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Original

Protective role of 27bp repeat polymorphism in intron 4 of eNOS gene in lacunar infarction

Pages 272-279 | Received 24 Oct 2008, Published online: 07 Jul 2009

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Ruozhuo Liu, Peiliang Geng, Minghui Ma, Shengyuan Yu, Xiaolin Wang, Wei Zhang & Hai Di. (2014) Association between endothelial nitric oxide synthase gene polymorphism (T-786C) and ischemic stroke susceptibility: a meta-analysis. International Journal of Neuroscience 124:9, pages 642-651.
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Kátia Cristina de Marco, Gilberto U. Braga & Fernando Barbosa Jr.. (2011) Determination of the Effects of eNOS Gene Polymorphisms (T-786C and Glu298Asp) on Nitric Oxide Levels in a Methylmercury-Exposed Population. Journal of Toxicology and Environmental Health, Part A 74:20, pages 1323-1333.
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Articles from other publishers (14)

Eugene I. Shorikov, Olena V. Zaliavska, Dina V. Shorikova, Olga M. Nika, Pavlo E. Shorikov & Oksana S. Khukhlina. (2022) ASSOCIATIONS OF POLYMORPHISMS NOS3-T-786C, MTHFR-C667T, P2RY12-T-744C, (GPIBΑ) -C482T AND GENE INTERACTIONS IN MACROANGIOPATHIES IN PATIENTS WITH COMBINED HYPERTENSION AND TYPE DIABETES MELLITUS 2. Wiadomości Lekarskie 75:4, pages 1002-1008.
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Leif Østergaard, Thorbjørn S Engedal, Fiona Moreton, Mikkel B Hansen, Joanna M Wardlaw, Turgay Dalkara, Hugh S Markus & Keith W Muir. (2015) Cerebral small vessel disease: Capillary pathways to stroke and cognitive decline. Journal of Cerebral Blood Flow & Metabolism 36:2, pages 302-325.
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B. V. Titov, N. A. Matveeva, M. Yu. Martynov & O. O. Favorova. (2015) Ischemic stroke as a complex polygenic disease. Molecular Biology 49:2, pages 195-216.
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Aysun Türkanoğlu ÖzçelikBirsen Can DemirdöğenŞeref DemirkayaOrhan Adalı. (2014) Importance of NOS3 Genetic Polymorphisms in the Risk of Development of Ischemic Stroke in the Turkish Population. Genetic Testing and Molecular Biomarkers 18:12, pages 797-803.
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Xiaolong Guo. (2014) Endothelial nitric oxide (eNOS) gene G894T and VNTR polymorphisms are closely associated with the risk of ischemic stroke development for Asians: meta-analysis of epidemiological studies. Molecular Biology Reports 41:4, pages 2571-2583.
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Ying-shui Yao, Wei-wei Chang, Yue-long Jin & Lian-ping He. (2013) An updated meta-analysis of endothelial nitric oxide synthase gene: Three well-characterized polymorphisms with ischemic stroke. Gene 528:2, pages 84-92.
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P.-P. Niu, G. Yang, B.-K. Zheng, Z.-N. Guo, H. Jin & Y. Yang. (2013) Relationship between endothelial nitric oxide synthase gene polymorphisms and ischemic stroke: a meta-analysis. Acta Neurologica Scandinavica 128:3, pages 202-212.
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Meiyun Wang, Xiubo Jiang, Wenlong Wu & Dongfeng Zhang. (2013) Endothelial NO Synthase Gene Polymorphisms and Risk of Ischemic Stroke in Asian Population: A Meta-Analysis. PLoS ONE 8:3, pages e60472.
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MEIYUN WANG, XIUBO JIANG, WENLONG WU & DONGFENG ZHANG. (2013) Association of G894T polymorphism in endothelial nitric oxide synthase gene with the risk of ischemic stroke: A meta-analysis. Biomedical Reports 1:1, pages 144-150.
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Lea M. Beaulieu & Jane E. Freedman. 2013. Platelets. Platelets 313 342 .
F. Parveen, R.M. Faridi, S. Alam & S. Agrawal. (2011) Genetic analysis of eNOS gene polymorphisms in association with recurrent miscarriage among North Indian women. Reproductive BioMedicine Online 23:1, pages 124-131.
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Claudia S. RobertsonShankar P. GopinathAlex B. ValadkaMai VanPaul R. SwankJ. Clay Goodman. (2011) Variants of the Endothelial Nitric Oxide Gene and Cerebral Blood Flow after Severe Traumatic Brain Injury. Journal of Neurotrauma 28:5, pages 727-737.
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Melih O. Babaoglu, Neslihan Dikmenoglu, Esin Ileri-Gurel, Nurten Seringec, Teuta Zoto, Umit Yasar, S. Oguz Kayaalp & Atilla Bozkurt. (2011) Functional Effects of Endothelial Nitric Oxide Synthase Genetic Polymorphisms on Haemorheological Parameters in Healthy Human Individuals. Basic & Clinical Pharmacology & Toxicology 108:3, pages 171-176.
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X Li, J An, R Guo, Z Jin, Y Li, Y Zhao, F Lu, H Lian, P Liu, Y Zhao & X Jin. (2010) Association of the genetic polymorphisms of the ACE gene and the eNOSgene with lupus nephropathy in northern Chinese population. BMC Medical Genetics 11:1.
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