Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: Atherosclerosis and CCL2[original query] |
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Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis.
The Journal of clinical investigation 2022 10 132 (24): . Hindy George, Tyrrell Daniel J, Vasbinder Alexi, Wei Changli, Presswalla Feriel, Wang Hui, Blakely Pennelope, Ozel Ayse Bilge, Graham Sarah, Holton Grace H, Dowsett Joseph, Fahed Akl C, Amadi Kingsley-Michael, Erne Grace K, Tekmulla Annika, Ismail Anis, Launius Christopher, Sotoodehnia Nona, Pankow James S, Thørner Lise Wegner, Erikstrup Christian, Pedersen Ole Birger, Banasik Karina, Brunak Søren, Ullum Henrik, Eugen-Olsen Jesper, Ostrowski Sisse Rye, , Haas Mary E, Nielsen Jonas B, Lotta Luca A, , Engström Gunnar, Melander Olle, Orho-Melander Marju, Zhao Lili, Murthy Venkatesh L, Pinsky David J, Willer Cristen J, Heckbert Susan R, Reiser Jochen, Goldstein Daniel R, Desch Karl C, Hayek Salim |
CCL2 polymorphisms are associated with serum monocyte chemoattractant protein-1 levels and myocardial infarction in the Framingham Heart Study. Circulation 2005 Aug 112 (8): 1113-20. McDermott DH, Yang Q, Kathiresan S, Cupples LA, Massaro JM, Keaney JF, Larson MG, Vasan RS, Hirschhorn JN, O'Donnell CJ, Murphy PM, Benjamin EJ |
Assessment of genetic effects of polymorphisms in the MCP-1 gene on serum MCP-1 levels and myocardial infarction in Japanese. Circulation journal : official journal of the Japanese Circulation Society 2006 Jul 70 (7): 805-9. Iwai Naoharu, Kajimoto Kazuaki, Kokubo Yoshihiro, Okayama Akira, Miyazaki Shunichi, Nonogi Hiroshi, Goto Yoichi, Tomoike Hitono |
Association between the -2518G/A polymorphism in the monocyte chemoattractant protein-1 (MCP-1) gene and hypertension in Tunisian patients. Clinical biochemistry 2009 Jan 42 (1-2): 34-7. Jemaa Riadh, Ben Ali Samir, Kallel Amani, Omar Souheil, Feki Moncef, Elasmi Monia, Haj-Taïeb Samah, Sanhaji Haïfa, Kaabachi Nazi |
Contribution of TNF-308A and CCL2-2518A to carotid intima-media thickness in obese mexican children and adolescents. Archives of medical research 2008 Nov 39 (8): 753-9. González-Enríquez Gracia Viviana, Rubio-Benítez Martha Imelda, García-Gallegos Víctor, Portilla-de Buen Eliseo, Troyo-Sanromán Rogelio, Leal-Cortés Caridad Aur |
Association between the -2518G/A polymorphism in the monocyte chemoattractant protein-1 (MCP-1) gene and myocardial infarction in Tunisian patients. Clinica chimica acta; international journal of clinical chemistry 2008 Apr 390 (1-2): 122-5. Jemaa Riadh, Rojbani Hajer, Kallel Amani, Ben Ali Samir, Feki Moncef, Chabrak Sonia, Elasmi Monia, Taieb Samah Haj, Sanhaji Haïfa, Souheil Omar, Mechmeche Rachid, Kaabachi Nazi |
Analysis of inflammation- and atherosclerosis-related gene polymorphisms in branch retinal vein occlusion. Molecular vision 2009 15 609-18. Steinbrugger Iris, Haas Anton, Maier Richard, Renner Wilfried, Mayer Monika, Werner Christoph, Wedrich Andreas, El-Shabrawi Yosuf, Schmut Otto, Weger Mart |
CCR2 and coronary artery disease: a woscops substudy. BMC research notes 2010 3 31. Dow David J, McMahon Alex D, Gray Ian C, Packard Chris J, Groot Pieter |
Lack of association of apoE e4 allele with insulin resistance. Acta diabetologica 2012 Feb 49 (1): 25-32. Ragogna Francesca, Lattuada Guido, Ruotolo Giacomo, Luzi Livio, Perseghin Gianlu |
Serum paraoxonase-3 concentration is associated with insulin sensitivity in peripheral artery disease and with inflammation in coronary artery disease. Atherosclerosis 2012 Feb 220 (2): 545-51. Rull Anna, García Raúl, Fernández-Sender Laura, García-Heredia Anabel, Aragonès Gerard, Beltrán-Debón Raúl, Marsillach Judit, Alegret Josep M, Martín-Paredero Vicente, Mackness Bharti, Mackness Michael, Joven Jorge, Camps Jor |
Identification of a potential proinflammatory genetic profile influencing carotid plaque vulnerability. Journal of vascular surgery 2015 Feb 61 (2): 374-81. Biscetti Federico, Straface Giuseppe, Bertoletti Giovanni, Vincenzoni Claudio, Snider Francesco, Arena Vincenzo, Landolfi Raffaele, Flex Andr |
A case-control study on proinflammatory genetic polymorphisms on sudden sensorineural hearing loss. The Laryngoscope 2015 Jan 125 (1): E28-32. Cadoni Gabriella, Gaetani Eleonora, Picciotti Pasqualina M, Arzani Dario, Quarta Miriam, Giannantonio Sara, Paludetti Gaetano, Boccia Stefan |
Combinations of Polymorphic Markers of Chemokine Genes, Their Receptors and Acute Phase Protein Genes As Potential Predictors of Coronary Heart Diseases. Acta naturae 0 8 (1): 111-6. Nasibullin T R, Yagafarova L F, Yagafarov I R, Timasheva Y R, Erdman V V, Tuktarova I A, Mustafina O |
Carriers of rare damaging CCR2 genetic variants are at lower risk of atherosclerotic disease. medRxiv : the preprint server for health sciences 2023 8 . Marios K Georgakis, Rainer Malik, Natalie R Hasbani, Gabrielle Shakt, Alanna C Morrison, Noah L Tsao, Renae Judy, Braxton D Mitchell, Huichun Xu, May E Montasser, Ron Do, Eimear E Kenny, Ruth J F Loos, James G Terry, John Jeffrey Carr, Joshua C Bis, Bruce M Psaty, W T Longstreth, Kendra A Young, Sharon M Lutz, Michael H Cho, Jai Broome, Alyna T Khan, Fei Fei Wang, Nancy Heard-Costa, Sudha Seshadri, Ramachandran S Vasan, Nicholette D Palmer, Barry I Freedman, Donald W Bowden, Lisa R Yanek, Brian G Kral, Lewis C Becker, Patricia A Peyser, Lawrence F Bielak, Farah Ammous, April P Carson, Michael E Hall, Laura M Raffield, Stephen S Rich, Wendy S Post, Russel P Tracy, Kent D Taylor, Xiuqing Guo, Michael C Mahaney, Joanne E Curran, John Blangero, Shoa L Clarke, Jeffrey W Haessler, Yao Hu, Themistocles L Assimes, Charles Kooperberg, Scott M Damrauer, Jerome I Rotter, Paul S de Vries, Martin Dichga |
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