15 research outputs found
Estrogen receptor 1 gene polymorphisms and coronary artery disease in the Brazilian population
Full text linkCoronary artery wall atherosclerosis in relation to the estrogen receptor 1 gene polymorphism: an autopsy study.
No full textPolymorphsims within the tumor necrosis factor locus and prevance of coronary artery disease in middle-aged men
No full textA functional variant of the iNOS gene flanking region is associated wirh LAD coronary artery disease: an autopsy study.
No full textMyeloperoxidase gene variation as a determinant of atherosclerosis progression in the abdominal and thoracic aorta: an autopsy study.
No full textAssociation of the endothelial nitric oxide synthase gene polymorphism with risk of coronary artery disease and myocardial infarction in middle-aged men.
No full textInfluence of genetic polymorphisms on bone disease of preterm infants.
No full textContains fulltext :
50866.pdf (publisher's version ) (Closed access)Bone disease is an important complication among very low birth weight (VLBW, 18] [odds ratio (OR): 0.17, 95% confidence interval (CI): 0.05-0.55]. A low number of repeats [(TA)(n) <19] was found more frequently in infants suffering from bone disease (OR: 6.00, 95% CI: 1.77-20.31). Significant interaction (p = 0.009) between VDR and COLIA1 genotypes was observed. In a logistic regression model, bone disorder of preterms significantly correlated with male gender (p = 0.002), lower gestational age (p = 0.015), homozygous allelic variants of high number of (TA)(n) repeats (p = 0.006), and interaction between VDR and COLIA1 genotype (p = 0.009)
Association between a dinucleotide repeat polymorphism of the estrogen receptor alpha gene and personality traits in women
No full textEndothelial nitric oxide synthase gene polymorphism is associated with sickle cell disease patients in India
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