Sentence examples for migration genes were from inspiring English sources
Leukocyte transendothelial migration genes were also downregulated, as discussed in our recent paper[7].
Sixty-six cellular invasion and migration genes were detectable in D283 cells using the mRNA miniarray.
Gene ontology (GO) analysis indicated that genes involved in the response to wound healing, including cell migration genes, were in the top 10 GO categories for both ATM and mutant p53 depleted samples.
There are no obvious explanations why signal transducer activity, multicellular organismal development and leukocyte trans-endothelial migration genes are down-regulated in parietal pleura.
It is therefore likely that migration genes are also found in the zebra finch genome even if they do not manifest themselves into a distinct migratory phenotype in contemporary zebra finch populations.
The mRNA expression of 94 cellular invasion and migration gene was analyzed using a ready-to-use Array Human Extracellular Matrix & Adhesion Molecules 96-well Plate (Applied Biosystems Catalogg number, 4414133) and the ABI 7500 Real-Time qPCR system.
To a minor extent our results also indicate that cell migration might be reduced on the nanorough surfaces, since a significantly lower gene expression of migration related genes were found on the roughest surfaces as compared to the flat reference.
In the non-Asian samples (GSE46581), there were 16 genes with significant expression changes related to cell migration, whereas 9 cell migration-related genes were found in the Asian samples (GSE33926) (Table 4).
A slightly lower number of stationary signature genes was found to be down-regulated (52 out of 105 – 49%), and 50% of migration signature genes were up-regulated (27 out of 54).
Most importantly, we found that several other cell migration-related genes were modulated secondary to treating human TEC with ITGA6 specific siRNA, thus pointing to the notion that intra-TEC expression of genes involved in controlling thymocyte migration by the thymic microenvironment should be regarded as complex networks.
Yet, there are a few limitations to our approach: Since our analysis is based on just two synthetic lethal screens, not all known spindle migration genes could be found.
