Production of Reactive Oxygen Species by Mitochondria

Generation of superoxide anion by the NADH dehydrogenase of bovine heart mitochondria

Turrens, J. F., & Boveris, A. (1980) · Biochemical Journal · doi:10.1042/bj1910421 · Cited by 1,601

Topology of superoxide production from different sites in the mitochondrial electron transport chain

St-Pierre, J., Buckingham, J. A., Roebuck, S. J., & Brand, M. D. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m207217200 · Cited by 1,545

Complete Structure of the 11-Subunit Bovine Mitochondrial Cytochrome bc 1 Complex

Iwata, S., Lee, J. W., Okada, K., Lee, J. K., Iwata, M., Rasmussen, B., Link, T. A., Ramaswamy, S., & Jap, B. K. (1998) · Science · doi:10.1126/science.281.5373.64 · Cited by 1,253

Ubisemiquinone is the electron donor for superoxide formation by complex III of heart mitochondria

Turrens, J. F., Alexandre, A., & Lehninger, A. L. (1985) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(85)90293-0 · Cited by 1,214

Oxygen activation and the conservation of energy in cell respiration

Babcock, Ǵ., & Wikström, M. K. F. (1992) · Nature · doi:10.1038/356301a0 · Cited by 1,126

Biochemical properties of subsarcolemmal and interfibrillar mitochondria isolated from rat cardiac muscle

Palmer, J. W., Tandler, B., & Hoppel, C. L. (1977) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)75283-1 · Cited by 830

Mitochondrial Dysfunction in Cardiac Disease: Ischemia–Reperfusion, Aging, and Heart Failure

Lesnefsky, E. J., Moghaddas, S., Tandler, B., Kerner, J., & Hoppel, C. L. (2001) · Journal of Molecular and Cellular Cardiology · doi:10.1006/jmcc.2001.1378 · Cited by 719

Voltage-dependent anion channels control the release of the superoxide anion from mitochondria to cytosol

Han, D., Antunes, F., Canali, R., Rettori, D., & Cadenas, E. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m210269200 · Cited by 711

The protonmotive Q cycle. Energy transduction by coupling of proton translocation to electron transfer by the cytochrome bc1 complex.

Trumpower, B. L. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)38410-8 · Cited by 598

Detection of catalase in rat heart mitochondria.

Radi, R., Turrens, J. F., Chang, L. Y., Bush, K. M., Crapo, J. D., & Freeman, B. A. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)54740-2 · Cited by 573

Cardiac-specific ablation of the E3 ubiquitin ligase Mdm2 leads to oxidative stress, broad mitochondrial deficiency and early death

Hauck, L., Stanley-Hasnain, S., Fung, A., Grothe, D., Rao, V., Mak, T. W., & Billia, F. (2017) · PLoS ONE · doi:10.1371/journal.pone.0189861 · Cited by 46

Disentangling oxidation/hydrolysis reactions of brain mitochondrial cardiolipins in pathogenesis of traumatic injury

Chao, H., Anthonymuthu, T. S., Kenny, E., Amoscato, A. A., Cole, L., Hatch, G. M., Ji, J., Kagan, V. E., & Bayır, H. (2018) · JCI Insight · doi:10.1172/jci.insight.97677 · Cited by 44

Hypercapnic tumor microenvironment confers chemoresistance to lung cancer cells by reprogramming mitochondrial metabolism in vitro

Kikuchi, R., Iwai, Y., Tsuji, T., Watanabe, Y., Koyama, N., Yamaguchi, K., Nakamura, H., & Aoshiba, K. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.01.014 · Cited by 44

Metformin preferentially provides neuroprotection following cardiac ischemia/reperfusion in non-diabetic rats

Benjanuwattra, J., Apaijai, N., Chunchai, T., Kerdphoo, S., Jaiwongkam, T., Arunsak, B., Wongsuchai, S., Chattipakorn, N., & Chattipakorn, S. C. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2020.165893 · Cited by 44

The Effects of Lead and Copper on the Cellular Architecture and Metabolism of the Red AlgaGracilaria domingensis

Gouveia, C., Kreusch, M., Schmidt, É. C., Felix, M. R. D. L., Osorio, L. K. P., Pereira, D. T., dos Santos, R. W., Ouriques, L. C., Martins, R. D. P., Latini, A., et al. (2013) · Microscopy and Microanalysis · doi:10.1017/s1431927613000317 · Cited by 44

A mitochondrial DNA mutation linked to colon cancer results in proton leaks in cytochrome c oxidase

Namslauer, I., & Brzezinski, P. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811450106 · Cited by 44

Age-Related Macular Degeneration: Cellular and Molecular Signaling Mechanisms

Jiang, F., Ma, J., Lei, C., Zhang, Y., & Zhang, M. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26136174 · Cited by 44

Molecular identification of the enzyme responsible for the mitochondrial NADH-supported ammonium-dependent hydrogen peroxide production

Kareyeva, A. V., Grivennikova, V. G., Cecchini, G., & Vinogradov, A. D. (2010) · FEBS Letters · doi:10.1016/j.febslet.2010.12.019 · Cited by 43

Cumulative mtDNA damage and mutations contribute to the progressive loss of RGCs in a rat model of glaucoma

Wu, J., Zhang, S.-H., Nickerson, J. M., Gao, F., Sun, Z., Chen, X.-Y., Zhang, S., Zhang, R., Gao, F., Chen, J., et al. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.11.014 · Cited by 44

HIV protease inhibitors elicit volume-sensitive Cl− current in cardiac myocytes via mitochondrial ROS

Deng, W., Baki, L., Yin, J., Zhou, H., & Baumgarten, C. M. (2010) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2010.08.013 · Cited by 43

Mitochondrial targets for volatile anesthetics against cardiac ischemia-reperfusion injury

Agarwal, B., Stowe, D. F., Dash, R. K., Bosnjak, Z. J., & Camara, A. K. S. (2014) · Frontiers in Physiology · doi:10.3389/fphys.2014.00341 · Cited by 43

Renal oncocytoma characterized by the defective complex I of the respiratory chain boosts the synthesis of the ROS scavenger glutathione

Kürschner, G., Zhang, Q., Clima, R., Xiao, Y., Busch, J. F., Kilic, E., Jung, K., Berndt, N., Bulik, S., Holzhütter, H., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.22413 · Cited by 45

Alteration of renal respiratory Complex-III during experimental type-1 diabetes

Munusamy, S., Saba, H., Mitchell, T., Megyesi, J. K., Brock, R. W., & MacMillan-Crow, L. A. (2009) · BMC Endocrine Disorders · doi:10.1186/1472-6823-9-2 · Cited by 46

Mitochondrial superoxide mediates labile iron level: evidence from Mn-SOD-transgenic mice and heterozygous knockout mice and isolated rat liver mitochondria

Ibrahim, W. H., Habib, H. M., Kamal, H., Clair, D. K. S., & Chow, C. K. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.06.026 · Cited by 44

Induction of Apoptosis-Like Mitochondrial Impairment Triggers Antioxidant and Bcl-2-Dependent Keratinocyte Differentiation

Tamiji, S., Beauvillain, J., Mortier, L., Jouy, N., Tual, M., Delaporte, E., Formstecher, P., Marchetti, P., & Polakowska, R. R. (2005) · Journal of Investigative Dermatology · doi:10.1111/j.0022-202x.2005.23885.x · Cited by 43

ROS scavenging before 27°C ischemia protects hearts and reduces mitochondrial ROS, Ca2+ overload, and changes in redox state

Camara, A. K. S., Aldakkak, M., Heisner, J. S., Rhodes, S. S., Riess, M. L., An, J., Heinen, A., & Stowe, D. F. (2007) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00231.2006 · Cited by 42

Saturated fatty acids accelerate linear motility through mitochondrial ATP production in bull sperm

Islam, M. M., Umehara, T., Tsujita, N., & Shimada, M. (2021) · Reproductive Medicine and Biology · doi:10.1002/rmb2.12381 · Cited by 42

Comprehensive evaluation of mitochondrial redox profile, calcium dynamics, membrane integrity and apoptosis markers in a preclinical model of severe penetrating traumatic brain injury

Pandya, J. D., Musyaju, S., Modi, H. R., Cao, Y. J., Flerlage, W. J., Huynh, L., Kociuba, B., Visavadiya, N. P., Kobeissy, F. H., Wang, K., et al. (2023) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2023.02.001 · Cited by 42

ROS Signalling of Inflammatory Cytokines During Trypanosoma cruzi Infection

Gupta, S., Dhiman, M., Jian-jun, W., & Garg, N. J. (2011) · Advances in Parasitology/Advances in parasitology · doi:10.1016/b978-0-12-385895-5.00007-4 · Cited by 42

Hydrogen Peroxide Accumulation in the Choroid During Intermittent Hypoxia Increases Risk of Severe Oxygen-Induced Retinopathy in Neonatal Rats

Beharry, K. D. A., Cai, C. L., Sharma, P., Bronshtein, V., Valencia, G. B., Lazzaro, D. R., & Aranda, J. V. (2013) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.13-13040 · Cited by 42

Synergistic effects of ascorbate and sorafenib in hepatocellular carcinoma: New insights into ascorbate cytotoxicity

Rouleau, L., Antony, A. N., Bisetto, S., Newberg, A. B., Doria, C., Levine, M., Monti, D., & Hoek, J. B. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.03.031 · Cited by 42

Mitochondrial Dysfunction in Cardiovascular Aging

Hoppel, C. L., Lesnefsky, E. J., Chen, Q., & Tandler, B. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-55330-6_24 · Cited by 44

Interconnections between dissociative electron attachment and electron-driven biological processes

Pshenichnyuk, S. A., Modelli, A., & Komolov, А. S. (2018) · International Reviews in Physical Chemistry · doi:10.1080/0144235x.2018.1461347 · Cited by 42

Hydrogen sulfide attenuates hyperhomocysteinemia-induced mitochondrial dysfunctions in brain

Kumar, M., & Sandhir, R. (2019) · Mitochondrion · doi:10.1016/j.mito.2019.11.004 · Cited by 42

Antioxidant role of amyloid β protein in cell-free and biological systems: implication for the pathogenesis of Alzheimerdisease

Sinha, M. S., Bhowmick, P., Banerjee, A., & Chakrabarti, S. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.09.036 · Cited by 45

The effect of different ubiquinones on lifespan in Caenorhabditis elegans

Yang, Y.-Y., Gangoiti, J. A., Sedensky, M. M., & Morgan, P. G. (2009) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2009.03.003 · Cited by 42

Dependence of Reactive Oxygen Species and FLICE Inhibitory Protein on Lipofectamine-Induced Apoptosis in Human Lung Epithelial Cells

Kongkaneramit, L., Sarisuta, N., Azad, N., Lu, Y., Iyer, A. K. V., Wang, L., & Rojanasakul, Y. (2008) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.107.136077 · Cited by 42

Wood Smoke Particle Sequesters Cell Iron to Impact a Biological Effect

Ghio, A. J., Soukup, J. M., Dailey, L. A., Tong, H., Kesic, M. J., Budinger, G. R. S., & Mutlu, G. M. (2015) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.5b00270 · Cited by 41

Thioether-Based Polymeric Micelles with Fine-Tuned Oxidation Sensitivities for Chemotherapeutic Drug Delivery

van der Vlies, A. J., Xu, J., Ghasemi, M., Bator, C. M., Bell, A., Rosoff-Verbit, B., Liu, B., Gomez, E. D., & Hasegawa, U. (2021) · Biomacromolecules · doi:10.1021/acs.biomac.1c01010 · Cited by 41

Inhibiting Succinate Release Worsens Cardiac Reperfusion Injury by Enhancing Mitochondrial Reactive Oxygen Species Generation

Milliken, A. S., Nadtochiy, S. M., & Brookes, P. S. (2022) · Journal of the American Heart Association · doi:10.1161/jaha.122.026135 · Cited by 41

Pretreatment with brain natriuretic peptide reduces skeletal muscle mitochondrial dysfunction and oxidative stress after ischemia-reperfusion

Talha, S., Bouitbir, J., Charles, A., Zoll, J., Marco, P. G.-D., Meziani, F., Piquard, F., & Gény, B. (2012) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00239.2012 · Cited by 41

Isoflurane modulates cardiac mitochondrial bioenergetics by selectively attenuating respiratory complexes

Agarwal, B., Dash, R. K., Stowe, D. F., Bosnjak, Z. J., & Camara, A. K. S. (2013) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2013.11.006 · Cited by 41

Heterogeneous Porphyromonas gingivalis LPS modulates immuno-inflammatory response, antioxidant defense and cytoskeletal dynamics in human gingival fibroblasts

Herath, T. D. K., Darveau, R. P., Seneviratne, C. J., Wang, C.-Y., Wang, Y., & Jin, L. (2016) · Scientific Reports · doi:10.1038/srep29829 · Cited by 41

A glyphosate-based herbicide induces sub-lethal effects in early life stages and liver cell line of rainbow trout, Oncorhynchus mykiss

Santos, S. W., Gonzalez, P., Cormier, B., Mazzella, N., Bonnaud, B., Morin, S., Clérandeau, C., Morin, B., & Cachot, J. (2019) · Aquatic Toxicology · doi:10.1016/j.aquatox.2019.105291 · Cited by 41

Antioxidant potential of CORM-A1 and resveratrol during TNF-α/cycloheximide-induced oxidative stress and apoptosis in murine intestinal epithelial MODE-K cells

Babu, D., Leclercq, G., Goossens, V., Remijsen, Q., Vandenabeele, P., Motterlini, R., & Lefebvre, R. A. (2015) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2015.07.007 · Cited by 42

Sepsis-Induced Cardiac Mitochondrial Dysfunction Involves Altered Mitochondrial-Localization of Tyrosine Kinase Src and Tyrosine Phosphatase SHP2

Zang, Q. S., Martinez, B., Yao, X., Maass, D. L., Ma, L., Wolf, S. E., & Minei, J. P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043424 · Cited by 41

Mitochondrial cytochrome redox states and respiration in acute pulmonary oxygen sensing

Sommer, N., Pak, O., Schorner, S., Derfuss, T., Krug, A., Gnaiger, E., Ghofrani, H. A., SCHERMULY, R. T., Huckstorf, C., Seeger, W., et al. (2010) · European Respiratory Journal · doi:10.1183/09031936.00013809 · Cited by 41

Diosmetin Induces Apoptosis of Acute Myeloid Leukemia Cells

Roma, A., Rota, S. G., & Spagnuolo, P. A. (2018) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.7b01151 · Cited by 41

Contribution of the FAD and quinone binding sites to the production of reactive oxygen species from Ascaris suum mitochondrial complex II

Paranagama, M. P., Sakamoto, K., Amino, H., Awano, M., Miyoshi, H., & Kita, K. (2010) · Mitochondrion · doi:10.1016/j.mito.2009.12.145 · Cited by 40

Improved transcription and translation with L-leucine stimulation of mTORC1 in Roberts syndrome

Xu, B., Gogol, M., Gaudenz, K., & Gerton, J. L. (2016) · BMC Genomics · doi:10.1186/s12864-015-2354-y · Cited by 40

Role of reactive oxygen species in cell physiology and pathology and their pharmacological regulation

Novikov, V. E., Левченкова, О. С., & Pozhilova, Y. V. (2014) · Reviews on Clinical Pharmacology and Drug Therapy · doi:10.17816/rcf12413-21 · Cited by 40

Inhibitory mechanism of phthalate esters on Karenia brevis

Liu, N., Wen, F., Li, F., Zheng, X., Liang, Z. C., & Zheng, H. (2016) · Chemosphere · doi:10.1016/j.chemosphere.2016.04.082 · Cited by 40

Natural Killer Cells Induce Eosinophil Activation and Apoptosis

Awad, A. I., Yassine, H., Barrier, M., Vorng, H., Marquillies, P., Tsicopoulos, A., & Duez, C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0094492 · Cited by 40

Mitochondrial respiration and reactive oxygen species in C. elegans

Sedensky, M. M., & Morgan, P. G. (2006) · Experimental Gerontology · doi:10.1016/j.exger.2006.06.056 · Cited by 40

Acute Isovolemic Hemodilution Triggers Proinflammatory and Procoagulatory Endothelial Activation in Vital Organs: Role of Erythrocyte Aggregation

Morariu, A. M., Maathuis, M.-H. J., Ásgeirsdóttir, S. A., Leuvenink, H. G. D., Boonstra, P. W., van Oeveren, W., Ploeg, R. J., Molema, I., & Rakhorst, G. (2006) · Microcirculation · doi:10.1080/10739680600745992 · Cited by 40

Xanthine Oxidase Contributes to Mitochondrial ROS Generation in an Experimental Model of Cocaine-Induced Diastolic Dysfunction

Vergeade, A., Mulder, P. G. H., Vendeville, C., Ventura‐Clapier, R., Thuillez, C., & Monteil, C. (2012) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0b013e318271223c · Cited by 40

Upregulation of BNIP3 and translocation to mitochondria mediates cyanide-induced apoptosis in cortical cells

Prabhakaran, K., Li, L., Zhang, L., Borowitz, J. L., & Isom, G. E. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.07.033 · Cited by 40

Localization of superoxide anion production to mitochondrial electron transport chain in 3-NPA-treated cells

Bácsi, A., Woodberry, M. W., Widger, W. R., Papaconstantinou, J., MITRA, S. P., Peterson, J. W., & Boldogh, I. R. (2006) · Mitochondrion · doi:10.1016/j.mito.2006.07.008 · Cited by 40

Regulation by the cAMP Cascade of Oxygen Free Radical Balance in Mammalian Cells

Bellomo, F., Piccoli, C., Cocco, T., Scacco, S., Papa, F., Gaballo, A., Boffoli, D., Signorile, A., D’Aprile, A., Scrima, R., et al. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2006.8.495 · Cited by 40

Nitric oxide protects against mitochondrial permeabilization induced by glutathione depletion: Role of S-nitrosylation?

Whiteman, M., Chua, Y. L., Zhang, D., Duan, W., Liou, Y., & Armstrong, J. S. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.10.200 · Cited by 40

Enhanced Generation of Mitochondrial Reactive Oxygen Species in Cybrids Containing 4977‐bp Mitochondrial DNA Deletion

Jou, M., Peng, T., WU, H., & Wei, Y. (2005) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1338.024 · Cited by 40

Air pollutants disrupt iron homeostasis to impact oxidant generation, biological effects, and tissue injury

Ghio, A. J., Soukup, J. M., Dailey, L. A., & Madden, M. C. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.02.007 · Cited by 39

Cardiac ageing: from hallmarks to therapeutic opportunities

Hastings, M. H., Zhou, Q., Wu, C., Shabani, P., Huang, S., Yu, X., Singh, A. P., Guseh, J. S., Li, H., Lerchenmüller, C., et al. (2024) · Cardiovascular Research · doi:10.1093/cvr/cvae124 · Cited by 42

Efficient Induction of Extrinsic Cell Death by Dandelion Root Extract in Human Chronic Myelomonocytic Leukemia (CMML) Cells

Ovadje, P., Hamm, C. M., & Pandey, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030604 · Cited by 40

Heat shock protein 27 mediates the effect of 1,3,5-trihydroxy-13,13-dimethyl-2H-pyran [7,6-b] xanthone on mitochondrial apoptosis in hepatocellular carcinoma

Fu, W.-M., Zhang, J.-F., Wang, H., Xi, Z., Wang, W.-M., Zhuang, P., Zhu, X. M., Chen, S., Chan, T.-M., Leung, K., et al. (2012) · Journal of Proteomics · doi:10.1016/j.jprot.2012.05.032 · Cited by 39

Ranolazine Inhibits An Oxidative Stress-induced Increase in Myocyte Sodium and Calcium Loading During Simulated-demand Ischemia

Zhang, X. Q., Yamada, S., & Barry, W. H. (2008) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0b013e318168e711 · Cited by 39

Dietary supplementation with N-acetyl cysteine, α-tocopherol and α-lipoic acid reduces the extent of oxidative stress and proinflammatory state in aged rat brain

Thakurta, I. G., Chattopadhyay, M., Ghosh, A., & Chakrabarti, S. (2012) · Biogerontology · doi:10.1007/s10522-012-9392-5 · Cited by 39

Overweight in the Elderly Induces a Switch in Energy Metabolism that Undermines Muscle Integrity

Potes, Y., Pérez-Martínez, Z., Bermejo-Millo, J. C., Rubio‐González, A., Fernández, M. F., Bermúdez, M., Arche-Coto, J. M., Solano, J. J., Boga, J. A., Oliván, M., et al. (2018) · Aging and Disease · doi:10.14336/ad.2018.0430 · Cited by 39

Sparc, an EPS-induced gene, modulates the extracellular matrix and mitochondrial function via ILK/AMPK pathways in C2C12 cells

Melouane, A., Yoshioka, M., Kanzaki, M., & St‐Amand, J. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.05.070 · Cited by 40

Decreased Mitochondrial DNA Content Drives OXPHOS Dysregulation in Chromophobe Renal Cell Carcinoma

Xiao, Y., Clima, R., Busch, J. F., Rabien, A., Kilic, E., Villegas, S. L., Timmermann, B., Attimonelli, M., Jung, K., & Meierhofer, D. (2020) · Cancer Research · doi:10.1158/0008-5472.can-20-0754 · Cited by 39

Polybrominated Diphenyl Ether Congener ( BDE ‐100) Induces Mitochondrial Impairment

Pereira, L. C., de Souza, A. O., & Dorta, D. J. (2013) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.12046 · Cited by 39

Reactive oxygen species generation in peripheral blood monocytes and oxidized LDL are increased in hyperlipidemic patients

Vasconcelos, E. M. D. A., Degasperi, G. R., Oliveira, H. C. F., Vercesi, A. E., de Faria, E. C., & Castilho, L. N. (2009) · Clinical Biochemistry · doi:10.1016/j.clinbiochem.2009.05.010 · Cited by 39

Blockade of electron transport before ischemia protects mitochondria and decreases myocardial injury during reperfusion in aged rat hearts

Tanaka‐Esposito, C., Chen, Q., & Lesnefsky, E. J. (2012) · Translational research · doi:10.1016/j.trsl.2012.01.024 · Cited by 39

Manganese ions induce H2O2 generation at the ubiquinone binding site of mitochondrial complex II

Bonke, E., Zwicker, K., & Dröse, S. (2015) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2015.06.011 · Cited by 39

Mitochondrial Targeted Antioxidant in Cerebral Ischemia

Ahmed, E., Donovan, T., Yujiao, L., & Zhang, Q. (2015) · Journal of Neurology and Neuroscience · doi:10.21767/2171-6625.100017 · Cited by 38

Electron flow into cytochrome c coupled with reactive oxygen species from the electron transport chain converts cytochrome c to a cardiolipin peroxidase: role during ischemia–reperfusion

Aluri, H. S., Simpson, D. C., Allegood, J. C., Hu, Y., Szczepanek, K., Gronert, S., Chen, Q., & Lesnefsky, E. J. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2014.07.017 · Cited by 38

Garlic extract attenuates brain mitochondrial dysfunction and cognitive deficit in obese-insulin resistant rats

Pintana, H., Sripetchwandee, J., Supakul, L., Apaijai, N., Chattipakorn, N., & Chattipakorn, S. C. (2014) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2014-0255 · Cited by 38

The leishmanicidal activity of artemisinin is mediated by cleavage of the endoperoxide bridge and mitochondrial dysfunction

Sarkar, S. D., Sarkar, D., Sarkar, A., Dighal, A., Chakrabarti, S., Staniek, K., Gille, L., & Chatterjee, M. (2018) · Parasitology · doi:10.1017/s003118201800183x · Cited by 38

Mitochondrial Dysfunction: Metabolic Drivers of Pulmonary Hypertension

Suliman, H. B., & Nozik‐Grayck, E. (2019) · Antioxidants and Redox Signaling · doi:10.1089/ars.2018.7705 · Cited by 38

Isoliquiritigenin Induces Mitochondrial Dysfunction and Apoptosis by Inhibiting mitoNEET in a Reactive Oxygen Species-Dependent Manner in A375 Human Melanoma Cells

Chen, X., Ren, H.-H., Wang, D., Chen, Y., Qu, C., Pan, Z., Liu, X., Hao, W., Wenjuan, X., Wang, K., et al. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/9817576 · Cited by 38

TRPC1 and ORAI1 channels in colon cancer

Villalobos, C., Hernández‐Morales, M., Gutiérrez, L. G., & Núñez, L. (2019) · Cell Calcium · doi:10.1016/j.ceca.2019.06.003 · Cited by 38

Mitochondrial bioenergetics links inflammation and cardiac contractility in endotoxemia

Vico, T. A., Marchini, T., Ginart, S., Lorenzetti, M. A., Areán, J. S. A., Calabró, V., Garcés, M., Ferrero, M. C., Mazo, T., D’Annunzio, V., et al. (2019) · Basic Research in Cardiology · doi:10.1007/s00395-019-0745-y · Cited by 38

Gentamicin Affects the Bioenergetics of Isolated Mitochondria and Collapses the Mitochondrial Membrane Potential in Cochlear Sensory Hair Cells

O’Reilly, M., Young, L., Kirkwood, N. K., Richardson, G. P., Kros, C. J., & Moore, A. L. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00416 · Cited by 38

Aberrant Upregulation of Compensatory Redox Molecular Machines May Contribute to Sperm Dysfunction in Infertile Men with Unilateral Varicocele: A Proteomic Insight

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Hypoglycemic activity of puerarin through modulation of oxidative stress and mitochondrial function via AMPK

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