The DOI matches its Crossref record; 175 of the 180 references it cites were found in a registry or an index.
Calcium and ROS: A mutual interplay
Open accessAbstract
Calcium is an important second messenger involved in intra- and extracellular signaling cascades and plays an essential role in cell life and death decisions. The Ca(2+) signaling network works in many different ways to regulate cellular processes that function over a wide dynamic range due to the action of buffers, pumps and exchangers on the plasma membrane as well as in internal stores. Calcium signaling pathways interact with other cellular signaling systems such as reactive oxygen species (ROS). Although initially considered to be potentially detrimental byproducts of aerobic metabolism, it is now clear that ROS generated in sub-toxic levels by different intracellular systems act as signaling molecules involved in various cellular processes including growth and cell death. Increasing evidence suggests a mutual interplay between calcium and ROS signaling systems which seems to have important implications for fine tuning cellular signaling networks. However, dysfunction in either of the systems might affect the other system thus potentiating harmful effects which might contribute to the pathogenesis of various disorders.
Overview
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
“However, sustained elevation in the cellular calcium signal stimulates higher mitochondrial reactive oxygen species (ROS) generation (28) due to enhanced electron flow through respiratory chain and subsequent inhibition of complexes I and III of ubiquinone (Q) cycle.”
From Mechanistic inferences on metabolic dysfunction in posttraumatic stress disorder from an integrated model and multiomic analysis: role of glucocorticoid receptor sensitivity (2019) · cites this paper as [28]
Experimental — accuracy not yet measured
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
Down-Regulation of Na+/K+ATPase Activity by Human Parvovirus B19 Capsid Protein VP1
Almilaji, A., Szteyn, K., Fein, E., Pakladok, T., Muñoz, C., Elvira, B., Towhid, S. T., Alesutan, I., Shumilina, E. V., Bock, C. –., et al. (2013) · Cellular Physiology and Biochemistry · doi:10.1159/000350083 · Cited by 8,700
How mitochondria produce reactive oxygen species
Murphy, M. P. (2009) · Biochemical Journal · doi:10.1042/bj20081386 · Cited by 8,207
The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
Bedard, K., & Krause, K.-H. (2007) · Physiological Reviews · doi:10.1152/physrev.00044.2005 · Cited by 6,989
Oxidants, antioxidants, and the degenerative diseases of aging.
Ames, B. N., Shigenaga, M. K., & Hagen, T. M. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.17.7915 · Cited by 5,958
Mitochondrial formation of reactive oxygen species
Turrens, J. F. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.049478 · Cited by 5,084
Meijer, L., Nelson, D. J., Riazanski, V., Gabdoulkhakova, A. G., Héry-Arnaud, G., Berre, R. L., Loaëc, N., Oumata, N., Galons, H., Nowak, E., et al. (2016) · Journal of Innate Immunity · doi:10.1159/000444256 · Cited by 5,008
Regulation of cell death: the calcium–apoptosis link
Orrenius, S., Zhivotovsky, B., & Nicotera, P. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1150 · Cited by 3,060
Physiological Roles of Mitochondrial Reactive Oxygen Species
Sena, L. A., & Chandel, N. S. (2012) · Molecular Cell · doi:10.1016/j.molcel.2012.09.025 · Cited by 2,632
Calcium, ATP, and ROS: a mitochondrial love-hate triangle
Brookes, P. S., Yoon, Y., Robotham, J. L., Anders, M. W., & Sheu, S.-S. (2004) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00139.2004 · Cited by 2,575
Cellular response to oxidative stress: Signaling for suicide and survival*
Martindale, J. L., & Holbrook, N. J. (2002) · Journal of Cellular Physiology · doi:10.1002/jcp.10119 · Cited by 2,314
Flagged first, then by citations
5 of the 180 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 101–200 of 999
SOD1 in ALS: Taking Stock in Pathogenic Mechanisms and the Role of Glial and Muscle Cells
Peggion, C., Scalcon, V., Massimino, M. L., Nies, K., Lopreiato, R., Rigobello, M. P., & Bertoli, A. (2022) · Antioxidants · doi:10.3390/antiox11040614 · Cited by 106
Nanoenabled Intracellular Metal Ion Homeostasis Regulation for Tumor Therapy
Xu, L., Peng, M., Gao, T., Wang, D., Lian, X., Sun, H., Shi, J., Wang, Y., & Wang, P. (2023) · Advanced Science · doi:10.1002/advs.202306203 · Cited by 98
Oxidative stress and proteasome inhibitors in multiple myeloma
Lipchick, B. C., Fink, E. E., & Nikiforov, M. A. (2016) · Pharmacological Research · doi:10.1016/j.phrs.2016.01.029 · Cited by 95
Sánchez-Cano, C., Romero‐Canelón, I., Yang, Y., Hands-Portman, I., Bohic, S., Cloetens, P., & Sadler, P. J. (2016) · Chemistry - A European Journal · doi:10.1002/chem.201605911 · Cited by 94
Yuan, R., Huang, L., Du, L., Feng, J., Li, J., Luo, Y., Xu, Q., Yang, S., Gao, H., & Feng, Y. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.02.017 · Cited by 95
Atrial fibrosis underlying atrial fibrillation (Review)
Li, C., Zhang, J., Hu, W., & Li, S. (2020) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2020.4842 · Cited by 98
Soglia, F., Petracci, M., Davoli, R., & Zappaterra, M. (2021) · Poultry Science · doi:10.1016/j.psj.2021.101180 · Cited by 96
Cellular mechanisms and signals that coordinate plasma membrane repair
Horn, A. J., & Jaiswal, J. K. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2888-7 · Cited by 96
Ablation of the stress protease OMA1 protects against heart failure in mice
Acín‐Pérez, R., Lechuga‐Vieco, A. V., Muñoz, M. D. M., Nieto-Arellano, R., Torroja, C., Sánchez‐Cabo, F., Jiménez, C., González-Guerra, A., Carrascoso, I., Benincá, C., et al. (2018) · Science Translational Medicine · doi:10.1126/scitranslmed.aan4935 · Cited by 91
Zhou, W., Qu, J., Xie, S.-Y., Sun, Y., & Yao, H.-W. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/5188306 · Cited by 97
Wang, Q., & Zennadi, R. (2021) · Antioxidants · doi:10.3390/antiox10101608 · Cited by 105
Andreadou, I., Schulz, R., Papapetropoulos, A., Turan, B., Ytrehus, K., Ferdinandy, P., Daiber, A., & Lisa, F. D. (2020) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.15279 · Cited by 92
Lee, J., & Song, C. (2021) · Antioxidants · doi:10.3390/antiox10060872 · Cited by 91
Mitochondrial Reactive Oxygen Species in Infection and Immunity
Mukherjee, A., Ghosh, K. K., Chakrabortty, S., Gulyás, B. Z., Padmanabhan, P., & Ball, W. B. (2024) · Biomolecules · doi:10.3390/biom14060670 · Cited by 99
Calcium Signaling During Meiotic Cell Cycle Regulation and Apoptosis in Mammalian Oocytes
Tiwari, M., Prasad, S., Shrivastav, T. G., & Chaube, S. K. (2016) · Journal of Cellular Physiology · doi:10.1002/jcp.25670 · Cited by 86
Gay, N. H., Phopin, K., Suwanjang, W., Songtawee, N., Ruankham, W., Wongchitrat, P., Prachayasittikul, S., & Prachayasittikul, V. (2018) · Neurochemical Research · doi:10.1007/s11064-017-2463-x · Cited by 88
Calcium Signaling in Liver Injury and Regeneration
Oliva‐Vilarnau, N., Hankeová, S., Vorrink, S. U., Mkrtchian, S., Andersson, E. R., & Lauschke, V. M. (2018) · Frontiers in Medicine · doi:10.3389/fmed.2018.00192 · Cited by 85
The calcium–iron connection in ferroptosis-mediated neuronal death
Gleitze, S., Paula-Lima, A. C., Núñez, M. T., & Hidalgo, C. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.08.231 · Cited by 84
Crosstalk between inflammatory mediators and endoplasmic reticulum stress in liver diseases.
Duvigneau, J., Luís, A., Gorman, A. M., Samali, A., Kaltenecker, D., Moriggl, R., & Kozlov, A. (2019) · Cytokine · doi:10.1016/j.cyto.2018.10.018 · Cited by 83
Nanomedicine‐Enabled/Augmented Cell Pyroptosis for Efficient Tumor Nanotherapy
Zhang, Z., Zhou, Y., Zhao, S., Ding, L., Chen, B., & Chen, Y. (2022) · Advanced Science · doi:10.1002/advs.202203583 · Cited by 84
Song, M., & Cubillos‐Ruiz, J. R. (2019) · Trends in Immunology · doi:10.1016/j.it.2018.12.001 · Cited by 82
Reactive Oxygen Species and Endothelial Ca2+ Signaling: Brothers in Arms or Partners in Crime?
Negri, S., Faris, P. S., & Moccia, F. D. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22189821 · Cited by 90
Organophosphorus Pesticides as Modulating Substances of Inflammation through the Cholinergic Pathway
Camacho-Pérez, M. R., Covantes‐Rosales, C. E., Toledo‐Ibarra, G. A., Mercado‐Salgado, U., Ponce-Regalado, M. D., Díaz‐Reséndiz, K. J. G., & Girón‐Pérez, M. I. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094523 · Cited by 88
Dufor, T., Grehl, S., Tang, A. D., Doulazmi, M., Traoré, M., Debray, N., Dubacq, C., Deng, Z., Mariani, J., Lohof, A. M., et al. (2019) · Science Advances · doi:10.1126/sciadv.aav9847 · Cited by 80
Noxious Iron–Calcium Connections in Neurodegeneration
Núñez, M., & Hidalgo, C. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00048 · Cited by 71
Intracellular Ca2 + Imbalance Critically Contributes to Paraptosis
Kim, E., Lee, D. M., Seo, M. J., Lee, H. J., & Choi, K. S. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.607844 · Cited by 80
Honey-Mediated Wound Healing: H2O2 Entry through AQP3 Determines Extracellular Ca2+ Influx
Martinotti, S., Laforenza, U., Patrone, M., Moccia, F. D., & Ranzato, E. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20030764 · Cited by 78
Wang, Q., Huang, L., & Yue, J. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2016.12.014 · Cited by 77
Cerebral Vascular Toxicity of Antiretroviral Therapy
Bertrand, L., Velichkovska, M., & Toborek, M. J. (2019) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-019-09858-x · Cited by 81
Molecular Mechanisms of Anticancer Activities of Puerarin
Ahmad, B., Khan, S., Liu, Y., Xue, M., Nabi, G., Kumar, S., Alshwmi, M., & Qarluq, A. W. (2020) · Cancer Management and Research · doi:10.2147/cmar.s233567 · Cited by 76
Mitochondrial dysfunction as a critical event in the pathophysiology of bipolar disorder
Scaini, G., Andrews, T., Lima, C. N. D. C., Benevenuto, D., STRECK, E. L., & Quevedo, J. (2020) · Mitochondrion · doi:10.1016/j.mito.2020.12.002 · Cited by 77
Li, X., Fang, P., Yang, W. Y., Chan, K., Lavallee, M., Xu, K., Gao, T., Wang, H., & Yang, X. (2016) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2016-0515 · Cited by 78
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
Subversion of host genome integrity by bacterial pathogens
Chumduri, C., Gurumurthy, R. K., Zietlow, R., & Meyer, T. F. (2016) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2016.100 · Cited by 81
The nuclear receptor RXRA controls cellular senescence by regulating calcium signaling
Ma, X., Warnier, M., Raynard, C., Ferrand, M., Kirsh, O., Defossez, P., Martin, N., & Bernard, D. (2018) · Aging Cell · doi:10.1111/acel.12831 · Cited by 82
Axonal degeneration induced by glutamate excitotoxicity is mediated by necroptosis
Hernández, D. E., Salvadores, N., Moya‐Alvarado, G., Catalán, R. J., Bronfman, F. C., & Court, F. A. (2018) · Journal of Cell Science · doi:10.1242/jcs.214684 · Cited by 75
Interplay of oxidative stress and antioxidant mechanisms in cancer development and progression
Jomová, K., Alomar, S. Y., Valko, R., Fresser, L., Nepovimová, E., Kuča, K., & Valko, M. (2025) · Archives of Toxicology · doi:10.1007/s00204-025-04146-5 · Cited by 103
Sonnay, S., Gruetter, R., & Duarte, J. M. N. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00288 · Cited by 74
Yap, J. L. Y., Tai, Y. K., Fröhlich, J., Fong, C. H. H., Yin, J. N., Foo, Z. L., Ramanan, S., Beyer, C., Toh, S. J., Casarosa, M., et al. (2019) · The FASEB Journal · doi:10.1096/fj.201900057r · Cited by 74
Lephatsi, M. M., Meyer, V., Piater, L. A., Dubery, I. A., & Tugizimana, F. (2021) · Metabolites · doi:10.3390/metabo11070457 · Cited by 74
Chen, X., Hocher, C., Shen, L., Krämer, B. K., & Hocher, B. (2023) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00177.2023 · Cited by 79
Genotoxic and neurotoxic potential of intracellular nanoplastics: A review
Casella, C., & Ballaz, S. (2024) · Journal of Applied Toxicology · doi:10.1002/jat.4598 · Cited by 77
The potential role of tubeimosides in cancer prevention and treatment
Islam, M. S., Wang, C., Zheng, J., Paudyal, N., Zhu, Y., & Sun, H. (2018) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2018.11.001 · Cited by 74
Low serum calcium and phosphorus and their clinical performance in detecting COVID‐19 patients
Yang, C., Ma, X., Wu, J., Han, J., Zheng, Z., Duan, H., Liu, Q., Wu, C., Dong, Y., & Dong, L. (2020) · Journal of Medical Virology · doi:10.1002/jmv.26515 · Cited by 73
Panagopoulos, D., Karabarbounis, A., Yakymenko, I., & Chrousos, G. (2021) · International Journal of Oncology · doi:10.3892/ijo.2021.5272 · Cited by 73
Diabetic Cardiomyopathy: An Immunometabolic Perspective
Mishra, P. K., Ying, W., Nandi, S. S., Bandyopadhyay, G. K., Patel, K. P., & Mahata, S. K. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00072 · Cited by 74
Vendrov, A. E., Stevenson, M., Alahari, S., Pan, H., Wickline, S. A., Madamanchi, N. R., & Runge, M. S. (2017) · Journal of the American Heart Association · doi:10.1161/jaha.117.006775 · Cited by 73
Abdallah, N. H., Baulies, A., Bouhlel, A., Béjaoui, M., Zaoualí, M. A., Mimouna, S. B., Messaoudi, I., Fernández-Checa, J. C., Ruiz, C. G., & Abdennebi, H. B. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.26747 · Cited by 73
Amaroli, A., Ferrando, S., & Benedicenti, S. (2018) · Photochemistry and Photobiology · doi:10.1111/php.13032 · Cited by 73
Zaibi, N., Li, P.-Y., & Xu, S.-Z. (2021) · PLoS ONE · doi:10.1371/journal.pone.0247234 · Cited by 66
Connecting Dots between Mitochondrial Dysfunction and Depression
Khan, M., Baussan, Y., & Hébert-Chatelain, É. (2023) · Biomolecules · doi:10.3390/biom13040695 · Cited by 77
Chang, J.-C., Lien, C., Lee, W., Chang, H.-R., Hsu, Y., Luo, Y., Jeng, J., Hsieh, J., & Yang, K. (2019) · Cells · doi:10.3390/cells8060564 · Cited by 70
Cellular calcium and redox regulation: the mediator of vertebrate environmental sex determination?
Castelli, M. A., Whiteley, S. L., Georges, A., & Holleley, C. E. (2020) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12582 · Cited by 75
Pathological and Inflammatory Consequences of Aging
García‐Domínguez, M. (2025) · Biomolecules · doi:10.3390/biom15030404 · Cited by 78
Choi, H., Kim, H. J., Kim, J., Kim, S., Yang, J., Lee, W., Park, Y., Hyeon, S. J., Lee, D.-S., Ryu, H., et al. (2017) · Molecular Neurodegeneration · doi:10.1186/s13024-017-0164-1 · 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
A Neurotoxic Ménage-à-trois: Glutamate, Calcium, and Zinc in the Excitotoxic Cascade
Granzotto, A., Canzoniero, L. M. T., & Sensi, S. L. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.600089 · Cited by 67
Luo, S., Zhang, C., Xiong, W., Song, Y., Wang, Q., Zhang, H., Guo, S., Yang, S., & Liu, H. (2024) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2024.06.009 · Cited by 75
Oxidative Stress and Redox Signaling in the Pathophysiology of Liver Diseases
Mooli, R. G. R., Mukhi, D., & Ramakrishnan, S. K. (2022) · Comprehensive physiology · doi:10.1002/cphy.c200021 · Cited by 134
Reactive Oxygen Species in intestinal stem cell metabolism, fate and function
Morris, O., & Jasper, H. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.02.015 · Cited by 70
Thoudam, T., Chanda, D., Lee, J. Y., Jung, M., Sinam, I. S., Kim, B., Park, B.-Y., Kwon, W. H., Kim, H., Kim, M., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-37214-4 · Cited by 74
Yang, Y.-C., Chien, Y., Yarmishyn, A. A., Lim, L.-Y., Tsai, H.-Y., Kuo, W., Tsai, P., Yang, S.-H., Hong, S.-I., Chen, S., et al. (2023) · Journal of Advanced Research · doi:10.1016/j.jare.2023.06.004 · Cited by 70
Mitochondria in Neurogenesis: Implications for Mitochondrial Diseases
Brunetti, D., Dykstra, W., Le, S., Zink, A., & Prigione, A. (2021) · Stem Cells · doi:10.1002/stem.3425 · Cited by 67
Madireddy, S., & Madireddy, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031844 · Cited by 76
STING Suppresses Mitochondrial VDAC2 to Govern RCC Growth Independent of Innate Immunity
Zhu, Z., Zhou, X., Du, H., Cloer, E. W., Zhang, J., Liu, M., Wang, Y., Tan, X. M., Hepperla, A. J., Simon, J. M., et al. (2022) · Advanced Science · doi:10.1002/advs.202203718 · Cited by 71
Recent Advances and Future Directions in Sonodynamic Therapy for Cancer Treatment
Datta, P., Moolayadukkam, S., Chowdhury, D., Rayes, A., Lee, N. S., Sahu, R. P., Zhou, Q., & Puri, I. K. (2024) · BME Frontiers · doi:10.34133/bmef.0080 · Cited by 69
Alkhalifa, A. E., Alkhalifa, O., Durdanovic, I., Ibrahim, D. R., & Maragkou, S. (2025) · Journal of Dementia and Alzheimer's Disease · doi:10.3390/jdad2020017 · Cited by 66
Bae, H., Lee, J., Yang, C., Song, G., & Lim, W. (2020) · Marine Drugs · doi:10.3390/md18010045 · Cited by 66
The role of NADPH oxidases in neuronal development
Terzi, A., & Suter, D. M. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.04.027 · Cited by 68
Cardioprotection from stress conditions by weak magnetic fields in the Schumann Resonance band
Elhalel, G., Price, C., Fixler, D., & Shainberg, A. (2019) · Scientific Reports · doi:10.1038/s41598-018-36341-z · Cited by 64
Mambro, T. D., Pellielo, G., Agyapong, E. D., Carinci, M., Chianese, D., Giorgi, C., Morciano, G., Patergnani, S., Pinton, P., & Rimessi, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24098181 · Cited by 68
Biomaterials-mediated targeted therapeutics of myocardial ischemia-reperfusion injury
Luo, Q., Sun, W., Li, Z., Sun, J., Xiao, Y., Zhang, J., Zhu, C., Liu, B., & Ding, J. (2023) · Biomaterials · doi:10.1016/j.biomaterials.2023.122368 · Cited by 67
Vitamin D deficiency induces the excitation/inhibition brain imbalance and the proinflammatory shift
Kasatkina, L. A., Tarasenko, A. S., Krupko, O., Kuchmerovska, T. M., Lisakovska, O., & Trikash, I. O. (2019) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2019.105665 · Cited by 65
González-Pleiter, M., Rioboo, C., Reguera, M., Abreu, I., Leganés, F., Cid, Á., & Fernández‐Piñas, F. (2017) · Aquatic Toxicology · doi:10.1016/j.aquatox.2017.02.021 · Cited by 64
Hao, X., Wang, B., Wang, L., Zeng, J., Yang, Y., & Wang, X. (2018) · Scientia Horticulturae · doi:10.1016/j.scienta.2018.06.008 · Cited by 64
Guo, Z., Gao, X., Lu, J., Li, Y., Jin, Z., Fahad, A., Pambe, N. U., Ejima, H., Sun, X., Wang, X., et al. (2024) · ACS Nano · doi:10.1021/acsnano.3c10173 · Cited by 65
Sun, Q., Liu, B., Zhao, R., Feng, L., Wang, Z., Dong, S., Dong, Y., Gai, S., Ding, H., & Yang, P. (2021) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.1c13304 · Cited by 63
Protective Effect of Natural Antioxidants on Reducing Cisplatin-Induced Nephrotoxicity
Zhou, J., Nie, R., Yin, Y., Cai, X., Xie, D., & Cai, M. (2022) · Disease Markers · doi:10.1155/2022/1612348 · Cited by 63
Zhang, H., Feng, Y., Si, Y., Lu, C., Wang, J., Wang, S., Li, L., Xie, W., Yue, Z., Jia, Y., et al. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102983 · Cited by 63
Major Oxidative and Antioxidant Mechanisms During Heat Stress-Induced Oxidative Stress in Chickens
Aryal, B., Kwakye, J., Ariyo, O. W., Ghareeb, A. F. A., Milfort, M. C., Fuller, A. L., Khatiwada, S., Rekaya, R., & Aggrey, S. E. (2025) · Antioxidants · doi:10.3390/antiox14040471 · Cited by 85
Therapeutic Effects of Cold Atmospheric Plasma on Solid Tumor
Min, T., Xie, X., Ren, K., Sun, T., Wang, H., Dang, C., & Zhang, H. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.884887 · Cited by 75
Signaling pathways in cutaneous wound healing
Križanová, O., Penesová, A., Sokol, J., Hokynková, A., Samadian, A., & Babula, P. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.1030851 · Cited by 66
Golovynska, I., Golovynskyi, S., Stepanov, Y. V., Stepanova, L. I., Qu, J., & Ohulchanskyy, T. Y. (2020) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2020.112088 · Cited by 62
Martínez‐Klimova, E., Aparicio‐Trejo, O. E., Gómez‐Sierra, T., Jiménez‐Uribe, A. P., Bellido, B., & Pedraza‐Chaverrí, J. (2020) · BioFactors · doi:10.1002/biof.1673 · Cited by 62
Lee, H., & José, P. A. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.670076 · Cited by 68
Nezhad‐Mokhtari, P., Javanbakht, S., Asadi, N., Ghorbani, M., Milani, M., Hanifehpour, Y., Gholizadeh, P., & Akbarzadeh, A. (2021) · Journal of Drug Delivery Science and Technology · doi:10.1016/j.jddst.2021.102789 · Cited by 61
Vascular calcium signalling and ageing
Harraz, O. F., & Jensen, L. J. (2021) · The Journal of Physiology · doi:10.1113/jp280950 · Cited by 62
Apoptosis and eryptosis: similarities and differences
Tkachenko, A. S. (2023) · APOPTOSIS · doi:10.1007/s10495-023-01915-4 · Cited by 66
Dietary magnesium supplementation improves lifespan in a mouse model of progeria
Villa‐Bellosta, R. (2020) · EMBO Molecular Medicine · doi:10.15252/emmm.202012423 · Cited by 65
Yang, C., Zhu, Z., Tong, B. C., Iyaswamy, A., Xie, W.-J., Zhu, Y., Sreenivasmurthy, S. G., Krishnamoorthi, S., Cheung, K., Song, J., et al. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101445 · Cited by 60
Endothelial dysfunction: mechanisms and contribution to diseases
Ajoolabady, A., Praticò, D., & Ren, J. T. (2024) · Acta Pharmacologica Sinica · doi:10.1038/s41401-024-01295-8 · Cited by 65
Linking mitochondrial dysfunction to neurodegeneration in lysosomal storage diseases
Saffari, A., Kölker, S., Hoffmann, G. F., & Ebrahimi‐Fakhari, D. (2017) · Journal of Inherited Metabolic Disease · doi:10.1007/s10545-017-0048-0 · Cited by 62
Cold atmospheric plasma causes a calcium influx in melanoma cells triggering CAP-induced senescence
Schneider, C., Gebhardt, L., Arndt, S., Karrer, S., Zimmermann, J. L., Fischer, M. J. M., & Bosserhoff, A. (2018) · Scientific Reports · doi:10.1038/s41598-018-28443-5 · Cited by 64
Shedding a New Light on Skin Aging, Iron- and Redox-Homeostasis and Emerging Natural Antioxidants
Pourzand, C., Albieri, A., & Raczek, N. N. (2022) · Antioxidants · doi:10.3390/antiox11030471 · Cited by 68
Anfray, A., Schaeffer, S., Hattori, Y., Santisteban, M. M., Casey, N., Wang, G., Strickland, M., Zhou, P., Holtzman, D. M., Anrather, J., et al. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01757-6 · Cited by 53
Gu, J., Dai, S., Liu, Y., Liu, H., Zhang, Y., Ji, X., Yu, F., Zhou, Y., Chen, L., Tse, W. K. F., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-19327-9 · Cited by 59
Role of GPCR signaling and calcium dysregulation in Alzheimer's disease
Sushma, & Mondal, A. C. (2019) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2019.103414 · Cited by 56
Hoorelbeke, D., Decrock, E., Smet, M. A. J. D., Bock, M. D., Descamps, B., Haver, V. V., Delvaeye, T., Krysko, D. V., Vanhove, C., Bultynck, G., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2392-5 · Cited by 59
Daiber, A., Steven, S., Vujačić-Mirski, K., Kalinovic, S., Oelze, M. W., Lisa, F. D., & Münzel, T. F. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103405 · Cited by 59
Özşen, N. K., Yılmaz, B., Alkım, C., Arslan, M., Topaloğlu, A., Kısakesen, H. İ., Gülsev, E., & Çakar, Z. P. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.822864 · Cited by 63
Metadata
- Authors
- Görlach, A., Bertram, K., Hudecova, S., & Krizanova, O.
- Affiliations
- German Centre for Cardiovascular Research (DE)
- Deutsches Herzzentrum München (DE)
- Corresponding author
- Görlach, Agnes
- ORCID
- Görlach, Agnes
- Venue
- Redox Biology
- Publisher
- Elsevier BV
- Published
- 2015-12
- Volume
- 6
- Pages
- 260-271
- ISSN
- 2213-2317 (ISSN-L)
- PMC
- PMC4556774
- OpenAlex
- W1165140024
- Cited by
- 1,546
- References
- 180
- Citations by year
- 2026: 128 · 2025: 188 · 2024: 195 · 2023: 184 · 2022: 177 · 2021: 179 · 2020: 141 · 2019: 133 · 2018: 115 · 2017: 72 · 2016: 30 · 2015: 3
- FWCI
- 7.11
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Redox Biology (publishedVersion, cc-by-nc-nd)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- mediaTUM (Technical University of Munich) (submittedVersion)
- Funders
- Bundesministerium für Bildung und Forschung (SAV 2/0074)
- Deutsches Zentrum für Herz-Kreislaufforschung
- Deutsche Forschungsgemeinschaft (DFG-GO709/4-5)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
- Life Sciences › Neuroscience › Sensory Systems › Ion Channels and Receptors
- Keywords
- calcium signaling, reactive oxygen species, second messengers, cell death, cell signaling networks, redox signaling, intracellular calcium stores
- MeSH terms
- Animals, Calcium, Cell Membrane, Endoplasmic Reticulum, Eukaryotic Cells, Gene Expression Regulation, Humans, Mitochondria, Calcium Channels, Cell Death, Reactive Oxygen Species, Oxidative Stress, NADPH Oxidases, Calcium Signaling, Plasma Membrane Calcium-Transporting ATPases
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
