Nitric oxide as an antioxidant

Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor

Palmer, R. M. J., Ferrige, A. G., & Moncada, S. (1987) · Nature · doi:10.1038/327524a0 · Cited by 10,704 · see citing works

A modification of the Lowry procedure to simplify protein determination in membrane and lipoprotein samples

Markwell, M. A. K., Haas, S. M., BIEBER, L. L., & Tolbert, N. E. (1978) · Analytical Biochemistry · doi:10.1016/0003-2697(78)90586-9 · Cited by 6,460 · see citing works

Oxygen-Derived Free Radicals in Postischemic Tissue Injury

Epstein, F. H., & McCord, J. M. (1985) · New England Journal of Medicine · doi:10.1056/nejm198501173120305 · Cited by 5,399 · see citing works

Nitric oxide: A cytotoxic activated macrophage effector molecule

Hibbs, J. B., Taintor, R. R., Vavrin, Z., & Rachlin, E. M. (1988) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(88)80015-9 · Cited by 2,030 · see citing works

Nitric oxide. A macrophage product responsible for cytostasis and respiratory inhibition in tumor target cells

Stuehr, D. J., & Nathan, C. F. (1989) · The Journal of Experimental Medicine · doi:10.1084/jem.169.5.1543 · Cited by 1,744 · see citing works

Macrophage oxidation of L-arginine to nitrite and nitrate: nitric oxide is an intermediate

Marletta, M. A., Yoon, P. S., Iyengar, R., Leaf, C. D., & Wishnok, J. S. (1988) · Biochemistry · doi:10.1021/bi00424a003 · Cited by 1,601 · see citing works

Biosynthesis And Metabolism Of Endothelium-Derived Nitric Oxide

Ignarro, L. J. (1990) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pa.30.040190.002535 · Cited by 1,300 · see citing works

Biosynthesis of nitric oxide from l-arginine

Moncada, S., Palmer, R. M. J., & Higgs, E. A. (1989) · Biochemical Pharmacology · doi:10.1016/0006-2952(89)90403-6 · Cited by 1,211 · see citing works

The importance of free radicals and catalytic metal ions in human diseases.

Halliwell, B., & Gutteridge, J. M. C. (1985) · Molecular Aspects of Medicine · doi:10.1016/0098-2997(85)90001-9 · Cited by 941 · see citing works

Correlation between nitric oxide formation during degradation of organic nitrates and activation of guanylate cyclase

Feelisch, M., & Noack, E. (1987) · European Journal of Pharmacology · doi:10.1016/0014-2999(87)90493-6 · Cited by 887 · see citing works

Spectrophotometric determination of serum iron at the submicrogram level with a new reagent (ferrozine)

Carter, P. M. (1971) · Analytical Biochemistry · doi:10.1016/0003-2697(71)90405-2 · Cited by 787 · see citing works

Initiation of lipid peroxidation in biological systems

Kanner, J., German, J. B., Kinsella, J., & Hultin, H. O. (1987) · C R C Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398709527457 · Cited by 382 · see citing works

Initiation of membranal lipid peroxidation by activated metmyoglobin and methemoglobin

Kanner, J., & Harel, S. (1985) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(85)90282-6 · Cited by 359 · see citing works

Electromagnetic Properties of Hemoproteins

Yonetani, T., Yamamoto, H., Erman, J. E., Leigh, J. S., & Reed, G. H. (1972) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)45449-5 · Cited by 345 · see citing works

On the participation of higher oxidation states of iron and copper in fenton reactions

Sutton, H. C., & Winterbourn, C. C. (1989) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(89)90160-3 · Cited by 340 · see citing works

Quantitative and kinetic characterization of nitric oxide and EDRF released from cultured endothelial cells

Kelm, M., Feelisch, M., Spahr, R., Piper, H. M., Noack, E., & Schrader, J. (1988) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(88)90675-4 · Cited by 339 · see citing works

Restoration of the responsiveness of purified guanylate cyclase to nitrosoguanidine, nitric oxide, and related activators by heme and hemeproteins. Evidence for involvement of the paramagnetic nitrosyl-heme complex in enzyme activation.

Craven, P. A., & DeRubertis, F. R. (1978) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)34310-7 · Cited by 328 · see citing works

Spectroscopic studies and bonding model for nitric oxide complexes of iron porphyrins

Wayland, B. B., & Olson, L. W. (1974) · Journal of the American Chemical Society · doi:10.1021/ja00826a013 · Cited by 293 · see citing works

Cooperativity in the dissociation of nitric oxide from hemoglobin.

Moore, E. G., & Gibson, Q. H. (1976) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)33557-3 · Cited by 292 · see citing works

Generation of nitric oxide by human neutrophils

Wright, C. D., Mülsch, A., Busse, R., & Oßwald, H. (1989) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(89)92506-0 · Cited by 292 · see citing works

Conformation, co-operativity and ligand binding in human hemoglobin

Cassoly, R., & Gibson, Q. H. (1975) · Journal of Molecular Biology · doi:10.1016/0022-2836(75)90382-4 · Cited by 259 · see citing works

Helichrome: synthesis and enzymic activity of a designed hemeprotein

Sasaki, T., & Kaiser, E. T. (1989) · Journal of the American Chemical Society · doi:10.1021/ja00183a065 · Cited by 244 · see citing works

Nitric oxide from L-arginine stimulates the soluble guanylate cyclase in adrenal glands

Palacios‐Callender, M., Knowles, R. G., Palmer, R. M. J., & Moncada, S. (1989) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(89)80037-3 · Cited by 237 · see citing works

Paramagnetic Resonance Study of Nitric Oxide Hemoglobin

Kon, H. (1968) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)93262-x · Cited by 230 · see citing works

Oxidizing intermediates in the reaction of ferrous EDTA with hydrogen peroxide. Reactions with organic molecules and ferrocytochrome c.

Rush, J. D., & Koppenol, W. H. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)62677-3 · Cited by 200 · see citing works

An Electron Spin Resonance Study of Some Complexes of Iron, Nitric Oxide, and Anionic Ligands

McDonald, C. C., Phillips, W. D., & Mower, H. F. (1965) · Journal of the American Chemical Society · doi:10.1021/ja01093a007 · Cited by 192 · see citing works

Vascular smooth muscle-derived relaxing factor (MDRF) and its close similarity to nitric oxide

Wood, K. S., Buga, G. M., Byrns, R. E., & Ignarro, L. J. (1990) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(90)91243-l · Cited by 177 · see citing works

Trapping of nitric oxide produced during denitrification by extracellular hemoglobin.

Goretski, J., & Hollocher, T. C. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)69208-7 · Cited by 175 · see citing works

Quantitation of the hydroxyl radical by reaction with dimethyl sulfoxide

Steiner, M. G., & Babbs, C. F. (1990) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(90)90288-a · Cited by 161 · see citing works

Enzymatic formation of nitrogen oxides from L-arginine in bovine brain cytosol

Schmidt, H. H. H. W., Wilke, P., Evers, B., & Böhme, E. (1989) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(89)91067-x · Cited by 157 · see citing works

Free radical‐induced pathology

Clark, I. A., Cowden, W. B., & Hunt, N. H. (1985) · Medicinal Research Reviews · doi:10.1002/med.2610050303 · Cited by 148 · see citing works

Developments in inorganic nitrogen chemistry

Colburn, C. B. (1966) · Medical Entomology and Zoology · Cited by 147 · see citing works

Picosecond and nanosecond geminate recombination of myoglobin with carbon monoxide, oxygen, nitric oxide and isocyanides

Jongeward, K. A., Magde, D., Taube, D. J., Marsters, J. C., Traylor, T. G., & Sharma, V. S. (1988) · Journal of the American Chemical Society · doi:10.1021/ja00210a011 · Cited by 133 · see citing works

The effect of pH on the conversion of superoxide to hydroxyl free radicals

Baker, M. S., & Gebicki, J. M. (1984) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(84)90348-5 · Cited by 127 · see citing works

The Generation of Ferryl or Hydroxyl Radicals During Interaction of Haemproteins with Hydrogen Peroxide

Harel, S., & Kanner, J. (1988) · Free Radical Research Communications · doi:10.3109/10715768809068555 · Cited by 110 · see citing works

Mechanisms of reoxygenation injury in myocardial infarction: Implications of a myoglobin redox cycle

Galaris, D., Eddy, L. J., Arduini, A., Cadenas, E., & Hochstein, P. (1989) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(89)80125-1 · Cited by 95 · see citing works

Formation of Bovine Nitrosylmyoglobin. I. pH 4.5-6.5*

Fox, J. B., & Thomson, J. S. (1963) · Biochemistry · doi:10.1021/bi00903a012 · Cited by 85 · see citing works

The interaction of oxymyoglobin with hydrogen peroxide: The formation of ferrylmyoglobin at moderate excesses of hydrogen peroxide

Whitburn, K. D. (1987) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(87)90195-0 · Cited by 80 · see citing works

The role of NADPH-cytochrome b5 reductase in microsomal lipid peroxidation

Bidlack, W. R., Okita, R. T., & Hochstein, P. E. (1973) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(73)90684-0 · Cited by 79 · see citing works

Iron Release from Metmyoglobin, Methaemoglobin and Cytochrome C by A System Generating Hydrogen Peroxide

Harel, S., Salan, M. A., & Kanner, J. (1988) · Free Radical Research Communications · doi:10.3109/10715768809068554 · Cited by 78 · see citing works

Co-oxidation of salicylate and cholesterol during the oxidation of metmyoglobin by H2O2

Galaris, D., Mira, D., Sevanian, A., Cadenas, E., & Hochstein, P. (1988) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(88)90184-1 · Cited by 63 · see citing works

Antioxidative effect of nitrite in cured meat products: nitric oxide-iron complexes of low molecular weight

Kanner, J., Harel, S., Shagalovich, J., & Berman, S. (1984) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf00123a023 · Cited by 61 · see citing works

Nitric‐oxide myoglobin as an inhibitor of lipid oxidation

Kanner, J., BEN‐GERA, I., & Berman, S. (1980) · Lipids · doi:10.1007/bf02534419 · Cited by 48 · see citing works

Haemoglobin and Myoglobin as Inhibitors of Hydroxyl Radical Generation in a Model System of “Iron Redox” Cycle

Harel, S., & Kanner, J. (1989) · Free Radical Research Communications · doi:10.3109/10715768909073422 · Cited by 30 · see citing works

Significance of peroxynitric acid in atmospheric chemistry of nitrogen oxides

Cox, R. A., Derwent, R. G., & HUTTON, A. J. L. (1977) · Nature · doi:10.1038/270328a0 · Cited by 29 · see citing works

Rates of OH radical reactions. II. The combination reaction OH+NO+M

Overend, R. P., Paraskevopoulos, G., & Black, C. (1976) · The Journal of Chemical Physics · doi:10.1063/1.431984 · Cited by 23 · see citing works

Gas-phase reactions of the hydroperoxide and peroxyformate anions

Bowie, J. H., DePuy, C. H., Sullivan, S. A., & Bierbaum, V. M. (1986) · Canadian Journal of Chemistry · doi:10.1139/v86-175 · Cited by 16 · see citing works

The ferritins: molecular properties, iron storage function and cellular regulation

Harrison, P. M., & Arosio, P. (1996) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(96)00022-9 · Cited by 2,667 · see citing works

Molecular mechanisms underlying chemopreventive activities of anti-inflammatory phytochemicals: down-regulation of COX-2 and iNOS through suppression of NF-κB activation

Surh, Y., Chun, K., Cha, H.-H., Han, S. S., Keum, Y., Park, K.-K., & Lee, S. S. (2001) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(01)00183-x · Cited by 1,620 · see citing works

Chemical biology of nitric oxide: insights into regulatory, cytotoxic, and cytoprotective mechanisms of nitric oxide

Wink, D. A., & Mitchell, J. B. (1998) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(98)00092-6 · Cited by 1,606 · see citing works

Nitric oxide regulation of superoxide and peroxynitrite-dependent lipid peroxidation. Formation of novel nitrogen-containing oxidized lipid derivatives

Rubbo, H., Radí, R., Trujillo, M., Telleri, R., Kalyanaraman, B., Barnes, S., KIRK, M. C., & Freeman, B. Α. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)47160-8 · Cited by 1,350 · see citing works

Perspectives series: host/pathogen interactions. Mechanisms of nitric oxide-related antimicrobial activity.

Fang, F. C. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119473 · Cited by 1,139 · see citing works

Nitric oxide release from a single cell measured in situ by a porphyrinic-based microsensor

Maliñski, T., & Taha, Z. (1992) · Nature · doi:10.1038/358676a0 · Cited by 1,071 · see citing works

Nitric Oxide: Pathophysiological Mechanisms

Gross, S. S., & Wolin, M. S. (1995) · Annual Review of Physiology · doi:10.1146/annurev.ph.57.030195.003513 · Cited by 888 · see citing works

Biologically relevant metal ion‐dependent hydroxyl radical generation An update

Halliwell, B. B., & Gutteridge, J. M. C. (1992) · FEBS Letters · doi:10.1016/0014-5793(92)80911-y · Cited by 884 · see citing works

Nitric Oxide: The Versatility of an Extensive Signal Molecule

Lamattina, L., García‐Mata, C., Graziano, M., & Pagnussat, G. C. (2003) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.54.031902.134752 · Cited by 877 · see citing works

Nitric oxide protects against cellular damage and cytotoxicity from reactive oxygen species.

Wink, D. A., Hanbauer, I., Krishna, M. C., DeGraff, W., Gamson, J., & Mitchell, J. B. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.21.9813 · Cited by 766 · see citing works

Oxidative processes in meat and meat products: Quality implications

Kanner, J. (1994) · Meat Science · doi:10.1016/0309-1740(94)90040-x · Cited by 737 · see citing works

Nitric oxide and cancer: a review

Choudhari, S. K., Chaudhary, M. S., Bagde, S., Gadbail, A. R., & Joshi, V. (2013) · World Journal of Surgical Oncology · doi:10.1186/1477-7819-11-118 · Cited by 638 · see citing works

Renal ischemia/reperfusion injury; from pathophysiology to treatment.

Malek, M., & Nematbakhsh, M. (2015) · PubMed Central · doi:10.12861/jrip.2015.06 · Cited by 593 · see citing works

Role of oxidants in microbial pathophysiology

Miller, R. A., & Britigan, B. E. (1997) · Clinical Microbiology Reviews · doi:10.1128/cmr.10.1.1 · Cited by 577 · see citing works

Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation

Tejero, J., Shiva, S., & Gladwin, M. T. (2019) · Physiological Reviews · doi:10.1152/physrev.00036.2017 · Cited by 541 · see citing works

Nitric Oxide Protects Cultured Rat Hepatocytes from Tumor Necrosis Factor-α-induced Apoptosis by Inducing Heat Shock Protein 70 Expression

Kim, Y., de Vera, M. E., Watkins, S. C., & Billiar, T. R. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.2.1402 · Cited by 524 · see citing works

Nitric Oxide: Cytotoxicity versus Cytoprotection— How, Why, When, and Where?

Kröncke, K., Fehsel, K., & Kolb-Bachofen, V. (1997) · Nitric Oxide · doi:10.1006/niox.1997.0118 · Cited by 511 · see citing works

Role of nitric oxide in gastrointestinal and hepatic function and disease

Stark, M. E., & Szurszewski, J. H. (1992) · Gastroenterology · doi:10.1016/0016-5085(92)91454-c · Cited by 481 · see citing works

Oxidative stress in schizophrenia: An integrated approach

Bitanihirwe, B. K. Y., & Woo, T.-U. W. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.10.008 · Cited by 474 · see citing works

A Role for Nitric Oxide in Muscle Repair: Nitric Oxide–mediated Activation of Muscle Satellite Cells

Anderson, J. E. (2000) · Molecular Biology of the Cell · doi:10.1091/mbc.11.5.1859 · Cited by 455 · see citing works

I. Physiological chemistry of nitric oxide and its metabolites: implications in inflammation

Grisham, M. B., Jourd’heuil, D., & Wink, D. A. (1999) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1999.276.2.g315 · Cited by 451 · see citing works

Mechanisms of nitric oxide-related antimicrobial activity

Fang, F. C. (1997) · Journal of Clinical Investigation · Cited by 446 · see citing works

Mechanisms of the Antioxidant Effects of Nitric Oxide

Wink, D. A., Miranda, K. M., Espey, M. G., Pluta, R. M., Hewett, S. J., Colton, C. A., Vitek, M. P., Feelisch, M., & Grisham, M. B. (2001) · Antioxidants and Redox Signaling · doi:10.1089/152308601300185179 · Cited by 400 · see citing works

Nitric oxide and lipid peroxidation

Hogg, N., & Kalyanaraman, B. (1999) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/s0005-2728(99)00027-4 · Cited by 380 · see citing works

[24] Nitric oxide assay using hemoglobin method

Murphy, M. E., & Noack, E. (1994) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(94)33027-1 · Cited by 361 · see citing works

Ferritin as a source of iron for oxidative damage

Reif, D. W. (1992) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(92)90091-t · Cited by 357 · see citing works

Modulation of Superoxide-dependent Oxidation and Hydroxylation Reactions by Nitric Oxide

Miles, A. M., Bohle, D. S., Glassbrenner, P. A., Hansert, B., Wink, D. A., & Grisham, M. B. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.1.40 · Cited by 352 · see citing works

Chronic oxidative stress and radiation‐induced late normal tissue injury: a review

Robbins, M. E. C., & Zhao, W. (2004) · International Journal of Radiation Biology · doi:10.1080/09553000410001692726 · Cited by 349 · see citing works

Biology of nitric oxide signaling

Liaudet, L., Soriano, F. G., & Szabó, C. (2000) · Critical Care Medicine · doi:10.1097/00003246-200004001-00005 · Cited by 326 · see citing works

Blood Radicals: Reactive Nitrogen Species, Reactive Oxygen Species, Transition Metal Ions, and the Vascular System

Darley-Usmar, V. M., & Halliwell, B. B. (1996) · Pharmaceutical Research · doi:10.1023/a:1016079012214 · Cited by 312 · see citing works

Evidence that Alzheimer’s disease is a microvascular disorder: the role of constitutive nitric oxide

de la Torre, J. C., & Stefano, G. B. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(00)00043-6 · Cited by 307 · see citing works

Endogenous nitric oxide enhances prostaglandin production in a model of renal inflammation.

Salvemini, D., Seibert, K., Masferrer, J. L., Misko, T. P., Currie, M. G., & Needleman, P. (1994) · Journal of Clinical Investigation · doi:10.1172/jci117185 · Cited by 306 · see citing works

Modulation of leukocyte–endothelial interactions by reactive metabolites of oxygen and nitrogen: relevance to ischemic heart disease

Grisham, M. B., Granger, D. N., & Lefer, D. J. (1998) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(98)00094-x · Cited by 293 · see citing works

Chemical biology of nitric oxide: Regulation and protective and toxic mechanisms

Wink, D. A., Hanbauer, I., Grisham, M. B., Laval, F., Nims, R. W., Laval, J., Cook, J. C., Pacelli, R., Liebmann, J., Krishna, M. C., et al. (1996) · Current topics in cellular regulation · doi:10.1016/s0070-2137(96)80006-9 · Cited by 288 · see citing works

Biological nitric oxide signalling: chemistry and terminology

Heinrich, T. A., da Silva, R. S., Miranda, K. M., Switzer, C., Wink, D. A., & Fukuto, J. M. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12217 · Cited by 287 · see citing works

Role of oxidative stress and nitric oxide in atherothrombosis

Lubos, E. (2008) · Frontiers in bioscience · doi:10.2741/3084 · Cited by 290 · see citing works

Plant Survival in a Changing Environment: The Role of Nitric Oxide in Plant Responses to Abiotic Stress

Simontacchi, M., Galatro, A., Ramos-Artuso, F., & Santa-Marı́a, G. E. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00977 · Cited by 278 · see citing works

Nitric oxide and peroxynitrite. The ugly, the uglier and the not so good

Halliwell, B. B., Zhao, K., & Whiteman, M. (1999) · Free Radical Research · doi:10.1080/10715769900301221 · Cited by 275 · see citing works

Nitric Oxide as a Unique Bioactive Signaling Messenger in Physiology and Pathophysiology

Tuteja, N., Chandra, M., Tuteja, R., & Misra, M. K. (2004) · BioMed Research International · doi:10.1155/s1110724304402034 · Cited by 269 · see citing works

Antioxidants, diabetes and endothelial dysfunction

Laight, D. W. (2000) · Cardiovascular Research · doi:10.1016/s0008-6363(00)00054-7 · Cited by 264 · see citing works

Role of nitric oxide in skeletal muscle: synthesis, distribution and functional importance

Reid, M. B. (1998) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.1998.0303f.x · Cited by 263 · see citing works

Nitric oxide, an inhibitor of lipid oxidation by lipoxygenase, cyclooxygenase and hemoglobin

Kanner, J., Harel, S., & Granit, R. (1992) · Lipids · doi:10.1007/bf02537058 · Cited by 247 · see citing works

The pharmacology of nitroxyl (HNO) and its therapeutic potential: Not just the janus face of NO11This review is dedicated to the career of Prof. Herbert T. Nagasawa, a pioneer in the field of HNO chemistry, biochemistry and pharmacology.

Paolocci, N., Jackson, M. I., Lopez, B., Miranda, K. M., Tocchetti, C. G., Wink, D. A., Hobbs, A. J., & Fukuto, J. M. (2006) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2006.11.002 · Cited by 243 · see citing works

Nitric Oxide and Myoglobins

Møller, J. K. S., & Skibsted, L. H. (2002) · Chemical Reviews · doi:10.1021/cr000078y · Cited by 228 · see citing works

Reactive oxygen species and reactive nitrogen species: Relevance to cyto(neuro)toxic events and neurologic disorders. An overview

Metodiewa, D., & Kośka, C. (1999) · Neurotoxicity Research · doi:10.1007/bf03033290 · Cited by 227 · see citing works

Superoxide anion and endothelial regulation of arterial tone

Katušić, Z. S. (1996) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(96)02116-8 · Cited by 211 · see citing works

The Cytotoxicity of Nitroxyl: Possible Implications for the Pathophysiological Role of NO

Wink, D. A., Feelisch, M., Fukuto, J. M., Chistodoulou, D., Jourd’heuil, D., Grisham, M. B., Yoram Vodovotz, B., Cook, J. A., Krishna, M. C., DeGraff, W., et al. (1998) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1997.0565 · Cited by 211 · see citing works

Nitric oxide, reactive oxygen species, and skeletal muscle contraction

Reid, M. B. (2001) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-200103000-00006 · Cited by 198 · see citing works

Nitric oxide and quality and safety of muscle based foods

Skibsted, L. H. (2011) · Nitric Oxide · doi:10.1016/j.niox.2011.03.307 · Cited by 201 · see citing works

Oxidative damage pathways in relation to normal tissue injury

Zhao, W., Diz, D. I., & Robbins, M. E. C. (2007) · British Journal of Radiology · doi:10.1259/bjr/18237646 · Cited by 201 · see citing works

Neuroprotective Properties of Nitric Oxide

Chiueh, C. C. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb08007.x · Cited by 200 · see citing works

Nitric Oxide Mechanism of Protection in Ischemia and Reperfusion Injury

Phillips, L., Toledo, A. H., López-Neblina, F., Anaya‐Prado, R., & Toledo-Pereyra, L. H. (2009) · Journal of Investigative Surgery · doi:10.1080/08941930802709470 · Cited by 192 · see citing works

Metal–organic frameworks for solar energy conversion by photoredox catalysis

Fang, Y., Ma, Y., Zheng, M., Yang, P., Asiri, A. M., & Wang, X. (2017) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2017.09.013 · Cited by 188 · see citing works

Direct and indirect effects of nitric oxide in chemical reactions relevant to biology

Wink, D. A., Grisham, M. B., Mitchell, J. B., & Ford, P. C. (1996) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(96)68006-9 · Cited by 182 · see citing works

Deficiency of Endothelial Nitric-Oxide Synthase Confers Susceptibility to Diabetic Nephropathy in Nephropathy-Resistant Inbred Mice

Kanetsuna, Y., Takahashi, K., Nagata, M., GANNON, M. A., Breyer, M. D., Harris, R. C., & Takahashi, T. (2007) · American Journal Of Pathology · doi:10.2353/ajpath.2007.060481 · Cited by 177 · see citing works

Nitric oxide (NO) protects against cellular damage by reactive oxygen species

Wink, D. A., Cook, J. A., Pacelli, R., Liebmann, J., Krishna, M. C., & Mitchell, J. B. (1995) · Toxicology Letters · doi:10.1016/0378-4274(95)03557-5 · Cited by 173 · see citing works

A Novel Hydrogen Sulfide Prodrug, SG 1002, Promotes Hydrogen Sulfide and Nitric Oxide Bioavailability in Heart Failure Patients

Polhemus, D. J., Li, Z., Pattillo, C. B., Gojon, G., Gojon, G., Giordano, T., & Krum, H. (2015) · Cardiovascular Therapeutics · doi:10.1111/1755-5922.12128 · Cited by 171 · see citing works

The Role of Nitric Oxide in Inflammation

Lyons, C. R. (1995) · Advances in immunology · doi:10.1016/s0065-2776(08)60589-1 · Cited by 169 · see citing works

The Physiological and Pathological Chemistry of Nitric Oxide

Beckman, J. S. (1996) · Elsevier eBooks · doi:10.1016/b978-012435555-2/50002-4 · Cited by 168 · see citing works

Neuroprotection by S ‐nitrosoglutathione of brain dopamine neurons from oxidative stress

Rauhala, P. V., Lin, A. M., & Chiueh, C. C. (1998) · The FASEB Journal · doi:10.1096/fasebj.12.2.165 · Cited by 166 · see citing works

Role of vascular nitric oxide in physiological and pathological conditions

Marı́n, J., & Rodríguez-Martínez, M. A. (1997) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(97)00051-x · Cited by 162 · see citing works

Nitric oxide protection of rat liver from lipid peroxidation, collagen accumulation, and liver damage induced by carbon tetrachloride

Muriel, P. (1998) · Biochemical Pharmacology · doi:10.1016/s0006-2952(98)00220-2 · Cited by 155 · see citing works

Is nitric oxide overproduction the target of choice for the management of septic shock?

Feihl, F., Waeber, B., & Liaudet, L. (2001) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(01)00155-3 · Cited by 151 · see citing works

Signaling and stress: The redox landscape in NOS2 biology

Thomas, D. D., Heinecke, J. L., Ridnour, L. A., Cheng, R. Y., Kesarwala, A. H., Switzer, C. H., McVicar, D. W., Roberts, D. D., Glynn, S., Fukuto, J. M., et al. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.06.002 · Cited by 150 · see citing works

Crosstalk between reactive oxygen species and nitric oxide in plants: Key role of S-nitrosoglutathione reductase

Lindermayr, C. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.11.027 · Cited by 147 · see citing works

Cellular antioxidant and pro-oxidant actions of nitric oxide

Joshi, M. S., Ponthier, J. L., & Lancaster, J. R. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(99)00179-3 · Cited by 147 · see citing works

Cyclooxygenase-derived products modulate the increased intrahepatic resistance of cirrhotic rat livers

Graupera, M., García‐Pagán, J. C., Abraldeṣ, J. G., Peralta, C., Bragulat, M., Corominola, H., Bosch, J., & Rodés, J. (2003) · Hepatology · doi:10.1053/jhep.2003.50004 · Cited by 145 · see citing works

Biochemistry of Nitric Oxide

Habib, S., & Ali, A. (2011) · Indian Journal of Clinical Biochemistry · doi:10.1007/s12291-011-0108-4 · Cited by 144 · see citing works

The oxidation of α‐tocopherol in human low‐density lipoprotein by the simultaneous generation of superoxide and nitric oxide

Hogg, N., Darley-Usmar, V. M., Wilson, M. T., & Moncada, S. (1993) · FEBS Letters · doi:10.1016/0014-5793(93)81790-7 · Cited by 144 · see citing works

Nitric oxide as a regulator of inflammatory processes

Wallace, J. L. (2005) · Memórias do Instituto Oswaldo Cruz · doi:10.1590/s0074-02762005000900002 · Cited by 142 · see citing works

The hydroxyl radical scavengers dimethylsulfoxide and dimethylthiourea protect rats against thioacetamide-induced fulminant hepatic failure

Bruck, R., Aeed, H., Shirin, H., Matas, Z., Zaidel, L., Avni, Y., & Halpern, Z. (1999) · Journal of Hepatology · doi:10.1016/s0168-8278(99)80160-3 · Cited by 141 · see citing works

Role of nitric oxide in the pathogenesis of muscular dystrophies: A “two hit” hypothesis of the cause of muscle necrosis

Rando, T. A. (2001) · Microscopy Research and Technique · doi:10.1002/jemt.1172 · Cited by 141 · see citing works

Nitric Oxide Levels and Lipid Peroxidation in Plasma of Patients with Gastric Cancer

Bakan, E. (2002) · Japanese Journal of Clinical Oncology · doi:10.1093/jjco/hyf035 · Cited by 136 · see citing works

Nitric oxide/nucleophile complexes inhibit the in vitro proliferation of A375 melanoma cells via nitric oxide release.

Maragos, C. M., Wang, J., Hrabie, J. A., Oppenheim, J. J., & Keefer, L. K. (1993) · PubMed · Cited by 135 · see citing works

Diazeniumdiolates:

Fitzhugh, A. L., & Keefer, L. K. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00251-3 · Cited by 132 · see citing works

Nitric oxide regulation of superoxide-dependent lung injury: Oxidant-protective actions of endogenously produced and exogenously administered nitric oxide

Gutierrez, H. H., Nieves, B., Chumley, P. H., Rivera, A., & Freeman, B. Α. (1996) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(95)02226-0 · Cited by 128 · see citing works

Oxidative Stress Promotes Blood Cell-Endothelial Cell Interactions in the Microcirculation

Cooper, D., Stokes, K. Y., Tailor, A., & Granger, D. N. (2002) · Cardiovascular Toxicology · doi:10.1007/s12012-002-0002-7 · Cited by 127 · see citing works

Cytotoxicity of nitric oxide in Fu5 rat hepatoma cells: evidence for co-operative action with hydrogen peroxide

IOANNIDIS, I., & de GROOT, H. (1993) · Biochemical Journal · doi:10.1042/bj2960341 · Cited by 126 · see citing works

Immune processes in the pathogenesis of Parkinson's disease - a potential role for microglia and nitric oxide.

Członkowska, A., Kurkowska‐Jastrzębska, I., Członkowski, A., Peter, D., & Stefano, G. B. (2002) · PubMed · Cited by 123 · see citing works

Reduction of Ferrylmyoglobin and Ferrylhemoglobin by Nitric Oxide: A Protective Mechanism against Ferryl Hemoprotein-Induced Oxidations

Gorbunov, N. V., Osipov, A. N., Day, B. W., Zayas-Rivera, B., Kagan, V. E., & Elsayed, N. M. (1995) · Biochemistry · doi:10.1021/bi00020a014 · Cited by 123 · see citing works

Human sperm endothelial nitric oxide synthase expression: correlation with sperm motility

O’Bryan, M. K., Zini, A. S., Cheng, C. Y., & Schlegel, P. N. (1998) · Fertility and Sterility · doi:10.1016/s0015-0282(98)00382-3 · Cited by 120 · see citing works

Modulation of ion channels by reactive oxygen and nitrogen species: a pathophysiological role in brain aging?

Annunziato, L., Pannaccione, A., Cataldi, M., Secondo, A., Castaldo, P., Renzo, G. F. D., & Taglialatela, M. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(02)00069-6 · Cited by 120 · see citing works

Nitric Oxide-induced Conversion of Cellular Chelatable Iron into Macromolecule-bound Paramagnetic Dinitrosyliron Complexes

Toledo, J. C., Bosworth, C. A., Hennon, S. W., Mahtani, H., Bergonia, H. A., & Lancaster, J. R. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m707862200 · Cited by 117 · see citing works

Therapeutic role of nitric oxide as emerging molecule

Kumar, S., Singh, R. K., & Bhardwaj, T. (2016) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2016.11.125 · Cited by 116 · see citing works

The redox pathway of S -nitrosoglutathione, glutathione and nitric oxide in cell to neuron communications

Chiueh, C. C., & Rauhala, P. V. (1999) · Free Radical Research · doi:10.1080/10715769900301211 · Cited by 115 · see citing works

Oxidation of low-density lipoproteins: questions of initiation, propagation, and the effect of antioxidants

Halliwell, B. B. (1995) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/61.3.670s · Cited by 114 · see citing works

Mechanisms of Cell Signaling by Nitric Oxide and Peroxynitrite: From Mitochondria to MAP Kinases

Levonen, A., Patel, R. P., Brookes, P. S., Go, Y., Jo, H., Parthasarathy, S., Anderson, P. G., & Darley-Usmar, V. M. (2001) · Antioxidants and Redox Signaling · doi:10.1089/152308601300185188 · Cited by 112 · see citing works

Cytokine stimulation of nitric oxide formation and differential regulation in hepatocytes and nonparenchymal cells of endotoxemic rats

Spitzer, J. A. (1994) · Hepatology · doi:10.1002/hep.1840190132 · Cited by 111 · see citing works

Cyclooxygenase-independent chemoprevention with an aspirin derivative in a rat model of colonic adenocarcinoma

Bak, A., McKnight, W., Li, P., Soldato, P. D., Calignano, A., Cirino, G., & Wallace, J. L. (1998) · Life Sciences · doi:10.1016/s0024-3205(98)00191-x · Cited by 110 · see citing works

[43] Antioxidant effects of nitric oxide

Wink, D. A., Yoram Vodovotz, B., Grisham, M. B., DeGraff, W., Cook, J. C., Pacelli, R., Krishna, M. C., & Mitchell, J. B. (1999) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(99)01105-2 · Cited by 109 · see citing works

Nitric oxide production in experimental alcoholic liver disease in the rat: Role in protection from injury

Nanji, A. A., Greenberg, S. S., Tahan, S. R., Fogt, F., Loscalzo, J., Sadrzadeh, S. M. H., Xie, J., & Stamler, J. S. (1995) · Gastroenterology · doi:10.1016/0016-5085(95)90400-x · Cited by 109 · see citing works

Regulation of Peroxiredoxins by Nitric Oxide in Immunostimulated Macrophages

Diet, A., Abbas, K., Bouton, C., Guillon, B., Tomasello, M. F., Fourquet, S., Tolédano, M. B., & Drapier, J. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m706420200 · Cited by 107 · see citing works

Diabetes-induced endothelial dysfunction in streptozotocin-treated rats

Dai, F. X., Diederich, A., Skopec, J., & Diederich, D. A. (1993) · Journal of the American Society of Nephrology · doi:10.1681/asn.v461327 · Cited by 106 · see citing works

Nitric Oxide Synthase and Xanthine Oxidase Activities in the Spermatic Vein of Patients with Varicocele: A Potential Role for Nitric Oxide and Peroxynitrite in Sperm Dysfunction

Mitropoulos, D., Deliconstantinos, G., Zervas, A., Villiotou, V., Dimopoulos, C., & Stavrides, J. C. (1996) · The Journal of Urology · doi:10.1016/s0022-5347(01)65403-x · Cited by 105 · see citing works

Apparent Role of Hydroxyl Radicals in Oxidative Brain Injury Induced by Sodium Nitroprusside

Rauhala, P. V., Khaldi, A., Mohanakumar, K. P., & Chiueh, C. C. (1998) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(97)00386-9 · Cited by 105 · see citing works

Vasoactive substances

Russo, G., Leopold, J. A., & Loscalzo, J. (2002) · Vascular Pharmacology · doi:10.1016/s1537-1891(02)00250-1 · Cited by 103 · see citing works

The Chemical Biology of Nitric Oxide

Wink, D. A., Feelisch, M., Yoram Vodovotz, B., Fukuto, J. M., & Grisham, M. B. (2006) · Kluwer Academic Publishers eBooks · doi:10.1007/0-306-46806-9_10 · Cited by 102 · see citing works

The Cardioprotective Actions of Hydrogen Sulfide in Acute Myocardial Infarction and Heart Failure

Polhemus, D. J., Calvert, J. W., Butler, J., & Lefer, D. J. (2014) · Scientifica · doi:10.1155/2014/768607 · Cited by 101 · see citing works

Effect of Nitric Oxide on Iron–Mediated Oxidative Stress in Primary Rat Hepatocyte Culture

Sergent, O., Griffon, B., Morel, I., Chevanne, M., Dubos, M., Cillard, P., & Cillard, J. (1997) · Hepatology · doi:10.1002/hep.510250123 · Cited by 101 · see citing works

Inhibition by interferon-gamma of human mononuclear cell-mediated low density lipoprotein oxidation. Participation of tryptophan metabolism along the kynurenine pathway.

Christen, S., Thomas, S. R., Garner, B., & Stocker, R. (1994) · Journal of Clinical Investigation · doi:10.1172/jci117211 · Cited by 99 · see citing works

Kinetic and mechanistic studies of the reactions of nitrogen monoxide and nitrite with ferryl myoglobin

Herold, S., & Rehmann, F. K. (2001) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s007750100231 · Cited by 80 · see citing works

Nitric‐oxide myoglobin as an inhibitor of lipid oxidation

Kanner, J., BEN‐GERA, I., & Berman, S. (1980) · Lipids · doi:10.1007/bf02534419 · Cited by 48 · see citing works

The modulation of ferryl myoglobin formation and its oxidative effects on low density lipoproteins by nitric oxide

Dee, G., Rice-Evans, C. A., Obeyesekera, S., Meraji, S., Jacobs, M., & Bruckdorfer, K. R. (1991) · FEBS Letters · doi:10.1016/0014-5793(91)81338-9 · Cited by 93 · see citing works

Reduction of Ferrylmyoglobin and Ferrylhemoglobin by Nitric Oxide: A Protective Mechanism against Ferryl Hemoprotein-Induced Oxidations

Gorbunov, N. V., Osipov, A. N., Day, B. W., Zayas-Rivera, B., Kagan, V. E., & Elsayed, N. M. (1995) · Biochemistry · doi:10.1021/bi00020a014 · Cited by 123 · see citing works

Does the Oxidation of Nitric Oxide by oxyMyoglobin Share an Intermediate with the metMyoglobin-Catalyzed Isomerization of Peroxynitrite?

Koebke, K. J., Pauly, D. J., Lerner, L., Liu, X., & Pacheco, A. A. (2013) · Inorganic Chemistry · doi:10.1021/ic400697a · Cited by 26 · see citing works