Figure 5.
Relative transcriptional levels of miR-146a in CD34+-derived erythroid cells, as evaluated by quantitative reverse-transcription PCR (qRT-PCR). Taqman qRT-PCR was used to evaluate the levels of miR-146a. Controls = CTRL (n = 3); subjects heterozygous for HPFH-2 = HPFH-2 (n = 2); patients heterozygous for Sicilian δβ-thalassemia = DB-Thal (n = 2)