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Amenable epigenetic traits of dental pulp stem cells underlie high capability of xeno free episomal reprogramming

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Figure

Table 1 Primer sequences used for quantitative polymerase chain reaction analysis
Fig. 1 Generation of clinically compatible DPSC-derived iPS cells using virus-free, xeno-free, and feeder-free approaches.of DiPS generation under xeno-free conditions and using small molecules.feeder-free conditions at post-transduction days (d)7 (i), d13
Table 2 Reprogramming efficiencies of DPSCs cultured underxeno-free and feeder-free conditions
Fig. 2 Pluripotent characterisation of clinically compatible DPSC-derived iPS cells using virus-free, xeno-free, and feeder-free approaches.pluripotency-related genes and mesenchymal genes of the H1 hES and DiPS cells relative to their isogeneic somatic ce
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