Life history of eNOS: Partners and pathways

Activation of nitric oxide synthase in endothelial cells by Akt-dependent phosphorylation

Dimmeler, S., Fleming, I., Fisslthaler, B., Hermann, C., Busse, R., & Zeiher, A. M. (1999) · Nature · doi:10.1038/21224 · Cited by 3,591

Regulation of endothelium-derived nitric oxide production by the protein kinase Akt

Fulton, D. J., Gratton, J., McCabe, T. J. D., Fontana, J. T., Fujio, Y., Walsh, K. X., Franke, T. F., Papapetropoulos, A., & Sessa, W. C. (1999) · Nature · doi:10.1038/21218 · Cited by 2,616

Caveolin, a protein component of caveolae membrane coats

Rothberg, K. G., Heuser, J. E., Donzell, W. C., Ying, Y., Glenney, J. R., & Anderson, R. G. W. (1992) · Cell · doi:10.1016/0092-8674(92)90143-z · Cited by 2,259

Protein S-nitrosylation: Purview and parameters

Hess, D. T., Matsumoto, A., Kim, S.-O., Marshall, H. E., & Stamler, J. S. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1569 · Cited by 2,153

Loss of Caveolae, Vascular Dysfunction, and Pulmonary Defects in Caveolin-1 Gene-Disrupted Mice

Dráb, M., Verkade, P., Elger, M., Kasper, M. E., Löhn, M., Lauterbach, B., Menne, J., Lindschau, C., Mende, F., Luft, F. C., et al. (2001) · Science · doi:10.1126/science.1062688 · Cited by 1,555

The HMG-CoA reductase inhibitor simvastatin activates the protein kinase Akt and promotes angiogenesis in normocholesterolemic animals.

Kureishi, Y., Luo, Z., Shiojima, I., Bialik, A., Fulton, D. J., Lefer, D. J., Sessa, W. C., & Walsh, K. X. (2000) · Nature Medicine · doi:10.1038/79510 · Cited by 1,438

Interaction of oestrogen receptor with the regulatory subunit of phosphatidylinositol-3-OH kinase

Simoncini, T., Hafezi‐Moghadam, A., Brazil, D. P., Ley, K. F., Chin, W. W., & Liao, J. K. (2000) · Nature · doi:10.1038/35035131 · Cited by 1,436

Insulin-mediated skeletal muscle vasodilation is nitric oxide dependent. A novel action of insulin to increase nitric oxide release.

Steinberg, H. O., Brechtel, G., Johnson, A., Fineberg, N. S., & Baron, A. (1994) · Journal of Clinical Investigation · doi:10.1172/jci117433 · Cited by 1,216

Dynamic activation of endothelial nitric oxide synthase by Hsp90

García‐Cardeña, G., Fan, R., Shah, V. H., Sorrentino, R., Cirino, G., Papapetropoulos, A., & Sessa, W. C. (1998) · Nature · doi:10.1038/33934 · Cited by 1,029

Modulation of Akt kinase activity by binding to Hsp90

Sato, S., Fujita, N., & Tsuruo, T. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.170276797 · Cited by 967

Novel Role of GPR35 (G-Protein–Coupled Receptor 35) in the Regulation of Endothelial Cell Function and Blood Pressure

Li, H., Nguyen, H. T., Venkata, S. P. M., Koh, J. Y., Kowluru, A., Li, L., Rossi, N. F., Chen, W., & Wang, J. (2021) · Hypertension · doi:10.1161/hypertensionaha.120.15423 · Cited by 19

Resveratrol Inhibits Angiogenic Response of Cultured Endothelial F-2 Cells to Vascular Endothelial Growth Factor, but Not to Basic Fibroblast Growth Factor

Uchiyama, T., Toda, K., & Takahashi, S. (2010) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.33.1095 · Cited by 19

Endothelial Caveolar Hub Regulation of Adenosine Triphosphate–Induced Endothelial Nitric Oxide Synthase Subcellular Partitioning and Domain-Specific Phosphorylation

Ramadoss, J., Liao, W.-X., Morschauser, T. J., Lopez, G. E., Patankar, M. S., Chen, D., & Magness, R. R. (2012) · Hypertension · doi:10.1161/hypertensionaha.111.189498 · Cited by 19

Hyperinsulinemia-induced KLF5 mediates endothelial angiogenic dysfunction in diabetic endothelial cells

Wang, X., Yan, C., & Liu, J. (2019) · Journal of Molecular Histology · doi:10.1007/s10735-019-09821-3 · Cited by 19

Pathophysiological Role of Caveolae in Hypertension

Lian, X., Matthaeus, C., Kaßmann, M., Daumke, O., & Gollasch, M. (2019) · Frontiers in Medicine · doi:10.3389/fmed.2019.00153 · Cited by 22

Pregnancy Programming and Preeclampsia: Identifying a Human Endothelial Model to Study Pregnancy-Adapted Endothelial Function and Endothelial Adaptive Failure in Preeclamptic Subjects

Boeldt, D. S., Hankes, A., Alvarez, R. E., Khurshid, N., Balistreri, M., Grummer, M. A., Yi, F.-X., & Bird, I. M. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-1-4939-1031-1_4 · Cited by 19

Inhibitory effect of 14,15-EET on endothelial senescence through activation of mTOR complex 2/Akt signaling pathways

Yang, C., Pan, S., Yan, S., Li, Z., Yang, J., Wang, Y., & Xiong, Y. H. (2014) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2014.02.020 · Cited by 19

Subcellular Localization Guides eNOS Function

Villadangos, L., & Serrador, J. M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252413402 · Cited by 21

Potential Roles of Endoplasmic Reticulum Stress and Cellular Proteins Implicated in Diabesity

Mustapha, S., Mohammed, M., Azemi, A. K., Yunusa, I. U., Shehu, A., Mustapha, L., Wada, Y., Ahmad, M. H., Ahmad, W. A. N. W., Rasool, A. H. G., et al. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/8830880 · Cited by 18

A20/TNFAIP3 Increases ENOS Expression in an ERK5/KLF2-Dependent Manner to Support Endothelial Cell Health in the Face of Inflammation

Angolano, C., Kaczmarek, E., Essayagh, S., Daniel, S., Choi, L. Y., Tung, B., Sauvage, G., Lee, A., Kipper, F. C., Arvelo, M. B., et al. (2021) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2021.651230 · Cited by 18

Regulatory effects of curcumin on nitric oxide signaling in the cardiovascular system

Abolfazli, S., Mortazavi, P., Kheirandish, A., Butler, A. E., Jamialahmadi, T., & Sahebkar, A. (2023) · Nitric Oxide · doi:10.1016/j.niox.2023.12.003 · Cited by 18

Mechanism of hyperhomocysteinemia-induced vascular endothelium dysfunction – Possible dysregulation of phosphatidylinositol-3-kinase and its downstream phosphoinositide dependent kinase and protein kinase B

Sharma, S., Singh, M., & Sharma, P. L. (2013) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2013.08.028 · Cited by 18

Angiotensin II dependent cardiac remodeling in the eel Anguilla anguilla involves the NOS/NO system

Filice, M., Amelio, D., Garofalo, F., David, S., Fucarino, A., Jensen, F. B., Imbrogno, S., & Cerra, M. C. (2017) · Nitric Oxide · doi:10.1016/j.niox.2017.02.007 · Cited by 18

Comparative effects of recombinant human activated protein C and dexamethasone in experimental septic shock

Bouazza, Y., Sennoun, N., Strub, C., Regnault, V., Gibot, S., Meziani, F., Lacolley, P. J., & Lévy, B. (2011) · Intensive Care Medicine · doi:10.1007/s00134-011-2327-9 · Cited by 20

Na+/H+ exchanger inhibitor induces vasorelaxation through nitric oxide production in endothelial cells via intracellular acidification-associated Ca2+ mobilization

Sasahara, T., Yayama, K., Matsuzaki, T., Tsutsui, M., & Okamoto, H. (2012) · Vascular Pharmacology · doi:10.1016/j.vph.2012.11.004 · Cited by 18

Supplemental l-arginine and vitamins E and C preserve xanthine oxidase activity in the lung of broiler chickens grown under hypobaric hypoxia

Bautista-Ortega, J., Cortés-Cuevas, A., Ellis, E. A., & Ruiz-Feria, C. A. (2014) · Poultry Science · doi:10.3382/ps.2013-03698 · Cited by 18

Beyond Antiangiogenesis: Vascular Modulation as an Anticancer Therapy—A Review

Oronsky, B. T., Scicinski, J. J., Reid, T. R., & Knox, S. J. (2012) · Translational Oncology · doi:10.1593/tlo.12118 · Cited by 18

Angiostatin Inhibition of Vascular Endothelial Growth Factor– Stimulated Nitric Oxide Production in Endothelial Cells

Takahashi, S., Shinya, T., & Sugiyama, A. (2010) · Journal of Pharmacological Sciences · doi:10.1254/jphs.10028fp · Cited by 17

Upregulation of caveolin-1 contributes to aggravated high-salt diet-induced endothelial dysfunction and hypertension in type 1 diabetic rats

Li, X., Xing, W., Wang, Y., Mi, C., Zhang, Z., Ma, H., Zhang, H., & Gao, F. (2014) · Life Sciences · doi:10.1016/j.lfs.2014.07.027 · Cited by 17

Functional inhibition of urea transporter UT-B enhances endothelial-dependent vasodilatation and lowers blood pressure via L-arginine-endothelial nitric oxide synthase-nitric oxide pathway

Sun, Y. X., Lau, C., Jia, Y., Li, Y., Wang, W., Ran, J., Li, F. Y., Huang, Y., Zhou, H., & Yang, B. (2016) · Scientific Reports · doi:10.1038/srep18697 · Cited by 17

Development of an Adverse Outcome Pathway for the Onset of Hypertension by Oxidative Stress-Mediated Perturbation of Endothelial Nitric Oxide Bioavailability

Lowe, F., Luettich, K., Talikka, M., Hoang, V., Haswell, L. E., Hoeng, J., & Gaça, M. (2017) · Applied In Vitro Toxicology · doi:10.1089/aivt.2016.0031 · Cited by 17

Recombinant human activated protein C improves endotoxemia-induced endothelial dysfunction: a blood-free model in isolated mouse arteries

Sennoun, N., Baron‐Menguy, C., Burban, M., Lecompte, T., Andriantsitohaina, R., Henrion, D., Mercat, A., Asfar, P., Lévy, B., & Meziani, F. (2009) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01133.2008 · Cited by 17

Effect of Selenium Supplementation on Redox Status of the Aortic Wall in Young Spontaneously Hypertensive Rats

Ruseva, B., Atanasova, M., Tsvetkova, R., Betova, T., Mollova, M., Alexandrova, M. L., Yordanova-Laleva, P., & Dimitrova, A. A. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/609053 · Cited by 16

Vitamin D in Oxidative Stress and Diseases

Uberti, F., Morsanuto, V., & Molinari, C. G. (2017) · InTech eBooks · doi:10.5772/64506 · Cited by 15

Inhibition potential of phenolic constituents from the aerial parts of Tetrastigma hemsleyanum against soluble epoxide hydrolase and nitric oxide synthase

Wang, C. Y., Lee, S., Jang, H., Su, X. D., Wang, H., Kim, Y. H., & Yang, S. Y. (2019) · Journal of Enzyme Inhibition and Medicinal Chemistry · doi:10.1080/14756366.2019.1584621 · Cited by 17

The rs12526453 Polymorphism in an Intron of the PHACTR1 Gene and Its Association with 5-Year Mortality of Patients with Myocardial Infarction

Szpakowicz, A., Kiliszek, M., Pepiński, W., Waszkiewicz, E., Franaszczyk, M., Skawrońska, M., Płoski, R., Niemcunowicz‐Janica, A., Burzyńska, B., Tulacz, D., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0129820 · Cited by 16

Suppressions of Serotonin-Induced Increased Vascular Permeability and Leukocyte Infiltration byBixa orellanaLeaf Extract

Yong, Y. K., Sulaiman, N., Hakim, M. N., Lian, G. E. C., Zakaria, Z. A., Othman, F., & Ahmad, Z. (2013) · BioMed Research International · doi:10.1155/2013/463145 · Cited by 16

Differential Effect of Resveratrol on Nitric Oxide Production in Endothelial F-2 Cells

Takahashi, S., Uchiyama, T., & Toda, K. (2009) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.32.1840 · Cited by 16

Stromal interaction molecule 1 modulates blood pressure via NO production in vascular endothelial cells

Nishimoto, M., Mizuno, R., Fujita, T., & Isshiki, M. (2018) · Hypertension Research · doi:10.1038/s41440-018-0045-1 · Cited by 16

Red fruit (Pandanus conoideus Lam) oil stimulates nitric oxide production and reduces oxidative stress in endothelial cells

Xia, N., Schirra, C., Hasselwander, S., Förstermann, U., & Li, H. (2018) · Journal of Functional Foods · doi:10.1016/j.jff.2018.10.014 · Cited by 16

Inhibition of endothelial nitric oxide synthase by the lipid phosphatase PTEN

Church, J. E., Qian, J., Kumar, S., Black, S. M., Venema, R. C., Papapetropoulos, A., & Fulton, D. J. (2009) · Vascular Pharmacology · doi:10.1016/j.vph.2009.11.007 · Cited by 16

Alpha7 nicotinic acetylcholine receptor mediates chronic nicotine inhalation-induced cardiopulmonary dysfunction

Whitehead, A., Fried, N. D., Li, Z., Neelamegam, K., Pearson, C. S., LaPenna, K. B., Sharp, T. E., Lefer, D. J., Lazartigues, E. D., Gardner, J. D., et al. (2022) · Clinical Science · doi:10.1042/cs20220083 · Cited by 15

Differential sensitivity of basal and acetylcholine‐induced activity of nitric oxide to blockade by asymmetric dimethylarginine in the rat aorta

AL-Zobaidy, M. J., Craig, J., & Martin, W. (2010) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2010.00802.x · Cited by 15

PHACTR1 and SLC22A3 gene polymorphisms are associated with reduced coronary artery disease risk in the male Chinese Han population

Zhao, Q., Wei, H., Liu, D., Shi, B., Li, L., Yan, M., Zhang, X., Wang, F., & Ouyang, Y. (2016) · Oncotarget · doi:10.18632/oncotarget.13506 · Cited by 14

Nitric oxide signaling comes of age: 20 years and thriving

Lamas, S., Lowenstein, C. J., & Michel, T. M. (2007) · Cardiovascular Research · doi:10.1016/j.cardiores.2007.05.023 · Cited by 15

Combination Therapy With Olmesartan and Azelnidipine Improves EDHF-Mediated Responses in Diabetic Apolipoprotein E-Deficient Mice

Hosoya, M., Ohashi, J., Sawada, A., Takaki, A., & Shimokawa, H. (2010) · Circulation Journal · doi:10.1253/circj.cj-09-0862 · Cited by 14

S-nitrosylation of endothelial nitric oxide synthase impacts erectile function

Kavoussi, P. K., Smith, R. P., Oliver, J. L., Costabile, R. A., Steers, W. D., Brown-Steinke, K., de Ronde, K., Lysiak, J. J., & Palmer, L. A. (2018) · International Journal of Impotence Research · doi:10.1038/s41443-018-0056-0 · Cited by 14

Preconditioning by inhaled nitric oxide prevents hyperoxic and ischemia/reperfusion injury in rat lungs

Waldow, T., Witt, W., Ulmer, A., Janke, A., Alexiou, K., & Matschke, K. (2007) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2007.10.005 · Cited by 14

Tetrahydrobiopterin improves cardiac and pulmonary function after cardiopulmonary bypass☆

Szabo, G. B., Seres, L., Soós, P., Gorenflo, M., Merkely, B. P., Horkay, F., Karck, M., & Radovits, T. (2011) · European Journal of Cardio-Thoracic Surgery · doi:10.1016/j.ejcts.2010.12.033 · Cited by 14

Synthesis of novel (−)-epicatechin derivatives as potential endothelial GPER agonists: Evaluation of biological effects

Sarmiento, V., Ramírez‐Sánchez, I., Moreno‐Ulloa, A., Romero‐Perez, D., Chávez, D., Ortíz-Flores, M., Nájera, N., Correa‐Basurto, J., Villarreal, F. J., & Ceballos, G. M. (2018) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2018.01.025 · Cited by 14

Biological effects of trans fatty acids and their possible roles in the lipid rafts in apoptosis regulation

Qiu, B., Wang, Q., Liu, W., Xu, T., Liu, L., Zong, A., Jia, M., Li, J., & Du, F. (2018) · Cell Biology International · doi:10.1002/cbin.10958 · Cited by 14

Association of eNOS and ACE gene polymorphisms as a genetic risk factor in gestational diabetes in Iranian women

Mirfeizi, M., Hasanzad, M., Sattari, M., Afshari, M., Abbasi, D., Ajoodani, Z., & Sheykheslam, A. B. (2018) · Journal of Diabetes & Metabolic Disorders · doi:10.1007/s40200-018-0348-4 · Cited by 13

Developmental acceleration of bradykinin-dependent relaxation by prenatal chronic hypoxia impedes normal development after birth

Blum‐Johnston, C., Thorpe, R. B., Wee, C., Romero, M., Brunelle, A. R., Blood, Q., Wilson, R. H., Blood, A. B., Francis, M., Taylor, M. S., et al. (2015) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00340.2015 · Cited by 13

Pivotal Cytoprotective Mediators and Promising Therapeutic Strategies for Endothelial Progenitor Cell‐Based Cardiovascular Regeneration

Kim, H., Kim, S., Baek, S. H., & Kwon, S. (2016) · Stem Cells International · doi:10.1155/2016/8340257 · Cited by 13

Genetics of Redox Systems and Their Relationship with Cardiovascular Disease

Farbstein, D., Soloveichik, Y. Z., Levy, N. S., & Levy, A. P. (2011) · Current Atherosclerosis Reports · doi:10.1007/s11883-011-0170-7 · Cited by 13

Circulating angiogenic cell population responses to 10 days of reduced physical activity

Guhanarayan, G., Jablonski, J., & Witkowski, S. (2014) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00087.2014 · Cited by 13

Alpha‐Asarone Protects Endothelial Cells from Injury by Angiotensin II

Shi, H., Yang, J., Yang, T., Xue, Y.-L., Liu, J., Li, Y., Zhang, D., Xu, J., & Bian, K. (2014) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2014/682041 · Cited by 13

Biological basis of neuroprotection and neurotherapeutic effects of Whole Body Periodic Acceleration (pGz)

Adams, J. A., Uryash, A., Bassuk, J. A., Sackner, M. A., & Kurlansky, P. A. (2014) · Medical Hypotheses · doi:10.1016/j.mehy.2014.02.031 · Cited by 13

Effects of tyrosine kinase inhibitor E7080 and eNOS inhibitor L-NIO on colorectal cancer alone and in combination.

Altun, A., Temiz, T. K., Balcı, E., Polat, Z. A., & Turan, M. (2013) · Europe PMC (PubMed Central) · doi:10.3978/j.issn.1000-9604.2013.10.10 · Cited by 13

Dexamethasone, tetrahydrobiopterin and uncoupling of endothelial nitric oxide synthase.

Tobias, S., Habermeier, A., Siuda, D., Reifenberg, G., Xia, N., Closs, E. I., Förstermann, U., & Li, H. (2015) · Europe PMC (PubMed Central) · doi:10.11909/j.issn.1671-5411.2015.05.013 · Cited by 12

Protein Kinase Cα Phosphorylates a Novel Argininosuccinate Synthase Site at Serine 328 during Calcium-dependent Stimulation of Endothelial Nitric-oxide Synthase in Vascular Endothelial Cells

Haines, R. J., Corbin, K. D., Pendleton, L. C., & Eichler, D. C. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.378794 · Cited by 13

ENOS and Stroke: Prevention, Treatment and Recovery

Gertz, K. R., & Endres, M. (2008) · Future Neurology · doi:10.2217/14796708.3.5.537 · Cited by 11

Research progress on signaling pathways in cirrhotic portal hypertension

Xu, W., Liu, P., & Mu, Y. (2018) · World Journal of Clinical Cases · doi:10.12998/wjcc.v6.i10.335 · Cited by 13

The N-terminal portion of autoinhibitory element modulates human endothelial nitric-oxide synthase activity through coordinated controls of phosphorylation at Thr495 and Ser1177

Wu, P., Chen, B.-R., Hsieh, C.-C., Lin, W.-C., Wu, K. K., Hwu, Y., & Chen, P. (2014) · Bioscience Reports · doi:10.1042/bsr20140079 · Cited by 12

Early intervention with Didang decoction delays macrovascular lesions in diabetic rats through regulating AMP-activated protein kinase signaling pathway

Dan-Dan, R. E. N., Li, J., Chang, B., Chun-shen, L., & Yang, J. (2017) · Chinese Journal of Natural Medicines · doi:10.1016/s1875-5364(18)30018-9 · Cited by 12

Endothelial Cells and the Cerebral Circulation

Lansdell, T. A., Chambers, L. C., & Dorrance, A. M. (2022) · Comprehensive physiology · doi:10.1002/cphy.c210015 · Cited by 22

Ex Vivo Treatment with a Polyphenol-Enriched Cocoa Extract Ameliorates Myocardial Infarct and Postischemic Mitochondrial Injury in Normotensive and Hypertensive Rats

Arbeláez, L. F. G., Pardo, A. C., Fantinelli, J. C., Caldiz, C. I., Ríos, J. L., Schinella, G. R., & Mosca, S. M. (2016) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.6b01669 · Cited by 11

TRPC channel-derived calcium fluxes differentially regulate ATP and flow-induced activation of eNOS

Muzorewa, T. T., Buerk, D. G., Jaron, D., & Barbee, K. A. (2021) · Nitric Oxide · doi:10.1016/j.niox.2021.03.005 · Cited by 11

Extremely low frequency electromagnetic stimulation reduces ischemic stroke volume by improving cerebral collateral blood flow

Kemps, H., Dessy, C., Dumas, L., Sonveaux, P., Alders, L., Broeckhoven, J. V., Font, L. P., Lambrichts, S. M. P., Foulquier, S., Hendrix, S., et al. (2022) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x221084410 · Cited by 10

Nitric Oxide-Releasing Nanomaterials and Skin Care

Seabra, A. B. (2011) · Springer eBooks · doi:10.1007/978-3-642-19792-5_13 · Cited by 11

Dysfonction endothéliale et risque cardiovasculaire. L’exercice protège la fonction endothéliale et prévient la maladie cardiovasculaire

Pellegrin, M., Mazzolai, L., Berthelot, A., & Laurant, P. (2008) · Science & Sports · doi:10.1016/j.scispo.2008.10.003 · Cited by 12

Short‐term (48 hours) intravenous serelaxin infusion has no effect on myogenic tone or vascular remodeling in rat mesenteric arteries

Jelinic, M., Leo, C. H., Marshall, S. A., Senadheera, S. N., Parry, L. J., & Tare, M. (2017) · Microcirculation · doi:10.1111/micc.12371 · Cited by 11

Long-term hypoxia uncouples Ca2+and eNOS in bradykinin-mediated pulmonary arterial relaxation

Blum‐Johnston, C., Thorpe, R. B., Wee, C., Opsahl, R., Romero, M., Murray, S. T., Brunelle, A. R., Blood, Q., Wilson, R. H., Blood, A. B., et al. (2018) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00311.2017 · Cited by 11

Plasma from Volunteers Breathing Helium Reduces Hypoxia-Induced Cell Damage in Human Endothelial Cells—Mechanisms of Remote Protection Against Hypoxia by Helium

Smit, K., Oei, G. T. M. L., Konkel, M., Augustijn, Q. J. J., Hollmann, M. W., Preckel, B., Patel, H. H., & Weber, N. C. (2019) · Cardiovascular Drugs and Therapy · doi:10.1007/s10557-019-06880-2 · Cited by 11

The Molecular Basis of Portal Hypertension.

Rockey, D. C. (2017) · Europe PMC (PubMed Central) · Cited by 11

Radioprotective Activity of the Nitric Oxide Synthase Inhibitor T1023. Toxicological and Biochemical Properties, Cardiovascular and Radioprotective Effects

Филимонова, М. В., Макарчук, В. М., Шевченко, Л. И., Saburova, A., Surinova, V., Изместьева, О. С., Lychagin, A., Saburov, V. O., Шегай, П. В., Каприн, А. Д., et al. (2020) · Radiation Research · doi:10.1667/rade-20-00046.1 · Cited by 11

Beneficial effect of insulin in hyperhomocysteinemia and diabetes mellitus-induced vascular endothelium dysfunction: role of phosphoinositide dependent kinase and protein kinase B

Sharma, S., Singh, M., & Sharma, P. L. (2010) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-010-0633-0 · Cited by 12

Post-translational Regulation of Endothelial Nitric Oxide Synthase (eNOS) by Estrogens in the Rat Vagina

Musicki, B., Liu, T., Strong, T. D., Lagoda, G. A., Bivalacqua, T. J., & Burnett, A. L. “. (2010) · The Journal of Sexual Medicine · doi:10.1111/j.1743-6109.2010.01750.x · Cited by 11

eNOS–ERα Complex Goes to Telomerase

Zeng, L., & Xu, Q. (2008) · Circulation Research · doi:10.1161/circresaha.108.179986 · Cited by 11

Therapeutic Antibody-Induced Vascular Toxicity Due to Off-Target Activation of Nitric Oxide in Cynomolgus Monkeys

Pai, R., Ma, N., Connor, A. V., Danilenko, D. M., Tarrant, J. M., Salvail, D., Wong, L., Hartley, D. P., Misner, D., Stefanich, E., et al. (2016) · Toxicological Sciences · doi:10.1093/toxsci/kfw037 · Cited by 9

Alpha 7‐nicotinic cholinoceptor regulation of pericyte‐containing retinal capillaries

Wu, K., Cheng, T., Zhai, Z., Jiang, C., & Zhou, X. (2023) · British Journal of Pharmacology · doi:10.1111/bph.16067 · Cited by 10

Lobe-Specific Calcium Binding in Calmodulin Regulates Endothelial Nitric Oxide Synthase Activation

Wu, P., Kuo, C.-C., Yet, S., Liou, J., Wu, K. K., & Chen, P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039851 · Cited by 10

Cardiovascular medications in angiogenesis—How to avoid the sting in the tail

Ma, C., Wang, Q., Man, Y., & Kemmner, W. (2012) · International Journal of Cancer · doi:10.1002/ijc.27576 · Cited by 10

Nitrooleate Mediates Nitric Oxide Synthase Activation in Endothelial Cells

Shin, E., Yeo, E.-J., Lim, J., Chang, Y. H., Park, H., Shim, E., Chung, H., Hwang, H. J., Chun, J., & Hwang, J. (2014) · Lipids · doi:10.1007/s11745-014-3893-8 · Cited by 10

Trifolium pratense isoflavones improve pulmonary vascular remodelling in broiler chickens

Jiang, Y. B., & Yang, Y. (2015) · Journal of Animal Physiology and Animal Nutrition · doi:10.1111/jpn.12424 · Cited by 10

Human microvascular reactivity: a review of vasomodulating stimuli and non-invasive imaging assessment

Troy, A. M., & Cheng, H. M. (2021) · Physiological Measurement · doi:10.1088/1361-6579/ac18fd · Cited by 12

Selective probing of a NADPH site controlled light‐induced enzymatic catalysis

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Reciprocal Modulation of Surface Expression of Annexin A2 in a Human Umbilical Vein Endothelial Cell-Derived Cell Line by Eicosapentaenoic Acid and Docosahexaenoic Acid

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Changes in eNOS phosphorylation contribute to increased arteriolar NO release during juvenile growth

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Potencial rol protector del óxido nítrico y Hsp70 asociado a alimentos funcionales en la aterosclerosis

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

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Cyanidin-3-glucoside phenolic metabolites, protocatechuic acid and vanillic acid, attenuate the adhesion of monocytes to endothelial cells in response to TNF-α by targeting NF-κB and Nrf2 pathways

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Role of nitric oxide and endothelial NO synthase in carcinogenesis

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