A single nucleotide polymorphism at the splice donor site of the human MYH base excision repair gene results in reduced translation efficiency of its transcripts

A single nucleotide polymorphism at the splice donor site of the human MYH base excision repair gene results in reduced translation efficiency of its transcripts
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人MYH碱基切除修复基因剪接供体位点的单核苷酸多态性导致其转录本翻译效率降低

DOI:
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发表时间:
2002
期刊:
影响因子:
2.1
通讯作者:
J. Yokota
J. Yokota
中科院分区:
生物学4区
文献类型:
--
作者:
S. Yamaguchi;K. Shinmura;T. Saitoh;S. Takenoshita;H. Kuwano;J. Yokota

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背景资料:腺嘌呤与8-羟基鸟嘌呤配对,是一种主要的氧化损伤DNA损伤,在人类细胞中被mutY同源物(MYH)碱基切除修复蛋白切除。由于DNA修复基因的遗传多态性与其产物的活性和表达水平相关,可能会调节个体的癌症易感性,因此我们研究了MYH基因中单核苷酸多态性(SNP)对其产物表达水平差异的影响。
Background: Adenine paired with 8‐hydroxyguanine, a major oxidatively damaged DNA lesion, is excised by mutY homologue (MYH) base excision repair protein in human cells. Since genetic polymorphisms of DNA repair genes associated with the activities and the expression levels of their products may modulate cancer susceptibility of individuals, we investigated the effect of a single nucleotide polymorphism (SNP) in the MYH gene on the difference in the expression levels of its products.
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影响因子: 11.1
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