Sentence examples for microarray study also from inspiring English sources

To investigate whether genes that had been found to be differentially expressed in deep-infiltrating endometriosis and matched eutopic endometrium in our previous complementary DNA microarray study also are differentially expressed in ovarian endometriosis and matched eutopic endometrium.

A previous microarray study also showed modest but consistent hypoxic reductions in mRNA levels of genes (Dicer, TARBP2 and AGO2) involved in miRNA biogenesis [ 36].

The microarray study also indicated that this transcript was regulated only within the heavy polysomal fraction, a result confirmed by the RT-PCR.

A human microarray study also showed AR gene down-regulation in the myometrium during preterm (0.4-fold) and term labour (0.3-fold) compared with non-labouring myometrium, but the protein expression was not determined (Bethin et al., 2003).

The microarray study also revealed a significant increase (by 2.8-fold) of the transcript of the gene for callose synthase (VvCasy, Vv_10001615), which is involved in the callose formation and the increase of three genes belonging to a cluster of β-1,3-glucanases (Vv_10000389, Vv_10010418, Vv_10002068), which hydrolyze β-1,3-glucans (4.3 to 11.0-fold increase).

While this finding derives from the analysis of immunohistochemical staining as a single technique, a recent expression microarray study also identified TPD52 overexpression as being associated with improved progression-free and overall survival in patients with serous and endometrioid tumours [ 24].

Microarray studies also suggest little change in the RNA pool under different conditions [17], [18].

Recent microarray studies also identified many CNVs in a variety of complex mental disorders such as mental retardation [3], [4], autism spectrum disorders [5] [8], and schizophrenia [9], [10].

Despite down-regulation of such genes by DAF-16 the two microarray studies also include many up-regulated DAF-16 innate immunity targets [23], [24].

Publicly available microarray studies also showed significant overexpression of Fbxl7 in LOAD brains compared to nondemented controls.

It is therefore likely that some of the 80 "selected negatives" which did not hybridize in our single channel microarray studies also represent rare transcripts.