How biology handles nitrite

Nitric oxide: physiology, pathophysiology, and pharmacology.

Moncada, S., Palmer, R. M., & Higgs, E. A. (1991) · Pharmacological Reviews · doi:10.1016/s0031-6997(25)06663-3 · Cited by 15,525 · see citing works

Analysis of nitrate, nitrite, and [15N]nitrate in biological fluids

Green, L. C., Wagner, D. A., Glogowski, J. A., Skipper, P. L., Wishnok, J. S., & Tannenbaum, S. R. (1982) · Analytical Biochemistry · doi:10.1016/0003-2697(82)90118-x · Cited by 12,061 · see citing works

Hydroperoxide metabolism in mammalian organs.

Chance, B., Sies, H., & Boveris, A. (1979) · Physiological Reviews · doi:10.1152/physrev.1979.59.3.527 · Cited by 5,827 · see citing works

Nitric oxide, superoxide, and peroxynitrite: the good, the bad, and ugly

Beckman, J. S., & Koppenol, W. H. (1996) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1996.271.5.c1424 · Cited by 5,513 · 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

Nitrogen cycles: Past, present, and future

Galloway, J. N., Dentener, F. J., Capone, D. G., Boyer, E. W., Howarth, R. W., Seitzinger, S. P., Asner, G. P., Cleveland, C. C., Green, P. A., Holland, E. A., et al. (2004) · Biogeochemistry · doi:10.1007/s10533-004-0370-0 · Cited by 5,315 · see citing works

Induction of Apoptotic Program in Cell-Free Extracts: Requirement for dATP and Cytochrome c

Liu, X., Kim, C. N., Yang, J., Jemmerson, R., & Wang, X. (1996) · Cell · doi:10.1016/s0092-8674(00)80085-9 · Cited by 5,167 · see citing works

Prevention of Apoptosis by Bcl-2: Release of Cytochrome c from Mitochondria Blocked

Yang, J., Liu, X., Bhalla, K. N., Kim, C. N., Ibrado, A. M., Cai, J., Peng, T.-I., Jones, D. P., & Wang, X. (1997) · Science · doi:10.1126/science.275.5303.1129 · Cited by 4,913 · see citing works

The Release of Cytochrome c from Mitochondria: A Primary Site for Bcl-2 Regulation of Apoptosis

Kluck, R. M., Bossy‐Wetzel, E., Green, D. R., & Newmeyer, D. D. (1997) · Science · doi:10.1126/science.275.5303.1132 · Cited by 4,715 · see citing works

Nitric oxide synthases: structure, function and inhibition

ALDERTON, W. K., COOPER, C. E., & KNOWLES, R. G. (2001) · Biochemical Journal · doi:10.1042/bj3570593 · Cited by 4,110 · see citing works

Nitric oxide synthases: structure, function and inhibition

ALDERTON, W. K., Cooper, C. E., & Knowles, R. G. (2001) · Biochemical Journal · doi:10.1042/0264-6021:3570593 · Cited by 4,106 · see citing works

The Free Radical Theory of Aging Matures

BECKMAN, K. B., & AMES, B. N. (1998) · Physiological Reviews · doi:10.1152/physrev.1998.78.2.547 · Cited by 3,879 · see citing works

Cell biology and molecular basis of denitrification

Zumft, W. G. (1997) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.61.4.533-616.1997 · Cited by 3,483 · see citing works

Isolation of an autotrophic ammonia-oxidizing marine archaeon

Könneke, M., Bernhard, A. E., de la Torre, J. R., Walker, C. B., Waterbury, J. B., & Stahl, D. A. (2005) · Nature · doi:10.1038/nature03911 · Cited by 2,864 · see citing works

The nitrate-nitrite-nitric oxide pathway in physiology and therapeutics

Lundberg, J. O., Weitzberg, E., & Gladwin, M. T. (2008) · Nature Reviews Drug Discovery · doi:10.1038/nrd2466 · Cited by 2,739 · see citing works

The Evolution and Future of Earth’s Nitrogen Cycle

Canfield, D. E., Glazer, A. N., & Falkowski, P. G. (2010) · Science · doi:10.1126/science.1186120 · Cited by 2,697 · see citing works

Handbook of methods for oxygen radical research

Greenwald, R. A. (1987) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(87)80012-6 · Cited by 2,384 · see citing works

The Whole Structure of the 13-Subunit Oxidized Cytochrome c Oxidase at 2.8 Å

Tomitake Tsukihara, A., Aoyama, H., Yamashita, E., Tomizaki, T., Yamaguchi, H., Shinzawa‐Itoh, K., Nakashima, R., Yaono, R., & Yoshikawa, S. (1996) · Science · doi:10.1126/science.272.5265.1136 · Cited by 2,102 · see citing works

Structure at 2.8 Å resolution of cytochrome c oxidase from Paracoccus denitrificans

Iwata, S., Ostermeier, C., Ludwig, B., & Michel, H. (1995) · Nature · doi:10.1038/376660a0 · Cited by 2,006 · see citing works

Mitochondria, oxidative stress and cell death

Ott, M., Gogvadze, V. G., Orrenius, S., & Zhivotovsky, B. (2007) · APOPTOSIS · doi:10.1007/s10495-007-0756-2 · Cited by 1,976 · see citing works

Nitrite-driven anaerobic methane oxidation by oxygenic bacteria

Ettwig, K. F., Butler, M. K., Paslier, D. L., Pelletier, É., Mangenot, S., Kuypers, M. M. M., Schreiber, F., Dutilh, B. E., Zedelius, J., de Beer, D., et al. (2010) · Nature · doi:10.1038/nature08883 · Cited by 1,864 · see citing works

Nitric oxide functions as a signal in plant disease resistance

Delledonne, M., Xia, Y., Dixon, R. A., & Lamb, C. J. (1998) · Nature · doi:10.1038/29087 · Cited by 1,859 · see citing works

Nitrite reduction to nitric oxide by deoxyhemoglobin vasodilates the human circulation

Cosby, K., Partovi, K. S., Crawford, J. H., Patel, R. P., Reiter, C. D., Martyr, S., Yang, B. K., Waclawiw, M. A., Zalos, G., Xu, X., et al. (2003) · Nature Medicine · doi:10.1038/nm954 · Cited by 1,807 · see citing works

The mononuclear molybdenum enzymes

Hille, R., Hall, J., & Basu, P. (2014) · Chemical Reviews · doi:10.1021/cr400443z · Cited by 1,738 · see citing works

Principles of structure, bonding, and reactivity for metal nitrosyl complexes

Enemark, J. H., & Feltham, R. D. (1974) · Coordination Chemistry Reviews · doi:10.1016/s0010-8545(00)80259-3 · Cited by 1,656 · see citing works

The therapeutic potential of carbon monoxide

Motterlini, R., & Otterbein, L. E. (2010) · Nature Reviews Drug Discovery · doi:10.1038/nrd3228 · Cited by 1,643 · see citing works

Hydrogen peroxide sensing and signaling

Veal, E. A., Day, A. M., & Morgan, B. A. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.03.016 · Cited by 1,604 · see citing works

S-nitrosohaemoglobin: a dynamic activity of blood involved in vascular control

Jia, L., Bonaventura, C., Bonaventura, J., & Stamler, J. S. (1996) · Nature · doi:10.1038/380221a0 · Cited by 1,586 · see citing works

Missing lithotroph identified as new planctomycete

Strous, M., Fuerst, J. A., Kramer, E. H. M., Logemann, S., Gerard Muyzer, C., van de Pas-Schoonen, K. T., Webb, R. I., Kuenen, J. G., & Jetten, M. S. M. (1999) · Nature · doi:10.1038/22749 · Cited by 1,578 · see citing works

The Mononuclear Molybdenum Enzymes

Hille, R. (1996) · Chemical Reviews · doi:10.1021/cr950061t · Cited by 1,501 · see citing works

Formation of nitric oxide-derived inflammatory oxidants by myeloperoxidase in neutrophils

Eiserich, J. P., Hristova, M., Cross, C. E., Jones, A. D., Freeman, B. A., Halliwell, B., & van der Vliet, A. (1998) · Nature · doi:10.1038/34923 · Cited by 1,496 · see citing works

S-nitrosylation of proteins with nitric oxide: synthesis and characterization of biologically active compounds.

Stamler, J. S., Simon, D. I., Osborne, J. A., Mullins, M. E., Jaraki, O., Michel, T. M., Singel, D. J., & Loscalzo, J. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.1.444 · Cited by 1,471 · see citing works

Structures of Metal Sites of Oxidized Bovine Heart Cytochrome c Oxidase at 2.8 Å

Tomitake Tsukihara, A., Aoyama, H., Yamashita, E., Tomizaki, T., Yamaguchi, H., Shinzawa‐Itoh, K., Nakashima, R., Yaono, R., & Yoshikawa, S. (1995) · Science · doi:10.1126/science.7652554 · Cited by 1,415 · see citing works

Mechanisms of cytochrome c release from mitochondria

Garrido, C., Galluzzi, L., Brunet, M., Puig, P., Mirjolet, C., & Kroemer, G. (2006) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401950 · Cited by 1,394 · see citing works

Detection and Imaging of Nitric Oxide with Novel Fluorescent Indicators: Diaminofluoresceins

Kojima, H., Nakatsubo, N., Kikuchi, K., Kawahara, S., Kirino, Y., Nagoshi, H., Hirata, Y., & Nagano, T. (1998) · Analytical Chemistry · doi:10.1021/ac9801723 · Cited by 1,391 · see citing works

A microbial consortium couples anaerobic methane oxidation to denitrification

Raghoebarsing, A. A., Pol, A., van de Pas-Schoonen, K. T., Smolders, A. J. P., Ettwig, K. F., Rijpstra, W. I. C., Stefan Schouten, A., Damsté, J. S. S., den Camp, H. J. M. O., Jetten, M. S. M., et al. (2006) · Nature · doi:10.1038/nature04617 · Cited by 1,364 · see citing works

Deciphering the evolution and metabolism of an anammox bacterium from a community genome

Strous, M., Pelletier, É., Mangenot, S., Rattei, T., Lehner, A., Taylor, M. W., Horn, M., Daims, H., Mavel, D., Wincker, P., et al. (2006) · Nature · doi:10.1038/nature04647 · Cited by 1,357 · see citing works

Febuxostat Compared with Allopurinol in Patients with Hyperuricemia and Gout

Becker, M. A., Schumacher, H. R., Wortmann, R. L., MacDonald, P. A., Eustace, D., Palo, W. A., Streit, J., & Joseph-Ridge, N. (2005) · New England Journal of Medicine · doi:10.1056/nejmoa050373 · Cited by 1,357 · see citing works

Enzyme promiscuity: A mechanistic and evolutionary perspective

Tawfik, O. K. A. D. S. (2010) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-030409-143718 · Cited by 1,355 · see citing works

The biological chemistry of the elements: the inorganic chemistry of life

(1992) · Choice Reviews Online · doi:10.5860/choice.30-0286 · Cited by 1,326 · see citing works

Defense gene induction in tobacco by nitric oxide, cyclic GMP, and cyclic ADP-ribose

Durner, J., Wendehenne, D., & Klessig, D. F. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.17.10328 · Cited by 1,320 · see citing works

Nitric oxide : biology and pathobiology

Ignarro, L. J. (2000) · Cited by 1,306 · see citing works

Cytochrome c acts as a cardiolipin oxygenase required for release of proapoptotic factors

Kagan, V. E., Tyurin, V. A., Jiang, J., Tyurina, Y. Y., Ritov, V. B., Amoscato, A. A., Osipov, A. N., Belikova, N. A., Kapralov, A. A., Kini, V., et al. (2005) · Nature Chemical Biology · doi:10.1038/nchembio727 · Cited by 1,256 · see citing works

Reversible inhibition of cytochrome c oxidase, the terminal enzyme of the mitochondrial respiratory chain, by nitric oxide: Implications for neurodegenerative diseases

Cleeter, M. W. J., Cooper, J. M., Darley-Usmar, V. M., Moncada, S., & Schapira, A. H. V. (1994) · FEBS Letters · doi:10.1016/0014-5793(94)00424-2 · Cited by 1,241 · see citing works

Nitric oxide circulates in mammalian plasma primarily as an S-nitroso adduct of serum albumin.

Stamler, J. S., Jaraki, O., Osborne, J., Simon, D. I., Keaney, J., Vita, J., Singel, D., Valeri, C. R., & Loscalzo, J. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.16.7674 · Cited by 1,238 · see citing works

Superoxide radicals in feline intestinal ischemia

Granger, D. N., Rutili, G., & McCord, J. M. (1981) · Gastroenterology · doi:10.1016/0016-5085(81)90648-x · Cited by 1,212 · see citing works

Hydrogen peroxide and nitric oxide as signalling molecules in plants

Neill, S. J. (2002) · Journal of Experimental Botany · doi:10.1093/jexbot/53.372.1237 · Cited by 1,202 · see citing works

OXYGEN DEFICIENCY AND ROOT METABOLISM: Injury and Acclimation Under Hypoxia and Anoxia

DREW, M. C. (1997) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.48.1.223 · Cited by 1,181 · see citing works

Hydrogen Peroxide: A Signaling Messenger

Stone, J. R., & Yang, S. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2006.8.243 · Cited by 1,175 · see citing works

Anammox bacteria: from discovery to application

Kuenen, J. G. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1857 · Cited by 1,166 · see citing works

Cytochrome c: functions beyond respiration

Ow, Y.-L. P., Green, D. R., Hao, Z., & Mak, T. W. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2434 · Cited by 1,111 · see citing works

Nitrite and nitrate determinations in plasma: a critical evaluation

Moshage, H. J., Kok, B., Huizenga, J. R., & Jansen, P. L. M. (1995) · Clinical Chemistry · doi:10.1093/clinchem/41.6.892 · Cited by 1,093 · see citing works

Red cell membrane: past, present, and future

Mohandas, N., & Gallagher, P. G. (2008) · Blood · doi:10.1182/blood-2008-07-161166 · Cited by 1,089 · see citing works

Signal interactions between nitric oxide and reactive oxygen intermediates in the plant hypersensitive disease resistance response

Delledonne, M., Zeier, J., Marocco, A., & Lamb, C. J. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.231178298 · Cited by 1,083 · see citing works

Acute Blood Pressure Lowering, Vasoprotective, and Antiplatelet Properties of Dietary Nitrate via Bioconversion to Nitrite

Webb, A. J., Patel, N., Loukogeorgakis, S., Okorie, M., Aboud, Z., Misra, S., Rashid, R., Miall, P., Deanfield, J., Benjamin, N., et al. (2008) · Hypertension · doi:10.1161/hypertensionaha.107.103523 · Cited by 1,078 · see citing works

Nanomolar concentrations of nitric oxide reversibly inhibit synaptosomal respiration by competing with oxygen at cytochrome oxidase

Brown, G. C., & Cooper, C. E. (1994) · FEBS Letters · doi:10.1016/0014-5793(94)01290-3 · Cited by 1,055 · see citing works

Blood Flow Regulation by <i>S</i> -Nitrosohemoglobin in the Physiological Oxygen Gradient

Stamler, J. S., Jia, L., Eu, J. P., McMahon, T. J., Demchenko, I. T., Bonaventura, J., Gernert, K., & Piantadosi, C. A. (1997) · Science · doi:10.1126/science.276.5321.2034 · Cited by 1,050 · see citing works

Quantitative Aspects of the Production of Superoxide Anion Radical by Milk Xanthine Oxidase

Fridovich, I. (1970) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)62884-4 · Cited by 1,035 · see citing works

A vertebrate globin expressed in the brain

Burmester, T., Weich, B., Reinhardt, S., & Hankeln, T. (2000) · Nature · doi:10.1038/35035093 · Cited by 1,025 · see citing works

ABA‐induced NO generation and stomatal closure in Arabidopsis are dependent on H 2 O 2 synthesis

Bright, J., Desikan, R., Hancock, J. T., Weir, I. S., & Neill, S. J. (2005) · The Plant Journal · doi:10.1111/j.1365-313x.2005.02615.x · Cited by 1,007 · see citing works

The Biological Chemistry of the Elements: The Inorganic Chemistry of Life

Fraústo da Silva, J. J. R., & Williams, R. J. P. (2001) · doi:10.1093/oso/9780198508472.001.0001 · Cited by 1,005 · see citing works

Mammalian nitric oxide synthases

Stuehr, D. J. (1999) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/s0005-2728(99)00016-x · Cited by 996 · see citing works

Cytochrome c release from mitochondria proceeds by a two-step process

Ott, M., Robertson, J. D., Gogvadze, V. G., Zhivotovsky, B., & Orrenius, S. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.241655498 · Cited by 955 · see citing works

Molecular mechanism of anaerobic ammonium oxidation

Kartal, B., Maalcke, W. J., de Almeida, N. M., Cirpus, I. E. Y., Gloerich, J., Geerts, W. J., den Camp, H. J. M. O., Harhangi, H. R., Janssen‐Megens, E. M., Françoijs, K., et al. (2011) · Nature · doi:10.1038/nature10453 · Cited by 952 · see citing works

Xanthine oxidoreductase and cardiovascular disease: molecular mechanisms and pathophysiological implications

Berry, C. E., & Hare, J. M. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.055913 · Cited by 925 · see citing works

Superoxide production by the mitochondrial respiratory chain

Turrens, J. F. (1997) · Bioscience Reports · doi:10.1023/a:1027374931887 · Cited by 903 · see citing works

Nitrate: nutrient and signal for plant growth.

Crawford, N. M. (1995) · The Plant Cell · doi:10.1105/tpc.7.7.859 · Cited by 903 · see citing works

The Production of Malignant Primary Hepatic Tumours in the Rat by Feeding Dimethylnitrosamine

Magee, P. N., & Barnes, J. M. (1956) · British Journal of Cancer · doi:10.1038/bjc.1956.15 · Cited by 900 · see citing works

Electronic structures of active sites in copper proteins: contributions to reactivity

Solomon, E. I., Baldwin, M. J., & Lowery, M. D. (1992) · Chemical Reviews · doi:10.1021/cr00012a003 · Cited by 896 · see citing works

Workgroup Report: Drinking-Water Nitrate and Health—Recent Findings and Research Needs

Ward, M. H., de Kok, T. M. C. M., Levallois, P., Brender, J. D., Guliš, G., Nolan, B. T., & VanDerslice, J. A. (2005) · Environmental Health Perspectives · doi:10.1289/ehp.8043 · Cited by 892 · see citing works

Identification of a Plant Nitric Oxide Synthase Gene Involved in Hormonal Signaling

Guo, F.-Q., Okamoto, M., & Crawford, N. M. (2003) · Science · doi:10.1126/science.1086770 · Cited by 889 · see citing works

Genome analysis of the smallest free-living eukaryote Ostreococcus tauri unveils many unique features

Derelle, É., Ferraz, C., Rombauts, S., Rouzé, P., Worden, A. Z., Robbens, S., Partensky, F., Degroeve, S., Echeynié, S., Cooke, R., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604795103 · Cited by 879 · 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

Molybdenum cofactors, enzymes and pathways

Schwarz, G., Mendel, R. R., & Ribbe, M. W. (2009) · Nature · doi:10.1038/nature08302 · Cited by 872 · see citing works

Nitric oxide signalling in plants

Neill, S. J., Desikan, R., & Hancock, J. T. (2003) · New Phytologist · doi:10.1046/j.1469-8137.2003.00804.x · Cited by 872 · see citing works

Persistent inhibition of cell respiration by nitric oxide: Crucial role of <i>S</i> -nitrosylation of mitochondrial complex I and protective action of glutathione

Clementi, E., Brown, G. C., Feelisch, M., & Moncada, S. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.13.7631 · Cited by 863 · see citing works

Novel genes for nitrite reductase and Amo‐related proteins indicate a role of uncultivated mesophilic crenarchaeota in nitrogen cycling

Treusch, A. H., Leininger, S., Kletzin, A., Schuster, S. C., Klenk, H., & Schleper, C. (2005) · Environmental Microbiology · doi:10.1111/j.1462-2920.2005.00906.x · Cited by 860 · see citing works

Oxidation of nitric oxide in aqueous solution to nitrite but not nitrate: comparison with enzymatically formed nitric oxide from L-arginine

Ignarro, L. J., Fukuto, J. M., Griscavage, J. M., Rogers, N. E., & Byrns, R. E. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.17.8103 · Cited by 856 · see citing works

The anaerobic oxidation of ammonium

Jetten, M. S. M., Strous, M., van de Pas-Schoonen, K. T., et al. (1998) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.1998.tb00379.x · Cited by 842 · see citing works

The role of abscisic acid in plant–pathogen interactions

Mauch‐Mani, B., & Mauch, F. (2005) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2005.05.015 · Cited by 839 · see citing works

The oxidative pentose phosphate pathway: structure and organisation

Kruger, N. J., & von Schaewen, A. (2003) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(03)00039-6 · Cited by 838 · see citing works

Tetrapyrrole Biosynthesis in Higher Plants

Tanaka, R., & Tanaka, A. (2007) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105448 · Cited by 823 · see citing works

Methods in nitric oxide research

Feelisch, M., & Stamler, J. S. (1996) · Wiley-Blackwell eBooks · Cited by 819 · see citing works

Production of NO 2 - and N 2 O by Nitrifying Bacteria at Reduced Concentrations of Oxygen

Goreau, T. J. F., Kaplan, W. A., Wofsy, S. C., McElroy, M. B., Valois, F. W., & Watson, S. W. (1980) · Applied and Environmental Microbiology · doi:10.1128/aem.40.3.526-532.1980 · Cited by 805 · see citing works

Regulation of nitric oxide (NO) production by plant nitrate reductase in vivo and in vitro

Rockel, P., Strube, F., Rockel, A., Wildt, J., & Kaiser, W. M. (2002) · Journal of Experimental Botany · doi:10.1093/jexbot/53.366.103 · Cited by 801 · see citing works

Complex regulation of ABA biosynthesis in plants

Seo, M., & Koshiba, T. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(01)02187-2 · Cited by 796 · see citing works

A Nitrospira metagenome illuminates the physiology and evolution of globally important nitrite-oxidizing bacteria

Lücker, S., Wagner, M., Maixner, F., Pelletier, É., Koch, H., Vacherie, B., Rattei, T., Damsté, J. S. S., Spieck, E., Paslier, D. L., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1003860107 · Cited by 792 · see citing works

Does nitric oxide modulate mitochondrial energy generation and apoptosis?

Moncada, S., & Erusalimsky, J. D. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm762 · Cited by 789 · see citing works

Enzyme-independent formation of nitric oxide in biological tissues

Zweier, J. L., Wang, P., Samouilov, A., & Kuppusamy, P. (1995) · Nature Medicine · doi:10.1038/nm0895-804 · Cited by 788 · see citing works

Structure and function of xanthine oxidoreductase: where are we now?

Harrison, R. (2002) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)00956-5 · Cited by 787 · see citing works

Formation of reactive nitrogen species during peroxidase-catalyzed oxidation of nitrite

van der Vliet, A., Eiserich, J. P., Halliwell, B., & Cross, C. E. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.12.7617 · Cited by 780 · see citing works

New processes and players in the nitrogen cycle: the microbial ecology of anaerobic and archaeal ammonia oxidation

Francis, C. A., Beman, J. M., & Kuypers, M. M. M. (2007) · The ISME Journal · doi:10.1038/ismej.2007.8 · Cited by 778 · see citing works

Mitochondrial control of apoptosis: the role of cytochrome c.

Cai, J.-Y., Yang, J., & Jones, D. P. (1998) · Biochimica et Biophysica Acta · doi:10.1016/s0005-2728(98)00109-1 · Cited by 777 · see citing works

NITRATE REDUCTASE STRUCTURE, FUNCTION AND REGULATION: Bridging the Gap between Biochemistry and Physiology

Campbell, W. H. (1999) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.50.1.277 · Cited by 775 · see citing works

Nitric Oxide Induces Stomatal Closure and Enhances the Adaptive Plant Responses against Drought Stress

García‐Mata, C., & Lamattina, L. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.126.3.1196 · Cited by 766 · see citing works

Nitric oxide and salicylic acid signaling in plant defense

Klessig, D. F., Durner, J., Noad, R. J., et al. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.16.8849 · Cited by 766 · see citing works

Hyperoxia increases oxygen radical production in rat lungs and lung mitochondria.

Freeman, B. Α., & Crapo, J. D. (1981) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)68544-3 · Cited by 762 · see citing works

The biological lifetime of nitric oxide: Implications for the perivascular dynamics of NO and O ₂

Thomas, D. D., Liu, X., Kantrow, S. P., & Lancaster, J. R. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.1.355 · Cited by 760 · see citing works

Nitric oxide, stomatal closure, and abiotic stress

Neill, S. J., Barros, R., Bright, J., Desikan, R., Hancock, J. T., Harrison, J., Morris, P. C., Ribeiro, D. M., & Wilson, I. D. (2008) · Journal of Experimental Botany · doi:10.1093/jxb/erm293 · Cited by 746 · see citing works

Nitrate, bacteria and human health

Lundberg, J. O., Weitzberg, E., Cole, J. A., & Benjamin, N. (2004) · Nature Reviews Microbiology · doi:10.1038/nrmicro929 · Cited by 739 · see citing works

Chemical generation of nitric oxide in the mouth from the enterosalivary circulation of dietary nitrate

Duncan, C., Dougall, H., Johnston, P., Green, S., Brogan, R., Leifert, C., Smith, L., Golden, M., & Benjamin, N. (1995) · Nature Medicine · doi:10.1038/nm0695-546 · Cited by 734 · see citing works

The Regulation of Rat Liver Xanthine Oxidase

Stirpe, F., Corte, E. D., & Lorenzoni, E. (1969) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)36428-1 · Cited by 733 · see citing works

Crystal structures of bovine milk xanthine dehydrogenase and xanthine oxidase: Structure-based mechanism of conversion

Enroth, C., Eger, B. T., Okamoto, K., Nishino, T., Nishino, T., & Pai, E. F. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.20.10723 · Cited by 733 · see citing works

Increased concentrations of nitrite in synovial fluid and serum samples suggest increased nitric oxide synthesis in rheumatic diseases.

Farrell, A. J., Blake, D. R., Palmer, R. M. J., & Moncada, S. (1992) · Annals of the Rheumatic Diseases · doi:10.1136/ard.51.11.1219 · Cited by 717 · see citing works

A new role for an old enzyme: Nitrate reductase-mediated nitric oxide generation is required for abscisic acid-induced stomatal closure in Arabidopsis thaliana

Desikan, R., Griffiths, R., Hancock, J. T., & Neill, S. J. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.252461999 · Cited by 711 · see citing works

Evidence for nitric oxide‐mediated oxidative damage in chronic inflammation Nitrotyrosine in serum and synovial fluid from rheumatoid patients

Kaur, H., & Halliwell, B. B. (1994) · FEBS Letters · doi:10.1016/0014-5793(94)00722-5 · Cited by 706 · see citing works

Apoptosis: a basic biological phenomenon with wide‐ranging implications in human disease

Fadeel, B., & Orrenius, S. (2005) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2005.01570.x · Cited by 699 · see citing works

Control of coronary vascular tone by nitric oxide.

Kelm, M., & Schrader, J. (1990) · Circulation Research · doi:10.1161/01.res.66.6.1561 · Cited by 697 · see citing works

Dietary Inorganic Nitrate Improves Mitochondrial Efficiency in Humans

Larsen, F. J., Schiffer, T. A., Borniquel, S., Sahlin, K., Ekblom, B., Lundberg, J. O., & Weitzberg, E. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.01.004 · Cited by 689 · see citing works

Simulation of the diffusion and reaction of endogenously produced nitric oxide.

Lancaster, J. R. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.17.8137 · Cited by 689 · see citing works

Ischemia-reperfusion injury: role of oxygen-derived free radicals.

Granger, D. N., Höllwarth, M. E., & Parks, D. A. (1986) · PubMed · Cited by 683 · see citing works

Nitric oxide stimulates seed germination and de-etiolation, and inhibits hypocotyl elongation, three light-inducible responses in plants

Beligni, M. V., & Lamattina, L. (2000) · Planta · doi:10.1007/pl00008128 · Cited by 680 · see citing works

Cytoprotective effects of nitrite during in vivo ischemia-reperfusion of the heart and liver

Duranski, M. R., Greer, J. J. M., Dejam, A., Jaganmohan, S., Hogg, N., Langston, W., Patel, R. P., Yet, S.-F., Wang, X., Kevil, C. G., et al. (2005) · Journal of Clinical Investigation · doi:10.1172/jci22493 · Cited by 674 · see citing works

A moderately thermophilic ammonia-oxidizing crenarchaeote from a hot spring

Hatzenpichler, R., Lebedeva, E. V., Spieck, E., Stoecker, K., Richter, A. A., Daims, H., & Wagner, M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708857105 · Cited by 674 · see citing works

Nitrate biosynthesis in man.

Green, L. C., Ruiz de Luzuriaga, K., Wagner, D. A., Rand, W., Istfan, N., Young, V. R., & Tannenbaum, S. R. (1981) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.78.12.7764 · Cited by 665 · see citing works

Stomach NO synthesis

Benjamin, N., O'Driscoll, F., Dougall, H., Duncan, C., Smith, L., Golden, M., & McKenzie, H. (1994) · Nature · doi:10.1038/368502a0 · Cited by 665 · see citing works

Intragastric nitric oxide production in humans: measurements in expelled air.

Lundberg, J. O., Weitzberg, E., Lundberg, J. M., & Alving, K. (1994) · Gut · doi:10.1136/gut.35.11.1543 · Cited by 661 · see citing works

Inorganic nitrate is a possible source for systemic generation of nitric oxide

Lundberg, J. O., & Govoni, M. (2004) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2004.04.027 · Cited by 657 · see citing works

15 N Kinetic Analysis of N 2 O Production by Nitrosomonas europaea : an Examination of Nitrifier Denitrification

Poth, M. A., & Focht, D. D. (1985) · Applied and Environmental Microbiology · doi:10.1128/aem.49.5.1134-1141.1985 · Cited by 657 · see citing works

The Assimilatory Nitrate-Reducing System and its Regulation

Guerrero, M. G., Vega, J. M., & Losada, M. (1981) · Annual Review of Plant Physiology · doi:10.1146/annurev.pp.32.060181.001125 · Cited by 654 · see citing works

Genomic studies of uncultivated archaea

Schleper, C., Jurgens, G., & Jonuscheit, M. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1159 · Cited by 645 · see citing works

Leghemoglobin and Rhizobium Respiration

Appleby, C. A. (1984) · Annual Review of Plant Physiology · doi:10.1146/annurev.pp.35.060184.002303 · Cited by 645 · see citing works

Oxidation of nitrogen-oxides by bound dioxygen in hemoproteins

Doyle, M. P., & Hoekstra, J. W. (1981) · Journal of Inorganic Biochemistry · doi:10.1016/s0162-0134(00)80291-3 · Cited by 643 · see citing works

Effects of dietary nitrate on oxygen cost during exercise

Larsen, F. J., Weitzberg, E., Lundberg, J. O., & Ekblom, B. (2007) · Acta Physiologica · doi:10.1111/j.1748-1716.2007.01713.x · Cited by 637 · see citing works

Inorganic Nitrate Supplementation Lowers Blood Pressure in Humans: Role for Nitrite-Derived NO

Kapil, V., Milsom, A. B., Okorie, M., Maleki-Toyserkani, S., Akram, F., Rehman, F., Arghandawi, S., Pearl, V., Benjamin, N., Loukogeorgakis, S., et al. (2010) · Hypertension · doi:10.1161/hypertensionaha.110.153536 · Cited by 621 · see citing works

The Nucleobase‐Cation‐Symport‐1 Family of Membrane Transport Proteins

Weyand, S. N., Ma, P., Saidijam, M., Baldwin, J. M., Beckstein, O., Jackson, S. M., Suzuki, S., Patching, S. G., Shimamura, T., Sansom, M. S. P., et al. (2004) · Handbook of Metalloproteins · doi:10.1002/0470028637.met268 · Cited by 619 · see citing works

Mechanism of NO-induced oxidation of myoglobin and hemoglobin

Eich, R. F., Li, T., Lemon, D. D., Doherty, D. H., Curry, S. R., Aitken, J. F., Mathews, A. J., Johnson, K. A., Smith, R. D., Phillips, et al. (1996) · Biochemistry · doi:10.1021/bi960442g · Cited by 613 · see citing works

Implication of free radical mechanisms in ethanol-induced cellular injury

Nordmann, R., Ribière, C., & Rouach, H. (1992) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(92)90030-k · Cited by 610 · see citing works

Reduction of nitrite to nitric oxide during ischemia protects against myocardial ischemia–reperfusion damage

Webb, A., Bond, R., McLean, P., Uppal, R., Benjamin, N., & Ahluwalia, A. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402927101 · Cited by 608 · see citing works

Measurement of endothelial cell free radical generation: evidence for a central mechanism of free radical injury in postischemic tissues.

Zweier, J. L., Kuppusamy, P., & Lutty, G. A. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.11.4046 · Cited by 601 · see citing works

Deoxymyoglobin Is a Nitrite Reductase That Generates Nitric Oxide and Regulates Mitochondrial Respiration

Shiva, S., Huang, Z., Grubina, R., Sun, J., Ringwood, L. A., MacArthur, P. H., Xu, X., Murphy, E., Darley-Usmar, V. M., & Gladwin, M. T. (2007) · Circulation Research · doi:10.1161/01.res.0000260171.52224.6b · Cited by 599 · see citing works

Influence of dietary nitrate on nitrite content of human saliva: Possible relevance to in vivo formation of N-nitroso compounds

Spiegelhalder, B., Eisenbrand, G., & Preussmann, R. (1976) · Food and Cosmetics Toxicology · doi:10.1016/s0015-6264(76)80005-3 · Cited by 596 · see citing works

Enzymes and associated electron transport systems that catalyse the respiratory reduction of nitrogen oxides and oxyanions

Berks, B. C., Ferguson, S. J., Moir, J. W. B., & Richardson, D. J. (1995) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(95)00092-5 · Cited by 596 · see citing works

Nitrate regulation of metabolism and growth

Stitt, M. D. (1999) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(99)80033-8 · Cited by 588 · see citing works

Effects of Dietary Nitrate on Blood Pressure in Healthy Volunteers

Larsen, F. J., Ekblom, B., Sahlin, K., Lundberg, J. O., & Weitzberg, E. (2006) · New England Journal of Medicine · doi:10.1056/nejmc062800 · Cited by 587 · see citing works

Plasma nitrite reflects constitutive nitric oxide synthase activity in mammals

Kleinbongard, P., Dejam, A., Lauer, T., Rassaf, T., Schindler, A., Picker, O., Scheeren, T., Gödecke, A., Schrader, J., Schulz, R., et al. (2003) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(03)00406-4 · Cited by 586 · see citing works

Protons and Anaerobiosis

Hochachka, P. W., & Mommsen, T. P. (1983) · Science · doi:10.1126/science.6298937 · Cited by 586 · see citing works

The increase in plasma nitrite after a dietary nitrate load is markedly attenuated by an antibacterial mouthwash

Govoni, M., Jansson, E. Å., Weitzberg, E., & Lundberg, J. O. (2008) · Nitric Oxide · doi:10.1016/j.niox.2008.08.003 · Cited by 585 · see citing works

Plasma nitrite rather than nitrate reflects regional endothelial nitric oxide synthase activity but lacks intrinsic vasodilator action

Lauer, T., Preik, M., Rassaf, T., Strauer, B. E., Deussen, A., Feelisch, M., & Kelm, M. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.221381098 · Cited by 585 · see citing works

Genomic Analysis of a Nutrient Response in Arabidopsis Reveals Diverse Expression Patterns and Novel Metabolic and Potential Regulatory Genes Induced by Nitrate

Wang, R., Guegler, K. J., LaBrie, S. T., & Crawford, N. M. (2000) · The Plant Cell · doi:10.1105/tpc.12.8.1491 · Cited by 585 · see citing works

Export by red blood cells of nitric oxide bioactivity

Pawloski, J. R., Hess, D. T., & Stamler, J. S. (2001) · Nature · doi:10.1038/35054560 · Cited by 579 · see citing works

Carbon Dioxide Enrichment Inhibits Nitrate Assimilation in Wheat and Arabidopsis

Bloom, A. J., Burger, M., Rubio-Asensio, J. S., et al. (2010) · Science · doi:10.1126/science.1186440 · Cited by 578 · see citing works

Biochemistry and molecular biology of anammox bacteria

Jetten, M. S. M., van Niftrik, L., Strous, M., Kartal, B., Keltjens, J. T., & den Camp, H. J. M. O. (2009) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409230902722783 · Cited by 575 · see citing works

Myoglobin-facilitated oxygen diffusion: role of myoglobin in oxygen entry into muscle.

Wittenberg, J. B. (1970) · Physiological Reviews · doi:10.1152/physrev.1970.50.4.559 · Cited by 573 · see citing works

Nitric oxide: comparative synthesis and signaling in animal and plant cells

Wendehenne, D., Pugin, A., Klessig, D. F., & Durner, J. (2001) · Trends in Plant Science · doi:10.1016/s1360-1385(01)01893-3 · Cited by 571 · see citing works

Nitric oxide dioxygenase: An enzymic function for flavohemoglobin

Gardner, P. R., Gardner, A. M., Martin, L. A., & Salzman, A. L. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.18.10378 · Cited by 569 · see citing works

Nitric Oxide Represses the Arabidopsis Floral Transition

He, Y., Tang, R., Hao, Y., Stevens, R. D., Cook, C. W., Ahn, S. M., Jing, L., Yang, Z., Chen, L., Guo, F., et al. (2004) · Science · doi:10.1126/science.1098837 · Cited by 565 · see citing works

Peroxynitrite reactivity with amino acids and proteins

Alvarez, B., & Radi, R. (2003) · Amino Acids · doi:10.1007/s00726-003-0018-8 · Cited by 560 · see citing works

Distribution and ecophysiology of the nitrifying bacteria emphasizing cultured species

Koops, H., & Pommerening-Röser, A. (2001) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2001.tb00847.x · Cited by 558 · see citing works

Superoxide Dismutases: Ancient Enzymes and New Insights

Miller, A.-F. (2012) · FEBS Letters · doi:10.1016/j.febslet.2011.10.048 · Cited by 557 · see citing works

Apoplastic Synthesis of Nitric Oxide by Plant Tissues

Bethke, P. C., Badger, M. R., & Jones, R. L. (2004) · The Plant Cell · doi:10.1105/tpc.017822 · Cited by 557 · see citing works

Nitrite augments tolerance to ischemia/reperfusion injury via the modulation of mitochondrial electron transfer

Shiva, S., Sack, M. N., Greer, J. J., Duranski, M., Ringwood, L. A., Burwell, L., Wang, X., MacArthur, P. H., Shoja, A., Raghavachari, N., et al. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070198 · Cited by 555 · see citing works

Complete Genome Sequence of the Ammonia-Oxidizing Bacterium and Obligate Chemolithoautotroph Nitrosomonas europaea

Chain, P., Lamerdin, J. E., Larimer, F. W., Regala, W., Lao, V., Land, M., Hauser, L., Hooper, A. B., Klotz, M. G., Norton, J. M., et al. (2003) · Journal of Bacteriology · doi:10.1128/jb.185.9.2759-2773.2003 · Cited by 552 · see citing works

Myoglobin function reassessed

Wittenberg, J. B., & Wittenberg, B. A. (2003) · Journal of Experimental Biology · doi:10.1242/jeb.00243 · Cited by 550 · see citing works

Simultaneous production of nitric oxide and peroxynitrite by plant nitrate reductase: in vitro evidence for the NR‐dependent formation of active nitrogen species

Yamasaki, H., & Sakihama, Y. (2000) · FEBS Letters · doi:10.1016/s0014-5793(00)01203-5 · Cited by 549 · see citing works

Linking crenarchaeal and bacterial nitrification to anammox in the Black Sea

Lam, P., Jensen, M. M., Lavik, G., McGinnis, D. F., Müller, B., Schubert, C. J., Amann, R., Thamdrup, B., & Kuypers, M. M. M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611081104 · Cited by 549 · see citing works

Anammox bacteria disguised as denitrifiers: nitrate reduction to dinitrogen gas via nitrite and ammonium

Kartal, B., Kuypers, M. M. M., Lavik, G., et al. (2006) · Environmental Microbiology · doi:10.1111/j.1462-2920.2006.01183.x · Cited by 548 · see citing works

Essential Roles of S-Nitrosothiols in Vascular Homeostasis and Endotoxic Shock

Liu, L., Yan, Y., Zeng, M., Zhang, J., Hanes, M. A., Ahearn, G. S., McMahon, T., Dickfeld, T. L., Marshall, H. E., Que, L. G., et al. (2004) · Cell · doi:10.1016/s0092-8674(04)00131-x · Cited by 546 · see citing works

Dissimilatory Nitrite and Nitric Oxide Reductases

Averill, B. A. (1996) · Chemical Reviews · doi:10.1021/cr950056p · Cited by 545 · see citing works

Nitric Oxide Is a Novel Component of Abscisic Acid Signaling in Stomatal Guard Cells

Neill, S. J., Desikan, R., Clarke, A., & Hancock, J. T. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.010707 · Cited by 542 · see citing works

Nitric oxide: a new player in plant signalling and defence responses

Wendehenne, D., Durner, J., & Klessig, D. F. (2004) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2004.04.002 · Cited by 540 · see citing works

Measurement of Nitric Oxide and Peroxynitrite Generation in the Postischemic Heart

Wang, P., & Zweier, J. L. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.46.29223 · Cited by 538 · see citing works

Greenhouse warming by CH ₄ in the atmosphere of early Earth

Pavlov, A. A., Kasting, J. F., Brown, L. L., Rages, K. A., & Freedman, R. (2000) · Journal of Geophysical Research: Planets · doi:10.1029/1999je001134 · Cited by 537 · see citing works

A Solution-Phase Chemical Approach to a New Crystal Structure of Cobalt

Dinega, D. P., & Bawendi, M. G. (1999) · Angewandte Chemie International Edition · doi:10.1002/(sici)1521-3773(19990614)38:12 · Cited by 526 · see citing works

Mechanistic aspects of the reactions of nitric oxide with transition-metal complexes

Ford, P. C., & Lorkovic, I. M. (2002) · Chemical Reviews · doi:10.1021/cr0000271 · Cited by 525 · see citing works

Oxidative stress, anti‐oxidant therapies and chronic kidney disease

Small, D. M., Coombes, J. S., Bennett, N. J., Johnson, D. W., & Gobe, G. C. (2012) · Nephrology · doi:10.1111/j.1440-1797.2012.01572.x · Cited by 524 · see citing works

Enzymatic function of hemoglobin as a nitrite reductase that produces NO under allosteric control

Huang, Z. (2005) · Journal of Clinical Investigation · doi:10.1172/jci24650 · Cited by 520 · see citing works

Nitrite is a signaling molecule and regulator of gene expression in mammalian tissues

Bryan, N. S., Fernandez, B. O., Bauer, S. M., Garcia-Saura, M. F., Milsom, A. B., Rassaf, T., Maloney, R. E., Bharti, A., Rodriguez, J., & Feelisch, M. (2005) · Nature Chemical Biology · doi:10.1038/nchembio734 · Cited by 518 · see citing works

ABA, hydrogen peroxide and nitric oxide signalling in stomatal guard cells

Desikan, R. (2003) · Journal of Experimental Botany · doi:10.1093/jxb/erh033 · Cited by 518 · see citing works

Vascular Oxidative Stress and Endothelial Dysfunction in Patients With Chronic Heart Failure

Landmesser, U., Spiekermann, S., Dikalov, S., Tatge, H., Wilke, R., Kohler, C., Harrison, D. G., Hornig, B., & Drexler, H. (2002) · Circulation · doi:10.1161/01.cir.0000041431.57222.af · Cited by 517 · see citing works

Nitric Reductase-Dependent Nitric Oxide Production Is Involved in Cold Acclimation and Freezing Tolerance in Arabidopsis

Zhao, M., Chen, L., Zhang, L., & Zhang, W. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.140996 · Cited by 515 · see citing works

Diffusion-limited reaction of free nitric oxide with erythrocytes

Liu, X., Miller, M. J. S., Joshi, M. S., Sadowska-Krowicka, H., Clark, D. A., & Lancaster, J. R. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.30.18709 · Cited by 512 · see citing works

Assimilatory Nitrate Reductase: Functional Properties and Regulation

Solomonson, L. P., & Barber, M. J. (1990) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.pp.41.060190.001301 · Cited by 511 · see citing works

Nitric oxide and iron proteins

Cooper, C. E. (1999) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/s0005-2728(99)00021-3 · Cited by 510 · see citing works

The Molecular Mechanism of the Catalase Reaction

Alfonso‐Prieto, M., Biarnés, X., Vidossich, P., & Rovira, C. (2009) · Journal of the American Chemical Society · doi:10.1021/ja9018572 · Cited by 504 · see citing works

Polyamines Induce Rapid Biosynthesis of Nitric Oxide (NO) in Arabidopsis thaliana Seedlings

Tun, N. N., Santa‐Catarina, C., Begum, T., Silveira, V., Handro, W., Floh, E. I. S., & Scherer, G. F. E. (2006) · Plant and Cell Physiology · doi:10.1093/pcp/pci252 · Cited by 503 · see citing works

Hypoxia, red blood cells, and nitrite regulate NO-dependent hypoxic vasodilation

Crawford, J. H. (2006) · Blood · doi:10.1182/blood-2005-07-2668 · Cited by 497 · see citing works

Determinants of a protein fold

Bashford, D., Chothia, C., & Lesk, A. M. (1987) · Journal of Molecular Biology · doi:10.1016/0022-2836(87)90521-3 · Cited by 496 · see citing works

Cytoglobin: A Novel Globin Type Ubiquitously Expressed inVertebrate Tissues

Burmester, T., Ebner, B., Weich, B., & Hankeln, T. (2002) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a004096 · Cited by 496 · see citing works

Mitochondrial cytochrome oxidase produces nitric oxide under hypoxic conditions: Implications for oxygen sensing and hypoxic signaling in eukaryotes

Castello, P. R., David, P. S., McClure, T., Crook, Z., & Poyton, R. O. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.02.011 · Cited by 495 · see citing works

A Tutorial on the Diffusibility and Reactivity of Free Nitric Oxide

Lancaster, J. R. (1997) · Nitric Oxide · doi:10.1006/niox.1996.0112 · Cited by 495 · see citing works

Relevance of nitrosamines to human cancer

Bartsch, H., & Montesano, R. (1984) · Carcinogenesis · doi:10.1093/carcin/5.11.1381 · Cited by 495 · see citing works

The Measurement of Pyridine Nucleotides by Enzymatic Cycling

Lowry, O. H., Passonneau, J. V., Schulz, D. W., & Rock, M. K. (1961) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)61729-1 · Cited by 494 · see citing works

Insights into the respiratory electron transfer pathway from the structure of nitrate reductase A

Bertero, M. G., Rothery, R. A., Palak, M., Hou, C., Lim, D., Blasco, F., Weiner, J. H., & Strynadka, N. C. J. (2003) · Nature Structural & Molecular Biology · doi:10.1038/nsb969 · Cited by 494 · see citing works

Reactive oxygen species, antioxidant systems and nitric oxide in peroxisomes

del Río, L. A., Corpas, F. J., Sandalio, L. M., Palma, J. M., Gómez, M., & Barroso, J. B. (2002) · Journal of Experimental Botany · doi:10.1093/jexbot/53.372.1255 · Cited by 494 · see citing works

Xanthine oxidoreductase catalyses the reduction of nitrates and nitrite to nitric oxide under hypoxic conditions

Millar, T. M., Stevens, C. R., Benjamin, N., Eisenthal, R., Harrison, R., & Blake, D. R. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)00430-x · Cited by 491 · see citing works

NO news is good news for plants

Delledonne, M. (2005) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2005.05.002 · Cited by 491 · see citing works

Copper Proteins and Copper Enzymes

Lontie, R. (2018) · CRC Press eBooks · doi:10.1201/9781351070898 · Cited by 487 · see citing works

A Tale of Two Controversies

Brennan, M.-L., Wu, W., Fu, X., Shen, Z., Song, W., Frost, H., Vadseth, C., Narine, L., Lenkiewicz, E., Borchers, M. T., et al. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m112400200 · Cited by 486 · see citing works

The Molecule of the Year

Guyer, R. L., & Koshland, D. E. (1989) · Science · doi:10.1126/science.2688087 · Cited by 482 · see citing works

Reactions of the bioregulatory agent nitric oxide in oxygenated aqueous media: Determination of the kinetics for oxidation and nitrosation by intermediates generated in the nitric oxide/oxygen reaction

Wink, D. A., Darbyshire, J. F., Nims, R. W., Saavedra, J. E., & Ford, P. C. (1993) · Chemical Research in Toxicology · doi:10.1021/tx00031a003 · Cited by 480 · see citing works

Crystal Structure of the Xanthine Oxidase-Related Aldehyde Oxido-Reductase from D. gigas

Romão, M. J., Archer, M., Moura, I., Moura, J. J. G., LeGall, J., Engh, R. A., Schneider, M., Hof, P., & Huber, R. (1995) · Science · doi:10.1126/science.270.5239.1170 · Cited by 480 · see citing works

Nitric oxide synthesis and signalling in plants

Wilson, I. D., Neill, S. J., & Hancock, J. T. (2007) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2007.01761.x · Cited by 479 · see citing works

Nitric Oxide in Biological Denitrification: Fe/Cu Metalloenzyme and Metal Complex NOx Redox Chemistry

Wasser, I. M., de Vries, S., Moënne‐Loccoz, P., Schröder, I., & Karlin, K. D. (2002) · Chemical Reviews · doi:10.1021/cr0006627 · Cited by 477 · see citing works

Anaerobic Metabolism in Plants

Kennedy, R., Rumpho, M. E., & Fox, T. C. (1992) · PLANT PHYSIOLOGY · doi:10.1104/pp.100.1.1 · Cited by 471 · see citing works

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Messerschmidt, A., Ladenstein, R., Huber, R., Bolognesi, M., Avigliano, L., Petruzzelli, R., Rossi, A., & Finazzi‐Agrò, A. (1992) · Journal of Molecular Biology · doi:10.1016/0022-2836(92)90583-6 · Cited by 471 · see citing works

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Risgaard‐Petersen, N., Langezaal, A. M., Høgslund, S. M., Schmid, M. C., Jetten, M. S. M., den Camp, H. J. M. O., Derksen, J. W. M., Piña-Ochoa, E., Eriksson, S. P., Nielsen, L. P., et al. (2006) · Nature · doi:10.1038/nature05070 · Cited by 469 · see citing works

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Wittenberg, B. A., & Wittenberg, J. B. (1989) · Annual Review of Physiology · doi:10.1146/annurev.ph.51.030189.004233 · Cited by 468 · see citing works

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Gogvadze, V. G., Orrenius, S., & Zhivotovsky, B. (2006) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2006.03.016 · Cited by 466 · see citing works

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

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Koch, C. D., Gladwin, M. T., Freeman, B. A., Lundberg, J. O., Weitzberg, E., & Morris, A. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.12.015 · Cited by 186 · see citing works

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(2016) · Advances in Microbial Physiology · doi:10.1016/bs.ampbs.2016.02.007 · Cited by 100 · see citing works

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Hawkins, D. (2017)

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Fang-zhon, L. (2013) · Journal of Sichuan University of Science & Engineering

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Jopson, B. (1998) · Optics and Photonics News · doi:10.1364/opn.9.9.000058

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Campe, R. (2014) · The Germanic Review Literature Culture Theory · doi:10.1080/00168890.2014.875787 · Cited by 1 · see citing works