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Baculoviral transduction facilitates TALEN-mediated targeted transgene integration and Cre/LoxP cassette exchange in human-induced pluripotent stem cells.

Zhu H, Lau CH, Goh SL, Liang Q, Chen C, Du S, Phang RZ, Tay FC, Tan WK, Li Z, Tay JC, Fan W, Wang S.

Nucleic Acids Res. 2013 Oct;41(19):e180. doi: 10.1093/nar/gkt721. Epub 2013 Aug 13.


Targeted transgene insertion into the AAVS1 locus driven by baculoviral vector-mediated zinc finger nuclease expression in human-induced pluripotent stem cells.

Tay FC, Tan WK, Goh SL, Ramachandra CJ, Lau CH, Zhu H, Chen C, Du S, Phang RZ, Shahbazi M, Fan W, Wang S.

J Gene Med. 2013 Oct;15(10):384-95. doi: 10.1002/jgm.2745.


Zinc finger nuclease-expressing baculoviral vectors mediate targeted genome integration of reprogramming factor genes to facilitate the generation of human induced pluripotent stem cells.

Phang RZ, Tay FC, Goh SL, Lau CH, Zhu H, Tan WK, Liang Q, Chen C, Du S, Li Z, Tay JC, Wu C, Zeng J, Fan W, Toh HC, Wang S.

Stem Cells Transl Med. 2013 Dec;2(12):935-45. doi: 10.5966/sctm.2013-0043. Epub 2013 Oct 28.


Efficient recombinase-mediated cassette exchange at the AAVS1 locus in human embryonic stem cells using baculoviral vectors.

Ramachandra CJ, Shahbazi M, Kwang TW, Choudhury Y, Bak XY, Yang J, Wang S.

Nucleic Acids Res. 2011 Sep 1;39(16):e107. doi: 10.1093/nar/gkr409. Epub 2011 Jun 17.


Generation of transgene-free mouse induced pluripotent stem cells using an excisable lentiviral system.

Varga E, Nemes C, Davis RP, Ujhelly O, Klincumhom N, Polgar Z, Muenthaisong S, Pirity MK, Dinnyes A.

Exp Cell Res. 2014 Apr 1;322(2):335-44. doi: 10.1016/j.yexcr.2014.02.006. Epub 2014 Feb 18.


Stable enhanced green fluorescent protein expression after differentiation and transplantation of reporter human induced pluripotent stem cells generated by AAVS1 transcription activator-like effector nucleases.

Luo Y, Liu C, Cerbini T, San H, Lin Y, Chen G, Rao MS, Zou J.

Stem Cells Transl Med. 2014 Jul;3(7):821-35. doi: 10.5966/sctm.2013-0212. Epub 2014 May 15.


Fluorescent labeling and visualization of human induced pluripotent stem cells with the use of transcription activator-like effector nucleases.

Sekine K, Takebe T, Taniguchi H.

Transplant Proc. 2014 May;46(4):1205-7. doi: 10.1016/j.transproceed.2014.02.003.


Chromatin structure of two genomic sites for targeted transgene integration in induced pluripotent stem cells and hematopoietic stem cells.

van Rensburg R, Beyer I, Yao XY, Wang H, Denisenko O, Li ZY, Russell DW, Miller DG, Gregory P, Holmes M, Bomsztyk K, Lieber A.

Gene Ther. 2013 Feb;20(2):201-14. doi: 10.1038/gt.2012.25. Epub 2012 Mar 22.


Baculoviral vector-mediated transient and stable transgene expression in human embryonic stem cells.

Zeng J, Du J, Zhao Y, Palanisamy N, Wang S.

Stem Cells. 2007 Apr;25(4):1055-61.


Improved transgene integration into the Chinese hamster ovary cell genome using the Cre-loxP system.

Inao T, Kawabe Y, Yamashiro T, Kameyama Y, Wang X, Ito A, Kamihira M.

J Biosci Bioeng. 2015 Jul;120(1):99-106. doi: 10.1016/j.jbiosc.2014.11.019. Epub 2015 Jan 22.


DICE, an efficient system for iterative genomic editing in human pluripotent stem cells.

Zhu F, Gamboa M, Farruggio AP, Hippenmeyer S, Tasic B, Schüle B, Chen-Tsai Y, Calos MP.

Nucleic Acids Res. 2014 Mar;42(5):e34. doi: 10.1093/nar/gkt1290. Epub 2013 Dec 4.


Site-specific integration of functional transgenes into the human genome by adeno/AAV hybrid vectors.

Recchia A, Perani L, Sartori D, Olgiati C, Mavilio F.

Mol Ther. 2004 Oct;10(4):660-70.


Establishment of medakafish as a model for stem cell-based gene therapy: efficient gene delivery and potential chromosomal integration by baculoviral vectors.

Yan Y, Du J, Chen T, Yi M, Li M, Wang S, Li CM, Hong Y.

Exp Cell Res. 2009 Aug 1;315(13):2322-31. doi: 10.1016/j.yexcr.2009.04.015. Epub 2009 May 3.


Establishment of transgene-free induced pluripotent stem cells reprogrammed from human stem cells of apical papilla for neural differentiation.

Zou XY, Yang HY, Yu Z, Tan XB, Yan X, Huang GT.

Stem Cell Res Ther. 2012 Oct 24;3(5):43. doi: 10.1186/scrt134.


Targeted transgene insertion into the CHO cell genome using Cre recombinase-incorporating integrase-defective retroviral vectors.

Kawabe Y, Shimomura T, Huang S, Imanishi S, Ito A, Kamihira M.

Biotechnol Bioeng. 2016 Jul;113(7):1600-10. doi: 10.1002/bit.25923. Epub 2016 Feb 7.


Site-specific chromosomal integration in mammalian cells: highly efficient CRE recombinase-mediated cassette exchange.

Feng YQ, Seibler J, Alami R, Eisen A, Westerman KA, Leboulch P, Fiering S, Bouhassira EE.

J Mol Biol. 1999 Oct 1;292(4):779-85.


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