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Yet, since both Y and ZSM-5 are used simultaneously in practice, the information on the relative rates of deactivation between the two zeolites is very important.
A two sample t-test was then run to determine the differences in deactivation between groups (HFA vs. Controls) for the prosodic listening condition.
Interestingly, these effects resulted from a relative difference in deactivation between conditions – with the target contrast (numbed hand>baseline during intensity trials) being the only condition that showed activation and all the other conditions showing deactivation.
Post-hoc tests by Fischer LSD confirmed that not only deactivation between different n-back-tasks is significantly different but also activation of the DMN in rest differs depending on the preceding n-back-task (Table 1).
To test whether the reason for this difference is that the molecular identity of the rate-limiting process of saturated photoresponse recovery changes (e.g. from PDE deactivation to rhodopsin deactivation) between 25°C and 37°C, we determined τD at three different temperatures (24 38°C) from two retinas in HEPES buffered Ringer.
There were small, but statistically significant, differences in the rates of deactivation between Δ2 25, Δ2 9 and GGSmut channels; e.g., at −120 mV the time constant for the fast component of deactivation was 11.4±0.3 ms (n = 14, for Δ2 9), 8.7±0.3 ms (n = 5, for Δ2 25) and 7.5±0.2 ms (n = 10, for GGS mut) compared to 33.7±1.0 ms (n = 11, for WT hERG channels).
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This discrepancy is mainly a result of the oil water interface effect on the deactivation reaction between propagating radicals and TEMPO.
We will study the activation and deactivation relationship between our gene of interest and different sets of coexpressed genes starting from these high-correlated nonlinear expression relationships.
Table 3 shows the thermal deactivation constants between 35°C and 90°C, obtained from angular coefficients of the curves shown in Figure 3, as well as the determination coefficients of regression and the half-life of enzymes at each temperature.
The ultimate goal of our approach is that researchers are able to know the networks of processes hidden in their experimental data, as well as the activation and deactivation relationships between all of these processes.
Half-blocking concentrations of 4-AP were correlated with the time constant of deactivation and varied between 26.2 and 102 microM.
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