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While all seven of the tested miRNAs were significantly upregulated in T2DM cases, there was no difference in the expressed levels between IGT cases and normal susceptible controls.
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To verify if the expression patterns observed could be attributed to differences in neural distribution or differences in the expressed levels of channels, the expression pattern of the pan-neuronal maker PGP 9.5 was tested.
While being aware of the limitations mentioned before, we consider species differences (e.g. dissimilar expansion of gene families) by chance or as a consequence of adaptation to slightly different ecological niches, or differences in the expressed repertoire of genes as most likely explanations.
The different physiological repertoire of CA3 and CA1 neurons in the hippocampus, as well as their differing behaviour after noxious stimuli are ultimately based upon differences in the expressed genome.
Differences in the expressed CD44 isoform also explain some of these controversies.
Differences were identified, and were related to differences in the expressed genome demonstrated in a microarray experiment using the same cell lines and conditions.
Our experiments show that individual differences in the expressed trait of loneliness are linked with variations in the gray matter volume of left pSTS.
They also noted that there was no longer a difference in the genes expressed in the frontal and temporal lobes in the brain.
Neither was there significant difference in the DNA expressed per g of tissue or in total DNA content in any of the analyzed depots between control and CR animals (Table 2).
This discrepancy could be explained by a difference in the isoforms expressed on 2-DE gels.
Vacuolation of the rostral colliculi was a feature of all of the brains studied and there was no significant difference in the (mildly expressed) clinical signs between pigs inoculated with rostral colliculi from different sources.
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