhao, Y., Zhou, Y., Zhang, Y., Chen, H., Lu, Z., Li, D., et al. (2025) · Protein & Cell · doi:10.1093/procel/pwaf109 · Cited by 2
MitoCommun: a database for decoding mitochondrial communication networks
Wu, X., Chen, D., Feng, J., Bu, X., Wu, S., & Qiao, J. (2026) · BMC Genomics · doi:10.1186/s12864-026-12549-6 · Cited by 2
Snapshot on Cell-to-Cell Communication Nanotubes: From Bacteria to Humans
Moro, L. (2026) · Biology · doi:10.3390/biology15060513 · Cited by 2
Lin, J., Wu, T., Wang, C., Zhou, W., Liu, Y., Yang, G., Zhou, H., Luo, J., Fan, Z., Da, Y., et al. (2026) · Metabolism · doi:10.1016/j.metabol.2026.156623 · Cited by 2
Looking Back to the Future of Mitochondrial Research
Bernardi, P. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.682467 · Cited by 3
A big picture of the mitochondria-mediated signals: From mitochondria to organism
Acar, N. V., & Özgül, R. K. (2023) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2023.08.032 · Cited by 2
Feng, Y., Wang, Z., Duan, H., & Shao, B. (2024) · Food and Chemical Toxicology · doi:10.1016/j.fct.2024.114506 · Cited by 2
Single molecule studies of dynamic platelet interactions with endothelial cells
Hauser, F., Naderer, C., Priglinger, E., Peterbauer, A., Fischer, M. B., Redl, H. R., & Jacak, J. (2024) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2024.1372807 · Cited by 2
Pasqualotto, B. A., Nelson, A., Deheshi, S., Sheldon, C. A., Vogl, A. W., & Rintoul, G. L. (2024) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2024.150119 · Cited by 2
Hanley‐Cook, G., Bastos-Moreira, Y., Martens, D. S., Dailey-Chwalibóg, T., Toe, L. C., de Kok, B., Ouédraogo, L. O., Argaw, A., Tesfamariam, K., Kolsteren, P. W., et al. (2024) · Food Science and Human Wellness · doi:10.26599/fshw.2024.9250304 · Cited by 3
Jiang, X., Wang, J., Ma, F., & Li, Y. (2024) · Journal of Cellular Biochemistry · doi:10.1002/jcb.30641 · Cited by 2
Exploring Mitochondrial Quality in Aging and Neurodegenerative Diseases
Jiao, X., Li, M., Na, D., Meng, M., Zhang, G., & Guo, Y. (2024) · Neurochemical Journal · doi:10.1134/s1819712424700016 · Cited by 2
Shirvani, P., Shirvani, A., & Holick, M. F. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb47020134 · Cited by 4
Zhao, M., Zhao, Y., Li, G., Zhang, L., Wang, H., Hong, Y., Yu, W., Song, W. J., & Zhang, Y. (2025) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.4c02357 · Cited by 2
Melittin-induced modulation of mitochondrial physiology: Beyond the antitumoral actions
de Oliveira, M. R. (2025) · Toxicon · doi:10.1016/j.toxicon.2025.108555 · Cited by 2
Metabolic reprogramming and immunity in cancer
Chen, Y., & Li, Y. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823397-9.00006-5 · Cited by 2
Yellow Fever Virus Infection Alters Mitochondrial Network DynamicsPreprint
Gomez, R. M., Tomatis, C., Scalise, M. L., Thomas, P., Aquila, S., Calderone, M., Fuentes, F., Eugenio Carrera Silva, A., & Ferrer, M. F. (2023) · doi:10.22541/au.167407899.97892667/v1 · Cited by 2
[Research progress of optic atrophy 1-mediated mitochondrial dynamics in skeletal system diseases].
Sun, K., Wu, Y., Zeng, Y., Li, M., Wu, L., & Shen, B. (2023) · PubMed Central · doi:10.7507/1002-1892.202302056 · Cited by 1
Valencia, A. P., Pharaoh, G. A., Brandao, A. F., & Marcinek, D. J. (2024) · Journal of Visualized Experiments · doi:10.3791/66863 · Cited by 1
Fang, Z., Li, Y., Chen, H., Lian, C., Zhang, X., Wang, J., & Zhou, Z. (2024) · Journal of Functional Foods · doi:10.1016/j.jff.2024.106291 · Cited by 2
Sima, Y., Shi, S., Min, Z., Chen, Y., Lu, Y., Sha, H., & Liu, S. (2025) · Journal of Assisted Reproduction and Genetics · doi:10.1007/s10815-025-03431-7 · Cited by 2
Yan, F., & Bao, L. (2025) · Journal of Cardiovascular Translational Research · doi:10.1007/s12265-025-10606-1 · Cited by 1
Wang, X., Li, H., Dong, Z., Lu, W., Chen, J., Zhang, H., Yuan, Z., Liu, Y., Weng, Q., & Han, Y. (2025) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2025.111927 · Cited by 1
Marcuzzo, M. B., Silveira, J. D. A., Pinheiro, C. V., ROSA, J. S. D., Zemniaçak, Â. B., Brondani, M., Kist, N. S., Hoffmann, C. I. H., Schiöth, H. B., Amaral, A. U., et al. (2025) · Neurotoxicity Research · doi:10.1007/s12640-025-00758-y · Cited by 1
Zhang, W., Xiao, H. J., Ma, Y., Lyu, X., Li, K., He, L., & Liu, S. (2025) · ACS Nano Medicine · doi:10.1021/acsnanomed.5c00057 · Cited by 2
Ganguly, A., Carter, C. M., Negron, A. R., Zhong, H., Moreira, A. G., Walters, M. S., Rogers, L. K., Prakash, Y. S., Tipple, T. E., & Richardson, A. (2025) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00205.2025 · Cited by 1
Gui, S., Gao, J., Tao, T., Wang, P., Huang, Z., She, Y., Li, J., Su, J., Lu, Z., Qiao, J., et al. (2026) · Interdisciplinary medicine · doi:10.1002/inmd.70085 · Cited by 1
Monitoring neuronal mitophagy and locomotion deficits in a C. elegans model of Alzheimer’s disease
Niforos-Garcia, G., Tsakiri, E., & Palikaras, K. (2026) · Methods in cell biology · doi:10.1016/bs.mcb.2025.12.001 · Cited by 1
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