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- W2479215566 endingPage "309" @default.
- W2479215566 startingPage "298" @default.
- W2479215566 abstract "The ability to reprogram somatic cells into induced pluripotent stem cells (iPSCs) using defined factors provides new tools for biomedical research. However, some iPSC clones display tumorigenic and immunogenic potential, thus raising concerns about their utility and safety in the clinical setting. Furthermore, variability in iPSC differentiation potential has also been described. Here we discuss whether these therapeutic obstacles are specific to transcription-factor-mediated reprogramming or inherent to every cellular reprogramming method. Finally, we address whether a better understanding of the mechanism underlying the reprogramming process might improve the fidelity of reprogramming and, therefore, the iPSC quality." @default.
- W2479215566 created "2016-08-23" @default.
- W2479215566 creator A5008637727 @default.
- W2479215566 creator A5078962332 @default.
- W2479215566 date "2016-09-01" @default.
- W2479215566 modified "2023-10-16" @default.
- W2479215566 title "Molecular Obstacles to Clinical Translation of iPSCs" @default.
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