Respiratory chain linked H2O2 production in pigeon heart mitochondria

DETERMINATION OF SERUM PROTEINS BY MEANS OF THE BIURET REACTION

Gornall, A. G., Bardawill, C. J., & David, M. M. (1949) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)57021-6 · Cited by 16,164 · see citing works

The Respiratory Chain and Oxidative Phosphorylation

Chance, B., & Williams, G. R. (1956) · Advances in enzymology and related areas of molecular biology/Advances in enzymology and related subjects · doi:10.1002/9780470122624.ch2 · Cited by 2,084 · see citing works

THE LARGE-SCALE SEPARATION OF PEROXISOMES, MITOCHONDRIA, AND LYSOSOMES FROM THE LIVERS OF RATS INJECTED WITH TRITON WR-1339

Leighton, F., Poole, B., Beaufay, H., Baudhuin, P., Coffey, J. W., Fowler, S., & Duve, C. D. (1968) · The Journal of Cell Biology · doi:10.1083/jcb.37.2.482 · Cited by 1,116 · see citing works

Flavin and Pyridine Nucleotide Oxidation-Reduction Changes in Perfused Rat Liver

Scholz, R., Thurman, R. G., WILLIAMSON, J. R., Chance, B., & Bücher, T. (1969) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)78228-3 · Cited by 254 · see citing works

Partial Resolution of the Enzymes Catalyzing Oxidative Phosphorylation

Hinkle, P. C., Butow, R. A., Racker, E., & Chance, B. (1967) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)99410-x · Cited by 195 · see citing works

A Sensitive Method for the Estimation of Hydrogen Peroxide in Biological Materials

Andreae, W. A. (1955) · Nature · doi:10.1038/175859a0 · Cited by 183 · see citing works

Succinic and Reduced Diphosphopyridine Nucleotide Oxidase Systems of Ascaris Muscle

Kmetec, E., & Bueding, E. (1961) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)64408-4 · Cited by 182 · see citing works

Antimycin-insensitive oxidation of succinate and reduced nicotinamide-adenine dinucleotide in electron-transport particles I. pH dependency and hydrogen peroxide formation

Pk, J. (1966) · Biochimica et Biophysica Acta (BBA) - Enzymology and Biological Oxidation · doi:10.1016/0926-6593(66)90057-9 · Cited by 147 · see citing works

Kinetics and mechanisms of catalase in peroxisomes of the mitochondrial fraction

Chance, B., & Oshino, N. (1971) · Biochemical Journal · doi:10.1042/bj1220225 · Cited by 139 · see citing works

Die Glutathionperoxidase: Enzymologie und biologische Aspekte

Floh�, L. (1971) · Journal of Molecular Medicine · doi:10.1007/bf01487101 · Cited by 136 · see citing works

CYTOCHROME c, CYTOCHROME OXIDASE, AND SUCCINOXIDASE ACTIVITIES OF HELMINTHS

Bueding, E., & CHARMS, B. L. (1952) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52396-1 · Cited by 98 · see citing works

Determination of Very Small Amounts of Hydrogen Peroxide

Perschke, H., & BRODA, E. E. (1961) · Nature · doi:10.1038/190257a0 · Cited by 97 · see citing works

The oxidase systems of Ascaris-muscle mitochondria

Cheah, K. S., & Chance, B. (1970) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(70)90131-3 · Cited by 45 · see citing works

Free Radicals in the Physiological Control of Cell Function

Dröge, W. (2002) · Physiological Reviews · doi:10.1152/physrev.00018.2001 · Cited by 9,855 · see citing works

How mitochondria produce reactive oxygen species

Murphy, M. P. (2009) · Biochemical Journal · doi:10.1042/bj20081386 · Cited by 8,207 · see citing works

Free radicals, metals and antioxidants in oxidative stress-induced cancer

Valko, M., Rhodes, C. J., Moncol, J., Izakovic, M., & Mazur, M. (2006) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2005.12.009 · Cited by 6,680 · see citing works

Mitochondria, Oxidants, and Aging

Balaban, R. S., Nemoto, S., & Finkel, T. (2005) · Cell · doi:10.1016/j.cell.2005.02.001 · Cited by 4,388 · see citing works

Oxidative Stress

Sies, H., Berndt, C., & Jones, D. P. (2017) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-061516-045037 · Cited by 3,520 · see citing works

Free Radicals: Properties, Sources, Targets, and Their Implication in Various Diseases

Phaniendra, A., Jestadi, D. B., & Periyasamy, L. (2015) · Indian Journal of Clinical Biochemistry · doi:10.1007/s12291-014-0446-0 · Cited by 2,886 · see citing works

The mitochondrial generation of hydrogen peroxide. General properties and effect of hyperbaric oxygen

Boveris, A., & Chance, B. (1973) · Biochemical Journal · doi:10.1042/bj1340707 · Cited by 2,626 · see citing works

High protonic potential actuates a mechanism of production of reactive oxygen species in mitochondria

Korshunov, S. S., Skulachev, V. P., & Starkov, A. A. (1997) · FEBS Letters · doi:10.1016/s0014-5793(97)01159-9 · Cited by 1,727 · see citing works

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 · see citing works

Dithiocarbamates as potent inhibitors of nuclear factor kappa B activation in intact cells.

Schreck, R., Meier, B., Männel, D. N., Dröge, W., & Baeuerle, P. A. (1992) · The Journal of experimental medicine · doi:10.1084/jem.175.5.1181 · Cited by 1,508 · see citing works

The Haber–Weiss reaction and mechanisms of toxicity

Kehrer, J. P. (2000) · Toxicology · doi:10.1016/s0300-483x(00)00231-6 · Cited by 1,418 · see citing works

Mitochondrial metabolism of reactive oxygen species

Andreyev, A. Y., Kushnareva, Y. E., & Starkov, A. A. (2005) · Biochemistry (Moscow) · doi:10.1007/s10541-005-0102-7 · Cited by 1,336 · see citing works

Generation of reactive oxygen species by the mitochondrial electron transport chain

Liu, Y., Fiskum, G., & Schubert, D. (2002) · Journal of Neurochemistry · doi:10.1046/j.0022-3042.2002.00744.x · Cited by 1,260 · see citing works

Application of glutathione depletion in cancer therapy: Enhanced ROS-based therapy, ferroptosis, and chemotherapy

Niu, B., Liao, K., Zhou, Y., Wen, T., Quan, G., Pan, X., & Wu, C. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.121110 · Cited by 1,168 · see citing works

Mitochondrial generation of superoxide and hydrogen peroxide as the source of mitochondrial redox signaling

Brand, M. D. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.04.001 · Cited by 1,063 · see citing works

Production of superoxide radicals and hydrogen peroxide by NADH-ubiquinone reductase and ubiquinol-cytochrome c reductase from beef-heart mitochondria

Cadenas, E., Boveris, A., Ragan, C. I., & Stoppani, A. O. M. (1977) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(77)90035-2 · Cited by 855 · see citing works

Signaling Functions of Reactive Oxygen Species

Forman, H. J., Maiorino, M., & Ursini, F. (2010) · Biochemistry · doi:10.1021/bi9020378 · Cited by 827 · see citing works

Role of mitochondrial <scp>ROS</scp> in the brain: from physiology to neurodegeneration

Angelova, P. R., & Abramov, A. Y. (2018) · FEBS Letters · doi:10.1002/1873-3468.12964 · Cited by 789 · see citing works

Role of ubiquinone in the mitochondrial generation of hydrogen peroxide

Boveris, A., Cadenas, E., & Stoppani, A. O. M. (1976) · Biochemical Journal · doi:10.1042/bj1560435 · Cited by 655 · see citing works

ΔΨ _m ‐Dependent and ‐independent production of reactive oxygen species by rat brain mitochondria

Votyakova, T. V., & Reynolds, I. J. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00548.x · Cited by 601 · see citing works

Mitochondrial Oxygen Radical Generation and Leak: Sites of Production in States 4 and 3, Organ Specificity, and Relation to Aging and Longevity

Barja, G. (1999) · Journal of Bioenergetics and Biomembranes · doi:10.1023/a:1005427919188 · Cited by 494 · see citing works

Mitochondrial reactive oxygen species production in excitable cells: Modulators of mitochondrial and cell function

Stowe, D. F., & Camara, A. K. S. (2009) · Antioxidants &amp; Redox Signaling · doi:10.1089/ars.2008.2331 · Cited by 471 · see citing works

Production of Reactive Oxygen Species in Brain Mitochondria: Contribution by Electron Transport Chain and Non–Electron Transport Chain Sources

Adam-Vizi, V. (2005) · Antioxidants &amp; Redox Signaling · doi:10.1089/ars.2005.7.1140 · Cited by 439 · see citing works

JNK1 and IKKβ: molecular links between obesity and metabolic dysfunction

Solinas, G., & Karin, M. (2010) · The FASEB Journal · doi:10.1096/fj.09-151340 · Cited by 347 · see citing works

Sites of superoxide and hydrogen peroxide production by muscle mitochondria assessed ex vivo under conditions mimicking rest and exercise

Goncalves, R. L. S., Quinlan, C. L., Perevoshchikova, I. V., Hey-Mogensen, M., & Brand, M. D. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.619072 · Cited by 329 · see citing works

On the history of oxidative stress: Concept and some aspects of current development

Sies, H. (2018) · Current Opinion in Toxicology · doi:10.1016/j.cotox.2018.01.002 · Cited by 285 · see citing works

Enhancement of hydrogen peroxide formation by protophores and ionophores in antimycin-supplemented mitochondria

Cadenas, E., & Boveris, A. (1980) · Biochemical Journal · doi:10.1042/bj1880031 · Cited by 275 · see citing works

Mitochondrial changes associated with glutathione deficiency

Meister, A. (1995) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/0925-4439(95)00007-q · Cited by 242 · see citing works

Respiration-dependent H2O2 removal in brain mitochondria via the thioredoxin/peroxiredoxin system

Drechsel, D. A., & Patel, M. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.101196 · Cited by 199 · 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

Redefining the major contributors to superoxide production in contracting skeletal muscle. The role of NAD(P)H oxidases

Sakellariou, G. K., Jackson, M. J., & Vasilaki, A. (2014) · Free Radical Research · doi:10.3109/10715762.2013.830718 · Cited by 184 · see citing works

The sites of superoxide anion generation in higher plant mitochondria

Rich, P. R., & Bonner, W. D. (1978) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(78)90373-9 · Cited by 146 · see citing works

Alterations in Oxygen Consumption, Respiratory Quotient, and Heat Production in Long-Lived GHRKO and Ames Dwarf Mice, and Short-Lived bGH Transgenic Mice

Westbrook, R., Bonkowski, M. S., Strader, A. D., & Bartke, A. (2009) · The Journals of Gerontology: Series A · doi:10.1093/gerona/gln075 · Cited by 143 · see citing works

Myxothiazol Induces H2O2 Production from Mitochondrial Respiratory Chain

Starkov, A. A., & Fiskum, G. (2001) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2001.4409 · Cited by 133 · see citing works

Respiration-dependent Removal of Exogenous H2O2 in Brain Mitochondria

Zoccarato, F., Cavallini, L., & Alexandre, A. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m308143200 · Cited by 130 · see citing works

Part of the Series: From Dietary Antioxidants to Regulators in Cellular Signalling and Gene ExpressionRole of reactive oxygen species and (phyto)oestrogens in the modulation of adaptive response to stress: Review

Vina, J., Borras, C., Gomez-Cabrera, M.-C., & Orr, W. C. (2006) · Free Radical Research · doi:10.1080/10715760500405778 · Cited by 125 · see citing works

H2O2 detection from intact mitochondria as a measure for one-electron reduction of dioxygen requires a non-invasive assay system11Dedicated to Prof. E. Elstner, on the occasion of his 60th anniversary.

Staniek, K., & Nohl, H. (1999) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/s0005-2728(99)00083-3 · Cited by 124 · see citing works

Mitochondrial (‘mild’) uncoupling and ROS production: Physiologically relevant or not?

Shabalina, I. G., & Nedergaard, J. (2011) · Biochemical Society Transactions · doi:10.1042/bst0391305 · Cited by 110 · see citing works

Reverse electron flow-induced ROS production is attenuated by activation of mitochondrial Ca²⁺-sensitive K⁺ channels

Heinen, A., Aldakkak, M., Stowe, D. F., Rhodes, S. S., Riess, M. L., Varadarajan, S. G., & Camara, A. K. S. (2007) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00198.2007 · Cited by 103 · see citing works

Generation of superoxide-radical by the NADH: Ubiquinone oxidoreductase of heart mitochondria

Vinogradov, A. D., & Grivennikova, V. G. (2005) · Biochemistry (Moscow) · doi:10.1007/s10541-005-0090-7 · Cited by 98 · see citing works

Effects of nitrite on modulating ROS generation following ischemia and reperfusion

Raat, N. J. H., Shiva, S., & Gladwin, M. T. (2009) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2009.02.002 · Cited by 79 · see citing works

Natural antioxidants’ effects on endoplasmic reticulum stress-related diseases

Reyes-Fermín, L. M., Aparicio-Trejo, O. E., Avila-Rojas, S. H., Gómez-Sierra, T., Martínez-Klimova, E., & Pedraza-Chaverri, J. (2020) · Food and Chemical Toxicology · doi:10.1016/j.fct.2020.111229 · Cited by 50 · see citing works

The ambiguous aspects of oxygen

Napolitano, G., Fasciolo, G., & Venditti, P. (2022) · Oxygen · doi:10.3390/oxygen2030027 · Cited by 30 · see citing works

Mitochondrial Targeted Coenzyme Q, Superoxide, and Fuel Selectivity in Endothelial Cells

Fink, B. D., O'Malley, Y., Dake, B. L., Ross, N. C., Prisinzano, T. E., & Sivitz, W. I. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004250 · Cited by 21 · see citing works

Susquehanna Chorale Spring Concert "Roots and Wings"

Hawkins, D. (2017)

Genentech taps Affimed’s antibodies

Cross, R. (2018) · C&EN Global Enterprise · doi:10.1021/cen-09635-buscon15

KOMPLIKASI REGIONAL ANESTESI PADA PEDIATRIK

Sari, D. (2023) · Jurnal Komplikasi Anestesi · doi:10.22146/jka.v5i1.7322

Enxerto livre de arteria epigastrica inferior: avaliacao hemodinamica e angiografica pre e pos-operatoria

Dib, A., Puig, L. B., Salvadori, D., et al. (1988) · Arquivos Brasileiros de Cardiologia

Interleucinas na encefalopatia hipóxico-isquêmica

Ceccon, M. E. J. R. (2003) · Jornal de Pediatria · doi:10.1590/s0021-75572003000400002 · Cited by 14 · see citing works