Figure 2: Concentration of MPs in 3 tissues of mice at different exposure times.
Levels of IL-33 in BAL fluids from wild type C57BL/6J mice at different time points after i.n.n
In vivo antimalarial efficacy was tested using Plasmodium berghei (NK65 resistant strain) infected swiss albino mice at different doses.
Wang, B. et al. Reprogramming efficiency and quality of induced Pluripotent Stem Cells (iPSCs) generated from muscle-derived fibroblasts of mdx mice at different ages.
All experimental conditions were reproduced with at least 3, most often up to 7 mice at different time points, representing individual biological repeats.
To address this, we first performed quantitative PCR on total RNA extracted from brains of mice at different days post infection with C. albicans (Fig. 3a).
We first evaluated IL-7 transcripts in the spleens and bone marrows (BM) harvested from mice at different time points after CTX treatment.
We estimated the percentage of PV cells that are enwrapped by WFA ECM structures in the hippocampus of mice at different time points following pump implantation.
This study was designed to evaluate the pharmacokinetics and tissue distribution of free and alginate-encapsulated antitubercular drugs in mice at different doses.
Table 1: Lectin staining, subjectively described from +++ (very strong) to − (absent) in infected, pzq-treated and reinfected mice at different weeks post-primary infection (wppi), compared with non-infected controls (0 wppi).
Muscle and spinal cord tissue was collected from WT, AR100 and AR20 control male mice at different stages of disease progression: presymptomatic mice (3 months old), symptomatic (12 months).
