The effect of the inhibitor diphenylene iodonium on the superoxide-generating system of neutrophils. Specific labelling of a component polypeptide of the oxidase

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

LAEMMLI, U. K. (1970) · Nature · doi:10.1038/227680a0 · Cited by 249,961

Short-Term Effects of Nose-Only Cigarette Smoke Exposure on Glutathione Redox Homeostasis, Cytochrome P450 1A1/2 and Respiratory Enzyme Activities in Mice Tissues

Raza, H., John, A., & Nemmar, A. (2013) · Cellular Physiology and Biochemistry · doi:10.1159/000350087 · Cited by 47,311

Oxygen-Dependent Microbial Killing by Phagocytes

BABIOR, B. M. (1978) · New England Journal of Medicine · doi:10.1056/nejm197803232981205 · Cited by 2,483

Oxidants from phagocytes: agents of defense and destruction

Babior, B. (1984) · Blood · doi:10.1182/blood.v64.5.959.959 · Cited by 804

Stimulated neutrophils from patients with autosomal recessive chronic granulomatous disease fail to phosphorylate a Mr-44,000 protein

Segal, A. W., Heyworth, P. G., Cockcroft, S., & Barrowman, M. M. (1985) · Nature · doi:10.1038/316547a0 · Cited by 281

Characteristics of the cofactor requirements for the superoxide-generating NADPH oxidase of human polymorphonuclear leukocytes

Light, D. R., Walsh, C. T., O'Callaghan, A. M., Goetzl, E. J., & Tauber, A. I. (1981) · Biochemistry · doi:10.1021/bi00509a010 · Cited by 249

The enzymic reduction and kinetics of oxidation of cytochrome b.245 of neutrophils

Cross, A. R., Higson, F. K., Jones, O. T. G., Harper, A., & Segal, A. W. (1982) · Biochemical Journal · doi:10.1042/bj2040479 · Cited by 246

Oxidation-reduction properties of the cytochrome b found in the plasma-membrane fraction of human neutrophils. A possible oxidase in the respiratory burst

Cross, A. R., Jones, O. T., Harper, A., & Segal, A. W. (1981) · Biochemical Journal · doi:10.1042/bj1940599 · Cited by 229

Polymorphonuclear Leukocyte-Mediated, Antibody-Dependent, Cellular Cytotoxicity against Tumor Cells: Dependence on Oxygen and the Respiratory Burst

Hafeman, D. G., & Lucas, Z. J. (1979) · The Journal of Immunology · doi:10.4049/jimmunol.123.1.55 · Cited by 142

The superoxide-generating oxidase of leucocytes. NADPH-dependent reduction of flavin and cytochrome b in solubilized preparations

Cross, A. R., Parkinson, J. F., & Jones, O. T. G. (1984) · Biochemical Journal · doi:10.1042/bj2230337 · Cited by 136

Regulatory roles of benzyl adenine and sucrose during wound response of the ribosomal protein gene, rpL34

Yu, G.-H., & An, G. (2000) · Plant Cell & Environment · doi:10.1046/j.1365-3040.2000.00656.x · Cited by 2

Inhibition of phase-1 biotransformation and cytostatic effects of diphenyleneiodonium on hepatoblastoma cell line HepG2 and a CYP3A4-overexpressing HepG2 cell clone

Schulz, C., Jung, F., & Küpper, J. (2021) · Clinical Hemorheology and Microcirculation · doi:10.3233/ch-219117 · Cited by 3

Free Radical Mechanisms for Chromosomal Instability in Bloom’s Syndrome

Nicotera, T. M. (1994) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-1833-4_3 · Cited by 2

Regulation of guard cell anion channels

Wang, Y. (2013) · Enlighten: Theses (The University of Glasgow) · Cited by 2

[Free radicals and antioxidant mechanisms. A general outline and its application in clinical practice].

Fernandez, A. D. L. P., & Bellón, P. R. (1997) · PubMed · Cited by 2

Characterization of wound-induced electrical signals and reactive oxygen species in chickpea (Cicer arietinum)

Deshpande, S. V., Pawar, S., & Kumari, A. (2025) · Plant Signaling & Behavior · doi:10.1080/15592324.2025.2567930 · Cited by 1

Diphenyleneiodonium exhibits protective effects against both nociception and gastrointestinal inflammation in vivo

Kouki, A., Souli, A., Bouzazi, D., Bouabdallah, S., Ferjani, W., Dang, P. M., Ben‐Attia, M., & Benna, J. E. (2025) · Inflammopharmacology · doi:10.1007/s10787-025-02046-9 · Cited by 1

Effect of NADPH Oxidase Inhibition on Heme Oxygenase-1 Expression in Human Hepatoma Cell Line HepG2

Lee, S.-K., Kim, K.-M., Park, K.-H., & Park, Y.-C. (2011) · Journal of Life Science · doi:10.5352/jls.2011.21.11.1625 · Cited by 1

Controle da produção muscular de espécies reativas e citocinas por ácido palmítico e eletroestimulação: possíveis implicações no envelhecimento.

Lambertucci, R. H. (2009) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2009.tde-01072009-120056 · Cited by 1

The Leishmania Donovani Lipophosphoglycan: Structure and Function

Turco, S. J. (1989) · Springer eBooks · doi:10.1007/978-1-4613-1575-9_79 · Cited by 1

The Neutrophil Respiratory Burst Oxidase

Quinn, M. T. (2013) · IMPERIAL COLLEGE PRESS eBooks · doi:10.1142/9781848168374_0002 · Cited by 1

Characterization of the ROS production in ischemia/reperfusion-induced lung injury

Sydykov, A. S., & Justus Liebig University Giessen (2009) · University writing server of the Justus Liebig University Giessen (Justus-Liebig-Universität Gießen) · doi:10.22029/jlupub-15539 · Cited by 1

Mitochondrial Diversity in the Vasculature: Implications for Vascular Oxygen Sensing

McMurtry, S., & Michelakis, E. D. (2006) · Kluwer Academic Publishers eBooks · doi:10.1007/1-4020-7858-7_17 · Cited by 1

The role of oxidative stress in the pathogenesis of epithelial ovarian cancer

Fletcher, N. M. (2013)

Relationships Between Reactive Oxygen Species and Reactive Nitrogen Oxide Species Produced by Macrophages

Espey, M. G. (2003) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-55742-2_13

Practical Applications of Polyvalent Iodine Compounds

Zhdankin, V. V. (2013) · Wiley eBooks · doi:10.1002/9781118341155.ch7

Role of HCV F/ARF protein and NAD(P)H oxidases in the RIG-I/MDA5-mediated interferon response in hepatocytes

Park, S. B. (2015) · eScholarship (California Digital Library)

Modulação do estado redox em ilhotas pancreáticas e sua implicação na secreção de insulina.

de Oliveira, E. R. L. (2010) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2010.tde-11082010-134632

Adrenergic signaling in insulin-sensitive tissues

Yamamoto, D. L. (2007) · KTH Publication Database DiVA (KTH Royal Institute of Technology)

Chemiluminescent picture of diphenyleneiodonium‐inhibited NADPH oxidase: a bimodal process and its logistic–exponential model‐based description

Kochel, B., Vocks, A., & Arnhold, J. (2007) · Luminescence · doi:10.1002/bio.961

CENTRO DE ENERGIA NUCLEAR NA AGRICULTURA

Borgo, L. (2010)

Wirkung von Hemmstoffen und Antioxidantien in Gliazellen bei Anoxie/Reoxygenierung und in der hepatischen Enzephalopathie

Widmer, R. (2007) · doi:10.14279/depositonce-1542

Evaluation of pharmacological properties of Danshen compounds by computational and biochemical approaches

Zhou, Z. (2016) · RMIT Research Repository (RMIT University Library) · doi:10.25439/rmt.27581778

Role of Intracellular Oxidant Release in Oxidised Low Lipoprotein - Induced U937 Cell Death

Chen, A. Y. (2012) · UC Research Repository (University of Canterbury) · doi:10.26021/9143

Genetic Defects of Phagocyte Nadph Oxidase Activity and Activation

Bellavite, P., Bazzoni, F., Scolaro, G., Poli, G., Dusi, S., & Cassatella, M. A. (1989) · International Journal of Immunopathology and Pharmacology · doi:10.1177/039463208900200204

Role of Myostatin in oxidative stress in skeletal muscle

Sandhya, S. (2013) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/53725

The Role Of Oxidative Stress In The Pathogenesis Of Epithelial Ovarian Cancer

King, N. M. (2013) · Human Biology

Composition of NADPH Oxidase of Phagocytes and Other Cell Types: Role of Flavoprotein in Proton Translocation and Oxidase Activity

Jones, O. T. G., & Cross, A. R. (1992) · Elsevier eBooks · doi:10.1016/b978-0-12-150404-5.50009-x

THE COMPONENTS OF THE RESPIRATORY BURST OXIDASE OF HUMAN NEUTROPHILS

BABIOR, B. M. (1991) · Elsevier eBooks · doi:10.1016/b978-0-08-041749-3.50118-2

Tumor necrosis factor triggers the expression and activation of matrix metalloproteinases through NADPH-dependent superoxide production

Awad, A. (2010) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r31m1r

Indications for the Involvement of a Hemoprotein as an Oxygen Pressure Sensor Protein in the Carotid Body

Acker, H. (1992) · Springer eBooks · doi:10.1007/978-3-642-77469-0_21

The NADPH oxidase-induced phagosomal environment of neutrophils and other phagocytes

Foote, J. R. (2019) · UCL Discovery (University College London)

鞘氨醇-1-磷酸通过提高蚕豆保卫细胞胞质pH和H2O2含量调节黑暗诱导气孔关闭

马, 引., 杨, 淑., & 佘, 小. (2012) · Scientia Sinica Vitae · doi:10.1360/zc2012-42-9-746

Generation and Roles of Nitric Oxide in Anaphylaxis

Ashkenazy, Y., Witzling, V., Abend, Y., Moshonov, S., & Zor, U. (1995) · Springer eBooks · doi:10.1007/978-1-4615-1903-4_22

Erratum: A late Neanderthal associated with Upper Palaeolithic artefacts

Hublin, J., Spoor, F., Braun, M., Zonneveld, F. W., & Condémi, S. (1998) · Nature · doi:10.1038/33734

Cellular Inflammation in Models of Acute Gout

Martin, W. J. (2008) · doi:10.26686/wgtn.16959223.v1

COMMUNICATIONS

(1990) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1990.tb16987.x

Redoxmodulation Hippokampaler Neurone

Gerich, F. J. (2007) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-238

Effect of Metabolic Inhibitors on the Size and Structure of Halos Induced by the Powdery Mildew Pathogen Blumeria graminis f. sp. tritici on Wheat Leaves

Babosha, A. V., & Avetisyan, T. V. (2023) · Biology Bulletin Reviews · doi:10.1134/s2079086423070022

E. coli Meningitis

Venketaraman, V., Hajjar, K., & Sheren, N. (2025) · Methods in molecular biology · doi:10.1007/978-1-0716-4674-8_2

Etude fonctionnelle du coeur catalytique membranaire d'enzymes de la famille NOX : Identification de la première NADPH oxydase procaryote

Hajjar, C. (2014) · theses.fr (ABES) · doi:10.70675/5072631eza040z42fez967bz09136cb3bb42

Impact d’extraits de plantes du désert Algérien sur le cytosquelette et la division cellulaire

hassoun, M. S. (2015) · theses.fr (ABES) · doi:10.70675/58573bbaz9e37z41cfz90c6zbed023f95eff

Neutrophil FcγRI expression as a determinant of oxidative responses in human blood

Huot, S., Fortin, P. R., Laflamme, C., & Pouliot, M. (2026) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiag048

Mammalian Heme Peroxidases

Nauseef, W. M. (2026) · Springer eBooks · doi:10.1007/978-3-032-21135-4_5

BindingDB Entry 50038757: Type II NADH dehydrogenase of the respiratory chain of Plasmodium falciparum and its inhibitors.

BindingDB (2012) · UC San Diego · doi:10.7270/q2z89dbx

Phagocytosis-Independent Chemiluminescence

Maly, F. E. (1989) · Springer eBooks · doi:10.1007/978-1-4613-0753-2_42

Homeostatic Regulation of Interleukin-4-Mediated Cell Signaling

Chakraborty, R. (2009) · EngagedScholarship @ Cleveland State University (Cleveland State University)

The inhibitory effects of some iodonium compounds on the superoxide generating system of neutrophils and their failure to inhibit diaphorase activity

Cross, A. R. (1987) · Biochemical Pharmacology · doi:10.1016/0006-2952(87)90356-x · Cited by 58

NADPH binding component of neutrophil superoxide-generating oxidase.

Umei, T., Takeshige, K., & Minakami, S. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)57201-5 · Cited by 61

Purification and some properties of the 45 kDa diphenylene iodonium-binding flavoprotein of neutrophil NADPH oxidase

Yea, C., Cross, A. R., & Jones, O. T. G. (1990) · Biochemical Journal · doi:10.1042/bj2650095 · Cited by 62

Diphenylene iodonium as an inhibitor of the NADPH oxidase complex of bovine neutrophils: Factors controlling the inhibitory potency of diphenylene iodonium in a cell‐free system of oxidase activation

DOUSSIÈRE, J., & VIGNAIS, P. V. (1992) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1992.tb17159.x · Cited by 153

The inhibition by diphenyleneiodonium and its analogues of superoxide generation by macrophages

Hancock, J. T., & Jones, O. T. (1987) · Biochemical Journal · doi:10.1042/bj2420103 · Cited by 208