Sentence examples for by evaluating gene expression from inspiring English sources

We analyzed EPO production by evaluating gene expression and confirming it by protein detection.

In the present study, we hypothesized that disease-associated molecular signatures linked to key host response, e.g., airway inflammation and mucus cell metaplasia, could be identified by evaluating gene expression in selected tissues from Scnn1b-Tg mice at critical time points.

Due to the robust morphological activation of macrophages in the Scnn1b-Tg mice, the tendency for genes involved in macrophage function to be up-regulated in whole lung (Additional file 3: Table S1), and the importance of this cell type in lung disease pathogenesis, we continued our studies by evaluating gene expression in purified pulmonary macrophages.

Indeed, the current data reinforce recent observations made by Roman-Perez and colleagues after evaluating gene expression patterns in 72 breast tissue samples [ 36].

Work by Allinen and coworkers evaluated gene expression profiles of breast cancer stromal cells which were isolated by negatively selecting out epithelial cells, lymphocytes and endothelial cells [ 12].

Cultivars TNG67, TNG72, SCTT and KSWSK, exhibiting diverse degrees of purple color, were selected to evaluate gene expression by real-time PCR.

To determine whether PLD1 gene expression correlates with either the basal or luminal CKs and/or ER status in breast tumour tissue, we isolated RNA from 30 frozen human breast carcinomas and evaluated gene expression by real-time RT PCR.

To validate our phase I findings, we evaluated gene expression by qRT−PCR (TaqMan primer probe assays) on the remaining 28 normal and 30 tumour tissue RNA specimens using a low-density array (LDA).

To evaluate gene expression by the Flow-FISH method we used a linear locked nucleic acid (LNA) probe, GACCACGCAAGAAGCAACAAGAGGG-5′FITC containing nucleic acid analogs with higher affinity for DNA and RNA [ 6].

Primer sequences used for real-time PCR to evaluate gene expression by mesenchymal precursor cells maintained in micromass cultures in the absence and presence of pentosan polysulfate for 7 and 10 days.

To better understand the molecular mechanisms underlying the dynamic alterations in offspring metabolism resulting from an HS maternal diet, we evaluated gene expression by quantitative real-time reverse transcriptase PCR (qRT-PCR).