Protein Kinase G Transmits the Cardioprotective Signal From Cytosol to Mitochondria

DETERMINATION OF SERUM PROTEINS BY MEANS OF THE BIURET REACTION

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

Inhibition of protein kinase C μ by various inhibitors. Inhibition from protein kinase c isoenzymes

Gschwendt, M., Dieterich, S., Rennecke, J., Kittstein, W., Mueller, H.-J., & Johannes, F.-J. (1996) · FEBS Letters · doi:10.1016/0014-5793(96)00785-5 · Cited by 644

Opposing cardioprotective actions and parallel hypertrophic effects of δPKC and ɛPKC

Chen, L., Hahn, H. S., Wu, G., Chen, C., Liron, T., Schechtman, D., Cavallaro, G., Banci, L., Guo, Y., Bolli, R., et al. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.191369098 · Cited by 537

Isoenzyme specificity of bisindolylmaleimides, selective inhibitors of protein kinase C

Wilkinson, S. E., Parker, P. J., & Nixon, J. (1993) · Biochemical Journal · doi:10.1042/bj2940335 · Cited by 522

Ischemic Preconditioning Induces Selective Translocation of Protein Kinase C Isoforms ε and η in the Heart of Conscious Rabbits Without Subcellular Redistribution of Total Protein Kinase C Activity

Ping, P., Zhang, J., Qiu, Y., Tang, X., Manchikalapudi, S., Cao, X., & Bolli, R. (1997) · Circulation Research · doi:10.1161/01.res.81.3.404 · Cited by 482

The Mitochondrial K Channel as a Receptor for Potassium Channel Openers

Garlid, K., Pauček, P., Yarov-Yarovoy, V. M., Sun, X., & Schindler, P. A. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.15.8796 · Cited by 445

Mitochondrial PKCε and MAPK Form Signaling Modules in the Murine Heart

Baines, C. P., Zhang, J., Wang, G.-W., Zheng, Y.-T., Xiu, J. X., Cardwell, E. M., Bolli, R., & Ping, P. (2002) · Circulation Research · doi:10.1161/01.res.0000012702.90501.8d · Cited by 429

A Selective ε-Protein Kinase C Antagonist Inhibits Protection of Cardiac Myocytes from Hypoxia-induced Cell Death

Gray, M. O., Karliner, J. S., & Mochly‐Rosen, D. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.49.30945 · Cited by 388

A Protein Kinase C Translocation Inhibitor as an Isozyme-selective Antagonist of Cardiac Function

Johnson, J. A., Gray, M. O., Chen, C., & Mochly‐Rosen, D. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.40.24962 · Cited by 377

Modulation of Mitochondrial ATP-Dependent K+Channels by Protein Kinase C

Sato, T., O'Rourke, B. P., & Marbán, E. (1998) · Circulation Research · doi:10.1161/01.res.83.1.110 · Cited by 366

Roles of mitochondrial Src tyrosine kinase and zinc in nitric oxide-induced cardioprotection against ischemia/reperfusion injury

Zhang, Y., Xing, F., Zheng, H., Xi, J., Cui, X., & Xu, Z. (2013) · Free Radical Research · doi:10.3109/10715762.2013.796044 · Cited by 16

Murine cardiac growth, TRPC channels, and cGMP kinase I

Domes, K., Patrucco, E., Loga, F., Dietrich, A., Birnbaumer, L., Wegener, J. W., & Hofmann, F. B. (2014) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-014-1682-0 · Cited by 16

The cardioprotective effect of sildenafil is mediated by the activation of malate dehydrogenase and an increase in the malate-aspartate shuttle in cardiomyocytes

Gevi, F., Campolo, F., Naro, F., & Zolla, L. (2016) · Biochemical Pharmacology · doi:10.1016/j.bcp.2016.12.017 · Cited by 16

Modulation of KATP currents in rat ventricular myocytes by hypoxia and a redox reaction

Yan, X.-S., Ma, J.-H., & Zhang, P.-H. (2009) · Acta Pharmacologica Sinica · doi:10.1038/aps.2009.134 · Cited by 18

Emerging therapy strategies for energy metabolism in acute myocardial infarction

Ma, R., Lu, D., Yang, Z., Ji, X., Tian, R., Xu, F., Chen, Y., & Li, C. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-07088-9 · Cited by 16

Treatment of Myocardial Ischemia/Reperfusion Injury by Ischemic and Pharmacological Postconditioning

Heusch, G. (2015) · Comprehensive physiology · doi:10.1002/j.2040-4603.2015.tb00650.x · Cited by 14

Connexins and Nitric Oxide Inside and Outside Mitochondria: Significance for Cardiac Protection and Adaptation

Shvedova, M., Anfinogenova, Y., Popov, S. V., & Atochin, D. N. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00479 · Cited by 15

The alpha1 isoform of soluble guanylate cyclase regulates cardiac contractility but is not required for ischemic preconditioning

Sips, P. Y., Brouckaert, P., & Ichinose, F. (2011) · Basic Research in Cardiology · doi:10.1007/s00395-011-0167-y · Cited by 13

Cell Survival Programs and Ischemia /Reperfusion: Hormesis, Preconditioning, and Cardioprotection

Krenz, M., Baines, C. P., Kalogeris, T. J., & Korthuis, R. J. (2013) · Colloquium Series on Integrated Systems Physiology From Molecule to Function · doi:10.4199/c00090ed1v01y201309isp044 · Cited by 13

Effects of sildenafil on nanostructural and nanomechanical changes in mitochondria in an ischaemia‐reperfusion rat model

Lee, K. H., Kwon, S. J., Woo, J., Lee, G., Lee, S., Jang, H., Kim, H. S., Kim, J., Park, H. K., Cho, K. S., et al. (2014) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.12290 · Cited by 13

Role of protein kinase C, PI3 kinase, tyrosine kinases, NO-synthase, KATP channels and MPT pore in the signaling pathway of the cardioprotective effect of chronic continuous hypoxia

Tsibulnikov, S. Y., Маслов, Л. Н., Naryzhnaya, N. V., Ma, H., Lishmanov, Y. B., Oeltgen, P. R., & Garlid, K. (2018) · General Physiology and Biophysics · doi:10.4149/gpb_2018013 · Cited by 13

Novel Findings and Therapeutic Targets on Cardioprotection of Ischemia/ Reperfusion Injury in STEMI

Li, J., Sun, D., & Li, Y. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666191105103417 · Cited by 13

PERK-Mediated Suppression of microRNAs by Sildenafil Improves Mitochondrial Dysfunction in Heart Failure

Shimizu, T., Taguchi, A., Higashijima, Y., Takubo, N., Kanki, Y., Urade, Y., & Wada, Y. (2020) · iScience · doi:10.1016/j.isci.2020.101410 · Cited by 13

Diabetes Abolishes Sildenafil-Induced cGMP-Dependent Protein Kinase-I Expression and Cardioprotection

Jamnicki, M., Weihrauch, D., Chiari, P. C., Krolikowski, J. G., Pagel, P. S., Warltier, D. C., & Kersten, J. R. (2007) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0b013e318157fd5b · Cited by 13

Pharmacological postconditioning with diazoxide attenuates ischemia/reperfusion-induced injury in rat liver

Tian, Y., RONG, T., Hong, Y., MIN, L., & Jian, P. (2013) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2013.941 · Cited by 12

Human muscle pathology is associated with altered phosphoprotein profile of mitochondrial proteins in the skeletal muscle

Sunitha, B., Kumar, M., Gowthami, N., Unni, S., Gayathri, N., Prasad, T. S. K., Nalini, A., Polavarapu, K., Vengalil, S., Preethish‐Kumar, V., et al. (2019) · Journal of Proteomics · doi:10.1016/j.jprot.2019.103556 · Cited by 12

Cardiovascular Pharmacology

Pagel, P. S., Farber, N. E., Pratt, P. F., & Warltier, D. C. (2010) · Elsevier eBooks · doi:10.1016/b978-0-443-06959-8.00023-6 · Cited by 12

Potent Cardioprotective Effect of the 4-Anilinoquinazoline Derivative PD153035: Involvement of Mitochondrial KATP Channel Activation

Cavalheiro, R. A., Marin, R. M., Rocco, S. A., Cerqueira, F. M., da Silva, C. C. C., Rittner, R., Kowaltowski, A. J., Vercesi, A. E., Franchini, K. G., & Castilho, R. F. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010666 · Cited by 12

NO/cGMP/PKG activation protects Drosophila cells subjected to hypoxic stress

Mahneva, O., Caplan, S. L., Ivko, P., Dawson-Scully, K. D., & Milton, S. (2019) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2019.05.013 · Cited by 11

Pharmacological preconditioning with gemfibrozil preserves cardiac function after heart transplantation

Benke, K., Mátyás, C., Sayour, A. A., Oláh, A., Németh, B. T., Ruppert, M., Szabo, G. B., Kökény, G., Horvath, E. M., Hartyánszky, I. L., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-14587-3 · 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

Mechanism of reactive oxygen species generation after opening of mitochondrial KATP channels

Kukreja, R. C. (2006) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00772.2006 · Cited by 11

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

Mitochondrial Ion Channels

O'Rourke, B. P. (2007) · Springer eBooks · doi:10.1007/978-0-387-69945-5_10 · Cited by 9

NO Better Way to Protect the Heart during Ischemia–Reperfusion: To be in the Right Place at the Right Time

Farah, C., & Reboul, C. (2015) · Frontiers in Pediatrics · doi:10.3389/fped.2015.00006 · Cited by 9

Remote ischemic preconditioning and outcome

Zarbock, A., Aken, H. V., & Schmidt, C. G. (2015) · Current Opinion in Anaesthesiology · doi:10.1097/aco.0000000000000161 · Cited by 8

Warm-blood cardioplegic arrest induces selective mitochondrial translocation of protein kinase Cε followed by interaction with 6.1 inwardly rectifying potassium channel subunit in viable myocytes overexpressing urocortin

Chen-Scarabelli, C. A., Faggian, G. G., Yuan, Z., Tessari, M. M., Rungatscher, A., Rezze, J. D., Scarabelli, G. M., Abounit, K., McCauley, R. B., Saravolatz, L. I. I., et al. (2009) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/j.jtcvs.2009.03.041 · Cited by 8

Acute treatment with copoazú fermented extract ameliorates myocardial ischemia-reperfusion injury via eNOS activation

Fantinelli, J. C., Álvarez, L. N. C., Arbeláez, L. F. G., Pardo, A. C., García, P., Schinella, G. R., & Mosca, S. M. (2017) · Journal of Functional Foods · doi:10.1016/j.jff.2017.05.010 · Cited by 8

Paradoxical mitochondrial effects of nitric oxide synthase inhibition following oxygen–glucose deprivation–reoxygenation (OGD/R) in endothelial cells and neurons

Sure, V. N. L. R., Sakamuri, S. S. V. P., Orgunati, L., Ageeli, R. Y., Murfee, W. L., & Katakam, P. V. G. (2025) · British Journal of Pharmacology · doi:10.1111/bph.70187 · Cited by 8

Dual role of cyclic GMP in cardiac cell survival

Xu, Z., Lee, S., & Han, J. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.04.027 · Cited by 7

Drug Candidate BGP-15 Prevents Isoproterenol-Induced Arrhythmias and Alters Heart Rate Variability (HRV) in Telemetry-Implanted Rats

Bernát, B., Erdélyi, R., Fazekas, L. Á., Garami, G., Szekeres, R., Takács, B., Bombicz, M., Varga, B., Sárkány, F., Ráduly, A. P., et al. (2023) · Pharmaceuticals · doi:10.3390/ph16030359 · Cited by 7

Stimulation of Oxytocin Receptor during Early Reperfusion Period Protects the Heart against Ischemia/Reperfusion Injury: the Role of Mitochondrial ATP-Sensitive Potassium Channel, Nitric Oxide, and Prostaglandins.

Imani, A., Khansari, M., Azizi, Y., Rakhshan, K., & Faghihi, M. (2015) · PubMed · Cited by 7

Role of ATP-Sensitive K+ Channels in Myocardial Infarct Size-Limiting Effect of Chronic Continuous Normobaric Hypoxia

Lishmanov, Y. B., Naryzhnaya, N. V., Tsibulnikov, S. Y., Wang, H., & Маслов, Л. Н. (2017) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-017-3728-8 · Cited by 7

Mitochondrial depolarization stimulates vascular repair‐relevant functions of CD34+ cells via reactive oxygen species‐induced nitric oxide generation

Joshi, S., & Jarajapu, Y. P. R. (2018) · British Journal of Pharmacology · doi:10.1111/bph.14529 · Cited by 7

Erythropoietin (EPO) Affords More Potent Cardioprotection by Activation of Distinct Signaling to Mitochondrial Kinases Compared with Carbamylated EPO

Sato, T., Tanno, M., Miki, T., Yano, T., Sato, T., Shimamoto, K., & Miura, T. (2010) · Cardiovascular Drugs and Therapy · doi:10.1007/s10557-010-6265-5 · 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

Nitric Oxide Donor NOC-18-Induced Changes of Mitochondrial Phosphoproteome in Rat Cardiac Ischemia Model

Umbrasas, D., Jokubka, R., Kaupinis, A., Valius, M., Arandarčikaitė, O., & Borutaitė, V. (2019) · Medicina · doi:10.3390/medicina55100631 · Cited by 6

Changes in gene expression following cardiac pacing-induced delayed cardioprotection in the canine heart

Kovács, M., Papp, R., Varga-Orvos, Z., Ménesi, D., Puskás, L. G., & Végh, Á. (2010) · Acta Biologica Hungarica · doi:10.1556/abiol.61.2010.4.7 · Cited by 6

Involvement of reperfusion injury salvage kinases in preconditioning depends critically on the preconditioning stimulus

Manintveld, O. C., Sluiter, W. J., Dekkers, D. H. W., Hekkert, M. T. L., Lamers, J. M. J., Verdouw, P. D., & Duncker, D. J. (2011) · Experimental Biology and Medicine · doi:10.1258/ebm.2011.010260 · Cited by 6

Open Access Animal Physiology

Koulen, P. (2012) · Open Access Animal Physiology · doi:10.2147/oaap · Cited by 3

Methods for Measuring the Regulation of Respiration by Nitric Oxide

Shiva, S., Brookes, P. S., & Darley-Usmar, V. M. (2007) · Methods in cell biology · doi:10.1016/s0091-679x(06)80020-8 · Cited by 5

An Inhibitor of the δPKC Interaction with the d Subunit of F1Fo ATP Synthase Reduces Cardiac Troponin I Release from Ischemic Rat Hearts: Utility of a Novel Ammonium Sulfate Precipitation Technique

Ogbi, M., Obi, I., & Johnson, J. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0070580 · Cited by 4

Ischemia and Reperfusion

Heger, J. (2016) · Springer eBooks · doi:10.1007/978-3-319-31251-4_8 · Cited by 4

Exploring PKG signaling as a therapeutic avenue for pressure overload, ischemia, and HFpEF

Zhazykbayeva, S., Budde, H., Kaçmaz, M., Zemedie, Y., Osman, H., Hassoun, R., Jaquet, K., Akın, İ., El‐Battrawy, I., Herwig, M., et al. (2024) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2024.2400093 · Cited by 3

Post-Genomics Cardiovascular Signaling Pathways

Marı́n-Garcı́a, J. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-404599-6.00003-2 · Cited by 3

The Mitochondrial Permeability Transition Pore – from Molecular Mechanism to Reperfusion Injury and Cardioprotection

Halestrap, A. P., Clarke, S. J., & Khalilin, I. (2007) · Springer eBooks · doi:10.1007/978-0-387-69945-5_11 · Cited by 3

Mitochondrial K ATP channels in skeletal muscle: are protein kinases C and G, and nitric oxide synthase involved in the fatigue process?

Sánchez-Duarte, E., Trujillo, X., Huerta, M., Ortiz-Mesina, M., Cortés-Rojo, C., Manzo‐Ávalos, S., Saavedra-Molina, A., & Montoya-Pérez, R. (2012) · Open Access Animal Physiology · doi:10.2147/oaap.s34818 · Cited by 4

Myocardial Ischemia and Infarction

Tomanek, R. J. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4887-7_10 · Cited by 3

A possible subcellular mechanism underlying the “French paradox”: the opening of mitochondrial KATP channels

Aiello, E. A., & Cingolani, H. E. (2011) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h11-089 · Cited by 3

Nitrite Therapy for Ischemic Syndromes

Kevil, C. G., & Lefer, D. J. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-373866-0.00018-6 · Cited by 4

The effect of cardioplegic supplementation with sildenafil on cardiac energetics in a piglet model of cardiopulmonary bypass and cardioplegic arrest with warm or cold cardioplegia

Skeffington, K. L., Ahmed, E. M., Rapetto, F., Chanoit, G. P. A., Bond, A., Vardeu, A., Ghorbel, M. T., Suleiman, M. S., & Caputo, M. (2023) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2023.1194645 · Cited by 2

Smooth Estimation and Inference with Interval Censored Data

van der Laan, M. J., & Peterson, D. R. (1997) · Collection of Biostatistics Research Archive · Cited by 2

Mitochondrial Reactive Oxygen Species (ROS): Which ROS is Responsible for Cardioprotective Signaling?

Garlid, A. O. (2000) · doi:10.15760/etd.1640 · Cited by 2

Reactive Oxygen and Nitrogen Species Production in Cardiomyoblasts During Hypoxia and Hypoxia/Reoxygenation

Kolamunne, R. T., Grant, M. M., Vernallis, A. B., & Griffiths, H. R. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.10.035 · Cited by 1

Role of caveolin-eNOS platform and mitochondrial ATP-sensitive potassium channel in abrogated cardioprotective effect of ischemic preconditioning in postmenopausal women

Goyal, A., Agrawal, N., Jain, A., Gupta, J. K., & Garabadu, D. (2022) · Brazilian Journal of Pharmaceutical Sciences · doi:10.1590/s2175-97902022e20081 · Cited by 1

Regulation, effects and monitoring of compartmented cGMP signalling in cardiomyocytes—current status

Andressen, K. W., Sedneva‐Lugovets, D., Ovesen, M., Calejo, A. I., Arunthavarajah, D., & Levy, F. O. (2025) · British Journal of Pharmacology · doi:10.1111/bph.70144 · Cited by 1

Mitochondrial Reactive Oxygen Species in Myocardial Pre- and Postconditioning

Cardoso, A. R., Queliconi, B. B., & Kowaltowski, A. J. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-600-9_5 · Cited by 1

Mitochondria and Their Role in Ischemia/Reperfusion Injury

Phillip, S., Downey, J. M., & Cohen, M. V. (2007) · Springer eBooks · doi:10.1007/978-0-387-69945-5_14 · Cited by 1

Efeitos redox e protetores do pré-condicionamento isquêmico e da abertura do canal mitocondrial de potássio sensível a ATP contra morte celular por isquemia e reperfusão cardíaca

Facundo, H. T. (2007) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.46.2007.tde-27052008-091351 · 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

Response to Letter by Tsuda

Zhang, F., Wang, S., Signore, A. P., & Chen, J. (2007) · Stroke · doi:10.1161/strokeaha.107.502302 · Cited by 1

Preconditioning in the Heart

Hausenloy, D. J., & Yellon, D. M. (2012) · Springer eBooks · doi:10.1007/978-1-4419-9695-4_4

Vulnérabilité cardiaque au stress au cours du remodelage ventriculaire pathologique : rôle de la mitochondrie et du pore de perméabilité transitionnelle (PTP)

Ascah, A. (2010) · doi:10.71781/28338

The Role of Mitochondria in Necrosis Following Myocardial Ischemia-Reperfusion

Murphy, E., & Steenbergen, C. (2007) · Springer eBooks · doi:10.1007/978-0-387-69945-5_13

Efeito de dietas hiperlipídicas sobre mitocôndrias de fígado de camundongos: bioenergética, transporte de K+ e estudo redox

Cardoso, A. R. (2009) · doi:10.11606/d.46.2009.tde-10122009-105758

A hipercolesterolemia abole o efeito cardioprotetor do pré e pós-condicionamento isquêmico em um modelo experimental de isquemia e reperfusão em ratos

Landim, M. B. P. (2009) · doi:10.11606/t.5.2009.tde-06042010-175143

The involvement of CaMKII in myocardial ischaemia-reperfusion injury

Llwyd, O. (2012) · ORCA Online Research @Cardiff (Cardiff University)

Further evidence for the role of nitric oxide in the antiarrhythmic effect of ischaemic preconditioning: the effect of peroxynitrite and changes in NOS-dependent NO production

Juhász, L. (2015) · SZTE Repository of Dissertations (University of Szeged) · doi:10.14232/phd.2643

Cardioprotective signaling cascade of A2adenosine receptor agonist 5'-N-ethylcarboxaminidoadenosine against myocardial reperfusion injury

Lee, Y. C., Jang, Y. H., Kim, C. J., & Kim, J. M. (2008) · Korean Journal of Anesthesiology · doi:10.4097/kjae.2008.55.6.716

From the organizers

Porter, R. K. (2008) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2008.05.440

Molecular and Cellular Signaling Mechanisms Elucidating Aldose Reductase Mediated Ischemia-Reperfusion Injury in the Myocardium

Abdillahi, M. (2012) · doi:10.7916/d8959qhc

Reducing infarct size by ischemic preconditioning versus insulin treatment in the heart : same outcome - similar mechanisms?

Fuglesteg, B. N. (2008) · NORA - Norwegian Open Research Archives

The role of protein phosphatases in myocardial ischaemia and reperfusion

Fan, W.-J. (2008) · SUNScholar (Stellenbosch University)

The role of cGMP and PKG in cardioprotection

Downey, J. M., Liu, Y., & Xin, W. (2009) · BMC Pharmacology · doi:10.1186/1471-2210-9-s1-s9

Systemic response to local ischaemia: the evolving concept of remote ischaemic preconditioning

Saxena, P. (2009) · UWA Profiles and Research Repository (University of Western Australia)

Role of Tumour Necrosis Factor Alpha (TNFa) in ischaemic and pharmacological postconditioning

Lacerda, L. (2010) · Open University of Cape Town (University of Cape Town)

Mitochondrial energetic metabolism in hereditary neuropathies associated with OPA1 and MFN2 genes mutations.

Guillet, V., & REYNIER, P. (2009) · OpenGrey (Institut de l'Information Scientifique et Technique)

Effect and Role of Post-conditioning During Coronary Angioplasty in Patients Affected by ST-Elevation Acute Myocardial Infarction

Favaretto, E. (2012) · Padua Research Archive (University of Padova)

Cardioprotective Signal Transduction to Mitochondria

Quinlan, C. L. (2008) · PDXScholar (Portland State University) · doi:10.15760/etd.7990

Cardiac Na/K-ATPase in ischemia-reperfusion injury and cardioprotection

Duan, Q. (2014) · OhioLink ETD Center (Ohio Library and Information Network)

Rolle der löslichen Guanylatzyklase im Modell der Herztransplantation in der Ratte

Loganathan, S., Korkmaz‐Icöz, S., Radovits, T., Li, S., Mikles, B., Barnucz, E., Hirschberg, K., Karck, M., & Szabo, G. B. (2016) · Zeitschrift für Herz- Thorax- und Gefäßchirurgie · doi:10.1007/s00398-016-0093-2

ROS , and ATP injury via pathway involving src kinase, mitoK Ouabain protects rat hearts against ischemia-reperfusion

Am, J., Costa, A. D. T., Pierre, S. V., Santos, P. D. D., Garlid, K., Pasdois, P., Quinlan, C. L., Rissa, A., Tariosse, L., & Jaspard‐Vinassa, B. (2016)

Role of Protein Kinase C in Mitochondrial Functions in Cardiac Ischemia- Reperfusion Injury

Ferreira, J. C. B., & Mochly‐Rosen, D. (2012) · Oxidative stress and disease · doi:10.1201/b12308-5

MYOCARDIAL ISCHAEMIC PRE-CONDITIONING in Open Heart surgery.

Essay, A. B., & Amin, S. R. (2013)

The use of pharmacological conditioning strategies to improve donor heart preservation in cardiac transplantation

Kumarasinghe, G. (2022) · UNSWorks (University of New South Wales, Sydney, Australia) · doi:10.26190/unsworks/19221

Factors Affecting The Cardioprotective Response To Remote Ischaemic Preconditioning In Patients Undergoing Cardiac Surgery

Suri, A. (2017) · UCL Discovery (University College London)

ROLE OF PKCBETA AND OXIDANT SIGNALING IN NEONATAL PULMONARY HYPERTENSION

Sheak, J. R. (2019) · UNM’s Digital Repository (University of New Mexico)

Evaluación de la cardioprotección de la harina de raíz de maca (Lepidium meyenii Walp) en la isquemia y reperfusión de ratas jóvenes y seniles

Matera, S. I. (2020) · El Servicio de Difusión de la Creación Intelectual (National University of La Plata) · doi:10.35537/10915/100600

Effect of Remote Ischemic Conditioning in Hemorrhagic Shock/Resuscitation

Leung, C. H. (2019) · TSpace (University of Toronto)

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