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Since GIRK activation kinetics could be influenced by the G protein deactivation cycle (Doupnik et al., 1997; Lambert et al., 2010), we did not put significant emphasis on the analysis of the differences in the raising phases of the response.
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Typically, bistable biological systems were described either at the level of gene expression due to the regulation of gene expression by transcription factors, or at the level of posttranslational modifications e.g., activation-deactivation cycle due to phosphorylation.
Furthermore, Ca2+ oscillations mediated during the activation-deactivation cycles are used for signal transduction by a majority of cells (2, 51).
Such severe processing conditions generally lead to rapid catalyst deactivation, shorter cycle lengths and reduced throughput.
Presently, a series of deactivation (reaction)–regeneration cycle tests were designed and carried out over a well-characterized 5 wt%Mo/HZSM-5 at practically required severe conditions (1073 K and 21,080 and 40,000 mL/g/h) to clarify the effect of CH4 and H2 exposure durations on the activity stability.
This could cause, for example, the deactivation of cell cycle checkpoints or enhanced exclusion of therapeutic reagents or increased expression of multidrug-resistance proteins, leading, as the name of the latter example already suggests, to resistance not only against already used therapeutic avenues but also against possible future approaches.
Therefore, the second alteration in cancer is deactivation of cell cycle checkpoints.
Conversely, as shown in many recent studies, these mitotic kinases also antagonize checkpoint signaling, and thereby promote checkpoint deactivation and cell cycle reentry, a process termed "checkpoint recovery".
Moreover, immobilized systems have shown that they are stable and do not present deactivation after several cycles of reuse, being readily applicable for continuous water treatment systems.
In particular, catalytic systems derived from resins containing ditopic groups being able to form stable pincer complexes have shown a very remarkable stability with no sign of deactivation after several cycles.
As compared with the 8% deactivation after 10 cycles of reaction in mono-aqueous phase [25], the fast deactivation might be attributed to the protein-denaturing role of the anionic surfactant SDS. Figure 3 Repeated use of the immobilized BsE.
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