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In a next set of experiments, we applied different chemoattractants (MIP-1α and PAF) and bacteria (E. coli) via microinjection and analyzed leukocyte adhesion, transmigration and interstitial migration.
In a next set of experiments, we then applied a place field specific spike episode obtained from a different in vivo granule cell recording (spike train 2) as published in Henze et al. [17].
In a next set of experiments, we examined the effect of PLD activity on the same initial SLBs, as described in Figure 3.
In a next set of experiments, we examined the differential miRNA expression in TNF-α treated, differentiated primary human and murine cell line myoblasts in vitro.
In a next set of experiments we tested the hypothesis that prolonged incubation with an established calcium channel activator can also promote cell death due to an overload in free cytosolic Ca2+ (Additional file 3).
In a next set of experiments, we were interested to know whether the observed activating effects were unique to the potassium salt or whether they could also be accomplished with other alkali hydroxide coatings.
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In the next set of experiments we investigated the signal enhancement of 1H and 19F and the magnetization transfer between both nuclei when applying the SABRE technique.
"Just be ready for the next set of experiments we have in 2 weeks".
In our next set of experiments, we further fine tune the value of μ to optimize the simulation execution time.
For the next set of experiments, we first run our method on the entire filtered dataset and without cross-validation.
In the next set of experiments, we separated the subjects used in the previous experiments (expression-based and illumination-based) to male and female face images.
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