Matrix metalloproteinases promote arterial remodeling in aging, hypertension, and atherosclerosis

Molecular Mechanisms of Stress-Responsive Changes in Collagen and Elastin Networks in Skin

Aziz, J., Shezali, H., Radzi, Z., Yahya, N. A., Abu Kassim, N. H., Czernuszka, J., & Rahman, M. T. (2016) · Skin Pharmacology and Physiology · doi:10.1159/000447017 · Cited by 7,323 · see citing works

Losartan, an AT1 Antagonist, Prevents Aortic Aneurysm in a Mouse Model of Marfan Syndrome

Habashi, J. P., Judge, D. P., Holm, T. M., Cohn, R. D., Loeys, B. L., Cooper, T. K., Myers, L., Klein, E. C., Liu, G., Calvi, C., et al. (2006) · Science · doi:10.1126/science.1124287 · Cited by 1,794 · see citing works

Pathophysiology of Atherosclerosis Plaque Progression

Sakakura, K., Nakano, M., Otsuka, F., Ladich, E. R., Kolodgie, F. D., & Virmani, R. (2013) · Heart Lung and Circulation · doi:10.1016/j.hlc.2013.03.001 · Cited by 471 · see citing works

Divergent effects of tissue inhibitor of metalloproteinase-1, -2, or -3 overexpression on rat vascular smooth muscle cell invasion, proliferation, and death in vitro. TIMP-3 promotes apoptosis.

Baker, A. H., Zaltsman, A. B., George, S. J., & Newby, A. C. (1998) · Journal of Clinical Investigation · doi:10.1172/jci1584 · Cited by 464 · see citing works

MicroRNA-29 in Aortic Dilation: Implications for Aneurysm Formation

Boon, R. A., Seeger, T., Heydt, S., Fischer, A., Hergenreider, E., Horrevoets, A. J. G., Vinciguerra, M., Rosenthal, N. A., Sciacca, S., Pilato, M., et al. (2011) · Circulation Research · doi:10.1161/circresaha.111.255737 · Cited by 365 · see citing works

Short Communication: Vascular Smooth Muscle Cell Stiffness As a Mechanism for Increased Aortic Stiffness With Aging

Qiu, H., Zhu, Y., Sun, Z., Trzeciakowski, J. P., Gansner, M., Depré, C., Resuello, R. R. G., Natividad, F. F., Hunter, W. C., Genin, G. M., et al. (2010) · Circulation Research · doi:10.1161/circresaha.110.221846 · Cited by 341 · see citing works

Elastin Degradation and Calcification in an Abdominal Aorta Injury Model

Basalyga, D. M., Simionescu, D. T., Xiong, W., et al. (2004) · Circulation · doi:10.1161/01.cir.0000148367.08413.e9 · Cited by 318 · see citing works

MicroRNA-21 Blocks Abdominal Aortic Aneurysm Development and Nicotine-Augmented Expansion

Mäegdefessel, L., Azuma, J., Toh, R., Deng, A. C., Merk, D. R., Raiesdana, A., Leeper, N. J., Raaz, U., Schoelmerich, A. M., McConnell, M. V., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003441 · Cited by 300 · see citing works

Angiotensin II–dependent TGF-β signaling contributes to Loeys-Dietz syndrome vascular pathogenesis

Gallo, E. M., Loch, D. C., Habashi, J. P., Calderón, J. F., Chen, Y., Bedja, D., van Erp, C., Gerber, E. E., Parker, S. J., Sauls, K., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci69666 · Cited by 250 · see citing works

Arterial stiffening with ageing is associated with transforming growth factor-β1-related changes in adventitial collagen: reversal by aerobic exercise

Fleenor, B. S., Marshall, K. D., Durrant, J., Lesniewski, L. A., & Seals, D. R. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2010.194753 · Cited by 212 · see citing works

Proinflammation: the key to arterial aging

Wang, M., Jiang, L., Monticone, R. E., & Lakatta, E. G. (2013) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2013.10.002 · Cited by 195 · see citing works

miR-29b Participates in Early Aneurysm Development in Marfan Syndrome

Merk, D. R., Chin, J. T., Dake, B. A., et al. (2011) · Circulation Research · doi:10.1161/circresaha.111.253740 · Cited by 195 · see citing works

Adventitial Mast Cells Contribute to Pathogenesis in the Progression of Abdominal Aortic Aneurysm

Tsuruda, T., Kato, J., Hatakeyama, K., et al. (2008) · Circulation Research · doi:10.1161/circresaha.108.173682 · Cited by 183 · see citing works

Deficiency of Gelatinase A Suppresses Smooth Muscle Cell Invasion and Development of Experimental Intimal Hyperplasia

Kuzuya, M., Kanda, S., Sasaki, T., Tamaya-Mori, N., Cheng, X. W., Itoh, T., Itohara, S., & Iguchi, A. (2003) · Circulation · doi:10.1161/01.cir.0000086463.15540.3c · Cited by 182 · see citing works

Angiotensin II Activates Matrix Metalloproteinase Type II and Mimics Age-Associated Carotid Arterial Remodeling in Young Rats

Wang, M., Zhang, J., Spinetti, G., Jiang, L., Monticone, R. E., Zhao, D., Cheng, L., Krawczyk, M., Talan, M. I., Pintus, G., et al. (2005) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)61229-1 · Cited by 178 · see citing works

Vascular Matrix Metalloproteinase-2–Dependent Cleavage of Calcitonin Gene-Related Peptide Promotes Vasoconstriction

Fernández-Patrón, C., Stewart, K., Zhang, Y., Koivunen, E., Radomski, M. W., & Davidge, S. T. (2000) · Circulation Research · doi:10.1161/01.res.87.8.670 · Cited by 175 · see citing works

Matrix metalloproteinases: influence on smooth muscle cells and atherosclerotic plaque stability

Johnson, J. L. (2007) · Expert Review of Cardiovascular Therapy · doi:10.1586/14779072.5.2.265 · Cited by 172 · see citing works

Immuno‐miRs: critical regulators of T‐cell development, function and ageing

Kroesen, B., Teteloshvili, N., Smigielska‐Czepiel, K., Brouwer, E., Boots, A. M. H., van den Berg, A., & Kluiver, J. L. (2014) · Immunology · doi:10.1111/imm.12367 · Cited by 168 · see citing works

Endothelial Cell–Specific Reactive Oxygen Species Production Increases Susceptibility to Aortic Dissection

Fan, L. M., Douglas, G., Bendall, J. K., McNeill, E., Crabtree, M. J., Hale, A., Mai, A., Li, J., McAteer, M. A., Schneider, J. E., et al. (2014) · Circulation · doi:10.1161/circulationaha.113.005062 · Cited by 134 · see citing works

Calpain-1 Regulation of Matrix Metalloproteinase 2 Activity in Vascular Smooth Muscle Cells Facilitates Age-Associated Aortic Wall Calcification and Fibrosis

Jiang, L., Zhang, J., Monticone, R. E., Telljohann, R. S., Wu, J. T., Wang, M., & Lakatta, E. G. (2012) · Hypertension · doi:10.1161/hypertensionaha.112.196840 · Cited by 130 · see citing works

MMP-2 and MMP-9 are prominent matrix metalloproteinases during atherosclerosis development in the Ldlr-/-Apob100/100 mouse

Wågsäter, D. (2011) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2011.693 · Cited by 127 · see citing works

MMP-2 Regulates Erk1/2 Phosphorylation and Aortic Dilatation in Marfan Syndrome

Xiong, W., Meisinger, T. M., Knispel, R., et al. (2012) · Circulation Research · doi:10.1161/circresaha.112.268268 · Cited by 122 · see citing works

Pathophysiology of vascular calcification: Pivotal role of cellular senescence in vascular smooth muscle cells

Burton, D. G. A., Matsubara, H., & Ikeda, K. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2010.07.005 · Cited by 121 · see citing works

Intraluminal abdominal aortic aneurysm thrombus is associated with disruption of wall integrity

Koole, D., Zandvoort, H. J. A., Schoneveld, A. H., Vink, A., Vos, J. A., van den Hoogen, L. L., de Vries, J. P. P. M., Pasterkamp, G., Moll, F. L., & van Herwaarden, J. A. (2012) · Journal of Vascular Surgery · doi:10.1016/j.jvs.2012.07.003 · Cited by 116 · see citing works

MicroRNA-24 Regulates Macrophage Behavior and Retards Atherosclerosis

Gregoli, K. D., Jenkins, N., Salter, R., White, S., Newby, A., & Johnson, J. L. (2014) · Arteriosclerosis, Thrombosis and Vascular Biology · doi:10.1161/atvbaha.114.304088 · Cited by 112 · see citing works

Role of miR-195 in Aortic Aneurysmal Disease

Zampetaki, A., Attia, R. Q., Mayr, U., et al. (2014) · Circulation Research · doi:10.1161/circresaha.115.304361 · Cited by 110 · see citing works

Chronic Matrix Metalloproteinase Inhibition Retards Age-Associated Arterial Proinflammation and Increase in Blood Pressure

Wang, M., Zhang, J., Telljohann, R. S., Jiang, L., Wu, J. T., Monticone, R. E., Kapoor, K., Talan, M. I., & Lakatta, E. G. (2012) · Hypertension · doi:10.1161/hypertensionaha.112.191270 · Cited by 106 · see citing works

CXCR3-dependent accumulation and activation of perivascular macrophages is necessary for homeostatic arterial remodeling to hemodynamic stresses

Zhou, J., Tang, P. C. Y., Qin, L., Gayed, P. M., Li, W., Skokos, E. A., Kyriakides, T. R., Pober, J. S., & Tellides, G. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20100098 · Cited by 102 · see citing works

MMP-2 Mediates Angiotensin II–Induced Hypertension Under the Transcriptional Control of MMP-7 and TACE

Odenbach, J., Wang, X., Cooper, S., Chow, F. L., Oka, T., Lopaschuk, G. D., Kassiri, Z., & Fernández-Patrón, C. (2010) · Hypertension · doi:10.1161/hypertensionaha.110.159525 · Cited by 99 · see citing works

Peripheral blood miRNAs as a biomarker for chronic cardiovascular diseases

Jiang, Y., Wang, H.-Y., Cao, H.-M., Wang, C.-Y., Zhang, L., Wang, H., Liu, L., Li, Y., & Cai, J.-H. (2014) · Scientific Reports · doi:10.1038/srep05026 · Cited by 98 · see citing works

Angiotensin-Converting Enzyme 2 Is a Critical Determinant of Angiotensin II–Induced Loss of Vascular Smooth Muscle Cells and Adverse Vascular Remodeling

Patel, V. B., Zhong, J., Dong, F., Basu, R., Morton, J. S., Parajuli, N., McMurtry, M. S., Davidge, S. T., Kassiri, Z., & Oudit, G. Y. (2014) · Hypertension · doi:10.1161/hypertensionaha.114.03388 · Cited by 97 · see citing works

Loss of matrix metalloproteinase 2 in platelets reduces arterial thrombosis in vivo

Momi, S., Falcinelli, E., Giannini, S., Ruggeri, L., Cecchetti, L., Corazzi, T., Libert, C., & Gresele, P. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20090687 · Cited by 88 · see citing works

The reality of aging viewed from the arterial wall ☆

Lakatta, E. G. (2013) · Artery Research · doi:10.1016/j.artres.2013.01.003 · Cited by 86 · see citing works

An important role of matrix metalloproteinase-8 in angiogenesis in vitro and in vivo

Fang, C., Wen, G., Zhang, L., Lin, L., Moore, A., Wu, S., Ye, S., & Xiao, Q. (2013) · Cardiovascular Research · doi:10.1093/cvr/cvt060 · Cited by 85 · see citing works

Doxycycline, a matrix metalloprotease inhibitor, reduces vascular remodeling and damage after cerebral ischemia in stroke-prone spontaneously hypertensive rats

Pires, P. W., Rogers, C. T., McClain, J. L., Garver, H. S., Fink, G. D., & Dorrance, A. M. (2011) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01206.2010 · Cited by 84 · see citing works

Matrix Metalloproteinase 7 Is Associated with Symptomatic Lesions and Adverse Events in Patients with Carotid Atherosclerosis

Abbas, A., Aukrust, P., Russell, D., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084935 · Cited by 80 · see citing works

Matrix metalloproteinases cleave the β2-adrenergic receptor in spontaneously hypertensive rats

Rodrigues, S. F., Tran, E. D., Fortes, Z. B., et al. (2010) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00620.2009 · Cited by 78 · see citing works

The Role of Extracellular Signal-Related Kinase During Abdominal Aortic Aneurysm Formation

Ghosh, A., DiMusto, P. D., Ehrlichman, L. K., Sadiq, O., McEvoy, B., Futchko, J. S., Henke, P. K., Eliason, J. L., & Upchurch, G. R. (2012) · Journal of the American College of Surgeons · doi:10.1016/j.jamcollsurg.2012.06.414 · Cited by 77 · see citing works

Activation of MMP-2, cleavage of matrix proteins, and adherens junctions during a snake venom metalloproteinase-induced endothelial cell apoptosis

Wu, W.-T. (2003) · Experimental Cell Research · doi:10.1016/s0014-4827(03)00183-6 · Cited by 75 · see citing works

Matrix Metalloproteinase-8 Promotes Vascular Smooth Muscle Cell Proliferation and Neointima Formation

Xiao, Q., Zhang, F., Grassia, G., Hu, Y., Zhang, Z., Xing, Q., Yin, X., Maddaluno, M., Drung, B., Schmidt, B., et al. (2013) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.113.301418 · Cited by 73 · see citing works

MicroRNA-21 is a unique signature associated with coronary plaque instability in humans by regulating matrix metalloproteinase-9 via reversion-inducing cysteine-rich protein with Kazal motifs

Fan, X., Wang, E., Wang, X., Cong, X., & Chen, X. (2014) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2014.02.009 · Cited by 70 · see citing works

Time course involvement of matrix metalloproteinases in the vascular alterations of renovascular hypertension

Ceron, C. S., Rizzi, É., Guimarães, D. A., et al. (2012) · Matrix Biology · doi:10.1016/j.matbio.2012.01.009 · Cited by 70 · see citing works

Exploring smooth muscle phenotype and function in a bioreactor model of abdominal aortic aneurysm

Riches‐Suman, K., Angelini, T. G., Mudhar, G. S., et al. (2013) · Journal of Translational Medicine · doi:10.1186/1479-5876-11-208 · Cited by 67 · see citing works

Doxycycline ameliorates 2K-1C hypertension-induced vascular dysfunction in rats by attenuating oxidative stress and improving nitric oxide bioavailability

de Castro, M. M., Rizzi, É., Ceron, C. S., et al. (2012) · Nitric Oxide · doi:10.1016/j.niox.2012.01.009 · Cited by 67 · see citing works

Matrix Metalloproteinase Enhances Big-Endothelin-1 Constriction in Mesenteric Vessels of Pregnant Rats With Reduced Uterine Blood Flow

Abdalvand, A., Morton, J. S., Bourque, S. L., Quon, A., & Davidge, S. T. (2013) · Hypertension · doi:10.1161/hypertensionaha.111.00055 · Cited by 67 · see citing works

Matrix metalloproteinase levels in chronic thoracic aortic dissection

Zhang, X., Wu, D., Choi, J. C.-B., et al. (2014) · Journal of Surgical Research · doi:10.1016/j.jss.2014.03.027 · Cited by 65 · see citing works

Validity of Dual MRI and 18F-FDG PET Imaging in Predicting Vulnerable and Inflamed Carotid Plaque

Saito, H., Kuroda, S., Hirata, K., Magota, K., Shiga, T., Tamaki, N., Yoshida, D., Terae, S., Nakayama, N., & Houkin, K. (2013) · Cerebrovascular Diseases · doi:10.1159/000348846 · Cited by 61 · see citing works

Nuclear Factor Kappa B and Matrix Metalloproteinase Induced Receptor Cleavage in the Spontaneously Hypertensive Rat

Wu, K.-I. S., & Schmid‐Schönbein, G. W. (2011) · Hypertension · doi:10.1161/hypertensionaha.110.158709 · Cited by 60 · see citing works

Angiotensin Type 1 Receptor Blocker Reduces Intimal Neovascularization and Plaque Growth in Apolipoprotein E–Deficient Mice

Cheng, X. W., Song, H., Sasaki, T., Hu, L., Inoue, A., Bando, Y., Shi, G., Kuzuya, M., Okumura, K., & Murohara, T. (2011) · Hypertension · doi:10.1161/hypertensionaha.110.168385 · Cited by 59 · see citing works

In vivo optical molecular imaging of matrix metalloproteinase activity in abdominal aortic aneurysms correlates with treatment effects on growth rate

Sheth, R. A., Maricevich, M., & Mahmood, U. (2010) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2010.05.012 · Cited by 56 · see citing works

The Synthetic Metalloproteinase Inhibitor Batimastat Suppresses Injury-Induced Phosphorylation of MAP Kinase ERK1/ERK2 and Phenotypic Modification of Arterial Smooth Muscle Cells in vitro

Lövdahl, C., Thyberg, J., & Hultgårdh‐Nilsson, A. (2000) · Journal of Vascular Research · doi:10.1159/000025750 · Cited by 55 · see citing works

Matrix Metalloproteinase-13 Predominates Over Matrix Metalloproteinase-8 as the Functional Interstitial Collagenase in Mouse Atheromata

Quillard, T., Araújo, H. A., Franck, G., Tesmenitsky, Y., & Libby, P. (2014) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.114.303326 · Cited by 55 · see citing works

Differential Effects of Mechanical and Biological Stimuli on Matrix Metalloproteinase Promoter Activation in the Thoracic Aorta

Ruddy, J. M., Jones, J. A., Stroud, R. E., Mukherjee, R. D., Spinale, F. G., & Ikonomidis, J. S. (2009) · Circulation · doi:10.1161/circulationaha.108.843581 · Cited by 54 · see citing works

Matrix Metalloproteinase-2 Proteolysis of Calponin-1 Contributes to Vascular Hypocontractility in Endotoxemic Rats

de Castro, M. M., Cena, J., Cho, W. J., et al. (2011) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.242685 · Cited by 54 · see citing works

Inactivation of Serum Response Factor Contributes To Decrease Vascular Muscular Tone and Arterial Stiffness in Mice

Galmiche, G., Labat, C., Mericskay, M., Ait‐Aissa, K., Blanc, J., Retailleau, K., Bourhim, M., Coletti, D., Loufrani, L., Gao-Li, J., et al. (2013) · Circulation Research · doi:10.1161/circresaha.113.301076 · Cited by 52 · see citing works

Proteomic Identification of Matrix Metalloproteinase Substrates in the Human Vasculature

Stegemann, C., Didangelos, A., Barallobre‐Barreiro, J., Langley, S. R., Mandal, K., Jahangiri, M., & Mayr, M. (2012) · Circulation Cardiovascular Genetics · doi:10.1161/circgenetics.112.964452 · Cited by 50 · see citing works

Inhibition of matrix metalloproteinase‐2 improves endothelial function and prevents hypertension in insulin‐resistant rats

Nagareddy, P. R., Rajput, P., Vasudevan, H., McClure, B. P., Kumar, U., MacLeod, K. M., & Jh, M. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01583.x · Cited by 49 · see citing works

Milk Fat Globule Epidermal Growth Factor VIII Signaling in Arterial Wall Remodeling

Wang, M., Wang, H. H., & Lakatta, E. G. (2013) · Current Vascular Pharmacology · doi:10.2174/1570161111311050014 · Cited by 49 · see citing works

Enhanced Endothelial Cell Senescence by Lithium-induced Matrix Metalloproteinase-1 Expression

Struewing, I. T., Durham, S. N., Barnett, C. D., & Mao, C. D. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.001735 · Cited by 47 · see citing works

Noncanonical Matrix Metalloprotease-1-Protease-activated Receptor-1 Signaling Triggers Vascular Smooth Muscle Cell Dedifferentiation and Arterial Stenosis

Austin, K. M., Nguyen, N., Javid, G., Covic, L., & Kuliopulos, A. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.467019 · Cited by 47 · see citing works

Hypertension Accelerated Experimental Abdominal Aortic Aneurysm Through Upregulation of Nuclear Factor κB and Ets

Shiraya, S., Miwa, K., Aoki, M., et al. (2006) · Hypertension · doi:10.1161/01.hyp.0000240266.26185.57 · Cited by 46 · see citing works

Sodium Intake Is Associated with Carotid Artery Structure Alterations and Plasma Matrix Metalloproteinase-9 Upregulation in Hypertensive Adults1–3

Ferreira-Sae, M. C., Cipolli, J. A., Cornélio, M. E., et al. (2011) · Journal of Nutrition · doi:10.3945/jn.110.135921 · Cited by 45 · see citing works

Impaired Vascular Contractility and Aortic Wall Degeneration in Fibulin-4 Deficient Mice: Effect of Angiotensin II Type 1 (AT1) Receptor Blockade

Moltzer, E., Riet, L. T., Swagemakers, S. M. A., van Heijningen, P. M., Vermeij, M., van Veghel, R., Bouhuizen, A. M., van Esch, J. H. M., Lankhorst, S., Ramnath, N. W. M., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023411 · Cited by 42 · see citing works

Matrix metalloproteinase-2 deficiency impairs aortic atherosclerotic calcification in ApoE-deficient mice

Sasaki, T., Nakamura, K., Sasada, K., et al. (2012) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2012.12.008 · Cited by 40 · see citing works

Quantitative assessment of glucose metabolism in the vessel wall of abdominal aortic aneurysms: correlation with histology and role of partial volume correction

Reeps, C., Bundschuh, R. A., Pellisek, J., et al. (2012) · International journal of cardiac imaging · doi:10.1007/s10554-012-0090-9 · Cited by 38 · see citing works

Angiotensin II Promotes Thoracic Aortic Dissections and Ruptures in Col3a1 Haploinsufficient Mice

Faugeroux, J., Nematalla, H., Li, W., Clément, M., Robidel, E., Frank, M., Curis, E., Ait‐Oufella, H., Caligiuri, G., Nicoletti, A., et al. (2013) · Hypertension · doi:10.1161/hypertensionaha.111.00974 · Cited by 37 · see citing works

Different activation forms of MMP-2 oppositely affect the fate of endothelial cells

Shapiro, S., Khodalev, O., Bitterman, H., et al. (2010) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00305.2009 · Cited by 30 · see citing works

Angiotensin-II induces phosphorylation of ERK1/2 and promotes aortic adventitial fibroblasts differentiating into myofibroblasts during aortic dissection formation

Wang, Z., Ren, Z.-L., Hu, Z., et al. (2013) · Journal of Molecular Histology · doi:10.1007/s10735-013-9558-8 · Cited by 30 · see citing works

Chronic Treatment with a Broad-Spectrum Metalloproteinase Inhibitor, Doxycycline, Prevents the Development of Spontaneous Aortic Lesions in a Mouse Model of Vascular Ehlers-Danlos Syndrome

Tae, H., Marshall, S. A., Zhang, J., Wang, M., Briest, W., & Talan, M. I. (2012) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.112.197020 · Cited by 29 · see citing works

Tumor Necrosis Factor-α Induces Aortic Intima-Media Thickening via Perivascular Adipose Tissue Inflammation

Moe, K. T., Naylynn, T. M., Yin, N. O., Khairunnisa, K., Allen, J. C., Wong, M. C., Chin-Dusting, J. P. F., & Wong, P. E. H. (2013) · Journal of Vascular Research · doi:10.1159/000350542 · Cited by 29 · see citing works

Inhibition of ERK1/2 Phosphorylation: A New Strategy to Stimulate Elastogenesis in the Aorta

Lannoy, M., Slove, S., Louedec, L., et al. (2014) · Hypertension · doi:10.1161/hypertensionaha.114.03352 · Cited by 27 · see citing works

TNF-α regulates vascular smooth muscle cell responses in genetic hypertension

Lee, S.-J., Kim, W., & Moon, S. (2009) · International Immunopharmacology · doi:10.1016/j.intimp.2009.03.010 · Cited by 24 · see citing works

Abrupt increase in rat carotid blood flow induces rapid alteration of artery mechanical properties

Monson, K. L., Matsumoto, M. M., Young, W. L., Manley, G. T., & Hashimoto, T. N. (2010) · Journal of the mechanical behavior of biomedical materials/Journal of mechanical behavior of biomedical materials · doi:10.1016/j.jmbbm.2010.08.003 · Cited by 12 · see citing works

Vascular receptors as new substrates for matrix metalloproteinases in hypertension and other inflammatory states

Kalogeris, T. J., & Korthuis, R. J. (2010) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00378.2010 · Cited by 3 · see citing works

Inflammageing: chronic inflammation in ageing, cardiovascular disease, and frailty

Ferrucci, L., & Fabbri, E. (2018) · Nature Reviews Cardiology · doi:10.1038/s41569-018-0064-2 · Cited by 3,690 · see citing works

Senescence-induced inflammation: an important player and key therapeutic target in atherosclerosis

Stojanović, S. D., Fiedler, J., Bauersachs, J., Thum, T., & Sedding, D. G. (2020) · European Heart Journal · doi:10.1093/eurheartj/ehz919 · Cited by 188 · see citing works

Mechanistic insights regarding the role of SGLT2 inhibitors and GLP1 agonist drugs on cardiovascular disease in diabetes

Garg, V., Verma, S., & Connelly, K. (2019) · Progress in Cardiovascular Diseases · doi:10.1016/j.pcad.2019.07.005 · Cited by 82 · see citing works

How the love of muscle can break a heart: Impact of anabolic androgenic steroids on skeletal muscle hypertrophy, metabolic and cardiovascular health

McCullough, D., Webb, R., Enright, K. J., Lane, K. E., McVeigh, J., Stewart, C. E., & Davies, I. G. (2021) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-020-09616-y · Cited by 62 · see citing works

Comparison of the effect of glucose-lowering agents on the risk of atrial fibrillation: A network meta-analysis

Shi, W., Zhang, W., Zhang, D., Ren, G., Wang, P., Gao, L., Chen, H., & Ding, C. (2021) · Heart Rhythm · doi:10.1016/j.hrthm.2021.03.007 · Cited by 54 · see citing works

ФОРМИРОВAНИЕ ГОТОВНОСТИ БУДУЩИХ ПЕДAГОГОВ К ОРГAНИЗAЦИИ РAБОТЫ ПО РAЗВИТИЮ ВAЛЕОЛОГИЧЕСКОЙ КУЛЬТУРЫ ШКОЛЬНИКОВ

БАЗАРБАЕВА, Ә. А., Майгельдиева, Ш. М., & ЖҮНДІБАЕВА, Т. Н. (2023) · Pedagogy and Psychology · doi:10.51889/2077-6861.2023.1.30.016

चितलवाना पंचायत समिति में मानव गरीबी सूचकांक - 2016 ( à¤à¤• गà¥à¤°à¤¾à¤® सà¥à¤¤à¤°à¥€à¤¯ à¤à¥Œà¤—ोलिक अधà¥à¤¯à¤¯à¤¨ )

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