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According to our microarray analyses, all MMP genes examined were down-regulated in nucleus pulposus cells with co-culture of synovial MSCs.
In the first analyses by differential cDNA hybridizations, expressed sequence tag sequencing, or microarray analyses, all identified ccgs were morning-specific (Bell-Pedersen et al. 1996; Loros et al. 1989; Nowrousian et al. 2003; Zhu et al. 2001), with evening-specific genes identified only later (Correa et al. 2003; Dong et al. 2008).
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RNA was pooled in equal amounts, and microarray analyses for all identified murine miRNAs (miRBase 9.0) were performed using the All-in-One™ miRNA qPCR Array (Exiqon, Denmark) (Sadoun & Reed, 2003).
TCGA analyzed 489 ovarian cancer tissues, and performed miRNA microarray analyses on all samples.
The response of A. tamarense after exposure to copepods and potential waterborne cues was assessed via screening of gene expression patterns through microarray analyses for all treatments and related to the PST measurements.
Only the treated leaf tissue was used in RNA extractions and microarray analyses (excluding all other green tissues).
The results represent the mean ± standard deviation of the relative expression in qPCR of seventeen differentially expressed genes identified in the microarray analyses with all data (main list), S. aureus (Sa list) or S. epidermidis data (Se list).
All microarray analyses were performed at the London Regional Genomics Centre and all sequencing was performed at the Robarts Sequencing Facility at the University of Western Ontario.
All microarray analyses were performed using BRB-Array Toolsoftwarere.
All microarray analyses were conducted at Exiqon Services (Denmark).
All microarray analyses were conducted by Phalanx Biotech (Taiwan).
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