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Calcium and ROS: A mutual interplay
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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.
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“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]
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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
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Items 301–400 of 999
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Staehlke, S., Bielfeldt, M., Zimmermann, J., Gruening, M., Barke, I., Freitag, T., Speller, S., van Rienen, U., & Nebe, B. J. (2022) · Cells · doi:10.3390/cells11172650 · Cited by 41
Bergamini, C., Leoni, I., Rizzardi, N., Melli, M., Galvani, G., Coadǎ, C. A., Giovannini, C., Monti, E., Liparulo, I., Valenti, F., et al. (2023) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-023-02718-w · Cited by 42
Chibani, K., Gherli, H., & Fan, M. (2025) · Frontiers in Plant Science · doi:10.3389/fpls.2025.1554281 · Cited by 46
SMYD2 glutathionylation contributes to degradation of sarcomeric proteins
Godage, D. N. P. M., VanHecke, G. C., Samarasinghe, K. T. G., Feng, H., Hiske, M. A., Holcomb, J., Yang, Z., Jin, J., Chung, C. S., & Ahn, Y. (2018) · Nature Communications · doi:10.1038/s41467-018-06786-x · Cited by 40
Shi, Y., Sun, H., Wang, X., Jin, W., Qianyi, C., Yuan, Z., & Yu, H. (2019) · PLoS ONE · doi:10.1371/journal.pone.0217204 · Cited by 41
Welcome, M. O. (2020) · PharmaNutrition · doi:10.1016/j.phanu.2020.100176 · Cited by 41
Zhang, X., Wang, Y., Chen, M., & Zeng, M. (2020) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2020.111391 · Cited by 41
Guo, Q., Bi, J., Wang, H., & Zhang, X. (2020) · Emerging Microbes & Infections · doi:10.1080/22221751.2020.1861913 · Cited by 40
Park, J.-M., Do, V. Q., Seo, Y.-S., Kim, H. J., Nam, J. H., Yin, M. Z., Kim, H. J., Kim, S. J., Griendling, K. K., & Lee, M.-Y. (2022) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.121.317239 · Cited by 42
Somvanshi, P. R., Mellon, S. H., Flory, J. D., Abu-Amara, D., PTSD Systems Biology Consortium;, Wolkowitz, O. M., Yehuda, R., Jett, M., Hood, L., Marmar, C., et al. (2019) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00065.2019 · Cited by 43
Poothong, J., Jang, I., & Kaufman, R. J. (2021) · Progress in molecular and subcellular biology · doi:10.1007/978-3-030-67696-4_6 · Cited by 41
Cadmium toxicity and autophagy: a review
Shao, Y., Zheng, L., & Jiang, Y. (2024) · BioMetals · doi:10.1007/s10534-023-00581-y · Cited by 41
Vakrou, S., Fukunaga, R., Foster, D. B., Sorensen, L. L., Liu, Y., Guan, Y., Woldemichael, K., Pineda-Reyes, R., Liu, T., Tardiff, J. C., et al. (2018) · JCI Insight · doi:10.1172/jci.insight.94493 · Cited by 40
Pfalzgraff, A., Bárcena‐Varela, S., Heinbockel, L., Gutsmann, T., Brandenburg, K., de Tejada, G. M., & Weindl, G. (2018) · British Journal of Pharmacology · doi:10.1111/bph.14425 · Cited by 40
ROS‐challenged keratinocytes as a new model for oxidative stress‐mediated skin diseases
Barygina, V. V., Becatti, M., Lotti, T., Moretti, S., Taddei, N., & Fiorillo, C. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.27485 · Cited by 40
Boulghobra, D., Coste, F., Gény, B., & Reboul, C. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.04.005 · Cited by 42
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Fontana, F., Raimondi, M., Marzagalli, M., Audano, M., Beretta, G., Procacci, P., Sartori, P., Mitro, N., & Limonta, P. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.07.009 · Cited by 40
Yao, D., Chen, E., Li, Y., Wang, K., Liao, Z., Li, M., & Huang, L. C. (2023) · Cellular Signalling · doi:10.1016/j.cellsig.2023.110986 · Cited by 39
Calcium's role as nuanced modulator of cellular physiology in the brain
Frazier, H. N., Maimaiti, S., Anderson, K. L., Brewer, L. D., Gant, J. C., Porter, N. M., & Thibault, O. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.08.105 · Cited by 40
Li, Y., Shi, J., Sun, X., Li, Y., Duan, Y., & Yao, H. (2019) · Journal of Natural Medicines · doi:10.1007/s11418-019-01333-4 · Cited by 39
Reactive Oxygen Species-Induced TRPM2-Mediated Ca2+ Signalling in Endothelial Cells
Ding, R., Yin, Y., & Jiang, L. (2021) · Antioxidants · doi:10.3390/antiox10050718 · Cited by 39
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Xun, Y., Zhou, P., Yang, Y., Li, C., Zhang, J., Hu, H., Qin, B., Zhang, Z., Wang, Q., Lu, Y., et al. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2020.8159 · Cited by 39
The “mitochondrial stress responses”: the “Dr. Jekyll and Mr. Hyde” of neuronal disorders
Rimessi, A., Patergnani, S., Morciano, G., Carinci, M., Leo, S., & Pinton, P. (2022) · Neural Regeneration Research · doi:10.4103/1673-5374.339473 · Cited by 41
Peng, D., Wang, Y.-X., Huang, T., Luo, D., Qiao, L., Wang, Q., Guan, L., Cai, Y., & Zhang, S. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/6664990 · Cited by 39
Sharma, S. K., Sardana, S., & Hamblin, M. R. (2023) · Journal of Photochemistry and Photobiology · doi:10.1016/j.jpap.2023.100160 · Cited by 39
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Motanova, E. S., Pirazzini, M., Negro, S., Rossetto, O., & Narici, M. V. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102586 · Cited by 43
Sheu, M., Shen, C.-C., Chen, Y.-S., & Chiang, C. (2016) · Oncotarget · doi:10.18632/oncotarget.14270 · Cited by 38
Chen, L.-D., Liu, Z., Zhang, L., Yao, J., & Wang, C. (2017) · Oncology Reports · doi:10.3892/or.2017.5912 · Cited by 38
Guidarelli, A., Fiorani, M., Cerioni, L., & Cantoni, O. (2018) · Redox Biology · doi:10.1016/j.redox.2018.10.015 · Cited by 38
Lee, H., Lee, G., Kim, H. K., & Chae, H. (2018) · Food and Chemical Toxicology · doi:10.1016/j.fct.2018.11.001 · Cited by 38
Tsamesidis, I., Pouroutzidou, G. K., Lymperaki, E., Kazeli, K., Lioutas, C. B., Christodoulou, E., Pério, P., Reybier, K., Pantaleo, A., & Kontonasaki, E. (2020) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2020.108974 · Cited by 38
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Orozco-Hernández, J. M., Gómez‐Oliván, L. M., Elizalde-Velázquez, G. A., Rosales-Pérez, K. E., Cardoso-Vera, J. D., Heredia-García, G., Islas‐Flores, H., García-Medina, S., & Galar‐Martínez, M. (2022) · NeuroToxicology · doi:10.1016/j.neuro.2022.03.007 · Cited by 38
Huang, J., He, J., Wang, J., Li, Y., Xu, Z., Zhang, L., Kang, Y., & Xue, P. (2023) · Biomaterials · doi:10.1016/j.biomaterials.2023.122340 · Cited by 37
Guo, M., Du, X., & Wang, X. (2024) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2024.117787 · Cited by 37
Berkowitz, B. A., Lenning, J. C., Khetarpal, N., Tran, C., Wu, J. Y., Berri, A. M., Dernay, K., Haacke, E. M., Khorassani, F. S., Podolsky, R. H., et al. (2017) · The FASEB Journal · doi:10.1096/fj.201700229r · Cited by 37
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Chan, S. M. H., Lau, Y. S., Miller, A. A., Ku, J., Potocnik, S. J., Ye, J., Woodman, O. L., & Herbert, T. P. (2017) · Endocrinology · doi:10.1210/en.2016-1879 · Cited by 37
Alevriadou, B. R., Shanmughapriya, S., Patel, A., Stathopulos, P. B., & Madesh, M. (2017) · Journal of The Royal Society Interface · doi:10.1098/rsif.2017.0672 · Cited by 41
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Warnock, A., Toomey, L. M., Wright, A. J., Fisher, K., Won, Y., Anyaegbu, C. C., & Fitzgerald, M. (2020) · Journal of Neurotrauma · doi:10.1089/neu.2019.6890 · Cited by 36
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Wu, J., Zhang, W., & Li, C. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.00653 · Cited by 39
Saatci, Ö., Alam, R., Huynh‐Dam, K., Işık, A., Üner, M., Belder, N., Ersan, P. G., Tokat, Ü. M., Ulukan, B., Çetįn, M., et al. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06814-3 · Cited by 41
Barnett, D., Zimmer, T. S., Booraem, C., Palaguachi, F., Meadows, S. M., Xiao, H., Wong, M. Y., Luo, W., Gan, L., Chouchani, E. T., et al. (2025) · Nature Metabolism · doi:10.1038/s42255-025-01390-y · Cited by 41
Chen, Y., Lan, K., Tsai, J.-R., Weng, T., Yang, C., & Liu, S. (2017) · Archives of Toxicology · doi:10.1007/s00204-017-1940-y · Cited by 36
Sadhu, A., Ghosh, I., Moriyasu, Y., Mukherjee, A., & Bandyopadhyay, M. (2018) · Mutagenesis · doi:10.1093/mutage/gey004 · Cited by 35
Jackson‐Weaver, O., Friedman, J. K., Rodriguez, L. A., Hoof, M. A., Drury, R. H., Packer, J., Smith, A., Guidry, C., & Duchesne, J. C. (2019) · The Journal of Trauma: Injury, Infection, and Critical Care · doi:10.1097/ta.0000000000002427 · Cited by 36
Ramírez-Moreno, I. G., Ibarra-Sánchez, A., Castillo-Arellano, J. I., Blank, U., & González‐Espinosa, C. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.1801430 · Cited by 37
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Morabito, C., Guarnieri, S., Cucina, A., Bizzarri, M., & Mariggiò, M. A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103638 · Cited by 37
Su, R., Chong, G., Dong, H., Gu, J., Zang, J., He, R., Sun, J., Zhang, T., Zhao, Y., Zheng, X. W., et al. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.121089 · Cited by 36
Morris, G., Sominsky, L., Walder, K. R., Berk, M., Marx, W., Carvalho, A. F., Bortolasci, C. C., Maes, M. H. J., & Puri, B. K. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02800-y · Cited by 38
Lee, W., Song, G., & Bae, H. (2022) · Marine Drugs · doi:10.3390/md20080473 · Cited by 37
Li, Y., Pan, Y., Chen, C., Li, Z., Du, S., Luan, X., Gao, Y., Han, X., & Song, Y. (2022) · Small · doi:10.1002/smll.202204244 · Cited by 36
Guo, S., Gong, L., Shen, Q., & Xing, D. (2020) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2020.112075 · Cited by 37
Costas‐Ferreira, C., & Faro, L. R. F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222413376 · Cited by 39
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Dong, X., Ye, L., Sheng, X., Zhou, W., Sun, A., & Dai, H. (2023) · Genes & Diseases · doi:10.1016/j.gendis.2023.03.019 · Cited by 38
Griffioen, G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241713243 · Cited by 36
Zhang, S., Cai, J., Yi, Y., Huang, L., Zheng, L., & Zhao, J. (2023) · Regenerative Biomaterials · doi:10.1093/rb/rbad078 · Cited by 38
Mahapatra, C., Thakkar, R., & Kumar, R. (2024) · Antioxidants · doi:10.3390/antiox13101172 · Cited by 37
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Zhou, J., Gao, G., Zhang, S., Wang, H., Ke, L., Zhou, J., Rao, P., Wang, Q., & Li, J. (2020) · Food Chemistry · doi:10.1016/j.foodchem.2020.126625 · Cited by 35
Singh, L., Singh, A. P., & Bhatti, R. (2021) · Pharmacological Reports · doi:10.1007/s43440-021-00261-z · Cited by 36
Doser, R. L., & Hoerndli, F. J. (2021) · Current Research in Neurobiology · doi:10.1016/j.crneur.2021.100012 · Cited by 35
Dvoriantchikova, G., Lypka, K. R., Adis, E. V., & Ivanov, D. (2022) · Scientific Reports · doi:10.1038/s41598-022-22140-0 · Cited by 36
Problems in evaluating the health impacts of radio frequency radiation
Ishai, P. B., Davis, D. L., Taylor, H. S., & Birnbaum, L. S. (2024) · Environmental Research · doi:10.1016/j.envres.2022.115038 · Cited by 36
Main, E. N., Cruz, T. M., & Bowlin, G. L. (2023) · Regenerative Biomaterials · doi:10.1093/rb/rbad070 · Cited by 34
Morabito, C., Guarnieri, S., Catizone, A., Schiraldi, C., Ricci, G., & Mariggiò, M. A. (2017) · Scientific Reports · doi:10.1038/s41598-017-15935-z · Cited by 34
Sudevan, S., Takiura, M., Kubota, Y., Higashitani, N., Cooke, M., Ellwood, R. A., Etheridge, T., Szewczyk, N. J., & Higashitani, A. (2019) · The FASEB Journal · doi:10.1096/fj.201802298r · Cited by 34
A mathematical model of calcium dynamics: Obesity and mitochondria-associated ER membranes
Han, J. M., & Periwal, V. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006661 · Cited by 34
Altshuler, P. J., Schiazza, A. R., Luo, L., Helmers, M. R., Chhay, B., Han, J. J., Hu, R., Herbst, D. A., Tsourkas, A., Cheng, Z., et al. (2021) · Advanced Therapeutics · doi:10.1002/adtp.202100036 · Cited by 35
Zhang, C., Guo, Y., Yan, Y., Du, Z., Fan, Y., Zhao, Y., & Yuan, S. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1118121 · Cited by 33
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Cinato, M., Andersson, L. K., Miljanovic, A., Laudette, M., Kunduzova, O., Borén, J., & Levin, M. C. (2024) · Antioxidants · doi:10.3390/antiox13020209 · Cited by 33
Nehme, J., Mesilmany, L., Varela-Eirín, M., Brandenburg, S. M., Altulea, A., Lin, Y., da Costa, M. G., Seelen, M. A., Hillebrands, J., van Goor, H., et al. (2024) · Nature Aging · doi:10.1038/s43587-024-00627-x · Cited by 34
Phua, S. Y., Yan, D., Chan, K. X., Estavillo, G. M., Nambara, E., & Pogson, B. J. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.01171 · Cited by 33
Covantes‐Rosales, C. E., Trujillo-Lepe, A. M., Díaz‐Reséndiz, K. J. G., Toledo‐Ibarra, G. A., Ventura‐Ramón, G. H., Ortiz‐Lazareno, P. C., & Girón‐Pérez, M. I. (2018) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2018.10.002 · Cited by 32
Lee, J., Bae, H., Yang, C., Park, S., Youn, B., Kim, H.-S., Song, G., & Lim, W. (2020) · Cancers · doi:10.3390/cancers12061459 · Cited by 33
Vilas‐Boas, E. A., Nalbach, L., Ampofo, E., Lucena, C. F., Naudet, L., Ortis, F., Carpinelli, Â. R., Morgan, B., & Roma, L. P. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.11.023 · Cited by 33
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Bon, R. S., Wright, D. J., Beech, D. J., & Sukumar, P. (2021) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-030121-122314 · Cited by 33
Li, X., Wang, W., Shao, Y., Zhou, J. Y., Huang, J., Xu, F., Gao, X., Wu, M., Dong, Y., Wu, W., et al. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-04437-6 · Cited by 34
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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
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