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Exact(10)
In this figure, the transmission rate is shown as a function of a and d, where the length steps variation of a and d are 1, and the incident angle is θ = 0.6720.
Furthermore, the rate of tension recovery after length steps depended on the phosphate concentration after stretches but not after rapid releases.
Thus, the tension response to temperature jumps seems to correspond to a slow phase of the tension relaxation in response to rapid length steps [ 225, 229, 230] and the overall rate of the tension response to length steps increases with temperature.
A direct identity of the force-generating transition associated with Pi release and length jumps was assumed in some early model studies [ 52, 107, 331] before the broad availability of data from perturbation studies other than length steps.
This "roll and lock" transition may both increase the effective attachment rate [ 75] and contribute to the translation of the thin filaments [ 71] as well as the tension recovery following rapid length steps [ 72, 74].
In terms of such a model, the tension response to length steps is due to very rapid transitions between mechanical/structural states (similar to those in Figure 5) without transitions between biochemical states (horizontal transitions in Figure 8).
Similar(50)
The spatial configuration of the sequence of stepping targets can be manipulated, requiring gait adjustments in terms of step length, step width and step-length symmetry.
Independent variables included variability of step length, step width, and step time.
The primary independent variables were the variability of step length, step width, and step time.
Gait parameters (stride length, step length, step width, gait velocity, and cadence) were evaluated while PF was measured with the Stroke Impact Scale (version 16).
Results show that most of these parameters had significant effects on the step length, step period and hip velocity of the passive walker.
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