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内皮型一氧化氮合酶/亚甲基四氢叶酸还原酶基因 Glu298Asp/677C-T 单核苷酸多态性与缺血性脑卒中血瘀证的关系。

Association between Glu298Asp/677C-T single nucleotide polymorphism in the eNOS/MTHRF gene and blood stasis syndrome of ischemic stroke.

机构信息

Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing 100700, China.

出版信息

Gene. 2012 Dec 15;511(2):475-9. doi: 10.1016/j.gene.2012.07.084. Epub 2012 Aug 25.

Abstract

Blood stasis syndrome of ischemic stroke (BSS-IS) is a common clinical phenotype that may be affected by certain mutagenic environmental factors or chemotherapeutic drugs; however, the role of susceptibility genes remains unclear. Previous studies have shown that ischemic stroke (IS) was closely associated with the Glu298Asp polymorphism in the eNOS gene and the 677C-T (Ala→Val) polymorphism in methylenetetrahydrofolate reductase (MTHRF) gene. Therefore, these two single nucleotide polymorphisms (SNPs) were selected to detect their associations with BSS-IS in this study. A SNP chip was employed to screen the SNP variation between both groups, and the results were verified using denaturing high-performance liquid chromatography (DHPLC) and restriction fragment length polymorphism (RFLP). The results confirmed that the TT genotype of Glu298Asp in the eNOS gene may be one of the risk factors associated with BSS-IS, while the genotype of 677C-T (Ala→Val) in the MTHRF gene may not be relevant to BSS-IS.

摘要

血瘀证型缺血性脑卒中(BSS-IS)是一种常见的临床表型,可能受到某些诱变环境因素或化疗药物的影响;然而,易感基因的作用仍不清楚。先前的研究表明,缺血性脑卒中(IS)与 eNOS 基因中的 Glu298Asp 多态性和亚甲基四氢叶酸还原酶(MTHFR)基因中的 677C-T(Ala→Val)多态性密切相关。因此,本研究选择这两个单核苷酸多态性(SNP)来检测它们与 BSS-IS 的关联。采用 SNP 芯片筛选两组之间的 SNP 变异,并用变性高效液相色谱(DHPLC)和限制性片段长度多态性(RFLP)验证结果。结果证实,eNOS 基因中 Glu298Asp 的 TT 基因型可能是与 BSS-IS 相关的危险因素之一,而 MTHFR 基因中 677C-T(Ala→Val)的基因型与 BSS-IS 无关。

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