We then evaluated expression of bphD.
When we evaluated expression of 1479 genes included in Dim1 by Darmanis et al. in our single neuron samples, we found a subset of the genes had enriched expression in our "matured" neuronal samples (Fig. S2).
Using the reverse transcription PCR, we evaluated expression levels of various antigen presentation-related genes, including LMP2, LMP7, MECL-1, PA28α, PA28β, TAP1, TAP2, and tapasin, in two oral squamous cell carcinoma cell lines, HSC5 and HSC7.
We next evaluated expression and secretion of the T3sVHHs by Western blot (WB).
We also evaluated expression of CD25, an additional marker of activated and regulatory T cells [32].
We also evaluated expression across the cortex gene set as a continuous variable.
We previously catalogued and evaluated expression of multiple splicing forms of TCF7L2 in several types of human tissue [21].
We have evaluated expression levels of candidate genes previously identified through genetic and protein interaction analyses [7].
In a fourth series of experiments, we evaluated expression patterns of connexin 26 and Na+/K+ ATPase in the cochlea of Slc26a4+/− and Slc26a4−/− mice.
Since Bowtie allocates isoform multireads to transcripts stochastically, we evaluated expression at the gene level rather than at the transcript level.
Since there can be a considerable degree of cell-specificity in the transcriptional response to glucocorticoids, we harvested multiple organs and evaluated expression and regulation of the mRNAs using multiple tissue in situ hybridisation.
