A nonviral minicircle vector for deriving human iPS cells.

A nonviral minicircle vector for deriving human iPS cells.
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DOI:
10.1038/nmeth.1426
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发表时间:
2010-03
期刊:
影响因子:
48
通讯作者:
Wu, Joseph C.
Wu, Joseph C.
中科院分区:
生物学1区
文献类型:
--
作者:
Jia, Fangjun;Wilson, Kitchener D.;Sun, Ning;Gupta, Deepak M.;Huang, Mei;Li, Zongjin;Panetta, Nicholas J.;Chen, Zhi Ying;Robbins, Robert C.;Kay, Mark A.;Longaker, Michael T.;Wu, Joseph C.

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由于插入突变的风险,病毒转导已越来越多地被非病毒方法取代以产生诱导多能干(iPS)细胞。尚未探索的一项技术是使用“小环”DNA,这是一种新型紧凑载体,不含细菌 DNA,能够在细胞中持续高水平表达。在这里,我们报道了使用单个小环载体从成人细胞中产生无转基因的 iPS 细胞。
Due to the risk of insertional mutagenesis, viral transduction has been increasingly replaced by non-viral methods to generate induced pluripotent stem (iPS) cells. One technique that has not yet been explored is the use of “minicircle” DNA, a novel compact vector that is free of bacterial DNA and capable of persistent high level expression in cells. Here, we report the use of a single minicircle vector to generate transgene-free iPS cells from adult human cells.
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