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Genetic variation in microRNA networks: The implications for cancer research

机译:microRNA网络中的遗传变异:对癌症研究的意义

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There were several mistakes in TABLES 1-3 of this article. In TABLE Ion page 385, for rs2910164 in hepatocelluar carcinoma the odds ratio data refer to males only. For rsll614913 in lung cancer the odds ratio is for both sexes and not for males only. Forrsll614913 in oesophageal cancer the reference genotype should be CC/CT and the analysed genotype should be TT. For rsll614913 in breast cancer the reference genotype should be CC and the analysed genotypes should be CT and then TT. For rs895819 in breast cancer the reference genotype should be CT. In TABLE 2 on page 396, for the SEDT8 alleles, the miRNA binds the derived alleles and not the ancestral alleles. For the BCTRP allele, the miRNA binds deletion alleles that are derived and not insertion alleles that are ancestral. For the BMPR1B allele, the miRNA binds the C allele and not the derived allele. For the CDS6 allele, the miRNA binds the ancestral allele and not the derived allele. In TABLE 3 on page 398, the odds ratio given for CEM/N4 rs7813 is for all cases of renal cell carcinoma, not just clear cell carcinoma as indicated. For CEMIN3 rsl97414 the cancer site should be bladder and not renal cell carcinoma and the reference is 35 and not 111. This has been corrected online.
机译:本文的表1-3中存在几个错误。在表离子第385页中,对于肝细胞癌中的rs2910164,比值比数据仅针对男性。对于rsll614913的肺癌,男女的比值比不仅是男性。食管癌的Forrsll614913参考基因型应为CC / CT,分析基因型应为TT。对于rsll614913的乳腺癌,参考基因型应为CC,分析的基因型应为CT,然后为TT。对于乳腺癌中的rs895819,参考基因型应为CT。在第396页的表2中,对于SEDT8等位基因,miRNA结合衍生的等位基因,而不结合祖先等位基因。对于BCTRP等位基因,miRNA结合衍生的缺失等位基因,而不是祖先的插入等位基因。对于BMPR1B等位基因,miRNA结合C等位基因,而不结合衍生等位基因。对于CDS6等位基因,miRNA结合祖先等位基因,而不结合衍生等位基因。在第398页的表3中,CEM / N4 rs7813的比值比适用于所有肾细胞癌病例,而不仅仅是所示的透明细胞癌。对于CEMIN3 rsl97414,癌症部位应为膀胱而非肾细胞癌,参考文献为35而并非111。此问题已在线纠正。

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