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For our analysis, we examined codon usage among 2,079 genes per organism and assessed gene expression using large-scale expressed sequenced tag (EST) data sets (279,323 and 453,559 ESTs for N. tetrasperma and N. discreta, respectively).
In order to directly assess the effect of Wnt/β-catenin signaling on the injury response, we assessed gene expression levels in blastema fin tissue in a transgenic line expressing heat shock-inducible Dickkopf (hsDKK1 GFP), a secreted inhibitor of Wnt/β-catenin signaling, and Wnt8a (hsWnt8a:GFP).
In the studies that assessed gene expression in a mixture of tumor cells and fibroblasts, we found three differentially expressed collagen genes: COL15A1, COL4A6, and COL4A5.
We assessed gene expression patterns by qPCR, global DNA methylation by ELISA, and proteome lysine acetylation status by Western blot in cardiac tissue from saline and DOX-treated rats.
To characterize developmental cues and benchmarks for differentiation toward limb vs. axial phenotypes, we dynamically loaded and treated TPCs with growth factors and assessed gene expression profiles as a function of developmental stage and anatomical origin.
who also assessed gene expression in SZ versus control LCLs.
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To assess gene expression, cells expressing CD14 were purified from endometrium and blood.
Assessing gene expression patterns using Genevestigator, it appears that RPD3/HDA1 histone deacetylases are expressed all throughout the plant parts and developmental stages of the plant.
Gene expression profiling of cells of the immune system isolated ex vivo is a unique tool to assess gene expression in vivo.
The comparative ΔCt method was used to assess gene expression stability.
A SSTR2-based reporter that can be imaged by a clinically approved radiopharmaceutical was used to assess gene expression.
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