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For instance, scaling up the chamber geometry seems to be mandatory to increase the reaction performance, which may promote this reactor concept as an alternative to common devices for continuous biphasic biocatalytic reactions.
The intrinsic bursting observed in SNc dopaminergic neurons at early postnatal stages may promote this process.
In the absence of Myb domain-directed binding, the basic domain of TRF2 may promote this process in a similar manner.
The natural history of C. elegans may promote this because as ephemeral food sources are exploited by a few dauer larvae, this may result in small, local clonal (or semi-clonal) populations [ 6].
Taken together, these results indicated that 4OHT may promote this ERα ligand-independent pathway in ERα-negative breast cancer cells, activating the MAPK-mediated phosphorylation of ERα, which may contribute to its own expression (autoregulation) [ 25].
Shortly after their identification in mammals, it was found that cyclin genes were overexpressed and amplified in a fraction of breast cancers, providing the first evidence that cyclin deregulation, in particular increased transcription, may promote this disease [ 2].
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This may promote the waste recycled and utilized in a more effective and integral way.
However, this may promote the aging of the nanomaterial in situ, modifying the sorption and hence the availability to test organisms.
This may promote the dehydrogenation step of chromophore maturation and transport abstracted proton transport outside the β-barrel, speeding up the chromophore's maturation [107].
This may promote the interaction of CC erythrocytes with splenic macrophages that remove them from the circulation.
This may promote the initial event of Wss1 activation.
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