Anatomical expression data revealed that BdCAD1 and BdCOMT4 were highly expressed in stems; therefore, we analyzed the expression levels of the target genes in stems of the selected transgenic lines for both BdCAD1 and BdCOMT4 in order to confirm silencing.
To investigate whether the expressed TLRs were functional in the breast cancer cells following LPS stimulation, we analyzed the expression levels of some pro-inflammatory genes that are known targets for NFκB.
We analyzed the expression levels of transcripts across all stages for each transcript group - known, partially annotated novel and completely novel transcripts and performed Wilcoxon rank sum test to study the distribution of expression levels between transcript groups for each developmental stage separately.
This study analyzed the expression levels of different splicing variants of the TGIF1 gene in OSCC compared with nontumoral epithelium (NT) and the relationship with clinical-pathologic features of tumors.
Since enhanced iron levels are discussed to participate in oxidative stress and neuronal death, we analyzed the expression levels of Fe-related mRNAs in a cell culture ALS model with the G93A mutation of SOD1.
We first analyzed the expression levels of the ATL9 family members ATL2-ACRE132, and6 ATL17Table(Table S1).
We next analyzed the expression levels of molecules that have been related to thymocyte selection and apoptosis.
To check this hypothesis, we analyzed the expression levels of tomato genes regulating cell cycle, in particular CDKA1, CycA1 and CycD3 [14], [14].
To confirm that PR1 expression does not correlate with transgenic MKS1oe levels, we next analyzed the expression levels of the different transgenic MKS1 versions.
We also analyzed the expression levels of HSP-40, a constitutive chaperone, and we found no differences between atx-3 and N2 animals.
Then, we analyzed the expression levels of the same receptor subunits of KA-injected WT (n = 9) and COX-2−/− mice (n = 9) compared with their respectively controls.
