To predict whether GPCRs in hES or hiPS cells are expressed, sufficiently above background we compared expression in these cells to other tissues.
To identify microRNAs that are aberrantly expressed in MM patient samples we compared expression levels with controls by ANOVA.
To establish whether the differentially expressed genes in each experiment were coordinately regulated, we compared expression ratios using cluster analysis.
Next, we transfected the pCI-β-cat plasmid expressing wt-β-catenin or mock control into KYSE140 cells and compared expression levels of PK-M2 and PDH.
The COXEN algorithm compared expression patterns among candidate genes between the two sets to find concordantly expressed genes between them.
We first compared expression profiles between the GMR-Gal4 × w1118 control and hINSWT- and hINSC96Y-expressing lines.
We also assessed and compared expression of p53 and a cell proliferation marker in these lesions.
Using real-time PCR (Fig. 4) and calculation of expression as the ratio relative to expression in mycelia grown in liquid culture, we compared expression patterns of individual multicopper oxidases in L. edodes.
The first analysis compared expression profiles between NASH and S3 patients.
We also compared expression levels in brains taken from animals at end stage prion disease (Chandler/RML) and uninfected controls.
Two multigene studies directly compared expression of 30 [30] and 100 [31] wildtype and sequence-optimized human genes in E.coli.
