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Different species or types of production systems were not differentiated in the data.
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Given the considerable literature supporting the involvement of glia in PD pathogenesis [26], [27], [30], [31] we might have expected glial markers to inversely differentiated in the SN data sets.
These data suggest that many Miscanthus genes have a closely related paralog that cannot be easily differentiated in the short read transcript data, but which assort independently.
Interestingly, in the data reported here, pro-asthmatic BMDCs from C3H mice were differentiated in the presence of GM-CSF.
Moreover, mir-64c is the most highly differentiated miRNA in this cluster among populations of C. remanei, also being one of the most highly differentiated miRNAs in our data set, and even more strongly differentiated among populations than 95% of non-miRNA reference genes in the genome.
The low UbcH10 levels detected in the differentiated thyroid malignancies would appear in contrast with the data showing an abundant UbcH10 expression in the cell lines deriving from differentiated carcinomas.
After differentiation, CD133-expressing cells declined from 89.20% in the spheroid populations to 40.5% in the differentiated adherent population (data not shown).
Again the interpretation in terms of three folding domains is clear when looking at the differentiated data in the Supporting Information.
Analysis of the cholinergic marker CHAT revealed a small population of positive CHAT neurons in the differentiated WT RGs (data not shown).
The expression of ChAT was not detected in differentiated ES-NS (data not shown).
No intranucleolar SUMO2 was found in differentiated fibre cells (data not shown), indicating that this reflects a cell feature characteristic of the epithelial layer.
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