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In regards to the GC-poor localization of the genes that are not expressed in any of the three adult mouse tissues considered here, the notion that they may be implicated in developmental processes is supported by several studies.
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Furthermore, among all analyzed human and mouse genes, the predicted target genes are characterized by consistently higher expression levels in all tissues considered.
Liu et al. [ 23] provided a comparison between many different microarrays and MPSS technology using mouse tissues but they did not consider as broad a range of biological samples for comparison as in our study.
The study is among the first to consider directly how dividing stem cells choose their fate in undamaged mouse tissues.
Next, we consider a dataset derived from proteomic analysis of the content of four cellular compartments in each of six mouse tissues.
Accumulation of hercynine in mouse tissues.
Uptake and accumulation of ET in various mouse tissues.
Biotinylated protein levels in mouse tissues were assessed by immunoblotting.
Accumulation of ergothioneine sulfonate (ET-SO3H) in mouse tissues.
Both of these cell lines were developed from mouse tissues.
Figure 6 Determination of MNPs mixed in different mouse tissues.
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