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In addition, we evaluated the activation of MAPK (p38, ERK1/2) and NF-κB signaling pathways required for the induction of proinflammatory responses in intestinal epithelial cells.
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In addition, to dissect the participation of cAMP we evaluated the activation of the chemotactic signaling by means of a gradient of db-cAMP, a membrane permeant cAMP analog (see experiment rationale below).
In addition, we evaluated the effect of milk proteins upon pbMEC activation, since MEC are in vivo exposed to milk.
In addition, we evaluated the effects of a background electrolyte on the rejection of dyes.
In addition, we evaluated the effect of exosome-mimetic nanovesicles in mice without partial hepatectomy.
In addition, we evaluated the incidence of complications of bracing.
In addition, we evaluated the number of fragments.
In addition, we evaluated group differences in amygdala activation to the US.
In addition, we evaluated whether VEGF levels in both types of plasma correlated with the presence of diabetes, glycemic control, markers of in vivo or ex vivo platelet activation, and degree of diabetic retinopathy and nephropathy.
Next, we performed phospho-kinase arrays, evaluating the activation of key innate immune pathways by HBV antigen and their suppression by HBV infection (Fig. 4a, b).
We used the cell surface marker fibroblast activation protein (FAP) to evaluate the activation of fibroblasts.
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