首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Genomic instability of human aberrant crypt foci measured by inter-(simple sequence repeat) PCR and array-CGH.
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Genomic instability of human aberrant crypt foci measured by inter-(simple sequence repeat) PCR and array-CGH.

机译:通过内部(简单序列重复)PCR和array-CGH测量的人类异常隐窝灶的基因组不稳定性。

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摘要

Aberrant crypt foci (ACF) are the earliest identifiable neoplastic lesions in the colon. Thirty-two ACFs were examined for genomic instability in forms detectable either by inter-(simple sequence repeat) PCR or by array comparative genomic hybridization [array-CGH]. One-fourth of ACFs revealed moderate instability by inter-(simple sequence repeat) PCR; none showed amplifications or deletions on array-CGH. The absence of genomic events detectible by BAC array-CGH indicates early events in colorectal tumor progression are typically smaller than the approximate 150 kb size of a BAC clone insert.
机译:隐窝灶(ACF)是结肠中最早可识别的肿瘤性病变。检查了32个ACF的基因组不稳定性,其形式可通过内部(简单序列重复)PCR或通过阵列比较基因组杂交[array-CGH]检测到。 ACF的四分之一通过间(简单序列重复)PCR显示出中等程度的不稳定性;没有显示在阵列-CGH上的扩增或缺失。 BAC阵列-CGH无法检测到基因组事件,这表明大肠肿瘤进展中的早期事件通常小于BAC克隆插入片段的大约150 kb。

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