The DOI matches its Crossref record; 229 of the 229 references it cites were found in a registry or an index.
Calcium, ATP, and ROS: a mitochondrial love-hate triangle
Abstract
The mitochondrion is at the core of cellular energy metabolism, being the site of most ATP generation. Calcium is a key regulator of mitochondrial function and acts at several levels within the organelle to stimulate ATP synthesis. However, the dysregulation of mitochondrial Ca(2+) homeostasis is now recognized to play a key role in several pathologies. For example, mitochondrial matrix Ca(2+) overload can lead to enhanced generation of reactive oxygen species, triggering of the permeability transition pore, and cytochrome c release, leading to apoptosis. Despite progress regarding the independent roles of both Ca(2+) and mitochondrial dysfunction in disease, the molecular mechanisms by which Ca(2+) can elicit mitochondrial dysfunction remain elusive. This review highlights the delicate balance between the positive and negative effects of Ca(2+) and the signaling events that perturb this balance. Overall, a "two-hit" hypothesis is developed, in which Ca(2+) plus another pathological stimulus can bring about mitochondrial dysfunction.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Peroxides produced by mitochondria can create nonenzymatic shunts in the TCA cycle (56, 121).”
From Mitochondrial reactive oxygen species production in excitable cells: Modulators of mitochondrial and cell function (2009) · cites this paper as [56]
In the citing paper
“In turn, an increased Ca 2ϩ load in the mitochondrial matrix has been linked to increased ROS production and increased permeability transition pore opening, leading to apoptosis (40,45).”
From Simvastatin Effects on Skeletal Muscle (2013) · cites this paper as [45]
Citations
Cites
Free radicals in biology and medicine
Gutteridge, J. M. C. (1991) · General Pharmacology The Vascular System · doi:10.1016/0306-3623(91)90478-o · Cited by 17,178
Free Radicals in the Physiological Control of Cell Function
Dröge, W. (2002) · Physiological Reviews · doi:10.1152/physrev.00018.2001 · Cited by 9,855
Green, D. R., & Reed, J. C. (1998) · Science · doi:10.1126/science.281.5381.1309 · Cited by 9,051
Induction of Apoptotic Program in Cell-Free Extracts: Requirement for dATP and Cytochrome c
Liu, X., Kim, C. N., Yang, J., Jemmerson, R., & Wang, X. (1996) · Cell · doi:10.1016/s0092-8674(00)80085-9 · Cited by 5,167
Mitochondrial formation of reactive oxygen species
Turrens, J. F. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.049478 · Cited by 5,084
Nitric oxide synthases: structure, function and inhibition
ALDERTON, W. K., COOPER, C. E., & KNOWLES, R. G. (2001) · Biochemical Journal · doi:10.1042/bj3570593 · Cited by 4,110
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
The mitochondrial permeability transition pore and its role in cell death
CROMPTON, M. (1999) · Biochemical Journal · doi:10.1042/bj3410233 · Cited by 2,432
Shimizu, S., Narita, M., Tsujimoto, Y., & Tsujimoto, Y. (1999) · Nature · doi:10.1038/20959 · Cited by 2,178
Nitric oxide mediates glutamate neurotoxicity in primary cortical cultures.
Dawson, V. L., Dawson, T. M., London, E. D., Bredt, D. S., & Snyder, S. H. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.14.6368 · Cited by 2,174
Flagged first, then by citations
Cited by
Sorted by citations
Items 501–600 of 1,005
Mitochondrial Ca2+ and ROS take center stage to orchestrate TNF-α–mediated inflammatory responses
Dada, L. A., & Sznajder, J. I. (2011) · Journal of Clinical Investigation · doi:10.1172/jci57748 · Cited by 81
Ascah, A., Khairallah, M., Daussin, F., Bourcier‐Lucas, C., Godin, R., Allen, B. G., Petrof, B. J., Rosiers, C. D., & Burelle, Y. (2010) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00522.2010 · Cited by 79
Presence of oxygen and mitochondria in skeletal muscle early postmortem
England, E. M., Matarneh, S. K., Mitacek, R. M., Abraham, A., Ramanathan, R., Wicks, J. C., Shi, H., Scheffler, T. L., Oliver, E. M., Helm, E. T., et al. (2018) · Meat Science · doi:10.1016/j.meatsci.2017.12.008 · Cited by 78
Yan, X., Zhang, Q., Ma, X., Zhong, Y., Tang, H., & Mai, S. (2023) · Japanese Dental Science Review · doi:10.1016/j.jdsr.2023.06.005 · Cited by 81
Kim, H. Y., Chung, J. M., & Chung, K. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.09.041 · Cited by 79
Zhang, J., Song, J. M., Wu, D., Wang, J., & Dong, W. (2015) · Medical Oncology · doi:10.1007/s12032-015-0516-z · Cited by 78
Mechanisms regulating cytochrome c release in pancreatic mitochondria
Odinokova, I. V., Sung, K.-F., Mareninova, O. A., Hermann, K., Evtodienko, Y. V., Andreyev, A. Y., Gukovsky, I., & Gukovskaya, A. S. (2008) · Gut · doi:10.1136/gut.2007.147207 · Cited by 79
Redox regulation: A new challenge for pharmacology
Frein, D., Schildknecht, S., Bachschmid, M. M., & Ullrich, V. (2005) · Biochemical Pharmacology · doi:10.1016/j.bcp.2005.04.012 · Cited by 78
Morris, G., Puri, B. K., Walder, K. R., Berk, M., Stubbs, B., Maes, M. H. J., & Carvalho, A. F. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1028-6 · Cited by 80
Mitochondria and sensory processing in inflammatory and neuropathic pain
Ribeiro, P. S. S., Willemen, H. L. D. M., & Eijkelkamp, N. (2022) · Frontiers in Pain Research · doi:10.3389/fpain.2022.1013577 · Cited by 88
Astrocytic Calcium Signaling: Mechanism and Implications for Functional Brain Imaging
Wang, X., Takano, T., & Nedergaard, M. (2008) · Methods in molecular biology · doi:10.1007/978-1-59745-543-5_5 · Cited by 78
Ye, J., Jiang, Z., Chen, X., Liu, M., Li, J., & Liu, N. (2015) · Experimental Cell Research · doi:10.1016/j.yexcr.2015.10.026 · Cited by 76
Lim, M. S., Lim, P. L. K., Gupta, R., & Boelsterli, U. A. (2006) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2006.09.012 · Cited by 77
Farfariello, V., Amantini, C., & Santoni, G. (2012) · Journal of Leukocyte Biology · doi:10.1189/jlb.0312123 · Cited by 78
Modes of Neuronal Calcium Entry and Homeostasis following Cerebral Ischemia
Cross, J. L., Meloni, B. P., Bakker, A. J., Lee, S., & Knuckey, N. (2010) · Stroke Research and Treatment · doi:10.4061/2010/316862 · Cited by 77
Chaiyarit, S., & Thongboonkerd, V. (2012) · Journal of Proteome Research · doi:10.1021/pr300018c · Cited by 78
Flahou, B., Haesebrouck, F., Chiers, K., Deun, K. V., Smet, L. D., Devreese, B. V., Vandenberghe, I. H. M., Favoreel, H. W., Smet, A., Pasmans, F., et al. (2011) · Cellular Microbiology · doi:10.1111/j.1462-5822.2011.01682.x · Cited by 76
Mitochondrial Ion Channels/Transporters as Sensors and Regulators of Cellular Redox Signaling
O‐Uchi, J., Ryu, S.-Y., Jhun, B. S., Hurst, S., & Sheu, S. (2013) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5681 · Cited by 76
Self-citationLu, Z., Zhang, C., Han, C., An, Q., Cheng, Y., Chen, Y., Meng, R., Zhang, Y., & Su, J. (2019) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.9b00121 · Cited by 76
Calcium regulation of T cell metabolism
Wang, Y., Tao, A. Y., Vaeth, M., & Feske, S. (2020) · Current Opinion in Physiology · doi:10.1016/j.cophys.2020.07.016 · Cited by 76
Concurrent diabetes and heart failure: interplay and novel therapeutic approaches
Karwi, Q. G., Ho, K. L., Pherwani, S., Ketema, E. B., Sun, Q., & Lopaschuk, G. D. (2021) · Cardiovascular Research · doi:10.1093/cvr/cvab120 · Cited by 80
Dey, K. K., Kumar, A., Shanker, R., Dhawan, A., Wan, M., Yadav, R. R., & Srivastava, A. K. (2011) · RSC Advances · doi:10.1039/c1ra00710f · Cited by 76
Increased mitochondrial Ca 2+ and decreased sarcoplasmic reticulum Ca 2+ in mitochondrial myopathy
Aydin, J., Andersson, D. C., Hänninen, S. L., Wredenberg, A., Tavi, P., Park, C. B., Larsson, N.-G., Bruton, J. D., & Westerblad, H. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddn355 · Cited by 75
Ayyappan, P., Vineetha, V. P., & Raghu, K. G. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096220 · Cited by 75
A chemical chaperone improves muscle function in mice with a RyR1 mutation
Lee, C. S., Hanna, A. D., Wang, H. J., Dagnino-Acosta, A., Joshi, A., Knoblauch, M. A., Xia, Y., Georgiou, D. K., Xu, J., Long, C., et al. (2017) · Nature Communications · doi:10.1038/ncomms14659 · Cited by 75
Inactivation of NUPR1 promotes cell death by coupling ER-stress responses with necrosis
Santofimia‐Castaño, P., Lan, W., Bintz, J., Gayet, O., Carrier, A., Lomberk, G. A., Neira, J. L., González, A., Urrutia, R. A., Soubeyran, P., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-35020-3 · Cited by 74
Mitochondrial Ca2+ Homeostasis: Emerging Roles and Clinical Significance in Cardiac Remodeling
Zhang, D., Wang, F., Li, P., & Gao, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23063025 · Cited by 81
Ma, T., Ding, Q., Liu, C., & Wu, H. K. (2023) · Stem Cell Research & Therapy · doi:10.1186/s13287-023-03303-w · Cited by 75
Suppression of KATP channel activity protects murine pancreatic β cells against oxidative stress
Gier, B., Krippeit‐Drews, P., Sheiko, T. V., Aguilar‐Bryan, L., Bryan, J., Düfer, M., & Drews, G. (2009) · Journal of Clinical Investigation · doi:10.1172/jci38817 · Cited by 76
Chojnacki, J. E., Liu, K., Yan, X., Toldo, S. A., Selden, T. M., Estrada, M., Rodríguez-Franco, M. I., Halquist, M. S., Ye, D., & Zhang, S. (2014) · ACS Chemical Neuroscience · doi:10.1021/cn500081s · Cited by 76
Watching the watcher: Regulation of p53 by mitochondria
Holley, A. K., & St Clair, D. K. (2009) · Future Oncology · doi:10.2217/14796694.5.1.117 · Cited by 75
Melatonin elevates apoptosis in human platelets via ROS mediated mitochondrial damage
Girish, K. S., Paul, M., Thushara, R. M., Hemshekhar, M., Sundaram, M. S., Rangappa, K. S., & Kemparaju, K. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.07.053 · Cited by 75
Nunn, A. V. W., Bell, J. D., & Guy, G. W. (2009) · Nutrition & Metabolism · doi:10.1186/1743-7075-6-16 · Cited by 77
Atypical pathways of NF-κB activation and aging
Kriete, A., & Mayo, K. L. (2009) · Experimental Gerontology · doi:10.1016/j.exger.2008.12.005 · Cited by 75
Control of innate and adaptive immunity by the inflammasome
Çıracı, C., Janczy, J. R., Sutterwala, F. S., & Cassel, S. L. (2012) · Microbes and Infection · doi:10.1016/j.micinf.2012.07.007 · Cited by 75
Infrared laser pulse triggers increased singlet oxygen production in tumour cells
Sokolovski, S. G., Zolotovskaya, S. A., Goltsov, A., Pourreyron, C., South, A. P., & Урихаевич, Р. Э. (2013) · Scientific Reports · doi:10.1038/srep03484 · Cited by 75
Heidari, R., Ghanbarinejad, V., Mohammadi, H., Ahmadi, A., Ommati, M. M., Abdoli, N., Aghaei, F., Esfandiari, A., Azarpira, N., & Niknahad, H. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2017.10.166 · Cited by 75
Mnatsakanyan, N., & Jonas, E. A. (2020) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2020.05.013 · Cited by 76
Lim, S., Lee, S., Seo, H., Ham, O., Lee, C., Park, J., Lee, J., Seung, M., Yun, I., Han, S. M., et al. (2014) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25016 · Cited by 77
Panagopoulos, D., Karabarbounis, A., Yakymenko, I., & Chrousos, G. (2021) · International Journal of Oncology · doi:10.3892/ijo.2021.5272 · Cited by 73
Lin, D., Huang, Y.-W., Ho, C., Hung, P., Hsu, M., Wang, T.-J., Wu, T., Lee, T., Huang, Z.-D., Chang, P.-C., et al. (2019) · Cells · doi:10.3390/cells8010065 · Cited by 74
Interactions of nanomaterials with ion channels and related mechanisms
Yin, S., Liu, J., Kang, Y., Lin, Y., Li, D., & Shao, L. (2019) · British Journal of Pharmacology · doi:10.1111/bph.14792 · Cited by 76
Saberi, M., Zhang, X., & Mobasheri, A. (2021) · GeroScience · doi:10.1007/s11357-021-00341-1 · Cited by 76
Bi, Y., Duan, W., Chen, J., You, T., Li, S., Jiang, W., Li, M., Wang, G., Pan, X., Wu, J., et al. (2021) · Advanced Functional Materials · doi:10.1002/adfm.202102912 · Cited by 74
Eike, L.-M., Yang, N., Rekdal, Ø., & Sveinbjørnsson, B. (2015) · Oncotarget · doi:10.18632/oncotarget.5308 · Cited by 77
Mitochondria Control Functional Ca V 1.2 Expression in Smooth Muscle Cells of Cerebral Arteries
Narayanan, D., Xi, Q., Pfeffer, L. M., & Jaggar, J. H. (2010) · Circulation Research · doi:10.1161/circresaha.110.224345 · Cited by 73
Kurochkin, I. O., Etzkorn, M., Buchwalter, D. B., Leamy, L. J., & Sokolova, I. M. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00279.2010 · Cited by 75
Specific surface area of titanium dioxide (TiO2) particles influences cyto- and photo-toxicity
Xiong, S., Tang, Y., Ng, H. S., Zhao, X., Jiang, Z., Chen, Z., Ng, K. W., & Loo, S. C. J. (2013) · Toxicology · doi:10.1016/j.tox.2012.12.015 · Cited by 75
Chen, N., Chiu, P. Y., & Ko, K. M. (2008) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.31.1387 · Cited by 73
Lin, M., Chen, S., Lu, Y.-C., Liang, R.-Y., Ho, Y.-T., Yang, C., & Chung, J. (2007) · PubMed · Cited by 73
Mitochondrial poly(ADP-ribose) polymerase: The Wizard of Oz at work
Brunyánszki, A., Szczęsny, B., Virág, L., & Szabó, C. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.02.024 · Cited by 73
Mitochondrial Ca2+-activated K+ channels and their role in cell life and death pathways
Krabbendam, I. E., Honrath, B., Culmsee, C., & Dolga, A. M. (2017) · Cell Calcium · doi:10.1016/j.ceca.2017.07.005 · Cited by 76
Ma, L., Liu, J., Dong, J., Xiao, Q., Zhao, J., & Jiang, F. (2017) · Toxicology Research · doi:10.1039/c7tx00204a · Cited by 73
Mitochondrial Dysfunction in Hepatitis C
Korenaga, M., Okuda, M., Otani, K., Wang, T., Li, Y., & Weinman, S. A. (2005) · Journal of Clinical Gastroenterology · doi:10.1097/01.mcg.0000155517.02468.46 · Cited by 73
Mitochondrial fragmentation enables localized signaling required for cell repair
Horn, A. J., Raavicharla, S., Shah, S., Cox, D., & Jaiswal, J. K. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.201909154 · Cited by 73
Sendtner, N., Seitz, R., Brandl, N., Müller, M., & Gülow, K. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262010240 · Cited by 81
Selenium and diabetes: an enigma?
Mueller, A. S., Mueller, K., Wolf, N. M., & Pallauf, J. (2009) · Free Radical Research · doi:10.1080/10715760903196925 · Cited by 74
Stanika, R. I., Winters, C. A., Pivovarova, N. B., & Andrews, S. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.10.020 · Cited by 72
Phosphorylated tau potentiates Aβ-induced mitochondrial damage in mature neurons
Quintanilla, R. A., Rommy von Bernhardi, M., Godoy, J. A., Inestrosa, N. C., & Johnson, G. V. W. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.08.016 · Cited by 70
In vivo cardioprotection by S-nitroso-2-mercaptopropionyl glycine
Nadtochiy, S. M., Burwell, L. S., Ingraham, C. A., Spencer, C. M., Friedman, A. E., Pinkert, C. A., & Brookes, P. S. (2009) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2009.01.012 · Cited by 74
Self-citationSmith, E. R., Holt, S. G., & Hewitson, T. D. (2017) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2017.09.009 · Cited by 75
Marcil, M., Bourduas, K., Ascah, A., & Burelle, Y. (2006) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00913.2005 · Cited by 71
Guo, S. J., Yang, C., Diao, B., Huang, X., Jin, M., Chen, L., Yan, W., Ning, Q., Zheng, L., Wu, Y., et al. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1005155 · Cited by 72
Yu, S., Zhang, L., Liu, C., Yang, J., Zhang, J., & Huang, L. J. (2019) · Experimental Cell Research · doi:10.1016/j.yexcr.2019.04.002 · Cited by 71
Michelucci, A., Chen, L., Protasi, F., & Dirksen, R. T. (2021) · Metabolites · doi:10.3390/metabo11070424 · Cited by 75
Mitochondrial Dynamics and Motility Inside Living Vascular Endothelial Cells: Role of Bioenergetics
Giedt, R. J., Pfeiffer, D. R., Anastasios Matzavinos, A., Kao, C., & Alevriadou, B. R. (2012) · Annals of Biomedical Engineering · doi:10.1007/s10439-012-0568-6 · Cited by 75
Ommati, M. M., Farshad, O., Niknahad, H., Arabnezhad, M., Azarpira, N., Mohammadi, H., Haghnegahdar, M., Mousavi, K., Akrami, S., Jamshidzadeh, A., et al. (2019) · Toxicology Letters · doi:10.1016/j.toxlet.2019.09.009 · Cited by 71
Min, H., Jang, H.-J., Park, K. H., Hyun, S. Y., Park, S. J., Kim, J. H., Son, J., Kang, S. S., & Lee, H. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-2041-z · Cited by 75
Soman, S. K., Bazała, M. A., Keatinge, M., Bandmann, O., & Kuźnicki, J. (2019) · Biology Open · doi:10.1242/bio.044347 · Cited by 72
Current Perspectives of Mitochondria in Sepsis-Induced Cardiomyopathy
Kuroshima, T., Kawaguchi, S., & Okada, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25094710 · Cited by 78
Martindale, J. J., & Metzger, J. M. (2013) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2013.12.008 · Cited by 69
Electron Transport Complex I Is Required for CD8+ T Cell Function
Yi, J. S., Holbrook, B. C., Michalek, R. D., Laniewski, N. G., & Grayson, J. M. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.2.852 · Cited by 69
Valente, M. J., Araújo, A. M., Silva, R., Bastos, M. D. L., Carvalho, F. D., de Pinho, P. G., & Carvalho, M. C. (2015) · Archives of Toxicology · doi:10.1007/s00204-015-1653-z · Cited by 70
Wang, W., Gong, G., Wang, X., Wei‐LaPierre, L., Cheng, H., Dirksen, R. T., & Sheu, S. (2016) · Antioxidants and Redox Signaling · doi:10.1089/ars.2016.6739 · Cited by 69
Self-citationNicolson, G. L., & Ash, M. E. (2017) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2017.04.013 · Cited by 75
Chen, L., Sun, Q., Zhou, D., Song, W., Yang, Q., Ju, B., Zhang, L., Xie, H., Zhou, L., Hu, Z., et al. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.09.020 · Cited by 70
Nguyen, E. K., Koval, O. M., Noble, P., Broadhurst, K., Allamargot, C., Wu, M., Strack, S., Thiel, W. H., & Grumbach, I. M. (2018) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.118.310951 · Cited by 70
He, Y., Gan, X., Zhang, L., Liu, B., Zhu, Z., Li, T., Zhu, J., Chen, J., & Yu, H. (2018) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00248.2017 · Cited by 70
Tian, J., Lu, Z., Wang, Y., Zhang, M., Wang, X., Tang, X., Peng, X., & Zeng, H. M. (2017) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2017.02.006 · Cited by 69
The Role and Study of Mitochondrial Impairment and Oxidative Stress in Cholestasis
Heidari, R., & Niknahad, H. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9420-5_8 · Cited by 69
Bathish, B., Robertson, H., Dillon, J. F., Dinkova‐Kostova, A. T., & Hayes, J. D. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.06.226 · Cited by 70
Advanced glycation end products (AGEs) activate mast cells
Sick, É., Brehin, S., André, P., Coupin, G., Landry, Y., Takeda, K., & Gies, J. (2010) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2010.00905.x · Cited by 70
Irigoín, F., Inada, N. M., Fernandes, M. P., Piacenza, L., Gadelha, F. R., Vercesi, A. E., & Radí, R. (2008) · Biochemical Journal · doi:10.1042/bj20081981 · Cited by 70
The role of protein O-linked β-N-acetylglucosamine in mediating cardiac stress responses
Chatham, J. C., & Marchase, R. B. (2009) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2009.07.004 · Cited by 69
Haynes, R. K., Cheu, K., Chan, H., Wong, H. N., Li, K., Tang, M. M., Chen, M., Guo, Z., Guo, Z., Sinniah, K., et al. (2012) · ChemMedChem · doi:10.1002/cmdc.201200383 · Cited by 69
Shi, J.-M., Bai, L., Zhang, D., Yiu, A., Yin, Z., Han, W., Liu, J.-S., Li, Y., Fu, D.-Y., & Ye, W. (2013) · Biochemical Pharmacology · doi:10.1016/j.bcp.2013.01.009 · Cited by 68
Mitochondrial Dysfunction in Kidney Disease and Uremic Sarcopenia
Takemura, K., Nishi, H., & Inagi, R. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.565023 · Cited by 68
A mitochondria-targeting near-infrared fluorescent probe for imaging hypochlorous acid in cells
Zheng, A., Liu, H., Peng, C., Gao, X., Xu, K., & Tang, B. (2021) · Talanta · doi:10.1016/j.talanta.2021.122152 · Cited by 68
Activation of an NLRP3 Inflammasome Restricts Mycobacterium kansasii Infection
Chen, C.-C., Tsai, S.-H., Lu, C., Hu, S.-T., Wu, T., Huang, T., Sadier, N. S., Ojcius, D. M., & Lai, H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036292 · Cited by 70
Calcium and Reactive Oxygen Species in Acute Pancreatitis: Friend or Foe?
Booth, D. M., Mukherjee, R., Sutton, R., & Criddle, D. N. (2011) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.3983 · Cited by 69
HCV infection induces mitochondrial bioenergetic unbalance: Causes and effects
Piccoli, C., Quarato, G., Ripoli, M. C., D’Aprile, A., Scrima, R., Cela, O., Boffoli, D., Moradpour, D., & Capitanio, N. (2008) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2008.11.008 · Cited by 68
Alcohol Induced Mitochondrial Oxidative Stress and Alveolar Macrophage Dysfunction
Liang, Y., Harris, F. L., & Brown, L. A. S. (2014) · BioMed Research International · doi:10.1155/2014/371593 · Cited by 67
Chen, C.-N., Huang, H.-H., Wu, C.-L., Lin, C. P. C., Hsu, J. T.-A., Hsieh, H., Chuang, S., & Lai, G. (2006) · Cancer Letters · doi:10.1016/j.canlet.2006.03.004 · Cited by 68
Pathak, T., Guéguinou, M., Walter, V., Delierneux, C., Johnson, M. T., Zhang, X., Xin, P., Yoast, R. E., Emrich, S. M., Yochum, G. S., et al. (2020) · eLife · doi:10.7554/elife.59686 · Cited by 72
Ca2+ Dysregulation Induces Mitochondrial Depolarization and Apoptosis
Miyamoto, S., Howes, A. L., Adams, J. W., Dorn, G. W., & Brown, J. H. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m505223200 · Cited by 70
Wang, H., Zhao, P., Huang, Q., Chi, Y., Dong, S., & Fan, J. (2019) · Chemosphere · doi:10.1016/j.chemosphere.2019.04.099 · Cited by 69
Márta, K., Hasan, P., Rodríguez-Prados, M., Paillard, M., & Hajnóczky, G. (2020) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2020.09.014 · Cited by 68
Effect of solanine on the membrane potential of mitochondria in HepG2cells and [Ca2+]iin the cells
Gao, S. (2006) · World Journal of Gastroenterology · doi:10.3748/wjg.v12.i21.3359 · Cited by 67
Khalek, W. A., Cortade, F., Ollendorff, V., Lapasset, L., Tintignac, L. A. J., Chabi, B., & Wrutniak‐Cabello, C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0114388 · Cited by 69
Oxygen sensors in hypoxic pulmonary vasoconstriction
Weißmann, N., Sommer, N., SCHERMULY, R. T., Ghofrani, H. A., Seeger, W., & Grimminger, F. (2006) · Cardiovascular Research · doi:10.1016/j.cardiores.2006.04.009 · Cited by 67
Metadata
- Authors
- Brookes, P. S., Yoon, Y., Robotham, J. L., Anders, M. W., & Sheu, S.-S.
- Affiliations
- University of Rochester Medicine (US)
- Venue
- American Journal of Physiology-Cell Physiology
- Publisher
- American Physiological Society
- Published
- 2004-10
- Volume
- 287
- Issue
- 4
- Pages
- C817-C833
- ISSN
- 0363-6143 (ISSN-L)
- 1522-1563
- OpenAlex
- W2068048197
- Cited by
- 2,575
- References
- 227
- Citations by year
- 2026: 72 · 2025: 112 · 2024: 126 · 2023: 138 · 2022: 144 · 2021: 177 · 2020: 162 · 2019: 134 · 2018: 125 · 2017: 125 · 2016: 122 · 2015: 125 · 2014: 124 · 2013: 129 · 2012: 124
- FWCI
- 5.61
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Physiology-Cell Physiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Medical Center, University of Rochester
- National Heart, Lung, and Blood Institute (HL 33333, R01HL033333, HL-71158-01, R01HL071158)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK-061991, R01DK061991)
- National Institute of Neurological Disorders and Stroke (NS-37710, R01NS037710)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Keywords
- mitochondrial calcium homeostasis, ATP production, reactive oxygen species, mitochondrial dysfunction, mitochondrial permeability transition pore, cytochrome c release, apoptosis, two-hit hypothesis, mitochondrial bioenergetics, calcium signaling
- MeSH terms
- Adenosine Triphosphate, Calcium, Energy Metabolism, Ion Channels, Mitochondria, Signal Transduction, Reactive Oxygen Species
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