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中国儿童PECAM-1基因多态性与川崎病的关联

Association of PECAM-1 Gene Polymorphisms with Kawasaki Disease in Chinese Children.

作者信息

Li Zhuoying, Han Dong, Jiang Jie, Chen Jia, Tian Lang, Yang Zuocheng

机构信息

Department of Pediatrics, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, China.

出版信息

Dis Markers. 2017;2017:2960502. doi: 10.1155/2017/2960502. Epub 2017 Apr 23.

DOI:10.1155/2017/2960502
PMID:28512385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5420431/
Abstract

Kawasaki disease (KD) is an acute systemic vasculitis complicated by development of coronary artery lesions. PECAM-1 is a kind of cell adhesion molecule, which plays an important role in coronary artery disease. The relationship between PECAM-1 gene polymorphisms and their susceptibility to Kawasaki diseases (KD) is still unclear. In our study, we examined the PECAM-1 gene polymorphisms in 44 KD patients and 59 healthy children and revealed the correlation of PECAM-1 gene polymorphisms in KD children with and without coronary artery lesions (CAL).

摘要

川崎病(KD)是一种急性全身性血管炎,可并发冠状动脉病变。血小板内皮细胞黏附分子-1(PECAM-1)是一种细胞黏附分子,在冠状动脉疾病中起重要作用。PECAM-1基因多态性与其对川崎病(KD)的易感性之间的关系仍不清楚。在我们的研究中,我们检测了44例KD患者和59例健康儿童的PECAM-1基因多态性,并揭示了KD患儿有无冠状动脉病变(CAL)时PECAM-1基因多态性的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2131/5420431/42dc70b77183/DM2017-2960502.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2131/5420431/5586fbabdf24/DM2017-2960502.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2131/5420431/42dc70b77183/DM2017-2960502.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2131/5420431/5586fbabdf24/DM2017-2960502.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2131/5420431/42dc70b77183/DM2017-2960502.002.jpg

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本文引用的文献

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Balkan J Med Genet. 2016 Aug 2;19(1):63-70. doi: 10.1515/bjmg-2016-0008. eCollection 2016 Jul 1.
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Roles of PECAM-1 in cell function and disease progression.血小板内皮细胞粘附分子-1在细胞功能和疾病进展中的作用。
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Association of miR-146a Gene Polymorphism at loci rs2910164 G/C, rs57095329 A/G, and rs6864584 T/C with Susceptibility to Kawasaki Disease in Chinese Children.中国儿童中,miR-146a基因rs2910164 G/C、rs57095329 A/G和rs6864584 T/C位点多态性与川崎病易感性的关联。
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