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To identify the direct target genes of EWS/WT1 −KTS), we have previously performed expression profiling analysis with an inducible cell line expressing EWS/WT1 −KTS) [23].
Given that the transcription factor NRL determines rod cell fate, we performed expression profiling of developing NRL-positive (rods) and NRL-negative (S-cone-like) mouse photoreceptors.
Furthermore, we performed expression profiling of identified genes.
To determine their expression patterns, we first performed expression analyses with transcriptional fusion genes.
Few studies have performed expression profiling of both miRNA and mRNA from the same primary breast carcinomas.
To obtain more quantitative information about the level of Wnt signaling, we performed expression profiling of Wnt pathway components in PDA with genechip microarray.
We confirmed 354 miRNA genes using miRNA microarrays and then performed expression profile analysis on these miRNAs for all developmental stages.
We performed expression profile analysis in five different conditions using a tiling array, in which we excluded repetitive regions and small untranslated regions (UTRs) from our analysis.
We performed expression profiling using Affymetrix whole human genome Gene Chips on infected cells incubated in the absence or presence of 30 µM LA for 60 hrs.
Three studies have performed expression analysis with microarrays using RNA extracted from peripheral blood monocytes (PBMCs) with the purpose of predicting response [13], [14], [15].
KD performed expression analyses.
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