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1 h an abnormal karyotype that included double minute chromosomes.
2 itial confirmation of the presence of double minute chromosomes.
3 h rearranged sequences present in the double minute chromosomes.
4 plification was localized to unstable double minute chromosomes and was uniquely found in mouse breas
8 xpanded chromosome regions (ECRs) and double minute chromosomes (DMs) that contained chromosome 20 ma
9 a strategy to purify amplified DNA on double minute chromosomes (DMs) to enable analysis of their pre
10 ired acentric chromatin bodies called double minute chromosomes (DMs), which can accumulate to a high
11 cation through chromothripsis-derived double-minute chromosome formation (MYC and MDM2) or breakage-f
12 ements are proposed as mechanisms for double minute chromosome formation and oncogene amplification,
13 ocus on Chromosome 10 responsible for double minute chromosome formation within this interspecific eu
15 ic chromosomes, chromatid breaks, and double minute chromosomes in Klf4(-/-) cells but in few, if any
16 lable, finding evidence for oncogenic double minute chromosomes in more than 20% of clinical specimen
22 cell component (DLLC) that displayed double minute chromosomes upon conventional karyotypic analysis
24 ion of HER2/neu, often in the form of double minute chromosomes, which correlated with recurring loss
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