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These results differ from previous studies that tested the expression of these receptors in RE.
To further validate this result, we treated LM2 cells with specific inhibitors for the ERK, p38 and JNK pathways and tested the expression of BCLM-associated genes.
Therefore, we tested the expression and solubility of the cloned BVMOs domains fused to an N-terminal His-tagged, cofactor regenerating protein; PTDH.
We have tested the expression of eight integral membrane pyrophosphatases in Saccharomyces cerevisiae, six from bacterial and archaeal sources and two from protozoa.
We then tested the expression of a few other markers by RT-PCR.
Therefore, we tested the expression profile of GSK3ß-related genes (Figure 3B) in these hyper-proliferative PASMCs.
First we tested the expression and subcellular localization of chimeras by fusing GFP to the C-termini.
We tested the expression of almost 20,000 transcripts on a recently developed microarray for linkage across the pig genome.
We confirmed these results using Q-RT-PCR, and also tested the expression of Hamp2, which was downregulated (Figure 1).
We also tested the expression of Foxp3, a master transcription factor for TGF-β-induced differentiation of T regulatory cells.
To determine how OsLIC affects BR signaling in rice, we tested the expression pattern of OsLIC with exogenous BR treatment.
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