Germline acquisition of Cas9/RNA-mediated gene modifications in monkeys.
作者信息
Chen Yongchang, Cui Yiqiang, Shen Bin, Niu Yuyu, Zhao Xiaoyang, Wang Lei, Wang Jianying, Li Wei, Zhou Qi, Ji Weizhi, Sha Jiahao, Huang Xingxu
机构信息
1] Yunnan Key Laboratory of Primate Biomedical Research, Kunming, Yunnan 650500, China [2] Kunming Biomed International and National Engineering Research Center of Biomedicine and Animal Science, Kunming, Yunnan 650500, China [3] Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan 650224, China.
State Key Laboratory of Reproductive Medicine, Department of Histology and Embryology, Nanjing Medical University, Nanjing, Jiangsu 210029, China.
出版信息
Cell Res. 2015 Feb;25(2):262-5. doi: 10.1038/cr.2014.167. Epub 2014 Dec 23.
Abstract
摘要
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本文引用的文献
1
CRISPR-Cas systems for editing, regulating and targeting genomes.用于编辑、调控和靶向基因组的CRISPR-Cas系统。
Nat Biotechnol. 2014 Apr;32(4):347-55. doi: 10.1038/nbt.2842. Epub 2014 Mar 2.
2
TALEN-mediated gene mutagenesis in rhesus and cynomolgus monkeys.TALEN介导的恒河猴和食蟹猴基因诱变。
Cell Stem Cell. 2014 Mar 6;14(3):323-328. doi: 10.1016/j.stem.2014.01.018. Epub 2014 Feb 13.
3
Generation of gene-modified cynomolgus monkey via Cas9/RNA-mediated gene targeting in one-cell embryos.通过 Cas9/RNA 介导的基因靶向在单细胞胚胎中生成基因修饰的食蟹猴。
Cell. 2014 Feb 13;156(4):836-43. doi: 10.1016/j.cell.2014.01.027. Epub 2014 Jan 30.
4
Precision gene editing paves way for transgenic monkeys.精准基因编辑为转基因猴子铺平了道路。
Nature. 2013 Nov 7;503(7474):14-5. doi: 10.1038/503014a.
5
Progress and prospects for genetic modification of nonhuman primate models in biomedical research.生物医学研究中非人类灵长类动物模型基因改造的进展与前景。
ILAR J. 2013;54(2):211-23. doi: 10.1093/ilar/ilt035.
6
Cas9 as a versatile tool for engineering biology.Cas9 作为一种通用的基因编辑工具。
Nat Methods. 2013 Oct;10(10):957-63. doi: 10.1038/nmeth.2649.
7
The available time window for embryo transfer in the rhesus monkey (Macaca mulatta).恒河猴（Macaca mulatta）胚胎移植的可用时间窗口。
Am J Primatol. 2012 Feb;74(2):165-73. doi: 10.1002/ajp.21017.
8
Transgenic rhesus monkeys produced by gene transfer into early-cleavage-stage embryos using a simian immunodeficiency virus-based vector.用基于猴免疫缺陷病毒的载体将基因转移到早期胚胎中，从而产生转基因恒河猴。
Proc Natl Acad Sci U S A. 2010 Oct 12;107(41):17663-7. doi: 10.1073/pnas.1006563107. Epub 2010 Sep 24.
9
MVH in piRNA processing and gene silencing of retrotransposons.MVH 在 piRNA 加工和逆转座子的基因沉默中的作用。
Genes Dev. 2010 May;24(9):887-92. doi: 10.1101/gad.1902110.
10
Generation of transgenic non-human primates with germline transmission.可进行种系传递的转基因非人灵长类动物的产生。
Nature. 2009 May 28;459(7246):523-7. doi: 10.1038/nature08090.
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