Single nucleotide polymorphisms

Polymorphisms in the vascular endothelial growth factor (VEGF) gene associated with asthma

H. Y. Lu, Zhao, G. L., Fu, M. F., Lu, H. Y., Zhao, G. L., and Fu, M. F., Polymorphisms in the vascular endothelial growth factor (VEGF) gene associated with asthma, vol. 15, p. -, 2016.

It has been proven that vascular endothelial growth factor (VEGF) is involved in airway restoration and the development of asthma. We sought to examine the relevance of VEGF gene polymorphisms to asthma in the Chinese Han population. We extracted the whole genomic DNA from the peripheral blood of 471 participants, including 226 patients with asthma and 245 healthy controls. Seven single nucleotide polymorphisms (SNPs) of the VEGF gene were genotyped using the MassARRAY system. The data were then analyzed using HaploView 4.0 and SPSS 20.0 softwares.

Association study between matrix metalloproteinase-9 gene (MMP9) polymorphisms and the risk of Henoch-Schönlein purpura in children

E. D. Xu, Xiao, Y. F., Wang, J. J., Dong, L., Xu, E. D., Xiao, Y. F., Wang, J. J., and Dong, L., Association study between matrix metalloproteinase-9 gene (MMP9) polymorphisms and the risk of Henoch-Schönlein purpura in children, vol. 15, p. -, 2016.

Henoch-Schönlein purpura nephritis (HSPN), the most serious long-term complication of Henoch-Schönlein purpura, is one of the most common renal diseases in children. Matrix metalloproteinase-9 (MMP-9) is implicated in the pathogenesis of renal diseases. Genomic DNA was isolated from the venous blood leukocytes of 220 unrelated patients with HSPN and 205 unrelated healthy individuals.

Association between NOS3 genetic variants and coronary artery disease in the Han population

G. L. Zhao, Li, Q. J., Lu, H. Y., Zhao, G. L., Li, Q. J., and Lu, H. Y., Association between NOS3 genetic variants and coronary artery disease in the Han population, vol. 15, p. -, 2016.

The enzyme endothelial nitric oxide synthase (NOS3) is an important mediator of atherosclerotic disease and is associated with coronary artery disease (CAD). There is growing evidence that polymorphisms in NOS3 influence the progression of CAD; however, there is also a controversy regarding the association of polymorphisms in the gene encoding NOS3 and CAD.

Correlation between polymorphisms in the visfatin gene and its expression in the serum and coronary artery calcification

L. W. Jin, Zheng, S. B., Zhou, Z. H., Pan, S. F., Zheng, Y., Jin, L. W., Zheng, S. B., Zhou, Z. H., Pan, S. F., and Zheng, Y., Correlation between polymorphisms in the visfatin gene and its expression in the serum and coronary artery calcification, vol. 15, p. -, 2016.

We investigated the association between serum visfatin levels and single nucleotide polymorphisms (SNPs; rs61330082, rs2058539) in the visfatin gene and coronary artery calcification (CAC) in patients from Wenzhou, China. CAC patients (N = 206) were divided into two groups: mild CAC (MCAC) and moderate and severe CAC (MSCAC). Volunteers without CAC (N = 70) were included in the control group. The serum visfatin level was analyzed by enzyme-linked immunosorbent assay.

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