Table 4.

Abnormal gene expression pattern detected in MDS: differentiation associated

DescriptionMDS1 fold changeMDS2 fold changeMDS3 fold changeMDS4 fold changeMDS5 fold change
α-globin3-150 −10.8 −100 — — −2.57 
β-globin −3.86 −89.3 — — −2.32 
δ-globin3-150 −5.34 −25.5 — — −2.11 
CAI −27.01 −103 — — −5.84 
Ad08c04 −2.00 −3.99 — — −1.65 
CD36 −7.95 — — — −4.32 
Actin — 1.72 −1.49 — — 
ERF-1 — 3.88 — — — 
TCTP3-150 — 1.75 — — — 
DescriptionMDS1 fold changeMDS2 fold changeMDS3 fold changeMDS4 fold changeMDS5 fold change
α-globin3-150 −10.8 −100 — — −2.57 
β-globin −3.86 −89.3 — — −2.32 
δ-globin3-150 −5.34 −25.5 — — −2.11 
CAI −27.01 −103 — — −5.84 
Ad08c04 −2.00 −3.99 — — −1.65 
CD36 −7.95 — — — −4.32 
Actin — 1.72 −1.49 — — 
ERF-1 — 3.88 — — — 
TCTP3-150 — 1.75 — — — 

Abnormal gene expression pattern in differentiation-associated category. Average MDS (Cy3) signal intensities for each gene (spotted 4 times per MDS chip) were compared with the mean NBM (Cy3) signal intensities from 40 spots (10 NBM chips × 4 spots per chip). The fold change in MDS mean Cy3 intensity compared with NBM Cy3 intensity for each chip is shown. Abnormal gene expression is defined as a mean MDS Cy3 intensity at least 2 SDs from the mean of the corresponding mean NBM Cy3 intensity.

F3-150

Genes that demonstrated a significant shift in the K562 signal intensity that correlated with shifts in MDS-probed intensities (K562 and MDS shifts in opposite directions) like those demonstrated in Figure 4. Other MDS interchip variations in K562 signal intensities were not statistically significant.

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