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The metabolic data also indicate further protective actions of NO in the isolated guinea pig hearts.
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On top of the already published work characterising metabolic phenotype variations during pregnancy, these data also provide a useful baseline and reference dataset to be compared to specific conditions (e.g. hypertensive disorders, diabetes mellitus) in pregnancy.
Nevertheless, our data also indicate that metabolic consequences of miRNA-122 inhibition may differ quantitatively between vertebrate species and that distinct direct molecular targets of miRNA-122 may mediate metabolic effects between vertebrate species, indicating that miRNA-122 - mRNA target relationships may have undergone species-specific evolutionary changes.
It enables the user to annotate multiple metagenomes at a time and also to compare the metabolic data [103].
Metabolic data from sepsis survivors and non-survivors were also pooled to compare patients with sepsis and non-infected SIRS.
A subset of the individuals (n = 864) with genotypic data also had detailed measures of metabolic traits related to obesity (Table 2).
Evaluation of these data also demonstrated a genotype specific regulation of distinct metabolic pathways, suggesting the importance of detection of metabolic patterns rather than specific metabolite changes when looking for metabolic markers differentially responding to pathogen infection.
We also did this for other (for example, metabolic) data.
Moreover, these data also suggest that other key components of metabolic syndrome are significantly improved by an increase of dairy food intake to an adequate level.
These data also underscore the strong influence of gender on metabolic traits in mice, an observation we have previously noted [34].
The microarray data also helped us to investigate the mechanisms of metabolic rate difference giving rise to divergent muscle growth and hypertrophy between broilers and layers.
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