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A paired t-test (two-tailed) was used for comparison of reconstructed counts in the lesions and the liver between the LD, FDAP, and FDVP reconstructions.
We performed a transcriptomic comparison of fatty liver between GF and RO-fed geese to gain insights into the molecular and cellular events mediating lipogenesis activity.
The only remaining plausible explanation in our view is to attribute the scatter to non-negligible inter- and intra-individual quantitative differences of FDG kinetics in the liver between different patients or scans.
Many of these CYP, XME and transporter genes are regulated by xeno-sensing nuclear receptors, and hierarchical clustering of CAR/PXR-regulated genes demonstrated the similarities of toxicogenomic responses in liver between all four triazoles and in testis between myclobutanil and triadimefon.
There was no statistical difference in mean bacterial burden in the liver between A1a and A1b infected mice.
No difference in COX activity was observed in muscle and liver between wild type and Fsp27−/− mice (Fig. 4B).
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We compared the size and morphology of livers between mice injected with control cells and stable Smad7 clones.
In mice, we did not observe any differences in body weight nor in the histology of the livers between Parp-1 genotypes.
Yellow cattle and water buffalo were sacrificed 7 weeks post infection and the differences in livers between yellow cattle and water buffalo were observed.
In summary, many genes are differentially-expressed between embryonic and adult liver, and between embryonic liver and embryo without liver.
This method adjusts for differences between liver lobes and between patients.
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