Sentence examples for rat liver compared from inspiring English sources
Consistent with this theory, it has been previously reported that macroH2A1 is up regulated in rat liver compared to rat brain [64].
However, due to the small size of rat livers compared with those of humans, it is a prerequisite to have a high resolution US machine as well as a high frequency probe for precise tumor measurement and US-guided injection.
Treatment with RADA16-I as an aqueous gel has been generally reported to accelerate coagulation; hemostasis was achieved in 6 s in a rat skin injury compared to 75 s for an untreated wound, 10 s in a rat liver injury compared to 204 s when treated with saline, and 10 s in a rat liver injury compared to 90 s with PBS.
Rodent liver had proportionally more HNF1B(A); comprising 65 and 64% total HNF1B expression in mouse and rat liver respectively compared with 36% in man (p = 0.04).
Preliminary experiments with MA, a potent orally active ovulation inhibitor, indicated that it was very resistant to metabolism in vitro by rat liver as compared with progesterone [ 56].
CCl4 administration in rats also increased APOP development in plasma and in liver compared to control rats significantly (p < 0.0001).
However, the JPJD-treated FRD-LC rats (with a concentration-dependent trend) exhibited a lower expression level of OATP1B2 mRNA in the liver compared with the FRD rats and FRD-LC rats.
DEN-treated gpt delta rats showed equivalent increases in the number and area of precancerous GST-P-positive foci in the liver compared to WT rats.
OLETF rats showed significantly lowered in vivo glucose uptake in glucose sensitive tissues such as BAT, WAT, soleus muscle and liver compared with LETO rats.
Similar to our in vitro results (Hu et al. 2002; Upham et al. 1998), PFOA decreased GJIC activity in the liver compared with the rats treated with the vehicle (control) for both the acute and long-term dosing schemes.
Although both high fat diets resulted in increased adiposity and hepatosteatosis, CAF-fed rats displayed remarkable inflammation in white fat, brown fat and liver compared to HFD and controls.
