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Despite these differences, only the bioluminescence approach can permit the quantification of changes in beta-cell mass in an individual mouse over time, which we believe can provide valuable insights into the kinetics of beta-cell regeneration that the more conventional approach cannot.
Mouse ID was included as a random effect to control for multiple samples per mouse over time.
CS790AM showed promise for monitoring labile copper in a single mouse over time, tracking different stages of health and disease.
Figure 2 shows sagittal T2-wi in an IVD Bgn−/0 mouse over time at 6, 11, 16 and 18 months of life.
The other important benefit of the fiber model is the ability to examine progression of cells to CRPC at various stages within the same host mouse over time, because the retrieval of a subset of fibers entails only minor surgery.
Tumor volume data from mouse experiments were analyzed using generalized estimating equations (GEEs) [ 8, 9] with an identity link function and exchangeable correlation structure, a regression model that accommodates the lack of independence among measures obtained from the same mouse over time.
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In mice, if you knock out the gene that encodes for an enzyme that regulates telomere length and function, these mice over time have decreased function and life expectancy.
The specificity of the OspC Ab response in experimentally infected mice over time was assessed to determine if domains shielded in the OspC homodimer become accessible and stimulate Ab production as infection progresses.
Multivisceral disease develops in Hq mice over time.
Results showed a drop in neurosphere number from the SVZ of WT and HD mice over time (Fig. 2A).
By quantifying luciferase expression using bioluminescent imaging, we were able to track MaSCs non-invasively in individual mice over time.
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