To verify the existence of an intermediate optimum, as indicated by a significant quadratic effect in the non-linear model, we visualized the relationship between parasite intensity and survival with the cubic spline technique [27].
To determine whether nuclear architecture or/and positioning are affected in our ALS fly model, we visualized nuclei in muscles overexpressing either DVAP-V260I or DVAP-WT transgenes using a nuclear marker and an anti-lamin antibody.
Because the ventricular structures are identical in both models, we can visualize differences in activation by plotting the difference in activation times at each point in the ventricles.
The Prussian blue staining revealed the presence of NPCP-BG-CTX well beyond the tumor boundary immediately after CED, but confined within the tumor at 48 h post CED. Figure 6 c displays a model for the behavior that we visualize here; upon completion of CED, NPCP-BG-CTX diffused outward beyond the tumor boundary.
We visualized models in the program ArcGIS 9.3 (ESRI Inc., Redlands, CA).
We visualized this model by plotting the relationship between the probability of death and SAPS-3 score for different categories of chloremia (Fig. 1).
In this study, using Xenopus laevis as a model, we therefore attempted to visualize MT dynamics by using EB3 (end binding 3) [17] proteins that bind the ends of MTs as the indicator of the intracellular events during convergent extension, and attempted to correlate it with the establishment of cell polarity.
We visualized the same model using MetDraw with no manual adjustments.
In the second part, we demonstrate how we can use our model to visualize which sequence positions are most informative about the classification.
Overall, the findings support the notion that CCR2 and CX3CR1 define functionally distinct monocyte subsets and for the first time we provide a model to visualize monocytes subsets in situ within brain infiltrates.
