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Growth and degradation reach an active equilibrium.
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Efforts to document dynamic equilibrium in active orogens require quantification of rates over time intervals significantly exceeding the scale of these millennial fluctuations in rate.
Evolutionary conservation and conformational plasticity of the kinase catalytic domain allow for a dynamic equilibrium between active and inactive kinase forms, which can facilitate regulation of the catalytic activity [15] [17].
One possibility is that His11 interacts with the sweet taste receptor directly to modulate its activation; the other is that His11 induces a conformational change in neoculin in a pH-dependent dynamic equilibrium between active and inactive forms, as described in our previous model [16].
These results suggest that the TAS1R3-R757C acido acid substitution may affect general functions of TAS1R1/TAS1R3 such as cell surface expression, dimerization of TAS1R1 and TAS1R3 or the dynamic equilibrium between the active and resting conformations modulated by the presence/absence of ligand as shown in mGluR1 [27], [27].
The proportion of active vs. inactive repeats appears to be established by a dynamic equilibrium reset at each cell cycle.
We define a small open emerging economy as an economy where the limited commitment problem is active in equilibrium.
In order to account for this deactivation, we need to consider that the active boron equilibrium concentration is modified by the presence of carbon in non-amorphized silicon region with high concentration of interstitials.
Thus, we cannot infer the exact inactive-state versus active-state equilibrium constant for the VSD at 0 V (even assuming that excision of the VSD from the rest of the channel does not alter this equilibrium).
In our numerical simulations, the inhibitory unit is always active at an equilibrium state regardless of the external input.
When both units are active in the equilibrium state, the state vector amplifies the difference in inputs according to widehat {u}_{1}-widehat {u}_{2} = frac{ widehat {b}_{1}- widehat {b}_{2}}{q- w^{0}{q- w^{
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