Sentence examples for mice generated from from inspiring English sources

F2 mice generated from the F1 mice showed a distribution of inflammatory responses extending between the two parental strains (Figures 1 and 2).

Transgene expression was analyzed by RT-PCR on total RNA extracted from different tissues of mice generated from founder A and D (indicated as TgA and TgD, respectively).

There was a difference observed, however, between the mice generated from B6 mothers and FVB fathers (BxF) as compared to those from FVB mothers and B6 fathers (FxB), suggesting an imprinted trait modifying the F1 phenotypes.

Compared with WT mice, the PR interval and QRS complex duration had a tendency of increase in both of the transgenic lines, but only the mice generated from founder 35 showed a significant increase in the QRS complex duration (P<0.05) in 7 mice with ECG recording.

F1 mice generated from crosses of B6 and FVB PECAM-deficient mice showed a phenotype most consistent with the B6 parents, i.e. they tended to display ongoing robust inflammatory responses to thioglycollate despite lack of PECAM (Figures 1 and 2; Supplemental Table S1).

The effects of CXCR4 inhibitors in vivo were determined on leukemic mice generated from these eight samples.

A Csrp2bp-null mouse, generated from 129-derived ES cells and maintained on the C57BL/6J background, has been reported to be embryonic-lethal at E9.5 [33].

L1−/y mice and L1+/y mice were generated from the mating of 129x1SvJ males and L1ki129 heterozygous females.

These transgenic mice were generated from FVB/N mice as reported earlier [ 11].

The Ago2-tetO mice were generated from a mouse Ago2 cDNA construct (a kind gift of G. Meister, University of Regensburg) (Nir et al., 2007).

TRα1/TRβ double KO mice were generated from TRα1−/−/TRβ+/− KO mice as previously described [17].