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Somatic microindels in human cancer: the insertions are highly error-prone and derive from nearby but not adjacent sense and antisense templates

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成果类型:
期刊论文
作者:
Scaringe, William A.;Li, Kai;Gu, Dongqing;Gonzalez, Kelly D.;Chen, Zhenbin;...
通讯作者:
Sommer, Steve S.
作者机构:
[Sommer, Steve S.] City Hope Natl Med Ctr, Beckman Res Inst, Dept Mol Genet, Duarte, CA 91010 USA.
[Li, Kai] Nanhua Univ, SNP Inst, Hengyang, Hunan, Peoples R China.
[Hill, Kathleen A.] Univ Western Ontario, Dept Biol, London, ON N6A 5B7, Canada.
[Sommer, Steve S.] City Hope Natl Med Ctr, Beckman Res Inst, Dept Mol Genet, 1500 E Duarte Rd, Duarte, CA 91010 USA.
通讯机构:
[Sommer, Steve S.] C
City Hope Natl Med Ctr, Beckman Res Inst, Dept Mol Genet, 1500 E Duarte Rd, Duarte, CA 91010 USA.
语种:
英文
期刊:
HUMAN MOLECULAR GENETICS
ISSN:
0964-6906
年:
2008
卷:
17
期:
18
页码:
2910-2918
基金类别:
NIH [R01AG19784]
机构署名:
本校为其他机构
院系归属:
药学与生物科学学院
摘要:
Somatic microindels (microdeletions with microinsertions) have been studied in normal mouse tissues using the Big Blue lacI transgenic mutation detection system. Here we analyze microindels in human cancers using an endogenous and transcribed gene, the TP53 gene. Microindel frequency, the enhancement of 1–2 microindels and other features are generally similar to that observed in the non-transcribed lacI gene in normal mouse tissues. The current larger sample of somatic microindels reveals recurroids: mutations in which deletions are identical ...

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