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Both short- and long-term post-transplantation human hepatocyte-like cells resided in the mouse host liver indicating parenchymal penetration and most likely functional engraftment.
To select the most likely functional AREs, we examined evolutionary conservation by phylogenetic footprinting.
This is in accordance with the expectation that the nsSNP is the most likely functional candidate.
We also defined our sample set to be the "most likely" functional equivalent.
In our work, we refer to such a sample as the most likely functional counterpart (MoLFunC) of each other.
Their most likely functional role appears to be related to local bending and possible binding sites for DNA packaging proteins such as HU [43].
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We found that, despite having originated before Brassicaceae radiation, MIR168a and MIR168b paralogs have been maintained, most likely as functional, throughout Brassicacea evolution, with MIR168b having undergone a partial sub-functionalization.
Therefore, we hypothesized that Phe/Tyr209 is most likely the functional SNP.
Our results confirm the presence of a novel F genome-specific ORF of significant length (>375 nt), located in VD1, that most likely has functional significance in marine mussels (Mytilus spp).
Concluding from our results we argue that the heterogeneity with respect to the Nanog concentrations is most likely a functional element to control the differentiation propensity of an ES cell population.
Our results confirm the presence of a novel F genome-specific mt ORF, of significant length (>100aa) and located in the control region, that most likely has functional significance in marine mussels.
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