Tumor Necrosis Factor-α Inhibits Endothelial Nitric-oxide Synthase Gene Promoter Activity in Bovine Aortic Endothelial Cells

Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor

Palmer, R. M. J., Ferrige, A. G., & Moncada, S. (1987) · Nature · doi:10.1038/327524a0 · Cited by 10,704

The hormone resistin links obesity to diabetes

Steppan, C. M., Bailey, S. T., Bhat, S., Brown, E. J., Banerjee, R. R., Wright, C. M., Patel, H. R., Ahima, R. S., & Lazar, M. A. (2001) · Nature · doi:10.1038/35053000 · Cited by 4,755

Isolation of nitric oxide synthetase, a calmodulin-requiring enzyme.

Bredt, D. S., & Snyder, S. H. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.2.682 · Cited by 3,308

Nitric oxide: an endogenous modulator of leukocyte adhesion.

Kubes, P., Suzuki, M., & Granger, D. N. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.11.4651 · Cited by 3,036

Elevated Circulating Levels of Tumor Necrosis Factor in Severe Chronic Heart Failure

Levine, B., Kalman, J., Mayer, L., Fillit, H. M., & Packer, M. (1990) · New England Journal of Medicine · doi:10.1056/nejm199007263230405 · Cited by 2,582

Peroxynitrite oxidation of sulfhydryls.

Radí, R., Beckman, J. S., Bush, K., & Freeman, B. Α. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(20)64313-7 · Cited by 2,492

Tumor necrosis factor signaling

Wajant, H., Pfizenmaier, K., & Scheurich, P. (2003) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401189 · Cited by 2,422

Nitric oxide-generating vasodilators and 8-bromo-cyclic guanosine monophosphate inhibit mitogenesis and proliferation of cultured rat vascular smooth muscle cells.

Garg, U. C., & Hassid, A. (1989) · Journal of Clinical Investigation · doi:10.1172/jci114081 · Cited by 2,154

A cytokine-responsive IκB kinase that activates the transcription factor NF-κB

DiDonato, J. A., Hayakawa, M., Rothwarf, D. M., Zandi, E., & Karin, M. (1997) · Nature · doi:10.1038/41493 · Cited by 2,125

IKK-1 and IKK-2: Cytokine-Activated IκB Kinases Essential for NF-κB Activation

Mercurio, F., Zhu, H., Murray, B. W., Shevchenko, A., Bennett, B. L., Li, J. W., Young, D. B., Barbosa, M. S., Mann, M., Manning, A. M., et al. (1997) · Science · doi:10.1126/science.278.5339.860 · Cited by 2,042

Nitric oxide and insulin resistance

(2015) · Immunoendocrinology · doi:10.14800/ie.657 · Cited by 16

Penile constitutive nitric oxide synthase expression in rats exposed to unpredictable chronic mild stress: role of inflammation

ŞAHİN, T. D., Yazır, Y., Utkan, T., Göçmez, S. S., & Bayramgürler, D. (2016) · International Journal of Impotence Research · doi:10.1038/ijir.2016.50 · Cited by 16

Delivery of small interfering RNA for inhibition of endothelial cell apoptosis by hypoxia and serum deprivation

Cho, S., Hartle, L., Son, S. M., Yang, F., Goldberg, M. S., Xu, Q., Langer, R., & Anderson, D. G. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.08.123 · Cited by 16

The structural and functional effects of fine particulate matter from cooking oil fumes on rat umbilical cord blood vessels

Zhu, X., Hou, L., Zhang, J., Yao, C., Liu, Y., Zhang, C., Xu, Y., & Cao, J. (2016) · Environmental Science and Pollution Research · doi:10.1007/s11356-016-6821-z · Cited by 15

Small-molecule Akt-activation in airway cells induces NO production and reduces IL-8 transcription through Nrf-2

Gopallawa, I., Kuek, L. E., Adappa, N. D., Palmer, J. N., & Lee, R. J. (2021) · Respiratory Research · doi:10.1186/s12931-021-01865-y · Cited by 15

Effects of IL-1β and IL-6 on tissue-type plasminogen activator expression in vascular endothelial cells

Larsson, P., Ulfhammer, E., Karlsson, L., Bokarewa, M. I., Wåhlander, K., & Jern, S. (2008) · Thrombosis Research · doi:10.1016/j.thromres.2008.03.013 · Cited by 15

Downregulation of human endothelial nitric oxide synthase promoter activity by p38 mitogen-activated protein kinase activation

Xing, F., Jiang, Y., Liu, J., Zhao, K., Mo, Y., Liu, Z., & Zeng, Y. (2006) · Biochemistry and Cell Biology · doi:10.1139/o06-092 · Cited by 15

How Perturbated Metabolites in Diabetes Mellitus Affect the Pathogenesis of Hypertension?

Ning, Z., Song, Z., Wang, C., Peng, S., Wan, X., Liu, Z., & Lü, A. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.705588 · Cited by 15

Phenolic Metabolites Protocatechuic Acid and Vanillic Acid Improve Nitric Oxide Bioavailability via the Akt-eNOS Pathway in Response to TNF-α Induced Oxidative Stress and Inflammation in Endothelial Cells

Festa, J., Hussain, A., Al-Hareth, Z., Bailey, S. J., Singh, H., & Boit, M. D. (2024) · Metabolites · doi:10.3390/metabo14110613 · Cited by 15

The effect of TNF-α inhibitor treatment on microRNAs and endothelial function in collagen induced arthritis

Gunter, S., Michel, F. S., Fourie, S., Singh, M., Roux, R. L., Manilall, A., Mokotedi, L. P., & Millen, A. M. E. (2022) · PLoS ONE · doi:10.1371/journal.pone.0264558 · Cited by 14

Autoantibodies and thrombophilia in RA: TNFα and TNFα blockers

Ferraccioli, G., & Gremese, E. (2004) · Annals of the Rheumatic Diseases · doi:10.1136/ard.2003.015586 · Cited by 14

Transcriptome analysis reveals fluid shear stress (FSS) and atherosclerosis pathway as a candidate molecular mechanism of short-term low salinity stress tolerance in abalone

Boamah, G. A., Huang, Z., Shen, Y., Lu, Y., Wang, Z., Su, Y., Xu, C., Luo, X., Ke, C., & You, W. (2022) · BMC Genomics · doi:10.1186/s12864-022-08611-8 · Cited by 13

Metastatic breast carcinoma induces vascular endothelial dysfunction in Balb-c mice: Role of the tumor necrosis factor-α and NADPH oxidase

Dalaklıoğlu, S., Taşatargil, A., Kale, Ş., Tanriover, G., Dilmaç, S., & Erin, N. (2013) · Vascular Pharmacology · doi:10.1016/j.vph.2013.07.008 · Cited by 13

Estradiol Modulates Tumor Necrosis Factor-Induced Endothelial Inflammation: Role of Tumor Necrosis Factor Receptor 2

Chakrabarti, S., & Davidge, S. T. (2012) · Journal of Vascular Research · doi:10.1159/000342736 · Cited by 12

Association of inflammatory biomarkers with morbidity and mortality risk in patients with peripheral artery disease: a systematic review and meta-analysis

Fragão-Marques, M., Francisca-Marques, M., Rocha-Neves, J. P., & Özben, T. (2025) · Critical Reviews in Clinical Laboratory Sciences · doi:10.1080/10408363.2025.2512472 · Cited by 12

The Inflammatory Pattern of Chronic Limb-Threatening Ischemia in Muscles: The TNF-α Hypothesis

Caicedo, D., Álvarez, C. V., Pérez-Romero, S., & Devesa, J. (2022) · Biomedicines · doi:10.3390/biomedicines10020489 · Cited by 11

The relationship between oxidative balance score and erectile dysfunction in the U.S. male adult population

Chen, M., Zhang, Z., Zhou, R., Li, B., Jiang, J., & Shi, B. (2024) · Scientific Reports · doi:10.1038/s41598-024-61287-w · Cited by 10

Phosphorylation of argininosuccinate synthase by protein kinase A

Corbin, K. D., Pendleton, L. C., Solomonson, L. P., & Eichler, D. C. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.10.056 · Cited by 10

Identification of monoclonal antibodies against human renal glomerular endothelial cells in lupus nephritis that induce endothelial interferon-alpha production

Hu, Y., Tsai, I., Hsu, H.-Y., Chiang, B., & Yang, Y. (2021) · Arthritis Research & Therapy · doi:10.1186/s13075-021-02552-5 · Cited by 10

Novel pathophysiological roles of α‐synuclein in age‐related vascular endothelial dysfunction

Takami, Y., Wang, C., Hironori Nakagami, A., Yamamoto, K. I., Nozato, Y., Imaizumi, Y., Nagasawa, M., Takeshita, H., Nakajima, T., Takeda, S., et al. (2022) · The FASEB Journal · doi:10.1096/fj.202101621r · Cited by 10

An Angiotensin Receptor Blocker Prevents Arrhythmogenic Left Atrial Remodeling in a Rat Post Myocardial Infarction Induced Heart Failure Model

Kim, H., No, C.-W., Goo, S.-H., & Cha, T. (2013) · Journal of Korean Medical Science · doi:10.3346/jkms.2013.28.5.700 · Cited by 10

Relationship Between Systemic Inflammatory Response Index and Erectile Dysfunction: A Cross-sectional Study

Lin, W., Wang, H., & Lin, M.-E. (2023) · Urology · doi:10.1016/j.urology.2023.08.015 · Cited by 9

Endothelial nitric oxide synthase in the vascular wall: Mechanisms regulating its expression and enzymatic function

Demosthenous, M., Antoniades, C. A., Tousoulis, D., Margaritis, M., Marinou, K., & Stefanadis, C. (2011) · Artery Research · doi:10.1016/j.artres.2011.03.003 · Cited by 9

Direct Effect of F12511, A Systemic Inhibitor of Acyl-CoA Cholesterol Acyltransferase on Bovine Aortic Endothelial Cells

Zamorano‐León, J. J., Fernández‐Sánchez, R., López-Farré, A. J., Lapuente-Tiana, L., Alonso‐Orgaz, S., Sacristán, D., Junquera, D., Delhon, A., Conesa, A., Mateos‐Cáceres, P. J., et al. (2006) · Journal of Cardiovascular Pharmacology · doi:10.1097/01.fjc.0000246263.67515.6a · Cited by 8

Nuclear Countermeasure Activity of TP508 Linked to Restoration of Endothelial Function and Acceleration of DNA Repair

Olszewska-Pazdrak, B., Mcvicar, S. D., Rayavara, K., Moya, S. M., Kantara, C., Gammarano, C., Olszewska, P., Fuller, G. M., Sower, L. E., & Carney, D. H. (2016) · Radiation Research · doi:10.1667/rr14409.1 · Cited by 8

Insulin Resistance and Endothelial Dysfunction: Macro and Microangiopathy

Arce‐Esquivel, A. A., Aaron, K. E., Catherine, R., & Laughli, M. H. (2013) · InTech eBooks · doi:10.5772/56475 · Cited by 9

Etanercept Prevents Endothelial Dysfunction in Cafeteria Diet-Fed Rats

Răzvan-Valentin, S., Güler, S. A., Utkan, T., ŞAHİN, T. D., Gacar, G., Yazır, Y., Rençber, S. F., Lupușoru, M. O. D., Bălălău, C., Popescu, B., et al. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph19042138 · Cited by 7

Circadian fluctuations of endothelial nitric oxide synthase activity in females with rheumatoid arthritis: a pilot study

Zaichko, K., Stanislavchuk, M., & Заічко, Н. В. (2020) · Rheumatology International · doi:10.1007/s00296-020-04525-4 · Cited by 7

Hydrogen Peroxide Mediates Endothelium‐Dependent Dilation of Coronary Arterioles in Obese Rats on a Low‐Carbohydrate Diet

Focardi, M., Picchi, A., Donnini, S., Cameli, M., Ziche, M., Marzilli, M., & Mondillo, S. (2013) · Microcirculation · doi:10.1111/micc.12058 · Cited by 6

Repetitive ischemia increases myocardial dimethylarginine dimethylaminohydrolase 1 expression

Zhang, P., Fassett, J. T., Zhu, G., Li, J., Hu, X., Xu, X., Chen, Y., & Bache, R. J. (2017) · Vascular Medicine · doi:10.1177/1358863x16681215 · Cited by 5

Jenseits der Immunpathogenese

Boehncke, W., Boehncke, S., & Buerger, C. (2012) · Der Hautarzt · doi:10.1007/s00105-011-2227-5 · Cited by 5

Elevated levels of pro-thrombotic eNOS-negative platelets in COVID-19 patients

Asgari, A., Franczak, A., Herchen, A., Jickling, G. C., & Jurasz, P. (2024) · Thrombosis Research · doi:10.1016/j.thromres.2024.109178 · Cited by 4

Oat-Protein-Based Diet Lowers Blood Pressure and Prevents Cardiac Remodeling and Dysfunction in Spontaneously Hypertensive Rats

Raj, P., Bouchard, J., Martineau-Côté, D., Malunga, L. N., L’Hocine, L., Yu, L., Sobhi, B., Achouri, A., Pitre, M., Thandapilly, S. J., et al. (2024) · Nutrients · doi:10.3390/nu16223870 · Cited by 4

Thrombin and Thrombin Peptides in Wound Healing and Tissue Repair

Olszewska-Pazdrak, B., Bergmann, J. S., Fuller, G. M., & Carney, D. H. (2008) · Springer eBooks · doi:10.1007/978-0-387-09637-7_7 · Cited by 4

Insulin Resistance and Erectile Dysfunction

Kim, S.-C. (2006) · Korean journal of urology · doi:10.4111/kju.2006.47.9.917 · Cited by 4

Endothelial dysfunction links cardiovascular disease to pediatric chronic kidney disease: the role of nitric oxide deficiency.

Tain, Y. (2007) · PubMed · Cited by 4

Kardiovaskuläre Manifestationen bei Rheumatoider Arthritis

Moritz, F., Wagner, U. G., Distler, O., Seidel, W., Gay, S., & Häntzschel, H. (2005) · Zeitschrift für Rheumatologie · doi:10.1007/s00393-005-0732-6 · Cited by 4

Insight into increased risk of portal vein thrombosis in nonalcoholic fatty liver disease

Gong, H., Zhong, H., Xu, H., Liu, X.-C., Liang-ping, L., & Zhang, D. (2023) · European Journal of Internal Medicine · doi:10.1016/j.ejim.2023.06.011 · Cited by 3

Vascular dysfunction and body mass index in African adults with HIV

Kaluba, L., Chikopela, T., Goma, F. M., Malambo, M., Mutale, W., Heimburger, D. C., & Koethe, J. R. (2023) · BMC Cardiovascular Disorders · doi:10.1186/s12872-023-03093-2 · Cited by 3

The effect of tumour necrosis factor-α and insulin on equine digital blood vessel function in vitro

Menzies‐Gow, N. J., Wray, H., Bailey, S. R., Harris, P. A., & Elliott, J. (2014) · Inflammation Research · doi:10.1007/s00011-014-0736-2 · Cited by 3

Nitric oxide synthase 3

Michel, T. M. (2009) · AfCS-Nature Molecule Pages · doi:10.1038/mp.a001660.01 · Cited by 3

C-Reactive Protein and Other Inflammatory Markers in Cardiovascular Disease

Arnold, N., & Köenig, W. (2007) · Humana Press eBooks · doi:10.1007/978-1-59745-533-6_5 · Cited by 3

Arterial endothelial injury due to infection in childhood: ticking bomb or innocent bystander?

Liuba, P. (2004) · Acta Paediatrica · doi:10.1111/j.1651-2227.2004.tb00240.x · Cited by 3

Advances in immune-inflammatory interactions within the testicular-penile microenvironment of varicocele patients: molecular mechanisms underlying erectile dysfunction and spermatogenic impairment

Xu, G., & Yu, Q.-F. (2026) · Frontiers in Endocrinology · doi:10.3389/fendo.2026.1813721 · Cited by 2

Molecular Action of Herbal Medicine in Physiology of Erection and its Dysfunction

Rizal, D. M., & Septiyorini, N. (2022) · BIO Web of Conferences · doi:10.1051/bioconf/20224902002 · Cited by 2

Arterial Wall Biology

Sumpio, B. E., & Huang, C. (2010) · Elsevier eBooks · doi:10.1016/b978-1-4160-5223-4.00003-2 · Cited by 2

The effect of different preparations of hormone therapy on tumor necrosis factor-α levels in women with surgical menopause

Somunkiran, A., Coşkun, A., Demirci, F., & Yücel, O. (2008) · Gynecological Endocrinology · doi:10.1080/09513590701718307 · Cited by 2

Network toxicology analysis reveals molecular mechanisms associated with noise exposure to multiple diseases

Taboada-Alquerque, M., & Olivero‐Verbel, J. (2025) · Toxicology Mechanisms and Methods · doi:10.1080/15376516.2025.2460591 · Cited by 1

The Biological Parallels Between Atherosclerosis and Cardiac Allograft Vasculopathy: Implications for Solid Organ Chronic Rejection

Otunla, A. A., Shanmugarajah, K., Davies, A. H., Madariaga, M. L. L., & Shalhoub, J. (2022) · Cardiology in Review · doi:10.1097/crd.0000000000000437 · Cited by 1

Adiponectin, Diabetes, and the Cardiovascular System

Gasbarrino, K., Boutari, C., Filippaios, A., Gianopoulos, I., Daskalopoulou, S. S., & Mantzoros, C. S. (2023) · Contemporary cardiology · doi:10.1007/978-3-031-13177-6_8 · Cited by 1

Multi-omics association study integrating GWAS and pQTL data revealed MIP-1α as a potential drug target for erectile dysfunction

Liu, J., & Pan, R. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1495970 · Cited by 1

Investigating the Role of In Utero Inflammation on Neurodevelopment in the Fetus and Offspring and the Neuroprotective Properties Afforded by Broccoli Sprouts

Nguyen, A. (2016) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3057d35z · Cited by 1

Impairment of Endothelial Thromboprotective Function by Haemodynamic and Inflammatory Stress Implications for hypertensive disease

Ulfhammer, E. (2007) · Gothenburg University Publications Electronic Archive (Gothenburg University)

The role of aryl hydrocarbon receptor in blood pressure regulation and vascular homeostasis

Zhang, N. (2009) · UNM’s Digital Repository (University of New Mexico)

The role and regulation of argininosuccinate synthase in endothelial function

Goodwin, B. L. (2005) · Digital Commons - University of South Florida (University of South Florida)

Interfering with Smoking‐Induced Pathophysiology

Csordás, A. (2011) · Wiley eBooks · doi:10.1002/9783527635320.ch16

Arginine transport and nitric oxide production: role in the inflammatory response

Barilli, A. (2008) · DSpaceUnipr (University of Parma)

The role of melatonin in cardioprotection : an investigation into the mechanisms involved in glucose homeostasis, microvascular endothelial function and mitochondrial function in normal and insulin resistant states

Nduhirabandi, F. (2014) · SUNScholar (Stellenbosch University)

Signaling in Diabetes and Metabolic Syndrome

Marín-García, J. (2011) · Springer eBooks · doi:10.1007/978-1-4419-9461-5_16

Functional topology and regulation of endothelial nitric oxide synthase and associated caveolar components

Flam, B. R. (2006) · Digital Commons - University of South Florida (University of South Florida)

New directions in diagnosis and treatment of canine acute pancreatitis

Mansfield, C. (2011) · Murdoch University Research Portal

Regulation of vascular endothelial t-PA expression in inflammation: Potential target for pharmacological modulation

Larsson, P. (2011) · Gothenburg University Publications Electronic Archive (Gothenburg University)

Régulation de protéine C-réactive vasculaire dans le diabète de type 2

Mugabo, Y. (2010) · doi:10.71781/27620

Vascular action of glycine in hypertensive rat models

Tripathy, S. (2011) · University Library - University of Saskatchewan (University of Saskatchewan)

The Role of Argininosuccinate Synthase Serine 328 Phosphorylation in Nitric Oxide Production

Thompson, R. J. (2012) · Digital Commons - University of South Florida (University of South Florida)

The role of Methylglyoxal in the pathogenesis of endothelial insulin resistance and vascular damage in type 2 diabetes

Nigro, C. (2011) · Università degli Studi di Napoli Federico II · doi:10.6092/unina/fedoa/8778

The anti-obesogenic effects of nitric oxide.

Sansbury, B. E. (2014) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/1262

Study of molecular and immunological factors that determine the sensitivity to the antitumor effect of Tumor Necrosis Factor

Huyghe, L. (2008) · Ghent University Academic Bibliography (Ghent University)

Hemodynamic Regulation of Endothelial Cell Gene Expression: Effects of p65 Expression Level on Constitutive and TNFα Induced NF-κB Signalling

Won, D. (2009) · TSpace (University of Toronto)

Mechanisms of soy isoflavones in the regulation of vascular function

Si, H. (2007) · VTechWorks (Virginia Tech)

Insulin Resistance may be a Central Pathogenetic Mechanism in the Development of Psoriatic Plaques

Boehncke, W., Boehncke, S., & Bürger, C. (2012) · Psoriasis Forum · doi:10.1177/247553031218a00206

The role of cannabinoid receptor type-1 in metabolic endotoxemia-induced metabolic dysfunctions

Grunewald, Z. I. (2016)

Biological activity of anthocyanins and their phenolic degradation products and metabolites in human vascular endothelial cells

Edwards, M. (2013) · UEA Digital Repository (University of East Anglia)

Brain Insulin Resistance, Nitric Oxide and Alzheimer’s Disease Pathology

Pei, Z., Lee, K.-C., Khan, A., & Wang, H.-Y. (2022) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815079814122010014

Diabetes, Prediabetes, Metabolic Syndrome, and Large Artery Vascular Ageing

Stehouwer, C. D. A., van der Heide, F. C. T., Kozàkovà, M., & Palombo, C. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15512-3.00007-6

Various Biological Activities of Citrus unshiu Flower Extracts

Lee, H.-M., Hong, S., Heo, H., Lee, H., & Lee, J. (2025) · Journal of the Korean Society of Food Science and Nutrition · doi:10.3746/jkfn.2025.54.10.822

Neutralizing endocan reduces blood pressure and improves endothelial function in angiotensin II-induced hypertensive mice

Oh, E. Y., Byeon, S., Choi, S.-K., & Lee, Y.-H. (2025) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2025.118910

Additional file 1 of Transcriptome analysis reveals fluid shear stress (FSS) and atherosclerosis pathway as a candidate molecular mechanism of short-term low salinity stress tolerance in abalone

Boamah, G. A., Huang, Z., Shen, Y., Lu, Y., Wang, Z., Su, Y., Xu, C., Luo, X., Ke, C., & You, W. (2022) · Figshare · doi:10.6084/m9.figshare.19862331

Additional file 1 of Small-molecule Akt-activation in airway cells induces NO production and reduces IL-8 transcription through Nrf-2

Gopallawa, I., Kuek, L. E., Adappa, N. D., Palmer, J. N., & Lee, R. J. (2022) · Figshare · doi:10.6084/m9.figshare.20375896

Effects of moderate-intensity aerobic exercise on coronary artery structure and function in type 2 diabetic rats

Wang, D., Guo, Y., Yin, L., Yan, Z., Li, C., Liu, X., & Liu, Y. (2026) · Scientific Reports · doi:10.1038/s41598-026-35082-8

Brachial artery flow‐mediated dilation is less repeatable in children with a chronic inflammatory disease compared to their healthy peers

Byra, M. M., Proudfoot, N. A., Currie, K. D., MacDonald, M. J., Timmons, B. W., & Obeid, J. (2026) · Clinical Physiology and Functional Imaging · doi:10.1111/cpf.70055

Rôle du tissu adipeux cutané dans la formation et la cicatrisation de plaies de compression au cours de l'obésité

Begey, A.-L. (2018) · theses.fr (ABES) · doi:10.70675/d27994bbz9ea0z4727za8f5zbb789d22105d

Effects of whole-body vibration training on resting blood pressure in adults: a systematic review and meta-analysis of randomised controlled trials

Pan, Y., Luo, P., Jia, B., & Pang, J. (2026) · Blood Pressure · doi:10.1080/08037051.2026.2648316

SGK1 inhibition exerts atheroprotective effects in vascular endothelial cells

Yamamoto, H., Hirose, A., Takada, N., & Kihara, S. (2026) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2026.102623

Nebivolol treatment improves hypertension-induced endothelial cell dysfunction by reducing TGF-β1-dependent senescence and normalizing mitochondrial indices

Uruski, P., Mikuła‐Pietrasik, J., Tykarski, A., & Książek, K. (2026) · Journal of Hypertension · doi:10.1097/hjh.0000000000004391

TNF-α induces a decrease in eNOS promoter activity

Neumann, P., Gertzberg, N., & Johnson, A. (2004) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00378.2002 · Cited by 118

The mechanism(s) of post-transcriptional regulation of the human constitutive endothelial nitric oxide synthase gene by tumor necrosis factor-alpha

Mohamed, F. (2000) · Spectrum Research Repository (Concordia University)

Tumor necrosis factor-α reduces argininosuccinate synthase expression and nitric oxide production in aortic endothelial cells

Goodwin, B. L., Pendleton, L. C., Levy, M. M., Solomonson, L. P., & Eichler, D. C. (2007) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01100.2006 · Cited by 110

Expression of an endothelial-type nitric oxide synthase isoform in human neutrophils: modification by tumor necrosis factor-alpha and during acute myocardial infarction

de Frutos, T., de Miguel, L. S., Farré, J., Rivas, J. G., Romero, J., Marcos‐Alberca, P., Nuñez, A., Rico, L., & López-Farré, A. J. (2001) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(00)01185-2 · Cited by 71

Transcriptional regulation of the endothelin-1 gene by TNF-alpha

Marsden, P. A., & Brenner, B. M. (1992) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1992.262.4.c854 · Cited by 288