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Association between polymorphisms of prokineticin receptor(PKR1 rs4627609 and PKR2 rs6053283) and recurrent pregnancy loss 被引量:1

前动力蛋白受体(PKR1 rs4627609和PKR2 rs6053283)的多态性与复发性流产的关系(英文)
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摘要 Recurrent pregnancy loss (RPL) is a condition with complex etiologies, to which both genetic and envi- ronmental factors may contribute. During the last decade, studies indicated that the expression patterns of the pro- kineticin receptor (PKR1 and PKR2) are closely related to early pregnancy. However, there are few studies on the role of PKR1 and PKR2 in RPL. In this study, we purpose to investigate the association between polymorphisms of the prokineticin receptor (PKR1 rs4627609 and PKR2 rs6053283) and RPL on a group of 93 RPL cases and 169 healthy controls. Genotyping of the single nucleotide polymorphisms (SNPs) was performed using a Sequenom MassARRAY iPLEX system. The results revealed a significant association between PKR2 rs6053283 polymorphism and RPL (P=0.003), whereas no association was observed between PKR1 rs4627609 polymorphism and RPL (P=-0.929) in the Chinese Han population. 目的:研究前动力蛋白受体PKR1 rs4627609和PKR2rs6053283的多态性与复发性流产的关系,并对其可能的作用机制进行预测。创新点:首次在中国汉族人群中进行前动力蛋白受体PKR1 rs4627609和PKR2 rs6053283的多态性与复发性流产关系的研究,并对其功能进行预测。方法:共收集了93例复发性流产和169例健康对照者血液样本,提取基因组DNA,对PKR1 rs4627609和PKR2 rs6053283两个位点进行基因多态性分析,在两组样本中分析不同基因型与复发性流产的关系,并对PKR2 rs6053283位点的不同等位基因进行生物功能预测。结论:PKR2 rs6053283的多态性与复发性流产相关;而PKR1 rs4627609的多态性与复发性流产之间不存在相关性。
出处 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2016年第3期218-224,共7页 浙江大学学报(英文版)B辑(生物医学与生物技术)
基金 Project supported by the National Natural Science Foundation of China(No.81571503)
关键词 Prokineticin receptor 1 (PKR1) PKR2 POLYMORPHISM Recurrent pregnancy loss 前动力蛋白受体1 前动力蛋白受体2 多态性 复发性流产
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  • 1Lewontin R. On measures of gametic disequilibrium. Genetics 1988; 120:849-52. 被引量:1
  • 2Chen WY, Shi YY, Zheng YL, et al. Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8. Hum Mol Genet 2004; 13:2991-5. 被引量:1
  • 3Shi Y, Zhao X, Yu L, et al. Genetic structure adds power to detect schizophrenia susceptibility at SLIT3 in the Chinese Han population. Genome Res 2004; 14:1345-9. 被引量:1
  • 4Zhao X, Shi Y, Tang J, et al. A case control and family based association study of the neuregulinl gene and schizophrenia. J Med Genet 2004; 41:31-4. 被引量:1
  • 5Guo S, Shi Y, Zhao X, et al. No genetic association between polymorphisms in the AMPA receptor subunit GluR4 gene (GRIA4) and schizophrenia in the Chinese population. Neurosci Lett 2004; 369:168-72. 被引量:1
  • 6Yang MS, Yu L, Guo TW, et al. Evidence for association between single nucleotide polymorphisms in T complex protein 1 gene and schizophrenia in the Chinese Han population. J Med Genet 2004; 41:e63. 被引量:1

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