A mouse control group receiving no drug was used for each drug treatment experiment.
In addition, in all E- and P-selectin-deficient scid mice, lung metastases were generally smaller than those in the scid mouse control group.
Rapid tumour growth was observed in the mouse control group; however, significant tumor growth suppression was demonstrated in mice treated with PEG-liposomal L-oHP.
FGF21KO and WT mice control groups (Ctrl) received citrate buffer alone.
We observed a significant increase in CD36 relative expression level in mice treated with LST with respect to mice control groups feeding on either chow or HFHC diet (p < 0.05 for both).
After being challenged with E. coli CVCC 1515 within 12 36 h, the survival ratio of the rOmpF-immunized mice was decreased from 60 to 40%, but kept to 30% at 48 h postchallenge, which was higher than that of the PBS-immunized mice (control group) (Fig. 6A).
The glutathione hepatic values in mice induced by intraperitoneal injection of the ester are superimposable with the GSH levels recorded in no-treated mice control group.
As a control, 5×106 Thy1.1+OT-1+cellsT cells from day 4 SubQ primed mice were adoptively transferred into naïve Thy1.2+ mice (control group).
To obtain Ts1Cje and wild type fetuses for RNA isolation, male +/+ mice (control group) or male Ts/+ mice (Down group) were bred with female breeding mice of the C3H/HeNHsd strain (Harlan, Horst, the Netherlands) at 8 10 weeks of age.
The histologic grading score indicated that KO mice (control group) had a poorer quality of cartilage compared with WT mice (control group).
