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. 2015 Apr 7;10(4):e0121567. doi: 10.1371/journal.pone.0121567

Fig 7. Expression of microRNA-210 and raptor mRNA in erythroid precursor cells.

Fig 7

Quantification by RT-qPCR of microRNA-210 (A, C) and raptor mRNA (B, D) in 9 healthy donors (US) (A, B) and 9 β-thalassemia patients (Th) (C, D). The untreated ErPC samples are depicted as circles and the treated (30 nM MTH) as squares; samples from a same subject are identified by the same color. Means and standard deviations are reported. RT-qPCR analysis was performed after four days of erythroid differentiation. MicroRNA-let-7c (equally expressed in these samples) and 18S were used as internal reference genes to normalize RNA input.