Concentration-dependent Effects of Nitric Oxide on Mitochondrial Permeability Transition and Cytochrome cRelease

PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT

Lowry, O. H., Rosebrough, N., Farr, A. L., & Randall, R. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52451-6 · Cited by 316,394

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

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.

Towbin, H., Staehelin, T., & Gordon, J. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.9.4350 · Cited by 53,218

Guide for the Care and Use of Laboratory Animals: Eighth Edition

(2011) · doi:10.17226/12910 · Cited by 16,199

Apparent hydroxyl radical production by peroxynitrite: Implications for endothelial injury from nitric oxide and superoxide

Beckman, J. S., Beckman, T. W., Chen, J., Marshall, P. A., & Freeman, B. A. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.4.1620 · Cited by 7,029

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

The mitochondrial permeability transition pore and its role in cell death

CROMPTON, M. (1999) · Biochemical Journal · doi:10.1042/bj3410233 · Cited by 2,432

Bcl-2 family proteins regulate the release of apoptogenic cytochrome c by the mitochondrial channel VDAC

Shimizu, S., Narita, M., Tsujimoto, Y., & Tsujimoto, Y. (1999) · Nature · doi:10.1038/20959 · Cited by 2,178

An APAF-1·Cytochrome c Multimeric Complex Is a Functional Apoptosome That Activates Procaspase-9

Zou, H., Li, Y., Liu, X., & Wang, X. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.17.11549 · Cited by 2,089

Mitochondrial control of nuclear apoptosis.

Zamzami, N., Susín, S. A., Marchetti, P., Hirsch, T., Gomez-Monterrey, I. M., Castedo, M., & Kroemer, G. (1996) · The Journal of Experimental Medicine · doi:10.1084/jem.183.4.1533 · Cited by 1,360

Pathophysiologic role of ischemia reperfusion injury: A review

Vishwakarma, V. K., Upadhyay, P. K., Gupta, J. K., & Yadav, H. N. (2017) · Journal of Indian College of Cardiology · doi:10.1016/j.jicc.2017.06.017 · Cited by 20

Mitochondrial modulation of apoptosis induced by low-dose radiation in mouse testicular cells.

Fang, F., Gong, P., Zhao, H., Bi, Y. J., Zhao, G., Gong, S. L., & Wang, Z. (2013) · PubMed · doi:10.3967/bes2013.005 · Cited by 19

Pharmacologic Preconditioning of Random-Pattern Skin Flap in Rats Using Local Cyclosporine and FK-506

Ghazinezami, B., Rahimpour, S., Gholipour, T., Ghasemi, M., Sadeghipour, H., Mehr, S. E., Emami-Razavi, S. H., & Dehpour, A. R. (2007) · Annals of Plastic Surgery · doi:10.1097/01.sap.0000258982.86308.f0 · Cited by 19

Injectable and self-healing hydrogel containing nitric oxide donor for enhanced antibacterial activity

Yang, Y., Zhou, Y., Li, Y., Guo, L., Zhou, J., & Chen, J. (2021) · Reactive and Functional Polymers · doi:10.1016/j.reactfunctpolym.2021.105003 · Cited by 18

Effect of R-(-)-Deprenyl and Harmaline on Dopamine- and Peroxynitrite-Induced Membrane Permeability Transition in Brain Mitochondria

Lee, C. S., Lee, C. S., Ko, H. H., Song, J. H., & Han, E. S. (2002) · Neurochemical Research · doi:10.1023/a:1014832520809 · Cited by 18

The role of nitric oxide in abnormal T cell signal transduction in systemic lupus erythematosus

Nagy, G., & Perl, A. (2006) · Clinical Immunology · doi:10.1016/j.clim.2005.10.016 · Cited by 18

The Liver-Selective Nitric Oxide Donor O2-Vinyl 1-(pyrrolidin-1-yl)diazen-1-ium-1,2-diolate (V-PYRRO/NO) Protects HepG2 Cells against Cytochrome P450 2E1-Dependent Toxicity

Gong, P., Cederbaum, A. I., & Nieto, N. (2004) · Molecular Pharmacology · doi:10.1124/mol.65.1.130 · Cited by 18

Mitochondrial function and nitric oxide production in hippocampus and cerebral cortex of rats exposed to enriched environment

Lores‐Arnaiz, S., Arnaiz, M. R. L., Czerniczyniec, A., Cuello, M. I., & Bustamante, J. (2010) · Brain Research · doi:10.1016/j.brainres.2010.01.017 · Cited by 17

miRNA-mRNA crosstalk in myocardial ischemia induced by calcified aortic valve stenosis

Duan, C., Cao, Z., Tang, F., Zhao, J. H., Liang, C., Liu, H., Xiao, Y., Liu, L., & Ma, R. (2019) · Aging · doi:10.18632/aging.101751 · Cited by 17

Nitric oxide‐mediated inhibition of NFκB regulates hyperthermia‐induced apoptosis

Aravindan, N., Mohan, S., Herman, T. S., & Natarajan, M. (2009) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22079 · Cited by 17

Nitric Oxide/Cyclic GMP-Dependent Calcium Signalling Mediates IL-6- and TNF-α-Induced Expression of Glial Fibrillary Acid Protein

Sticozzi, C., Belmonte, G., Frosini, M., & Pessina, F. (2020) · Journal of Molecular Neuroscience · doi:10.1007/s12031-020-01708-3 · Cited by 16

The higher susceptibility of congenital analbuminemic rats to Ca2+-induced mitochondrial permeability transition is associated with the increased expression of cyclophilin D and nitrosothiol depletion

Figueira, T. R., Castilho, R. F., Saito, Â., Oliveira, H. C. F., & Vercesi, A. E. (2011) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2011.08.031 · Cited by 16

Reactive oxygen species are key mediators of the nitric oxide apoptotic pathway in anterior pituitary cells

Machiavelli, L. I., Poliandri, A., Quinteros, F. A., Cabilla, J. P., & Duvilanski, B. H. (2006) · Nitric Oxide · doi:10.1016/j.niox.2006.08.002 · Cited by 16

S-nitrosothiol-terminated poly(vinyl alcohol): Nitric oxide release and skin blood flow response

Giglio, L. P., Picheth, G. F., Løvschall, K. B., Zelikin, A. N., & de Oliveira, M. G. (2020) · Nitric Oxide · doi:10.1016/j.niox.2020.03.002 · Cited by 15

Nitric Oxide: Regulation and Function in Neutrophil Immune Responses

Kumar, S., & Dikshit, M. (2024) · Antioxidants and Redox Signaling · doi:10.1089/ars.2022.0220 · Cited by 17

New perspectives of nitric oxide donors in cardiac arrest and cardiopulmonary resuscitation treatment

Kružliak, P., Pecháňová, O., & Kára, T. (2013) · Heart Failure Reviews · doi:10.1007/s10741-013-9397-4 · Cited by 14

SECOND-GENERATION SULFONYLUREAS PRESERVE INHIBITION OF MITOCHONDRIAL PERMEABILITY TRANSITION BY THE MITOCHONDRIAL K+ ATP OPENER NICORANDIL IN EXPERIMENTAL MYOCARDIAL INFARCTION

Argaud, L., Garrier, O., Loufouat, J., Gomez, L., Couture-Lepetit, E., Gateau-Roesch, O., Robert, D., & Ovize, M. (2009) · Shock · doi:10.1097/shk.0b013e31819c3794 · Cited by 14

Transient injury to rat lung mitochondrial DNA after exposure to hyperoxia and inhaled nitric oxide

Lightfoot, R. T., Khov, S., & Ischiropoulos, H. (2004) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00352.2002 · Cited by 14

Lysosomal Fe2+contributes to myofibrillar protein degradation through mitochondrial-dysfunction-induced apoptosis

Chen, C., Guo, Z., Ma, G., Ma, J., Zhang, Z., Yu, Q., & Han, L. (2021) · LWT · doi:10.1016/j.lwt.2021.111197 · Cited by 13

Reactive Oxygen Species and the Cardiovascular System

Montezano, A. C. I., & Touyz, R. M. (2012) · Colloquium Series on Integrated Systems Physiology From Molecule to Function · doi:10.4199/c00043ed1v01y201112isp032 · Cited by 14

LEUKOCYTE MITOCHONDRIAL ALTERATIONS AFTER CARDIAC SURGERY INVOLVING CARDIOPULMONARY BYPASS: CLINICAL CORRELATIONS

Kong, C., Huang, C.-H., Hsu, T.-G., Tsai, K. K., Hsu, C.-F., Huang, M.-C., & Chen, L.-C. (2004) · Shock · doi:10.1097/00024382-200404000-00005 · Cited by 13

Cardiac mitochondrial function and tissue remodelling are improved by a non-antihypertensive dose of enalapril in spontaneously hypertensive rats

Piotrkowski, B., Koch, O. R., de Cavanagh, E. M. V., & Fraga, C. G. (2009) · Free Radical Research · doi:10.1080/10715760902801517 · Cited by 13

Arginase, Nitric Oxide Synthase, and Novel Inhibitors of L-arginine Metabolism in Immune Modulation

Chioda, M., Marigo, I., Mandruzzato, S., D, S. M. M., & Bronte, V. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-394296-8.00034-8 · Cited by 14

Cardiac mitochondrial cGMP stimulates cytochrome c release

Seya, K., Motomura, S., & Furukawa, K. (2006) · Clinical Science · doi:10.1042/cs20060144 · Cited by 13

Regulation of soluble VEGFR-2 secreted by microvascular endothelial cells derived from human BPH

Aweimer, A., Stachon, T., Tannapfel, A., Köller, M., Truß, M. C., & Stachon, A. (2011) · Prostate Cancer and Prostatic Diseases · doi:10.1038/pcan.2011.63 · Cited by 13

Opioid receptor-independent protection of ischemic rat hepatocytes by morphine

Kim, J., & Lemasters, J. J. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.10.153 · Cited by 13

Switching off HSP70 and i-NOS to study their role in normal and H2O2-stressed human fibroblasts.

Renis, M., Cardile, V., Grasso, S., Palumbo, M., & Scifo, C. (2003) · Life Science · doi:10.1016/j.lfs.2003.07.016 · Cited by 14

The Renin-Angiotensin-Aldosterone System as a Therapeutic Target in Late Injury Caused by Ischemia-Reperfusion

Rodríguez-Lara, S. Q., García‐Benavides, L., & Miranda‐Díaz, A. G. (2018) · International Journal of Endocrinology · doi:10.1155/2018/3614303 · Cited by 12

Mitochondrial contribution to the molecular mechanism of heart acclimatization to chronic hypoxia: role of nitric oxide

Zaobornyj, T. (2006) · Frontiers in bioscience · doi:10.2741/2143 · Cited by 12

Ca(2+)N It Be Measured? Detection of Extramitochondrial Calcium Movement With High-Resolution FluoRespirometry

Nászai, A., Terhes, E., Kaszaki, J., Boros, M., & Juhász, L. (2019) · Scientific Reports · doi:10.1038/s41598-019-55618-5 · Cited by 12

Nitric Oxide/cGMP Signaling Pathway Protects RAW264 Cells Against Nitric Oxide-Induced Apoptosis by Inhibiting the Activation of p38 Mitogen-Activated Protein Kinase

Yoshioka, Y., Yamamuro, A., & Maeda, S. (2006) · Journal of Pharmacological Sciences · doi:10.1254/jphs.fpj06001x · Cited by 12

Multifunctional Role of Fas-Associated Death Domain Protein in Apoptosis

Kim, K. (2002) · BMB Reports · doi:10.5483/bmbrep.2002.35.1.001 · Cited by 13

Hypoxia and nitric oxide exposure promote apoptotic signaling in contractile pulmonary arterial smooth muscle but not in pulmonary epithelium

Postolow, F., Fediuk, J., Nolette, N., Hinton, M., & Dakshinamurti, S. (2011) · Pediatric Pulmonology · doi:10.1002/ppul.21491 · Cited by 11

Heart Mitochondrial Nitric Oxide Synthase

Zaobornyj, T., & Valdez, L. B. (2014) · Vitamins and hormones · doi:10.1016/b978-0-12-800254-4.00003-9 · Cited by 11

S3/7 Intramitochondrial signaling — Interactions among mitoKATP, PKCε, ROS, and MPT

Garlid, K., & Costa, A. D. T. (2008) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2008.05.106 · Cited by 11

Nitric Oxide, Cell Death, and Heart Failure

Oyama, J., Frantz, S., Blais, C., Kelly, R. A., & Bourcier, T. (2002) · Heart Failure Reviews · doi:10.1023/a:1020758300499 · Cited by 11

Mitochondrial Signal Transduction Abnormalities in Systemic Lupus Erythematosus

Nagy, G., Koncz, Á., Phillips, P., & Perl, A. (2005) · Current Immunology Reviews · doi:10.2174/1573395052952932 · Cited by 11

Inactivation of multiple targets by nitric oxide in CD95‐triggered apoptosis

Bernassola, F., Catani, M. V., Corazzari, M., Rossi, A., & Melino, G. (2001) · Journal of Cellular Biochemistry · doi:10.1002/jcb.1143 · Cited by 11

Interaction of the nitric oxide signaling system with the Sphingomyelin cycle and Peroxidation on transmission of toxic signal of tumor necrosis factor-α in ischemia-reperfusion

Shupik, M. A., Vanin, A. F., & Alessenko, A. V. (2011) · Biochemistry (Moscow) · doi:10.1134/s0006297911110010 · Cited by 10

Mechanism of Ischemia and Reperfusion Injury to the Heart: From the Viewpoint of Nitric Oxide and Mitochondria

Ha, S. J., & Kim, W. (2010) · Chonnam Medical Journal · doi:10.4068/cmj.2010.46.3.129 · Cited by 10

Electroencephalographic Response to Sodium Nitrite May Predict Delayed Cerebral Ischemia After Severe Subarachnoid Hemorrhage

Garry, P. S., Rowland, M. J., Ezra, M., Herigstad, M., Hayen, A., SLEIGH, J. W., Westbrook, J., Warnaby, C. E., & Pattinson, K. T. S. (2016) · Critical Care Medicine · doi:10.1097/ccm.0000000000001950 · Cited by 8

Nitric oxide donors prevent while the nitric oxide synthase inhibitor l-NAME increases arachidonic acid plus CYP2E1-dependent toxicity

Wu, D., & Cederbaum, A. I. (2006) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2006.05.019 · Cited by 9

Integrated analysis of the involvement of nitric oxide synthesis in mitochondrial proliferation, mitochondrial deficiency and apoptosis in skeletal muscle fibres

Rodrigues, G. S., Godinho, R. O., Kiyomoto, B. H., Gamba, J., Oliveira, A. S. B., Schmidt, B., & Tengan, C. H. (2016) · Scientific Reports · doi:10.1038/srep20780 · Cited by 9

Function and regulation of mitochondrially produced nitric oxide in cardiomyocytes

Kanai, A., & Peterson, J. (2004) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00776.2003 · Cited by 9

Ventricular but not atrial electro-mechanical delay of the embryonic heart is altered by anoxia-reoxygenation and improved by nitric oxide

Maury, P., Sarre, A., Terrand, J., Rosa, A., Kučera, P., KAPPENBERGER, L. J., & Raddatz, E. (2004) · Molecular and Cellular Biochemistry · doi:10.1023/b:mcbi.0000044391.97857.4d · Cited by 9

Catalase-Like Antioxidant Activity is Unaltered in Hypochlorous Acid Oxidized Horse Heart Myoglobin

Ahmad, G., Chami, B., Kazzi, M. E., Wang, X., Moreira, M. T. S., Hamilton, N. A., Maw, A. M., Hambly, T. W., & Witting, P. K. (2019) · Antioxidants · doi:10.3390/antiox8090414 · Cited by 6

Formation of dinitrosyl iron complexes in cardiac mitochondria

Шумаев, К. Б., Sviryaeva, I. V., Gubkina, S. A., Krivova, T. S., Topunov, A. F., Vanin, A. F., & Ruuge, E. K. (2010) · BIOPHYSICS · doi:10.1134/s0006350910030097 · Cited by 7

5.3 Mitochondrial Production of Oxidants and Their Role in the Regulation of Cellular Processes

Brookes, P. S. (2007) · Springer eBooks · doi:10.1007/978-0-387-30411-3_19 · Cited by 7

Pharmacological Targeting of the Mitochondrial Permeability Transition Pore for Cardioprotection

Silva, F. S. G., Costa, C. F., Marques, R., Oliveira, P. J., & Pereira, G. C. (2018) · Springer eBooks · doi:10.1007/978-3-319-73344-9_20 · Cited by 7

Postanoxic functional recovery of the developing heart is slightly altered by endogenous or exogenous nitric oxide

Terrand, J., Felley‐Bosco, E., Courjault-Gautier, F., Rochat, A.-C., Kučera, P., & Raddatz, E. (2003) · Molecular and Cellular Biochemistry · doi:10.1023/a:1025565126250 · Cited by 6

Rôle pro- et anti-apoptotique du monoxyde d’azote, NO

Kolb, J. (2001) · Comptes Rendus de l Académie des Sciences - Series III - Sciences de la Vie · doi:10.1016/s0764-4469(01)01315-4 · Cited by 6

Role of ADAMTS-13 and nNOS expression in neuropathogenesis of listeric encephalitis of small ruminants

Karayığıt, M. Ö., & Dinçel, G. Ç. (2020) · Biotechnic & Histochemistry · doi:10.1080/10520295.2020.1743359 · Cited by 5

Examination of the Changes in Calcium Homeostasis in the Delayed Antiarrhythmic Effect of Sodium Nitrite

Demeter‐Haludka, V., Kovács, M., Prorok, J., Nagy, N., Varró, A., & Végh, Á. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20225687 · Cited by 5

Hemodynamic responses induced by modulation of the nitric oxide system and mitochondrial permeability in the medullary cardiovascular nuclei of rats

Shapoval, L. N., Dmytrenko, O. V., Pobegailo, L. S., Stepanenko, L. G., & Сагач, В. Ф. (2007) · Neurophysiology · doi:10.1007/s11062-007-0027-4 · Cited by 5

The role of nitric oxide in mitochondria. Focus on “Modulation of mitochondrial Ca2+ by nitric oxide in cultured bovine vascular endothelial cells”

Davidson, S. M., & Yellon, D. M. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00277.2005 · Cited by 5

The interaction between the renin-angiotensin system and peroxisome proliferator activated receptors: a hypothesis including the participation of mitochondria in aging

V., D. C. E. M. (2006) · Frontiers in bioscience · doi:10.2741/2125 · Cited by 5

Modulated nitric oxide delivery in three-dimensional biomaterials for vascular functionality

Wang, Z., Wen, F., Zhang, R., & Zhang, Q. (2017) · MRS Communications · doi:10.1557/mrc.2017.40 · Cited by 5

Injectable protein hydrogel microspheres with reactive oxygen species-responsive nitric oxide release for cardiac protection against ischemia/reperfusion injury

Zheng, H., Jia, F., Gao, Y. H., Deng, K., Shen, L., Zheng, C., Xie, X., Gao, C., Ren, T., & Zhu, Y. (2025) · Acta Biomaterialia · doi:10.1016/j.actbio.2025.08.040 · Cited by 6

Nitric Oxide Synthesis in the Mitochondria of Animal Cells

Rőszer, T. (2012) · Springer eBooks · doi:10.1007/978-94-007-2819-6_10 · Cited by 4

Nitric Oxide: Immune Modulation of Tumor Growth

Janakiram, N. B., & Rao, C. V. (2015) · Springer eBooks · doi:10.1007/978-3-319-13611-0_11 · Cited by 4

Mitochondria permeability transition as a target for ischemic preconditioning

Hoshovs'ka, I., Tv, S., Rudyk, O., IuP, K., & Sahach, V. F. (2011) · Fìzìologìčnij žurnal · doi:10.15407/fz57.04.034 · Cited by 4

THE FUNCTIONAL STATE OF THE RAT HEART DURING ISCHEMIA-REPERFUSION, THE SENSITIVITY OF CALCIUM-INDUCED MITOCHONDRIAL PERMEABILITY TRANSITION PORE OPENING AND THE UNCOUPLING PROTEIN 3 EXPRESSION FOLLOWING LONG EXERCISE TRAINING

Chorna, S. V., Talanov, S. O., Strutynska, N. A., Vavilova, G. L., Kotsuruba, A. V., Gaidai, N. M., & Sagach, V. F. (2010) · Fìzìologìčnij žurnal · doi:10.15407/fz56.01.013 · Cited by 4

Mito-controversies

Patel, H. H., Tsutsumi, Y. M., & Roth, D. M. (2008) · Anesthesiology · doi:10.1097/01.anes.0000299750.34472.93 · Cited by 5

Nitrite-Mediated Modulation of HL-60 Cell Cycle and Proliferation: Involvement of Cyclin-Dependent Kinase 2 Activation

Kumar, S., Barthwal, M. K., & Dikshit, M. (2011) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.110.177444 · Cited by 3

Impact of Swimming Exercise Training on the Effects of Modulation of Mitochondrial Permeability Transition and NOS-1 Activation in Medullary Cardiovascular Neurons of Rats

Shapoval, L., Pobegailo, L. S., Stepanenko, L., Dmytrenko, O., Bouryi, V., & Sagach, V. (2011) · Neurophysiology (New York) · doi:10.1007/s11062-011-9230-4 · Cited by 3

Cytokines in liver, biliary, and pancreatic disease

Weiss, M. J. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4377-1454-8.00010-2 · Cited by 3

Bleaching of the Cnidarian-Dinoflagellate Symbiosis: Aspects of Innate Immunity and the Role of Nitric Oxide

Hawkins, T. D. (2013) · Open Access Victoria University of Wellington | Te Herenga Waka (Figshare) · doi:10.26686/wgtn.17005798.v1 · Cited by 2

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Elbeheiry, H. M., & Schulz, M. (2024) · Chemistry - A European Journal · doi:10.1002/chem.202400709 · Cited by 2

Nitric Oxide Synthases in Brain Function

Murphy, S. P., & Coughlan, T. C. (2006) · Springer eBooks · doi:10.1007/0-387-30395-2_11 · Cited by 2

Nitrite and Nitrate in Ischemia–Reperfusion Injury

Lefer, D. J., Bryan, N. S., & Organ, C. L. (2017) · Springer eBooks · doi:10.1007/978-3-319-46189-2_16 · Cited by 2

The Renin-Angiotensin System and the Aging Process

Ferder, L., & Martínez–Maldonado, M. (2007) · Springer eBooks · doi:10.1007/978-0-387-72659-5_12 · Cited by 2

Nitrite and Nitrate in Ischemia-Reperfusion Injury

Lavu, M., Gundewar, S., & Lefer, D. J. (2011) · Humana Press eBooks · doi:10.1007/978-1-60761-616-0_14 · Cited by 2

Changes in the mitochondrial permeability in medullary cardiovascular neurons influence the hemodynamics in rats

Shapoval, L. N., Dmytrenko, O. V., Pobegailo, L. S., Stepanenko, L. G., & Сагач, В. Ф. (2007) · Neurophysiology · doi:10.1007/s11062-007-0052-3 · Cited by 2

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Soane, L., Solenski, N. J., & Fiskum, G. M. (2007) · Springer eBooks · doi:10.1007/978-0-387-30411-3_26 · Cited by 1

Effect of Hepatic Steatosis on Bioenergetic Function During Hepatic Ischemia-reperfusion: A Systematic Review

Chu, M. J. J. (2013) · The Open Transplantation Journal · doi:10.2174/1874418420130513001 · Cited by 1

Effect of Sildenafil on Heart Nitric Oxide Metabolism and Mitochondrial Function

Zaobornyj, T., Valdez, L. B., & Boveris, A. (2012) · Oxidative stress and disease · doi:10.1201/b12308-12 · Cited by 1

Biochemistry and Physiology of Heart Mitochondrial Nitric Oxide Synthase

Zaobornyj, T., Iglesias, D. E., Bombicino, S. S., Rukavina-mikusic, I. A., & Valdez, L. B. (2016) · Springer eBooks · doi:10.1007/978-3-319-45865-6_4 · Cited by 1

Arginase, Nitric Oxide Synthase, and Novel Inhibitors of L-Arginine Metabolism in Immune Modulation

Mandruzzato, S., D, S. M. M., & Bronte, V. (2007) · Elsevier eBooks · doi:10.1016/b978-012372551-6/50084-5 · Cited by 1

The use of the Petri net method in the simulation modeling of mitochondrial swelling

Danylovych, I. V., Chunikhin, A., Danylovych, G. V., & Kolomiets, O. V. (2016) · The Ukrainian Biochemical Journal · doi:10.15407/ubj88.04.066 · Cited by 1

Identification of Differentially Expressed Genes in Murine Hippocampus by Modulation of Nitric Oxide in Kainic Acid-induced Neurotoxic Animal Model

Suh, Y.-A., Kwon, O.-M., Yim, S., Lee, H. J., & Kim, S. (2007) · Korean Journal of Physiology and Pharmacology · Cited by 1

APOPTOTIC AND CYTOTOXIC EFFECT OF ORIGANUM MINUTIFLORUM ON NB2A NEUROBLASTOMA CELLS

Sarı, İ., Dönmez, G., Özkan, O., Aydemir, I., Özbey, C., & Tuğlu, M. İ. (2020) · Ankara Universitesi Eczacilik Fakultesi Dergisi · doi:10.33483/jfpau.707277 · Cited by 1

Chapter 10 The Interaction of Mitochondrial Membranes with Reactive Oxygen and Nitrogen Species

(2008) · Current topics in membranes · doi:10.1016/s1063-5823(08)00210-x · Cited by 1

Papel de las especies reactivas del oxígeno en el daño al miocardio inducido por isquemia/reperfusión

Delgado-Roche, L., & Martı́nez-Sánchez, G. (2010) · Redalyc (Universidad Autónoma del Estado de México) · Cited by 1

Testosterona induz migração de células da musculatura lisa vascular de ratos espontaneamente hipertensos por mecanismos dependentes de EROs e ativação da NADPH oxidase via c-Src.

Chignalia, A. Z. (2009) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2009.tde-02022010-114821 · Cited by 1

Endotoxin and Cytokines in Liver and Biliary Tract Disease

McAuliffe, P. F., & Moldawer, L. L. (2007) · Elsevier eBooks · doi:10.1016/b978-1-4160-3256-4.50018-1 · Cited by 1

Cyclophilin D ‐Dependent Necrosis

Mehta, J., & Mandal, C. C. (2018) · Wiley eBooks · doi:10.1002/9781119432463.ch18 · Cited by 1

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