Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Coronary Artery Disease and MMP9[original query] |
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Matrix metalloproteinase circulating levels, genetic polymorphisms, and susceptibility to acute myocardial infarction among patients with coronary artery disease. American heart journal 2007 Dec 154 (6): 1043-51. Hlatky Mark A, Ashley Euan, Quertermous Thomas, Boothroyd Derek B, Ridker Paul, Southwick Audrey, Myers Richard M, Iribarren Carlos, Fortmann Stephen P, Go Alan S, |
[Association of MMP9 gene -1562 C/T polymorphism with myocardial infarction in Uighur population of Xinjiang]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2011 Apr 28 (2): 180-4. WANG Lei, MA Yi-tong, XIE Xiang, YANG Yi-ning, FU Zhen-yan, LIU Fen, LI Xiao-mei, CHEN Bang-da |
Association of matrix metalloproteinases (MMP2, MMP7 and MMP9) genetic variants with left ventricular dysfunction in coronary artery disease patients. Clinica chimica acta; international journal of clinical chemistry 2012 Oct 413 (19-20): 1668-74. Mishra Avshesh, Srivastava Anshika, Mittal T, Garg N, Mittal |
Matrix metalloproteinase family gene polymorphisms and risk for coronary artery disease: systematic review and meta-analysis. Heart (British Cardiac Society) 2012 Oct 98 (20): 1483-91. Niu Wenquan, Qi Y |
Variations in matrix metalloproteinase-1, -3, and -9 genes and the risk of acute coronary syndrome and coronary artery disease in the Chinese Han population. Coronary artery disease 2013 Jan . Xu X, Wang L, Xu C, Zhang P, Yong F, Liu H, Wang J, Shi Y |
Genetic predisposition to left ventricular dysfunction: a multigenic and multi-analytical approach. Gene 2014 Aug 546 (2): 309-17. Mishra Avshesh, Srivastava Anshika, Mittal Tulika, Garg Naveen, Mittal Balr |
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.
Circulation research 2017 Jan 120 (2): 341-353. Jones Gregory T, Tromp Gerard, Kuivaniemi Helena, Gretarsdottir Solveig, Baas Annette F, Giusti Betti, Strauss Ewa, Van't Hof Femke N G, Webb Thomas R, Erdman Robert, Ritchie Marylyn D, Elmore James R, Verma Anurag, Pendergrass Sarah, Kullo Iftikhar J, Ye Zi, Peissig Peggy L, Gottesman Omri, Verma Shefali S, Malinowski Jennifer, Rasmussen-Torvik Laura J, Borthwick Kenneth M, Smelser Diane T, Crosslin David R, de Andrade Mariza, Ryer Evan J, McCarty Catherine A, Böttinger Erwin P, Pacheco Jennifer A, Crawford Dana C, Carrell David S, Gerhard Glenn S, Franklin David P, Carey David J, Phillips Victoria L, Williams Michael J A, Wei Wenhua, Blair Ross, Hill Andrew A, Vasudevan Thodor M, Lewis David R, Thomson Ian A, Krysa Jo, Hill Geraldine B, Roake Justin, Merriman Tony R, Oszkinis Grzegorz, Galora Silvia, Saracini Claudia, Abbate Rosanna, Pulli Raffaele, Pratesi Carlo, Saratzis Athanasios, Verissimo Ana R, Bumpstead Suzannah, Badger Stephen A, Clough Rachel E, Cockerill Gillian, Hafez Hany, Scott D Julian A, Futers T Simon, Romaine Simon P R, Bridge Katherine, Griffin Kathryn J, Bailey Marc A, Smith Alberto, Thompson Matthew M, van Bockxmeer Frank M, Matthiasson Stefan E, Thorleifsson Gudmar, Thorsteinsdottir Unnur, Blankensteijn Jan D, Teijink Joep A W, Wijmenga Cisca, de Graaf Jacqueline, Kiemeney Lambertus A, Lindholt Jes S, Hughes Anne, Bradley Declan T, Stirrups Kathleen, Golledge Jonathan, Norman Paul E, Powell Janet T, Humphries Steve E, Hamby Stephen E, Goodall Alison H, Nelson Christopher P, Sakalihasan Natzi, Courtois Audrey, Ferrell Robert E, Eriksson Per, Folkersen Lasse, Franco-Cereceda Anders, Eicher John D, Johnson Andrew D, Betsholtz Christer, Ruusalepp Arno, Franzén Oscar, Schadt Eric E, Björkegren Johan L M, Lipovich Leonard, Drolet Anne M, Verhoeven Eric L, Zeebregts Clark J, Geelkerken Robert H, van Sambeek Marc R, van Sterkenburg Steven M, de Vries Jean-Paul, Stefansson Kari, Thompson John R, de Bakker Paul I W, Deloukas Panos, Sayers Robert D, Harrison Seamus C, van Rij Andre M, Samani Nilesh J, Bown Matthew |
A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors. Scientific reports 2017 Aug 7 (1): 10252. Brænne Ingrid, Willenborg Christina, Tragante Vinicius, Kessler Thorsten, Zeng Lingyao, Reiz Benedikt, Kleinecke Mariana, von Ameln Simon, Willer Cristen J, Laakso Markku, Wild Philipp S, Zeller Tanja, Wallentin Lars, Franks Paul W, Salomaa Veikko, Dehghan Abbas, Meitinger Thomas, Samani Nilesh J, Asselbergs Folkert W, Erdmann Jeanette, Schunkert Heribe |
Association of R279Q and C1562T polymorphisms of matrix metalloproteinase 9 gene and increased risk for myocardial infarction in patients with premature coronary artery disease. Journal of clinical laboratory analysis 2017 Apr . Sheikhvatan Mehrdad, Boroumand Mohammad Ali, Behmanesh Mehrdad, Ziaee Shay |
Plasma concentration, genetic variation, and gene expression levels of matrix metalloproteinase 9 in Iranian patients with coronary artery disease. Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences 2017 22 8. Mahmoodi Khalil, Kamali Koorosh, Karami Elham, Soltanpour Mohammad Soleim |
Association between matrix metalloproteinase 9 C-1562T polymorphism and the risk of coronary artery disease: an update systematic review and meta-analysis. Oncotarget 2018 Feb 9 (10): 9468-9479. Zhang Ming-Ming, Chang Xue-Wei, Hao Xue-Qin, Wang Hao, Xie Xiang, Zhang Shou-Y |
Association of the Polymorphism rs3918242 of the Matrix Metalloproteinase-9 Gene with Coronary Artery Disease in a Younger Population. Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki) 2023 7 44 (2): 31-39. Marjan Boshev, Svetlana Stankovic, Sasho Panov, Slavica Josifovska, Antonio Georgiev, Lidija Poposka, Hristo Pejk |
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- Page last updated:Apr 29, 2024
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