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Although MSCs can be greatly expanded in vitro and induced to differentiate into multiple mesenchymal cell types, however, differentiation to nonmesenchymal fate has been demonstrated.
However, differentiation to contracting cardiomyocytes was very rare, and instead we frequently observed cells with neural morphology, particularly when extending the differentiation cultures beyond two weeks.
However, differentiation of true odontoblasts is still more speculative, and the approach is largely limited to immature teeth with open apices.
However, differentiation would have been faster if residual variation had been simulated.
Treatment of mice with BF increased tumor uptake of [125I]IBG by 56%; however, differentiation of tumors with and without AGT still was not possible.
However, differentiation of RPE cells from iPSCs is inefficient, time-consuming, and variable among different iPSC lines (Buchholz et al., 2009).
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However, late differentiation timepoints produce statistically significant hierarchies that reflect cell-state diversity along the differentiation process (Supplementary Text).
However, the differentiation from PAB to SAB is likely controlled by a precise molecular network like most cell differentiation processes.
However, robust differentiation into specific lineages remains a stumbling block.
However, marketing differentiation is less effective.
However, the differentiation potential was lost in these cells.
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