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Subsequent studies indicate that EH networks promote myoblastic cell attachment and proliferation as well as delivers functional insulin-like growth factor-1 to an in vitro population of skeletal myoblasts.
Later, mice exhibit increased startle reactivity and reduced threshold for in vitro population spikes.
The identification of the factors accounting for the differentiation within this condensed in vitro population is an interesting subject of further investigation.
In contrast to bacteria grown in culture, which do not experience natural death, M. tb bacilli growing in an immunocompetent host are frequently killed through adaptive or innate immune responses and thus a host bacillary population of a given size is likely to have undergone far more replication events than an in vitro population of the same size.
The authors' goal is an in vitro population of 'glutamatergic cortical neurons'.
Of these, 37 genes were exclusively expressed in the in vivo population and 10 genes were exclusively expressed in the in vitro population.
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Therefore, we surveyed the basal in vitro population-spike threshold and the effects of partial Na+ channel blockade on fEPSPs.
Importantly, we have demonstrated the feasibility of using an in vitro population-based model system for assessment of individual variability in next-generation risk assessment (Zeise et al. 2013).
Our study extends these observations by identifying a number of alternatively spliced genes between in vivo and in vitro populations.
Our set of in vitro populations showed that mutation rates detected for nine VNTR loci used for VTEC O157 subtyping were according to those reported previously for other bacterial VNTRs, with a similar proportion between single and multiple repeat changes.
We performed similar PSPEs on 9 E. coli O157 H7 strains (Table 1), generating a set of in vitro populations representing ~211.500 total generations (23.5 generations/colony × 100 lineages × 10 passages × 9 PSPEs).
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