Generation of an ICF syndrome model by efficient genome editing of human induced pluripotent stem cells using the CRISPR system
Genome manipulation of human induced pluripotent stem (iPS) cells is essential to achieve their full potential as tools for regenerative medicine. To date, however, gene targeting in human pluripotent stem cells (hPSCs) has proven to be extremely difficult. Recently, an efficient genome manipulation...
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Veröffentlicht in: | International journal of molecular sciences 2013-09, Vol.14 (10), p.19774-19781 |
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Sprache: | eng |
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