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MTHFR promoter hypermethylation in testicular biopsies of patients with non-obstructive azoospermia: the role of epigenetics in male infertility

机译:非梗阻性无精症患者睾丸活检中MTHFR启动子甲基化过高:表观遗传学在男性不育症中的作用

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摘要

BACKGROUND The causative mechanisms of male infertility are still poorly understood. Mutations in the Methylenetetrahydrofolate reductase (MTHFR) gene have been shown to be involved in male infertility; however, other mechanisms of pathogenesis, like promoter hyper-methylation, could also play a role. Therefore, in this study we compared the methylation status of the promoter region of MTHFR in male patients with non-obstructive azoospermia (NOA) and obstructive azoospermia without anomalies of spermatogenesis.
机译:背景技术关于男性不育的病因机制仍知之甚少。亚甲基四氢叶酸还原酶(MTHFR)基因的突变已被证明与男性不育有关;然而,其他发病机制,如启动子甲基化过高,也可能起作用。因此,在这项研究中,我们比较了患有非阻塞性无精子症(NOA)和无精子发生异常的阻塞性无精子症的男性患者中MTHFR启动子区域的甲基化状态。

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  • 来源
    《Human Reproduction》 |2009年第9期|p.2361-2364|共4页
  • 作者单位

    1Department of Medical Genetics and Hematology, Tarbiat Modares University, Tehran, Iran 2Sarem Cell Research Center (SCRC), Tehran, Iran 3Service de Génétique Médicale, Inserm 896, CHU de Arnaud-de-Villeneuve, 371, avenue du Doyen-Gaston-Giraud, 34295 Montpellier Cedex, France;

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