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首页> 外文期刊>Leukemia and lymphoma >Absence of somatic hypermutation in the open reading frame of the bcl-2 gene participating in the t(14;18) chromosomal translocation in follicular lymphoma.
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Absence of somatic hypermutation in the open reading frame of the bcl-2 gene participating in the t(14;18) chromosomal translocation in follicular lymphoma.

机译:bcl-2基因的开放阅读框中参与滤泡性淋巴瘤的t(14; 18)染色体易位的体细胞高突变的缺乏。

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摘要

The information concerning potential effects of somatic hypermutation on bcl-2 sequences translocated to the immunoglobulin heavy chain gene (IgH) locus in follicular lymphoma (FL) is rather limited. We analysed the complete open reading frame (ORF) of the bcl-2 gene for the presence of mutations in 24 bcl-2/IgH-positive diagnostic FL samples by the single strand conformation polymorphism (SSCP) technique. A prior analysis on many of these FL samples had revealed a consistent pattern of somatic hypermutation in IgH genes. Abnormally migrating bands on SSCP gels were identified only in 4/24 samples. This result provides strong support for the notion that in FL the translocated bcl-2 coding region is not targeted by somatic hypermutation.
机译:关于体细胞高突变对滤泡性淋巴瘤(FL)中易位至免疫球蛋白重链基因(IgH)基因座的bcl-2序列的潜在影响的信息相当有限。我们通过单链构象多态性(SSCP)技术分析了24个bcl-2 / IgH阳性诊断性FL样本中bcl-2基因的完整开放阅读框(ORF)突变的存在。对许多此类FL样品的先前分析显示,IgH基因的体细胞超突变具有一致的模式。仅在4/24个样品中发现了SSCP凝胶上的异常迁移带。该结果为以下观点提供了有力的支持:在FL中,易位bcl-2编码​​区域不受体细胞超突变的影响。

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