Sentence examples for mice we assayed from inspiring English sources

To confirm that Cre Recombinase was functioning in these mice we assayed for the deletion of exon 2 of the AR in SMARKO testes by RT-PCR.

To further investigate the ontogeny of abnormal ureteric tip cell gene expression in Ptc1−/−UB mice, we assayed Ret and Wnt11 expression in isolated ureteric bud tissue using quantitative real-time PCR.

To evaluate the extent to which pheromones which increase uterine mass are produced by different strains of laboratory mice, we assayed male urine from BALB/cJ, C57BL/6J, and CD-1 lineages.

In order to determine whether expression of genes in the chondrocyte differentiation and maturation pathways was altered in Hoxc8- or Hoxd4-transgenic mice, we assayed the prevalence of transcripts for genes known to participate in regulation of the chondrocyte differentiation pathway.

To investigate the adverse effects of AV-65 in treated mice, we assayed colony-forming activity in BM and other biochemical parameters in AV-65 and vehicle-treated mice.

To determine if this could be due a deviated immune response against hFIX protein in BALB/c F9−/Y mice, we assayed for TH1 (IgG2andand TH2 (IgG1 -associated antIgG1 -associatedbulin (IgG).

In the Fgfr3-iCre-ERT2 Ai14 tdTomato Fgfr3-iCre-ERT2 Ai14 tdTomato Fgfr3-iCre-ERT2 Ai14 tdTomato following tamoxifen adoubletransgenictween P2 and P4.

Because PGE2 was significantly increased in the pleural lavages of 7 days S. pneumoniae-infected WT mice, we next assayed PGE2 levels in the pleural lavages of 3 day infected WT and PAI-1−/− mice.

Based on the hypothesis that calcium signaling may be compromised in nBmp2NLStm mice, we next assayed for defects in calcium mobilization within the cells of wild type and mutant mice.

To ask whether this could result from changes in the level of Gli activity in Pax6 Olig2 mutant mice, we first assayed Tg(GBS-GFP) activity in this genetic background.

To exclude the possibility that these findings were an artefact of clonal selection or adaptation to the xeno-environment resulting from passage through the mice, we also assayed primary blasts sorted for CD20 or CD34 expression and transplanted at low cell dose.