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b Whole abdomen imaging of representative control (left) and tumor-bearing (right) mice.
As a representative control scheme, impulsive control has received much attention from various fields.
We review the most representative control strategies, discuss their theoretical background and experimental realization.
Corresponding post-mortem autoradiography and immunohistochemistry on the coronal sections in the representative control and KASE (severe SE) rats, 7 days post-SE induction are shown.
The two alternatives are evaluated through simulated execution of representative control software with detailed modeling of cache/memory effects and bus contention.
As with CASP-8p18 antibody, the commercial antibody-labeled neurons in all AD cases, while showing a relative paucity of staining in representative control cases.
The review is also extended with model generalizations and the implications on system design, especially the heat transfer effects and the representative control designs are discussed in detail.
Compounds 7 and 9 exhibited stronger inhibitory effects on the EBV-EA activation than that of the representative control, oleanolic acid, at the highest measured concentration.
TACs were expressed as the percentage injected dose per milliliter (%ID/ml) of plasma and several brain regions in the representative control (a) and KASE (severe SE) (b) rats.
[125I]-CLINDE autoradiography images of the representative control and KASE (severe SE) rats and quantitative analysis of [125I]-CLINDE specific binding (kBq/mg) in the control (N = 4) and KASE (N = 5) groups of dorsal hippocampal sections are shown.
In vitro and ex vivo TSPO autoradiography on sagittal sections in representative control and KASE (medium SE) animals demonstrating higher signal in the hippocampus, piriform cortex, amygdala and thalamic nuclei post-KASE.
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