Figure 5
Figure 5. Expression profiling in R174Q and R139X RUNX1 mutated patients CD34+ cells. Expression fold-change analysis of genes selected from array data (supplemental Table 2) in independent samples by Q-PCR. RNA was directly extracted and reverse-transcribed from sorted CD34+ cells obtained from AII-1, AII-2 (R174Q mutation) and BI-1, BII-2 (R139X mutation) patients and healthy donors peripheral blood. Gene expression was normalized to 18S and results are expressed as fold changes related to healthy control.

Expression profiling in R174Q and R139X RUNX1 mutated patients CD34+ cells. Expression fold-change analysis of genes selected from array data (supplemental Table 2) in independent samples by Q-PCR. RNA was directly extracted and reverse-transcribed from sorted CD34+ cells obtained from AII-1, AII-2 (R174Q mutation) and BI-1, BII-2 (R139X mutation) patients and healthy donors peripheral blood. Gene expression was normalized to 18S and results are expressed as fold changes related to healthy control.

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