Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: Hypertension and MMP9[original query] |
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Coronary artery complicated lesion area is related to functional polymorphism of matrix metalloproteinase 9 gene: an autopsy study. Arteriosclerosis, thrombosis, and vascular biology 2001 Sep 21 (9): 1446-50. Pöllänen P J, Karhunen P J, Mikkelsson J, Laippala P, Perola M, Penttilä A, Mattila K M, Koivula T, Lehtimäki |
Matrix metalloproteinase3 and 9 gene promoter polymorphisms: joint action of two loci as a risk factor for coronary artery complicated plaques. Atherosclerosis 2005 May 180 (1): 73-8. Pöllänen Perttu J, Lehtimäki Terho, Mikkelsson Jussi, Ilveskoski Erkki, Kunnas Tarja, Perola Markus, Penttilä Antti, Mattila Kari M, Nikkari Seppo T, Syrjäkoski Kirsi, Karhunen Pekka |
Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury. Human genetics 2007 Jan 120 (5): 671-80. Fornage Myriam, Mosley Thomas H, Jack Clifford R, de Andrade Mariza, Kardia Sharon L R, Boerwinkle Eric, Turner Stephen |
Polymorphisms in MMP family and TIMP genes and carotid artery intima-media thickness. Stroke; a journal of cerebral circulation 2007 Nov 38 (11): 2895-9. Armstrong Christine, Abilleira Sonia, Sitzer Matthias, Markus Hugh S, Bevan Ste |
Pharmacogenetic associations of MMP9 and MMP12 variants with cardiovascular disease in patients with hypertension. PloS one 2011 6 (8): e23609. Tanner Rikki M, Lynch Amy I, Brophy Victoria H, Eckfeldt John H, Davis Barry R, Ford Charles E, Boerwinkle Eric, Arnett Donna |
Gene panels to help identify subgroups at high and low risk of coronary heart disease among those randomized to antihypertensive treatment: the GenHAT study. Pharmacogenetics and genomics 2012 May 22 (5): 355-66. Lynch Amy I, Eckfeldt John H, Davis Barry R, Ford Charles E, Boerwinkle Eric, Leiendecker-Foster Catherine, Arnett Donna |
Associations of MMP1, 3, 9 and TIMP3 genes polymorphism with isolated systolic hypertension in Chinese Han population. International journal of medical sciences 2013 10 (7): 840-7. Huang Rong, Deng Liehua, Shen AnNa, Liu Jian, Ren Hao, Xu Ding- |
Genetic predisposition to essential hypertension in children: analysis of 17 single nucleotide polymorphisms. Fiziolohichny? zhurnal (Kiev, Ukraine : 1994) 2013 59 (6): 12-24. Goncharov S V, Gurianova V L, Stroy D O, Drevytska T I, Kaplinskii S P, Nastenko E A, Litvinenko M, Terletskiy R V, Khaitovych M V, Moibenko O O, Dosenko V |
Genetic variations of MMP9 gene and intracerebral hemorrhage susceptibility: a case-control study in Chinese Han population. Journal of the neurological sciences 2014 Jun 341 (1-2): 55-7. Yang Jie, Wu Bo, Lin Sen, Zhou Junshan, Li Yingbin, Dong Wei, Arima Hisatomi, Zhang Chanfei, Liu Yukai, Liu Ming, |
Polymorphisms in the RAC1 gene are associated with hypertension risk factors in a Chilean pediatric population. American journal of hypertension 2014 Mar 27 (3): 299-307. Tapia-Castillo Alejandra, Carvajal Cristian A, Campino Carmen, Vecchiola Andrea, Allende Fidel, Solari Sandra, García Lorena, Lavanderos Sergio, Valdivia Carolina, Fuentes Cristobal, Lagos Carlos F, Martínez-Aguayo Alejandro, Baudrand Rene, Aglony Marlene, García Hernán, Fardella Carlos |
DNA methylation of hypertension-related genes and effect of riboflavin supplementation in adults stratified by genotype for the MTHFR C677T polymorphism. International journal of cardiology 2020 Sep . Amenyah Sophia D, Ward Mary, McMahon Amy, Deane Jennifer, McNulty Helene, Hughes Catherine, Strain J J, Horigan Geraldine, Purvis John, Walsh Colum P, Lees-Murdock Diane |
Dataset of allele and genotype frequencies of the three functionally significant polymorphisms of the MMP genes in Russian patients with primary open-angle glaucoma, essential hypertension and peptic ulcer. Data in brief 2020 Aug 31 106004. Minyaylo Oksana, Starikova Dina, Moskalenko Maria, Ponomarenko Irina, Reshetnikov Evgeny, Dvornyk Volodymyr, Churnosov Mikha |
MMP9 rs17576 Is Simultaneously Correlated with Symptomatic Intracranial Atherosclerotic Stenosis and White Matter Hyperintensities in Chinese Population. Cerebrovascular diseases (Basel, Switzerland) 2020 Dec 1-8. Feng Xianjing, Yu Fang, Zhou Xiaoqing, Liu Zeyu, Liao Di, Huang Qin, Li Xi, Jin Xin, Xia Ji |
Polymorphisms of the matrix metalloproteinase genes are associated with essential hypertension in a Caucasian population of Central Russia. Scientific reports 2021 Mar 11 (1): 5224. Moskalenko Maria, Ponomarenko Irina, Reshetnikov Evgeny, Dvornyk Volodymyr, Churnosov Mikha |
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 |
[Assessment of environmental and genetic risk factors for the development of primary open-angle glaucoma]. Vestnik oftalmologii 2023 11 139 (5): 74-80. A N Samoylov, D Yu Plotnikov, P A Tumano |
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- Page last updated:May 28, 2024
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