Degradation of phospholipids by oxidative stress—Exceptional significance of cardiolipin

PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT

Lowry, O. H., Rosebrough, N., Farr, A. L., & Randall, R. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52451-6 · Cited by 315,771 · see citing works

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

Bradford, M. M. (1976) · Analytical Biochemistry · doi:10.1016/0003-2697(76)90527-3 · Cited by 255,302 · see citing works

A SIMPLE METHOD FOR THE ISOLATION AND PURIFICATION OF TOTAL LIPIDES FROM ANIMAL TISSUES

Folch, J., Lees, M., & Stanley, G. H. S. (1957) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)64849-5 · Cited by 65,189 · see citing works

A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

Bligh, E. G., & Dyer, W. J. (1959) · Canadian Journal of Biochemistry and Physiology · doi:10.1139/o59-099 · Cited by 54,751 · see citing works

Two dimensional thin layer chromatographic separation of polar lipids and determination of phospholipids by phosphorus analysis of spots

Rouser, G., Fleischer, S., & Yamamoto, A. (1970) · Lipids · doi:10.1007/bf02531316 · Cited by 3,280 · see citing works

Strategies of antioxidant defense

SIES, H. (1993) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1993.tb18025.x · Cited by 1,976 · see citing works

Biochemistry of Oxidative Stress

Sies, H. (1986) · Angewandte Chemie International Edition in English · doi:10.1002/anie.198610581 · Cited by 1,316 · see citing works

Mitochondrial Oxidative Stress: Implications for Cell Death

Orrenius, S., Gogvadze, V. G., & Zhivotovsky, B. (2006) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.47.120505.105122 · Cited by 1,266 · see citing works

Cardiolipin Stabilizes Respiratory Chain Supercomplexes

Pfeiffer, K., Gohil, V., Stuart, R. A., Hunte, C., Brandt, U., Greenberg, M. L., & Schägger, H. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m308366200 · Cited by 843 · see citing works

The biosynthesis and functional role of cardiolipin

Schlame, M., Rua, D., & Greenberg, M. L. (2000) · Progress in Lipid Research · doi:10.1016/s0163-7827(00)00005-9 · Cited by 810 · see citing works

Improved analysis of malondialdehyde in human body fluids

Jentzsch, A. M., Bachmann, H., Fürst, P., & Biesalski, H. K. (1996) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(95)02043-8 · Cited by 805 · see citing works

Role of cardiolipin alterations in mitochondrial dysfunction and disease

Chicco, A. J., & Sparagna, G. C. (2006) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00243.2006 · Cited by 641 · see citing works

Cytochrome c/cardiolipin relations in mitochondria: a kiss of death

Kagan, V. E., Bayır, H., Belikova, N. A., Kapralov, A. A., Tyurina, Y. Y., Tyurin, V. A., Jiang, J., Stoyanovsky, D. A., Wipf, P., Kochanek, P. M., et al. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.03.004 · Cited by 445 · see citing works

Cardiolipin membrane domains in prokaryotes and eukaryotes

Mileykovskaya, E., & Dowhan, W. (2009) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2009.04.003 · Cited by 391 · see citing works

Oxidative lipidomics of apoptosis: redox catalytic interactions of cytochrome c with cardiolipin and phosphatidylserine

Kagan, V. E., Borisenko, G. G., Tyurina, Y. Y., Tyurin, V. A., Jiang, J., Potapovich, A. I., Kini, V., Amoscato, A. A., & Fujii, Y. (2004) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2004.08.016 · Cited by 342 · see citing works

Cardiolipin defines the interactome of the major ADP/ATP carrier protein of the mitochondrial inner membrane

Claypool, S. M., Oktay, Y., Boontheung, P., Loo, J. A., & Koehler, C. M. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200801152 · Cited by 318 · see citing works

Functional binding of cardiolipin to cytochromec oxidase

Robinson, N. C. (1993) · Journal of Bioenergetics and Biomembranes · doi:10.1007/bf00762857 · Cited by 265 · see citing works

Role of cardiolipin peroxidation and Ca2+ in mitochondrial dysfunction and disease

Paradies, G., Petrosillo, G., Paradies, V., & Ruggiero, F. M. (2009) · Cell Calcium · doi:10.1016/j.ceca.2009.03.012 · Cited by 261 · see citing works

The role of cardiolipin in the structural organization of mitochondrial membranes

Schlame, M., & Ren, M. (2009) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2009.04.019 · Cited by 248 · see citing works

O2 solubility in aqueous media determined by a kinetic method

Reynafarje, B., Costa, L. E., & Lehninger, A. L. (1985) · Analytical Biochemistry · doi:10.1016/0003-2697(85)90381-1 · Cited by 226 · see citing works

Medical, biochemical and chemical aspects of free radicals

(1990) · General Pharmacology The Vascular System · doi:10.1016/0306-3623(90)91041-o · Cited by 226 · see citing works

Oxidative damage and phospholipid fatty acyl composition in skeletal muscle mitochondria from mice underexpressing or overexpressing uncoupling protein 3

BRAND, M. D., PAMPLONA, R., PORTERO-OTÍN, M., REQUENA, J. R., ROEBUCK, S. J., BUCKINGHAM, J. A., CLAPHAM, J. C., & CADENAS, S. (2002) · Biochemical Journal · doi:10.1042/bj20021077 · Cited by 184 · see citing works

Shotgun Lipidomics Identifies Cardiolipin Depletion in Diabetic Myocardium Linking Altered Substrate Utilization with Mitochondrial Dysfunction

Han, X., Yang, J., Cheng, H., Yang, K., Abendschein, D. R., & Gross, R. W. (2005) · Biochemistry · doi:10.1021/bi051908a · Cited by 181 · see citing works

Apoptotic interactions of cytochrome c: Redox flirting with anionic phospholipids within and outside of mitochondria

Bayir, H., Fadeel, B., Palladino, M. J., Witasp, E., Kurnikov, I. V., Tyurina, Y. Y., Tyurin, V. A., Amoscato, A. A., Jiang, J., Kochanek, P. M., et al. (2006) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2006.03.002 · Cited by 175 · see citing works

Oxidative stress and mitochondrial dysfunction in neurodegeneration; cardiolipin a critical target?

Pope, S. A. S., Land, J. M., & Heales, S. (2008) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2008.03.011 · Cited by 154 · see citing works

Voltage Gating of VDAC Is Regulated by Nonlamellar Lipids of Mitochondrial Membranes

Rostovtseva, T. K., Kazemi, N., Weinrich, M., & Bezrukov, S. M. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m602548200 · Cited by 136 · see citing works

Quantitative and Compositional Study of Cardiolipin in Platelets by Electrospray Ionization Mass Spectrometry: Application for the Identification of Barth Syndrome Patients

Valianpour, F., Wanders, R. J. A., Barth, P. G., Overmars, H., & Gennip, A. H. (2002) · Clinical Chemistry · doi:10.1093/clinchem/48.9.1390 · Cited by 112 · see citing works

Mitochondria‐targeted disruptors and inhibitors of cytochrome c /cardiolipin peroxidase complexes: A new strategy in anti‐apoptotic drug discovery

Kagan, V. E., Bayır, A. G., Bayır, H., Stoyanovsky, D. A., Borisenko, G. G., Tyurina, Y. Y., Wipf, P., Atkinson, J., Greenberger, J. S., Chapkin, R. S., et al. (2008) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.200700402 · Cited by 90 · see citing works

Mitochondrial dysfunction associated with cardiac ischemia/reperfusion can be attenuated by oxygen tension control. Role of oxygen-free radicals and cardiolipin

Petrosillo, G., Venosa, N. D., Ruggiero, F. M., Pistolese, M., D’Agostino, D., Tiravanti, E., Fiore, T., & Paradies, G. (2005) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2005.10.003 · Cited by 88 · see citing works

Mitochondrial Function In Ischaemia And Reperfusion Of The Ageing Heart

Pepe, S. (2000) · Clinical and Experimental Pharmacology and Physiology · doi:10.1046/j.1440-1681.2000.03326.x · Cited by 80 · see citing works

Cardiolipin Molecular Species in Rat Heart Mitochondria are Sensitive to Essential Fatty Acid-Deficient Dietary Lipids

Yamaoka, S., Urade, R., & Kito, M. (1990) · Journal of Nutrition · doi:10.1093/jn/120.5.415 · Cited by 79 · see citing works

Formation of phosphatidic acid, ceramide, and diglyceride on radiolysis of lipids: identification by MALDI-TOF mass spectrometry

Шадыро, О. И., Yurkova, I. L., Kisel, M. A., Brede, O., & Arnhold, J. (2004) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2004.03.013 · Cited by 78 · see citing works

Oxidative stress is involved in the permeabilization of the inner membrane of brain mitochondria exposed to hypoxia/reoxygenation and low micromolar Ca2+

Schild, L., & Reiser, G. (2005) · FEBS Journal · doi:10.1111/j.1742-4658.2005.04781.x · Cited by 78 · see citing works

Microanalysis of cardiolipin in small biopsies including skeletal muscle from patients with mitochondrial disease

Schlame, M., Shanske, S., Doty, S. B., König, T., Sculco, T. P., DiMauro, S., & Blanck, T. J. J. (1999) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)33404-0 · Cited by 71 · see citing works

Molecular species of cardiolipin in relation to other mitochondrial phospholipids

Schlame, M., Beyer, K., Hayer-Hartl, M. K., & Klingenberg, M. (1991) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1991.tb16144.x · Cited by 70 · see citing works

Initiation of Apoptotic Signal by the Peroxidation of Cardiolipin of Mitochondria

Nakagawa, Y. (2004) · Springer eBooks · doi:10.1007/978-3-662-41088-2_18 · Cited by 61 · see citing works

Initiation of Apoptotic Signal by the Peroxidation of Cardiolipin of Mitochondria

NAKAGAWA, Y. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1293.018 · Cited by 60 · see citing works

Cardiolipin activates cytochrome c peroxidase activity since it facilitates H2O2 access to heme

IuA, V., Proskurnina, E. V., Izmailov, D. Y., Novikov, A. A., Brusnichkin, A. V., Osipov, A. N., & Kagan, V. E. (2006) · Biochemistry (Moscow) · doi:10.1134/s0006297906090082 · Cited by 59 · see citing works

Transbilayer Lipid Diffusion Promoted by Bax: Implications for Apoptosis

Epand, R. F., Martinou, J., Montessuit, S., & Epand, R. M. (2003) · Biochemistry · doi:10.1021/bi035348w · Cited by 58 · see citing works

Formation of phosphatidic acid in stressed mitochondria

Yurkova, I. L., Stuckert, F., Kisel, M. A., Шадыро, О. И., Arnhold, J., & Hüster, D. (2008) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2008.09.007 · Cited by 33 · see citing works

Differential effects of endothelial cell fatty acid modification on the sensitivity of their membrane phospholipids to peroxidation

Vossen, R. C. R. M., van Dam-Mieras, M. C. E., Hornstra, G., & Zwaal, R. F. A. (1995) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/0952-3278(95)90036-5 · Cited by 30 · see citing works

Rapid isocratic method for the separation and quantification of major phospholipid classes by high-performance liquid chromatography

Shafiq‐ur‐Rehman (1991) · Journal of Chromatography B Biomedical Sciences and Applications · doi:10.1016/0378-4347(91)80306-w · Cited by 27 · see citing works

Injury of mitochondrial respiration and membrane potential during iron/ascorbate-induced peroxidation

Wiswedel, I., Trümper, L., Schild, L., & Augustin, W. (1988) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(88)90122-3 · Cited by 26 · see citing works

Dietary Essential Fatty Acids Change the Fatty Acid Profile of Rat Neural Mitochondria Over Time

Dyer, J. R., & Greenwood, C. E. (1991) · Journal of Nutrition · doi:10.1093/jn/121.10.1548 · Cited by 17 · see citing works

Influence of Mg2+-ions on the properties of rat heart mitochondria in dependence on the preparation.

Schaller, H., Letko, G., & Kunz, W. S. (1978) · PubMed · Cited by 12 · see citing works

Redox regulation of mitochondrial function

Handy, D. E., & Loscalzo, J. (2012) · Antioxidants & Redox Signaling · doi:10.1089/ars.2011.4123 · Cited by 588 · see citing works

First‐in‐class cardiolipin‐protective compound as a therapeutic agent to restore mitochondrial bioenergetics

Szeto, H. H. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12461 · Cited by 550 · see citing works

The Mitochondrial-Targeted Compound SS-31 Re-Energizes Ischemic Mitochondria by Interacting with Cardiolipin

Birk, A. V., Liu, S., Soong, Y., Mills, W., Singh, P. K., Warren, J. D., Seshan, S. V., Pardee, J. D., & Szeto, H. H. (2013) · Journal of the American Society of Nephrology · doi:10.1681/asn.2012121216 · Cited by 486 · see citing works

Mitochondrial oxidative stress in aging and healthspan

Dai, D., Chiao, Y. A., Marcinek, D. J., Szeto, H. H., & Rabinovitch, P. S. (2014) · Longevity & Healthspan · doi:10.1186/2046-2395-3-6 · Cited by 481 · see citing works

Manganese Superoxide Dismutase: Guardian of the Powerhouse

Holley, A. K., Bakthavatchalu, V., Velez-Roman, J. M., & St. Clair, D. K. (2011) · International Journal of Molecular Sciences · doi:10.3390/ijms12107114 · Cited by 358 · see citing works

Mitochondrial Dysfunction and β -Cell Failure in Type 2 Diabetes Mellitus

Ma, Z. A., Zhao, Z., & TURK, J. W. (2011) · Experimental Diabetes Research · doi:10.1155/2012/703538 · Cited by 214 · see citing works

Mitochondria and Reactive Oxygen Species. Which Role in Physiology and Pathology?

Lenaz, G. (2011) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-2869-1_5 · Cited by 214 · see citing works

Impaired Autophagy Induces Chronic Atrophic Pancreatitis in Mice via Sex- and Nutrition-Dependent Processes

Diakopoulos, K. N., Lesina, M., Wörmann, S. M., Song, L., Aichler, M., Schild, L., Artati, A., Römisch‐Margl, W., Wartmann, T., Fischer, R., et al. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.12.003 · Cited by 177 · see citing works

Advances in methods for the determination of biologically relevant lipid peroxidation products

Spickett, C. M., Wiswedel, I., Siems, W., Žarković, K., & Žarković, N. (2010) · Free Radical Research · doi:10.3109/10715762.2010.498476 · Cited by 152 · see citing works

Phase 2a Clinical Trial of Mitochondrial Protection (Elamipretide) During Stent Revascularization in Patients With Atherosclerotic Renal Artery Stenosis

Saad, A., Herrmann, S. M., Eirin, A., Ferguson, C. M., Glockner, J. F., Bjarnason, H., McKusick, M. A., Misra, S., Lerman, L. O., & Textor, S. C. (2017) · Circulation Cardiovascular Interventions · doi:10.1161/circinterventions.117.005487 · Cited by 125 · see citing works

Mitochondrial dynamics, a key executioner in neurodegenerative diseases

Panchal, K., & Tiwari, A. K. (2018) · Mitochondrion · doi:10.1016/j.mito.2018.11.002 · Cited by 127 · see citing works

Reduced Iron-Containing Clay Minerals as Antibacterial Agents

Wang, X., Dong, H., Zeng, Q., Xia, Q., Zhang, L., & Zhou, Z. (2017) · Environmental Science & Technology · doi:10.1021/acs.est.7b00726 · Cited by 99 · see citing works

Improved health-span and lifespan in mtDNA mutator mice treated with the mitochondrially targeted antioxidant SkQ1

Shabalina, I. G., Vyssokikh, M. Y., Gibanova, N. V., Csikasz, R. I., Edgar, D., Waldemarson, A. H., Rozhdestvenskaya, Z., Bakeeva, L. E., Vays, V. B., Pustovidko, A. V., et al. (2017) · Aging · doi:10.18632/aging.101174 · Cited by 96 · see citing works

Alcohol-induced oxidative/nitrosative stress alters brain mitochondrial membrane properties

Reddy, V. D., Padmavathi, P., Kavitha, G., Bulle, S., & Nallanchakravarthula, V. (2012) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-012-1526-1 · Cited by 86 · see citing works

Multistep and multitask Bax activation

Ghibelli, L., & Diederich, M. F. (2010) · Mitochondrion · doi:10.1016/j.mito.2010.08.003 · Cited by 84 · see citing works

Cyclosporine A-induced apoptosis in renal tubular cells is related to oxidative damage and mitochondrial fission

de Arriba, G., Calvino, M., Martínez, S. B., & Parra, T. (2013) · Toxicology Letters · doi:10.1016/j.toxlet.2013.01.007 · Cited by 83 · see citing works

Origins of metabolic complications in obesity

Carobbio, S., Rodríguez‐Cuenca, S., & Vidal‐Puig, A. (2011) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e32834ad966 · Cited by 64 · see citing works

Lipid metabolism and oxidative stress in patients with Alzheimer's disease and amnestic mild cognitive impairment

Nie, Y., Chu, C., Qin, Q., Shen, H., Wen, L., Tang, Y., & Qu, M. (2023) · Brain Pathology · doi:10.1111/bpa.13202 · Cited by 63 · see citing works

Methylglyoxal induces oxidative stress and mitochondrial dysfunction in osteoblastic MC3T3-E1 cells

Suh, K. S., Choi, E. M., Rhee, S. Y., & Kim, Y. S. (2013) · Free Radical Research · doi:10.3109/10715762.2013.859387 · Cited by 57 · see citing works

Mechanisms of Enhanced Antibacterial Activity by Reduced Chitosan-Intercalated Nontronite

Xia, Q., Wang, X., Zeng, Q., Guo, D., Zhu, Z., Chen, H., & Dong, H. (2020) · Environmental Science & Technology · doi:10.1021/acs.est.9b07185 · Cited by 49 · see citing works

The Role of Peroxidation of Mitochondrial Membrane Phospholipids in Pancreatic β -Cell Failure

Ma, Z. A. (2011) · Current Diabetes Reviews · doi:10.2174/157339912798829232 · Cited by 45 · see citing works

Prevention of free fatty acid-induced lipid accumulation, oxidative stress, and cell death in primary hepatocyte cultures by a Gynostemma pentaphyllum extract

Müller, C., Gardemann, A., Keilhoff, G., Peter, D., Wiswedel, I., & Schild, L. (2012) · Phytomedicine · doi:10.1016/j.phymed.2011.12.002 · Cited by 46 · see citing works

Peroxiredoxin 6 Confers Protection Against Nonalcoholic Fatty Liver Disease Through Maintaining Mitochondrial Function

Lee, D. H., Jung, Y. Y., Park, M. H., Jo, M. R., Han, S., Yoon, D. Y., Roh, Y. S., & Hong, J. T. (2019) · Antioxidants and Redox Signaling · doi:10.1089/ars.2018.7544 · Cited by 45 · see citing works

Three Classes of Antioxidant Defense Systems and the Development of Postmenopausal Osteoporosis

Yang, K., Cao, F., Xue, Y., Tao, L., & Zhu, Y. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.840293 · Cited by 46 · see citing works

Quality control systems in cardiac aging

Quarles, E. K., Dai, D., Tocchi, A., Basisty, N., Gitari, L., & Rabinovitch, P. S. (2015) · Ageing Research Reviews · doi:10.1016/j.arr.2015.02.003 · Cited by 40 · see citing works

Acute Hypoxia and Exercise-Induced Blood Oxidative Stress

McGinnis, G. R., Kliszczewicz, B. M., Barberio, M. D., Ballmann, C. G., Peters, B. A., Slivka, D. R., Dumke, C., Cuddy, J. S., Hailes, W. S., Ruby, B. C., et al. (2014) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.2013-0188 · Cited by 39 · see citing works

Amorphous solid dispersion of Berberine mitigates apoptosis via iPLA 2 β/Cardiolipin/Opa1 pathway in db/db mice and in Palmitate-treated MIN6 β-cells

Li, J., Du, H., Zhang, M., Zhang, Z., Teng, F., Zhao, Y., Zhang, W., Yu, Y., Feng, L., Cui, X., et al. (2019) · International Journal of Biological Sciences · doi:10.7150/ijbs.32020 · Cited by 37 · see citing works

Effects of Organic Ligands on the Antibacterial Activity of Reduced Iron-Containing Clay Minerals: Higher Extracellular Hydroxyl Radical Production Yet Lower Bactericidal Activity

Xia, Q., Chen, J., & Dong, H. (2023) · Environmental Science & Technology · doi:10.1021/acs.est.3c00033 · Cited by 34 · see citing works

Regulation of adipose tissue energy availability through blood flow control in the metabolic syndrome

Alemany, M. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.03.003 · Cited by 35 · see citing works

Peroxidative permeabilization of liposomes induced by cytochrome c/cardiolipin complex

Firsov, A. M., Kotova, Е. А., Korepanova, E. A., Osipov, A. N., & Antonenko, Y. N. (2014) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2014.11.027 · Cited by 33 · see citing works

Caveolin‐3 deficiency associated with the dystrophy P104L mutation impairs skeletal muscle mitochondrial form and function

Shah, D. S., Nisr, R. B., Stretton, C., Krasteva‐Christ, G., & Hundal, H. S. (2020) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12541 · Cited by 33 · see citing works

Dietary Docosahexaenoic Acid (22:6) Incorporates into Cardiolipin at the Expense of Linoleic Acid (18:2): Analysis and Potential Implications

Cortie, C. H., & Else, P. L. (2012) · International Journal of Molecular Sciences · doi:10.3390/ijms131115447 · Cited by 33 · see citing works

PLIN2 Mediates Neuroinflammation and Oxidative/Nitrosative Stress via Downregulating Phosphatidylethanolamine in the Rostral Ventrolateral Medulla of Stressed Hypertensive Rats

Zhang, S., Hu, L., Han, C., Huang, R., Ooi, K., Qian, X., Ren, X., Chu, D., Zhang, H., Du, D., et al. (2021) · Journal of Inflammation Research · doi:10.2147/jir.s329230 · Cited by 29 · see citing works

Exendin-4 Protects Mitochondria from Reactive Oxygen Species Induced Apoptosis in Pancreatic Beta Cells

Li, Z., Zhou, Z., Huang, G., Hu, F., Xiang, Y., & He, L.-N. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076172 · Cited by 29 · see citing works

Biochemical disorders associated with antiproliferative effect of dehydroepiandrosterone in hepatoma cells as revealed by LC-based metabolomics

Cheng, M., Shiao, M., Chiu, D. T.-Y., Weng, S.-F., Tang, H.-Y., & Ho, H. (2011) · Biochemical Pharmacology · doi:10.1016/j.bcp.2011.07.104 · Cited by 28 · see citing works

Flavonoids affect the endophytic bacterial community in Ginkgo biloba leaves with increasing altitude

Fu, S., Deng, Y., Zou, K., Zhang, S., Liu, X., & Liang, Y. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.982771 · Cited by 26 · see citing works

Sequential Detection of Lipids, Metabolites, and Proteins in One Tissue for Improved Cancer Differentiation Accuracy

Lu, H., Zhang, H., Chingin, K., Wei, Y., Xu, J., Ke, M., Huang, K., Feng, S., & Chen, H. (2019) · Analytical Chemistry · doi:10.1021/acs.analchem.9b01507 · Cited by 26 · see citing works

Mitochondrial ROS and Apoptosis

El-Osta, H., & Circu, M. (2016) · Springer eBooks · doi:10.1007/978-3-319-42139-1_1 · Cited by 23 · see citing works

Lipidomic analysis of molecular cardiolipin species in livers exposed to ischemia/reperfusion

Martens, J.-C., Keilhoff, G., Halangk, W., Wartmann, T., Gardemann, A., Päge, I., & Schild, L. (2014) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-014-2282-1 · Cited by 22 · see citing works

Effects of NMDA-Receptor Antagonist on the Expressions of Bcl-2 and Bax in the Subventricular Zone of Neonatal Rats with Hypoxia–Ischemia Brain Damage

Fan, H., Li, X., Wang, W., Lai, Q., Tang, X., Gao, D., Yin, X., & Xu, T. (2015) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-015-0586-8 · Cited by 20 · see citing works

Electrochemical Signals of Mitochondria: A New Probe of Their Membrane Properties

Hermes, M., Scholz, F., Härdtner, C., Walther, R., Schild, L., Wolke, C., & Lendeckel, U. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201101235 · Cited by 18 · see citing works

Links between Insulin Resistance, Lipoprotein Metabolism and Amyloidosis in Alzheimer’s Disease

Martins, I. J., & Creegan, R. (2014) · Health · doi:10.4236/health.2014.612190 · Cited by 17 · see citing works

Mono- and Polyunsaturated Fatty Acids Counter Palmitate-Induced Mitochondrial Dysfunction in Rat Skeletal Muscle Cells

Nisr, R. B., Shah, D. S., & Hundal, H. S. (2020) · Cellular Physiology and Biochemistry · doi:10.33594/000000282 · Cited by 17 · see citing works

Targeting Mitochondria during Cold Storage to Maintain Proteasome Function and Improve Renal Outcome after Transplantation

Lo, S., Blaszak, R. T., & Parajuli, N. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103506 · Cited by 15 · see citing works

Mineral and/or milk supplementation of fruit beverages helps in the prevention of H2O2-induced oxidative stress in Caco-2 cells.

Cilla, A., Laparra, J. M., Alegrı́a, A., & Barberá, R. (2011) · PubMed · doi:10.1590/s0212-16112011000300027 · Cited by 11 · see citing works

The protective effects of sciadopitysin against methylglyoxal‐induced cytotoxicity in cultured pancreatic β‐cells

Suh, K. S., Chon, S., & Choi, E. M. (2018) · Journal of Applied Toxicology · doi:10.1002/jat.3620 · Cited by 10 · see citing works

Maintaining Mitochondrial Morphology in AKI

Hall, A. M. (2013) · Journal of the American Society of Nephrology · doi:10.1681/asn.2013050519 · Cited by 9 · see citing works

Impact of acute heat stress on mitochondrial function, ultrastructure and cardiolipin distribution in Arabidopsis

Wang, Y., Pan, R., & Hu, J. (2024) · aBIOTECH · doi:10.1007/s42994-024-00151-x · Cited by 7 · see citing works

Long-term Exposure to Acetaminophen is a Crucial for Activity of Selected Antioxidative Enzymes and Level of Lipid Peroxidation Process in Rat Liver

Polaniak, R., Bułdak, R. J., & Jacheć, W. (2011) · Journal of Bioequivalence & Bioavailability · doi:10.4172/jbb.1000082 · Cited by 7 · see citing works

Oxidation of cardiolipin is involved in functional impairment and disintegration of liver mitochondria by hypoxia/reoxygenation in the presence of increased Ca2+ concentrations

Martens, J.-C., Keilhoff, G., Gardemann, A., & Schild, L. (2014) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-014-2087-2 · Cited by 6 · see citing works

Palmitate protects hepatocytes from oxidative stress and triacylglyceride accumulation by stimulation of nitric oxide synthesis in the presence of high glucose and insulin concentration

Müller, C., Gardemann, A., Keilhoff, G., Peter, D., Wiswedel, I., Kropf, S., & Schild, L. (2010) · Free Radical Research · doi:10.3109/10715762.2010.512919 · Cited by 5 · see citing works

Electrochemical Signals of Mitochondria: A New Probe of Their Membrane Properties

Hermes, M., Scholz, F., Härdtner, C., Walther, R., Schild, L., Wolke, C., & Lendeckel, U. (2011) · Angewandte Chemie · doi:10.1002/ange.201101235 · Cited by 3 · see citing works

The link between pediatric heart failure and mitochondrial lipids

Fillmore, N., & Lopaschuk, G. D. (2014) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2014.08.002 · Cited by 3 · see citing works

Comment on “The effects of mercury exposure on Amazonian fishes: An investigation of potential biomarkers”

Hussain, S., Saadi, S., & Hassan, W. (2023) · Chemosphere · doi:10.1016/j.chemosphere.2023.138564 · Cited by 3 · see citing works

Oxidative Stress, Metabolism and Photoaging – The Role of Mitochondria

Jackson, M. J., Naidoo, K., & Birch‐Machin, M. A. (2019) · Royal Society of Chemistry eBooks · doi:10.1039/9781788015981-00105 · Cited by 2 · see citing works

The Effects of High Fat Diets With and Without N-Acetylcysteine Supplementation on the Lipin-1 Levels of Serum and Various Tissues in Rats

Kural, B. V., Alver, A., Canpolat, S., Kahraman, C., Altay, D. U., Kara, H., & Akçan, B. (2014) · Turkish Journal of Biochemistry · doi:10.5505/tjb.2014.78941 · Cited by 2 · see citing works

Autophagy and Proteostasis in Cardiac Aging

Dai, D., & Rabinovitch, P. S. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-805253-2.00015-8 · Cited by 2 · see citing works

Pulmonary Hypertension Is a Probable NO/ONOO−Cycle Disease: A Review

Pall, M. L. (2012) · ISRN Hypertension · doi:10.5402/2013/742418 · Cited by 2 · see citing works

Manganese Superoxide Dismutase (MnSOD) and Its Importance in Mitochondrial Function and Cancer

Holley, A. K., & Clair, D. K. S. (2016) · Oxidative stress in applied basic research and clinical practice · doi:10.1007/978-3-319-30705-3_3 · Cited by 2 · see citing works

Les cardiolipides, des phospholipides clés pour la fonction mitochondriale. Relation avec les apports lipidiques et la physiopathologie

Feillet‐Coudray, C., Fouret, G., Casas, F., & Coudray, C. (2015) · Cahiers de Nutrition et de Diététique · doi:10.1016/j.cnd.2015.04.002 · Cited by 1 · see citing works

Investigations of peroxidation of membrane phospholipids

Cortie, C. H. (2015) · Research Online (University of Wollongong) · Cited by 1 · see citing works

Induction of Oxidative Stress by Iron/Ascorbate in Isolated Mitochondria and by UV Irradiation in Human Skin

Wiswedel, I., Augustin, W., Quist, S., Gollnick, H. P. M., & Gardemann, A. (2011) · Humana Press eBooks · doi:10.1007/978-1-60761-956-7_20

Papel do inflamassoma NLRP3 nas alterações vasculares promovidas pelo diabetes tipo 1 em modelo induzido por estreptozotocina

Pereira, C. A. (2019) · doi:10.11606/t.17.2019.tde-08112018-150821

Untargeted metabolic profiling of dogs with a suspected toxic mitochondrial myopathy using liquid chromatography-mass spectrometry

Hunt, H., Fraser, K., Cave, N., Gartrell, B. D., Petersen, J., & Roe, W. (2019) · Toxicon · doi:10.1016/j.toxicon.2019.05.007

Discovery and investigation of a novel role for mitochondrial prohibitin in mitigating acute heart failure in endotoxic shock

Mattox, T. A. (2014) · The Scholarship East Carolina University's Institutional Repository (East Carolina University)

Protective Role of Citric Acid Against Arsenic, Mercury, Lead, Iron and Sodium Nitroprusside Induced Phospholipids DegradationPreprint

Hussain, S., Saadi, S., & Hassan, W. (2023) · SSRN Electronic Journal · doi:10.2139/ssrn.4603445

Peptide pACC1-nano complex suppresses ACC1-mediated lipogenesis 5 in breast cancer cells via altering p53/NF-κB pathway of signallingPreprint

Manimaran, D., & Palanisamy, V. (2025) · Research Square · doi:10.21203/rs.3.rs-6273696/v1

Mitochondrial cardiolipin and other structural changes mediating cardiac dysfunction in the reperfused myocardium

Zhang, L. T., Groenewald, A., Ward, M., & Power, A. (2026) · Current Opinion in Physiology · doi:10.1016/j.cophys.2026.100961

High‐Cholesterol Diet Supplemented With Methionine During Pregnancy Modulates Hepatic MMP‐2 and MMP‐9 Activities and Aggravates Iron Overload and Fatty Liver Development in Rabbits

Ait-Benali, S., Fernane, A., Benazzoug, Y., & Othmani-Mecif, K. (2026) · ChemistrySelect · doi:10.1002/slct.74180

Oxidation of cardiolipin is involved in functional impairment and disintegration of liver mitochondria by hypoxia/reoxygenation in the presence of increased Ca2+ concentrations

Martens, J.-C., Keilhoff, G., Gardemann, A., & Schild, L. (2014) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-014-2087-2 · Cited by 6 · see citing works

Metabolism and Biological Function of Cardiolipin

Nakagawa, Y. (2013) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.13-00052 · Cited by 9 · see citing works

Identification of oxidation products of cardiolipin using mass spectrometry

Maciel, E. A. (2010) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · Cited by 1 · see citing works

Profiling of cardiolipins and their hydroperoxides in HepG2 cells by LC/MS

Chen, Z., Wu, Y., Ma, Y., Kobayashi, Y., Zhao, Y., Miura, Y., Chiba, H., & Hui, S. (2017) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-017-0515-3 · Cited by 19 · see citing works

Cardiolipin: characterization of distinct oxidized molecular species

Kim, J. H., Minkler, P. E., Salomon, R. G., Anderson, V. E., & Hoppel, C. L. (2010) · Journal of Lipid Research · doi:10.1194/jlr.m010520 · Cited by 67 · see citing works