Using our microarray data, we confirmed that the expression of this gene is not significantly different among the groups.
Using microarray data, we verified that 102 of 328 genes commonly upregulate in hESCs.
Using circRNA microarray data, we compared the circRNA expression profiles in lung tissues between these 6 rats.
By analyzing the microarray data, we found that the expression of EPB41L4A-AS2 wasignificantlylowerwer (Student's t-test, P = 0.042, Fig. 5D) in the resistant group than the non-resistant group.
To further confirm the microarray data, we performed real-time PCR analysis.
METHODS: Using in vitro drug sensitivity data, coupled with microarray data, we developed gene expression signatures predicting sensitivity to cisplatin and pemetrexed.
In order to confirm and extend the microarray data, we used quantitative RT-PCR.
Based upon microarray data, we first evaluate the correlation between genes and the phenotype response.
To corroborate the AMFR microarray data, we followed up by Western blot analysis.
To independently assess the microarray data, we conducted QPCR on RNA from purified spermatocytes and spermatids.
To validate these microarray data, we next performed real-time PCR on selected gene targets.
