Sentence examples for assessing the induction of from inspiring English sources

The present study sought to further investigate the in vitro and in vivo anticancer effects of a representative omega-3 fatty acid, docosahexaenoic acid (DHA), with a focus on assessing the induction of oxidative stress and apoptosis as an important mechanism for its anticancer actions.

In the present study, we sought to further investigate the anticancer efficacy of omega-3 FAs, DHA in particular, on the growth of MCF-7 human breast cancer cells in vitro and in vivo (as xenografts in athymic nude mice), with a focus on assessing the induction of oxidative stress and apoptosis as a crucial mechanistic element for their anticancer activity.

TCDF exposure in the Ahr /– mice was confirmed using dichloromethane extracts of liver and assessing the induction of AHR signaling in a Hepa 1.1 stable reporter cell line (see Supplemental Material, Figure S1).

Since it has been hypothesised that induction of T-cell apoptosis by FasL is linked to the loss or decrease of TcR/CD3- ζ expression (Rabinowich et al, 1998), the capability of FasL-expressing 'exosomes' to induce apoptosis was examined by assessing the induction of DNA fragmentation.

To assess the acute pro-inflammatory response to TLR stimulation, we treated the three subsets with LPS for 2 h, and assessed the induction of TNF-α from baseline, at the mRNA level.

In order to better assess the induction of inflammatory activity in CNS cell populations, we also studied the expression of the pro-inflammatory mitogen activated protein kinase (MAPK) p38 in its active form (phosphorylated) in glial and neuronal cells.

For information, in children who had T cell responses assessed, the induction of anti-CS antibodies (data not shown) showed a similar pattern to what has been described for children in the B cell subset.

We first assessed the induction of pathological Tau-forms in brains in vivo following Tau-seeding.

We next assessed the induction of IP-10 expression mediated by the interaction of FLSs and leukocytes (monocytes or PMNs).

To decipher the sequence of these events, we assessed the induction of γH2AX in a cell cycle-dependent manner.

To assess the induction of apoptosis by ARG098, implanted tissues were fixed in formalin 24 h after antibody injection.