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 401–500 of 999
El‐Shoura, E. A. M., Salem, M. A., Ahmed, Y. H., Ahmed, L. K., & Zaafar, D. K. (2023) · Environmental Science and Pollution Research · doi:10.1007/s11356-023-27021-1 · Cited by 32
Yang, J., Du, Y., Yao, Y., Liao, Y., Wang, B., Yu, X., Yuan, K., Zhang, Y., He, F., & Yang, P. (2024) · Advanced Science · doi:10.1002/advs.202307130 · Cited by 30
The Influence of MicroRNAs on Mitochondrial Calcium
de Giusti, C. J., Román, B., & Das, S. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01291 · Cited by 32
Exploring paraptosis as a therapeutic approach in cancer treatment
Chang, L., Chiang, S.-K., Chen, S., & Hung, M. (2024) · Journal of Biomedical Science · doi:10.1186/s12929-024-01089-4 · Cited by 36
Stress is an agonist for the induction of programmed cell death: A review
Zhou, D. R., Eid, R., Boucher, É. L., Miller, K. A., Mandato, C. A., & Greenwood, M. T. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2018.12.001 · Cited by 32
Hu, M., & Carraway, K. L. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.605361 · Cited by 33
Structural and Functional Characterization of a Na v 1.5-Mitochondrial Couplon
Pérez-Hernández, M., Leo‐Macías, A., Keegan, S., Jouni, M., Kim, J., Agulló-Pascual, E., Vermij, S. H., Zhang, M., Liang, F., Burridge, P. W., et al. (2020) · Circulation Research · doi:10.1161/circresaha.120.318239 · Cited by 33
Zhong, Q., Roumeliotis, T. I., Kozik, Z., Cepeda-Molero, M., Fernández, L. Á., Shenoy, A. R., Bakal, C., Frankel, G. M., & Choudhary, J. S. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000986 · Cited by 31
Mijares, A., Allen, P. D., & Lopez, J. R. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2020.601189 · Cited by 31
Huang, T.-I., & Hsieh, C. (2021) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2021/6624976 · Cited by 31
Liang, Y., Chu, P. H., Tian, L., Ho, K., Ip, M., & Mak, J. (2021) · Environmental Pollution · doi:10.1016/j.envpol.2021.118720 · Cited by 31
Xie, W., Ye, J., Guo, Z., Lu, J., Xu, W., Gao, X., Huang, H., Hu, R., Mao, L., Wei, Y., et al. (2022) · Chemical Engineering Journal · doi:10.1016/j.cej.2022.135372 · Cited by 31
Uzhachenko, R. V., Boyd, K. L., Olivares–Villagómez, D., Zhu, Y., Goodwin, J. S., Rana, T., Shanker, A., Tan, W. J. T., Bondar, T., Medzhitov, R. M., et al. (2017) · Aging · doi:10.18632/aging.101213 · Cited by 29
Fan, H., Huang, H.-J., Hu, L., Zhu, W., Yu, Y.-F., Lou, J., Hu, L.-L., & Chen, F. (2018) · Toxicology Letters · doi:10.1016/j.toxlet.2018.04.030 · Cited by 23
Huang, K., Ma, K., Chang, Y., Lo, L., Jhap, T., Su, Y., Liu, P., & Chueh, S. (2019) · Experimental Dermatology · doi:10.1111/exd.13912 · Cited by 30
Dehydroepiandrosterone (DHEA) and its Sulphate (DHEAS) in Alzheimer’s Disease
Štrac, D. Š., Konjevod, M., Perković, M. N., Tudor, L., Erjavec, G. N., & Pivac, N. (2020) · Current Alzheimer Research · doi:10.2174/1567205017666200317092310 · Cited by 31
Zinc regulates reactive oxygen species generation in platelets
Pires, M. E. L., Ahmed, N. S., Vara, D. S., Gibbins, J. M., Pula, G., & Pugh, N. (2020) · Platelets · doi:10.1080/09537104.2020.1742311 · Cited by 30
Verma, N., Pink, M., & Schmitz‐Spanke, S. (2021) · Archives of Toxicology · doi:10.1007/s00204-021-03032-0 · Cited by 30
β-amyrin-induced apoptosis in Candida albicans triggered by calcium
Kwun, M. S., Lee, H. J., & Lee, D. G. (2021) · Fungal Biology · doi:10.1016/j.funbio.2021.03.006 · Cited by 30
Li, Y., Zhu, Y., Zhao, B., Yao, Q., Xu, H., Lv, S., Wang, J., Sun, Z., Li, Y., & Guo, C. (2022) · Nanotoxicology · doi:10.1080/17435390.2022.2144774 · Cited by 30
Liu, L., Chang, X., Zhang, Y., Wu, C., Li, R., Tang, L., & Zhou, Z. (2017) · Toxicology in Vitro · doi:10.1016/j.tiv.2017.12.006 · Cited by 30
Bello-Medina, P. C., Prado-Alcalá, R. A., & Rivas-Arancibia, S. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.01.018 · Cited by 29
Photobiomodulation Response From 660 nm is Different and More Durable Than That From 980 nm
Fuchs, C., Schenk, M. S., Pham, L., Cui, L., Anderson, R. R., & Tam, J. (2021) · Lasers in Surgery and Medicine · doi:10.1002/lsm.23419 · Cited by 29
Translational reprogramming as a driver of antimony-drug resistance in Leishmania
Guarnizo, S. A. G., Tikhonova, E. B., Karamyshev, A. L., Muskus, C., & Karamysheva, Z. N. (2023) · Nature Communications · doi:10.1038/s41467-023-38221-1 · Cited by 32
Reactive oxygen species-mediated signal transduction and utilization strategies in microalgae
Tang, D., Li, X., Zhang, L., Xiao, P., Nie, Y., Qiu, F., Cheng, Z., Li, W., & Zhao, Y. (2024) · Bioresource Technology · doi:10.1016/j.biortech.2024.132004 · Cited by 32
Oxidative Stress in Health and Disease: Mechanisms and Therapeutic Perspectives
Anwar, S., Alharbi, H. O. A., Babiker, A. Y., & Rahmani, A. H. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27062681 · Cited by 40
Morimoto, M., Waller‐Evans, H., Ammous, Z., Song, X., Strauss, K. A., Pehli̇van, D., Gonzaga-Jauregui, C. G., Puffenberger, E. G., Holst, C. R., Karaca, E., et al. (2018) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2018.09.014 · Cited by 29
Mitochondrial Calcium Signaling as a Therapeutic Target for Alzheimer’s Disease
Wu, A. J., Tong, B. C., Huang, S., Li, M., & Cheung, K. (2019) · Current Alzheimer Research · doi:10.2174/1567205016666191210091302 · Cited by 30
Jang, E., Kim, I. Y., Kim, H., Lee, D. M., Seo, D. Y., Lee, J. A., Choi, K. S., & Kim, E. (2020) · Biochemical Pharmacology · doi:10.1016/j.bcp.2020.114098 · Cited by 30
Molecular mechanisms of anticancer activities of polyphyllin VII
Ahmad, B., Rehman, S. U., Azizullah, A., Khan, M. F., Din, S. R. U., Ahmad, M., Ali, A., Tahir, N., Azam, N., Gamallat, Y., et al. (2020) · Chemical Biology & Drug Design · doi:10.1111/cbdd.13818 · Cited by 29
Ahmad, B., Gamallat, Y., Khan, M. F., Din, S. R. U., Israr, M., Ahmad, M., Tahir, N., Azam, N., Rahman, K. U., Wang, X., et al. (2021) · OncoTargets and Therapy · doi:10.2147/ott.s287354 · Cited by 30
Cid‐Castro, C., & Morán, J. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/8832863 · Cited by 29
Dang, D., Stafford, C. D., Taylor, M. J., Buhler, J. F., Thornton, K. J., & Matarneh, S. K. (2021) · Meat Science · doi:10.1016/j.meatsci.2021.108646 · Cited by 29
Chaanine, A. H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910579 · Cited by 31
Huang, W., Liu, Y., Luz, A. L., Berrong, M., Meyer, J. N., Zou, Y., Swann, E., Sundaramoorthy, P., Kang, Y., Jauhari, S., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.754083 · Cited by 27
Pang, K.-L., Mai, C., & Chin, K. (2023) · Nutrients · doi:10.3390/nu15081854 · Cited by 29
Pang, Y., Lv, J., He, C., Ju, C., Lin, Y., Zhang, C., & Li, M. C. (2024) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2024.01.217 · Cited by 29
Hu, F. Z., Hui, Z., Wei, W., Yang, J., Chen, Z., Guo, B., Xing, F., Zhang, X., Pan, L., & Xu, J. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.03.008 · Cited by 29
Dufor, T., Lohof, A. M., & Sherrard, R. M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242216456 · Cited by 28
Membrane Dynamics and Cation Handling in Ferroptosis
Hirata, Y., & Mishima, E. (2024) · Physiology · doi:10.1152/physiol.00029.2023 · Cited by 33
Mitochondrial connexin40 regulates mitochondrial calcium uptake in coronary endothelial cells
Guo, R., Si, R., Scott, B. T., & Makino, A. (2017) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00283.2016 · Cited by 28
Ahmadi‐Zeidabadi, M., Akbarnejad, Z., Esmaeeli, M., Masoumi‐Ardakani, Y., Mohammadipoor‐Ghasemabad, L., & Eskandary, H. (2019) · Electromagnetic Biology and Medicine · doi:10.1080/15368378.2019.1625784 · Cited by 28
The roles of calcium-sensing receptor (CaSR) in heavy metals-induced nephrotoxicity
Kosiba, A. A., Wang, Y., Chen, D., Wong, C. K. C., Gu, J., & Shi, H. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.117183 · Cited by 28
Heart failure and the glutathione cycle: an integrated view
Bachhawat, A. K., Yadav, S., Jainarayanan, A., & Dubey, P. (2020) · Biochemical Journal · doi:10.1042/bcj20200429 · Cited by 28
The ER-mitochondria Ca2+ signaling in cancer progression: Fueling the monster
Bustos, G., Ahumada-Castro, U., Silva-Pavez, E., Puebla, A., Lovy, A., & Cárdenas, C. (2021) · International review of cytology · doi:10.1016/bs.ircmb.2021.03.006 · Cited by 28
Kwak, M. S., Lim, J. W., & Kim, H. (2021) · Mediators of Inflammation · doi:10.1155/2021/5587297 · Cited by 28
Genome-wide activation screens to increase adeno-associated virus production
Barnes, C. R., Lee, H., Ojala, D. S., Lewis, K. K., Limsirichai, P., & Schaffer, D. V. (2021) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2021.06.026 · Cited by 28
Butterfield, D. A., Favia, M., Spera, I., Campanella, A., Lanza, M., & Castegna, A. (2022) · Molecules · doi:10.3390/molecules27030951 · Cited by 29
Bielfeldt, M., Rebl, H., Peters, K., Sridharan, K., Staehlke, S., & Nebe, B. J. (2022) · Biomedical Materials & Devices · doi:10.1007/s44174-022-00028-x · Cited by 29
Shin, Y. K., & Seol, G. H. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1233977 · Cited by 28
Sun, L., Liu, Y., Ye, F., Xie, J., Zeng, J., Li, Q., Xue, J., Wang, Y.-T., Guo, K.-M., Ma, M.-M., et al. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.08.018 · Cited by 29
Potential roles of natural products in the targeting of proteinopathic neurodegenerative diseases
Dash, R., Jahan, I., Ali, M. C., Mitra, S., Munni, Y. A., Timalsina, B., Hannan, M. A., & Moon, I. S. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.105011 · Cited by 28
Huang, K.-F., Ma, K.-H., Jhap, T.-Y., Liu, P.-S., & Chueh, S.-H. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.06.020 · Cited by 27
Trujillo, M., Odle, A. K., Aykin‐Burns, N., & Allen, A. R. (2022) · Biology of Reproduction · doi:10.1093/biolre/ioac222 · Cited by 27
Zhang, X.-Y., Han, P.-P., Zhao, Y., Shen, X.-Y., & Bi, X. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e28959 · Cited by 28
Environmental Exposome and Atrial Fibrillation: Emerging Evidence and Future Directions
Wass, S. Y., Hahad, O., Asad, Z. U. A., Li, S., Chung, M. K., Benjamin, E. J., Nasir, K., Rajagopalan, S., & Al-Kindi, S. G. (2024) · Circulation Research · doi:10.1161/circresaha.123.323477 · Cited by 27
Buendía, I., Tenti, G., Michalska, P., Méndez‐López, I., Luengo, E., Satriani, M., Padín, J. F., López, M. G., Ramos, M. T., Garcı́a, A. G., et al. (2016) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.6b00181 · Cited by 27
Yan, X., Xun, M., Dou, X., Wu, L., Zhang, F., & Zheng, J. (2017) · APOPTOSIS · doi:10.1007/s10495-016-1342-2 · Cited by 27
Alhazzani, A. A., Rajagopalan, P., Albarqi, Z., Devaraj, A., Mohamed, M. H., Al‐Hakami, A. M., & Chandramoorthy, H. C. K. (2018) · Cells · doi:10.3390/cells7120250 · Cited by 27
Free-radical and biochemical reactions involving polar part of glycerophospholipids
Шадыро, О. И., Самович, С. Н., & Edimecheva, I. P. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.02.033 · Cited by 31
Lee, J., Lim, W., Ham, J., Kim, J., You, S., & Song, G. (2019) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2019.06.009 · Cited by 27
Pino, A. M. D., Guiducci, M., D’Amato, R., Michele, A. D., Tosti, G., Datti, A., & Palmerini, C. A. (2019) · Scientific Reports · doi:10.1038/s41598-019-49760-3 · Cited by 28
Pedersen, S. F., Flinck, M., & Pardo, L. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22105209 · Cited by 27
Characterizing SERCA Function in Murine Skeletal Muscles after 35–37 Days of Spaceflight
Braun, J. L., Geromella, M. S., Hamstra, S. I., Messner, H. N., & Fajardo, V. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111764 · Cited by 27
TRPC Channels in the Physiology and Pathophysiology of the Renal Tubular System: What Do We Know?
Englisch, C. N., Paulsen, F. P., & Tschernig, T. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010181 · Cited by 26
Paraneoplastic cerebellar degeneration: Yo antibody alters mitochondrial calcium buffering capacity
Panja, D., Vedeler, C. A., & Schubert, M. (2018) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12492 · Cited by 26
Thioredoxin Modulates Protein Arginine Deiminase 4 (PAD4)-Catalyzed Citrullination
Nagar, M., Tilvawala, R. R., & Thompson, P. R. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00244 · Cited by 27
Xiong, Y., Huang, W., Ling, X., Zhou, S. Y., Wang, X., Li, X., & Zhou, L. (2024) · Acta Pharmacologica Sinica · doi:10.1038/s41401-024-01298-5 · Cited by 28
Bravo, A., Sánchez, R., Zambrano, F., & Uribe, P. (2024) · Antioxidants · doi:10.3390/antiox13060739 · Cited by 29
Lee, J.-R., Lee, J.-Y., Kim, H., Hahn, M., Kang, J., & Cho, H. (2019) · Experimental & Molecular Medicine · doi:10.1038/s12276-019-0279-2 · Cited by 26
Redox control of vascular biology
Obradovic, M. M., Essack, M., Zafirovic, S. S., Sudar-Milovanovic, E. M., Bajić, V., Neste, C. V., Trpković, A., Stanimirović, J., Bajić, V. B., & Isenović, E. R. (2019) · BioFactors · doi:10.1002/biof.1559 · Cited by 26
Reactive Oxygen Species Modulate Activity-Dependent AMPA Receptor Transport in C. elegans
Doser, R. L., Amberg, G. C., & Hoerndli, F. J. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0902-20.2020 · Cited by 28
The role of reactive oxygen species in cognitive impairment associated with sleep apnea
Xu, L., Yang, Y., & Chen, J. (2020) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2020.9132 · Cited by 27
The Synaptic Dysregulation in Adolescent Rats Exposed to Maternal Immune Activation
Cieślik, M., Gąssowska-Dobrowolska, M., Zawadzka, A., Frontczak‐Baniewicz, M., Gewartowska, M., Dominiak, A., Czapski, G. A., & Adamczyk, A. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.555290 · Cited by 25
Zakyrjanova, G. F., Tsentsevitsky, A. N., Kuznetsova, E. A., & Petrov, A. M. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.08.013 · Cited by 26
Sun, Z., Li, X., Liu, Y., Dong, X., Han, Y., Li, Y., Luo, J., & Li, W. (2022) · Molecular Neurobiology · doi:10.1007/s12035-021-02717-y · Cited by 29
CaCO3-MnSiOx hybrid particles to enable CO2-mediated combinational tumor therapy
Xie, C., Zhang, T., Fu, Y., Han, G., & Li, X. (2022) · Nano Research · doi:10.1007/s12274-022-4471-7 · Cited by 26
Prasad, K., Yogendra, K. N., Sanivarapu, H., Rajasekaran, K., Cary, J. W., Sharma, K. K., & Bhatnagar‐Mathur, P. (2023) · Toxins · doi:10.3390/toxins15050319 · Cited by 26
Guo, H., Dong, Q., Li, S., Cha, X., Sun, L., Duan, H., Li, S., Jin, Y., & Zhang, M. (2023) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2023.107860 · Cited by 26
Hong, S., Yang, Y., Wang, S., & Qin, B. (2023) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2023.110636 · Cited by 25
Mitochondrial ROS versus ER ROS: Which Comes First in Myocardial Calcium Dysregulation?
Chaube, R., & Werstuck, G. H. (2016) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2016.00036 · Cited by 27
Grimm, A., Cummins, N., & Götz, J. (2018) · iScience · doi:10.1016/j.isci.2018.07.015 · Cited by 26
Shao, Z., Zhang, X., Fan, H.-H., Wang, X.-S., Wu, H., Zhang, L., Cheng, W., & Zhu, J. (2019) · Journal of Nutrition · doi:10.1093/jn/nxz199 · Cited by 25
Abu-Salah, A., Cesur, M. F., Anchan, A., Ay, M., Langley, M. R., Shah, A., Reina-Gonzalez, P., Strazdins, R., Çakır, T., & Sarkar, S. (2024) · Environmental Science & Technology · doi:10.1021/acs.est.4c05472 · Cited by 26
Vascular defects of DYRK1A knockouts are ameliorated by modulating calcium signaling in zebrafish
Cho, H.-J., Lee, J.-G., Kim, S., Kim, S., Huh, Y. H., Kim, H., Lee, K., Yu, K., & Lee, J.-S. (2019) · Disease Models & Mechanisms · doi:10.1242/dmm.037044 · Cited by 25
Mapping glutathione utilization in the developing zebrafish (Danio rerio) embryo
Rastogi, A., Clark, C. W., Conlin, S. M., Brown, S. E., & Timme‐Laragy, A. R. (2019) · Redox Biology · doi:10.1016/j.redox.2019.101235 · Cited by 25
Bello-Medina, P. C., González-Franco, D. A., Vargas-Rodríguez, I., & Díaz-Cintra, S. Y. (2019) · Neurología · doi:10.1016/j.nrl.2019.06.002 · Cited by 25
Zhang, Y., Zhang, W., Zeng, K., Ao, Y., Wang, M., Yu, Z., Qi, F., Yu, W., Mao, H., Tao, L., et al. (2020) · Small · doi:10.1002/smll.201906797 · Cited by 25
Shabani, F., Mahdavi, M., Imani, M., Feizi, M. A. H., & Gheibi, N. (2020) · Human & Experimental Toxicology · doi:10.1177/0960327120909530 · Cited by 25
Role of mitochondrial calcium in hypochlorite induced oxidative damage of cells
Cheshchevik, V. T., Крылова, Н. Г., Cheshchevik, N. G., Lapshina, E. A., Семенкова, Г. Н., & Zavodnik, I. B. (2021) · Biochimie · doi:10.1016/j.biochi.2021.02.009 · Cited by 24
Amyloid-β 25-35 Induces Neurotoxicity through the Up-Regulation of Astrocytic System Xc−
D’Ezio, V., Colasanti, M., & Persichini, T. (2021) · Antioxidants · doi:10.3390/antiox10111685 · Cited by 26
Boulghobra, D., Dubois, M., Alpha‐Bazin, B., Coste, F., Olmos, M., Gayrard, S., Bornard, I., Meyer, G., Gaillard, J., Armengaud, J., et al. (2021) · Basic Research in Cardiology · doi:10.1007/s00395-021-00906-3 · Cited by 25
Bioactive Chitosan-Based Organometallic Scaffolds for Tissue Engineering and Regeneration
Zakhireh, S., Barar, J., Adibkia, K., Beygi‐Khosrowshahi, Y., Fathi, M., Omidain, H., & Omidi, Y. (2022) · Topics in Current Chemistry · doi:10.1007/s41061-022-00364-y · Cited by 25
Guéguinou, M., Ibrahim, S., Bourgeais, J., Robert, A., Pathak, T., Zhang, X., Crottès, D., Dupuy, J., Ternant, D., Monbet, V., et al. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04311-4 · Cited by 28
Boyer, M., Baudin, P., Stengel, C., Valero‐Cabré, A., Lohof, A. M., Charpier, S., Sherrard, R. M., & Mahon, S. (2022) · The Journal of Physiology · doi:10.1113/jp283244 · Cited by 25
Oliveira, M. C., Verswyvel, H., Smits, E., Cordeiro, R. M., Bogaerts, A., & Lin, A. G. (2022) · Redox Biology · doi:10.1016/j.redox.2022.102503 · Cited by 26
Roles of Mitochondria in Oral Squamous Cell Carcinoma Therapy: Friend or Foe?
Bai, J., Wu, L., Wang, X., Wang, Y., Shang, Z., Jiang, E., & Shao, Z. (2022) · Cancers · doi:10.3390/cancers14235723 · Cited by 27
Graziani, M., Sarti, P., Arese, M., Magnifico, M., Badiani, A., & Saso, L. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/3034245 · Cited by 24
Shen, L., Sun, Z., Chu, S., Cai, Z., Nie, P., Wu, C., Yuan, R., Hu, L., & He, B. (2017) · PLoS ONE · doi:10.1371/journal.pone.0188841 · Cited by 25
Calcium Signaling During Brain Aging and Its Influence on the Hippocampal Synaptic Plasticity
Kumar, A. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-12457-1_39 · Cited by 25
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