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Analyzing this expression, we can observe that for any s ≠ s', |h sn /h s'n | = 1.
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To validate whether Grhl3 expression is controlled by Wnt signaling, we first analyzed this expression in Dkk1-deficient embryos (Fig. 7A E′).
ARSER identified 96% of the cycling transcripts identified by COSOPT, suggesting our methodology efficiently reproduced the original results, while Fisher's G-test merely identified only 15%, implying it may not efficiently analyze this circadian expression data.
To our knowledge, there are no available reports analyzing the expression of this gene in the uterine cervix or in cervical carcinoma.
Analyzing this pathway we found altered expression of the genes Rasa1 (decreased levels), STAT1 and STAT3 (increased levels).
Since CDKN1C is poorly expressed in lymphoblasts (data not shown), we analyzed the expression of this gene in the skin fibroblasts by qRT-PCR.
To assess the specificity of the decrease in Mrp1 found in CPs, we analyzed the expression of this transporter in the spleen, an organ that highly expresses Mrp1.
To examine this hypothesis, we analyzed the expression of genes hypomethylated both in E14.5 NPCs and astrocytes.
This study analyzed the expression of TGIF1 transcripts and protein in oral squamous cell carcinoma (OSCC).
For this, we analyzed the expression of RAGE mRNA in lung brush cells and BALF cells obtained from ventilated patients.
To further address this, we analyzed the expression of atrial specific markers ANF/Nppa and Shox2, which mark the whole atrium and the right atrial wall, respectively.
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