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When either input frame (Rec[t] and Rec[t + S]) is coded by 'Skip' mode, the target frame (frame[t + S/2]) is coded by skip mode, and only one 'Skip' indication bit is transmitted.
It is well known that, when a Pulse-Doppler radar operates in high pulse repetition frequency (HPRF) mode, the target range information is ambiguous due to the aliasing range [1].
Comparisons of the computed far-field results with the measured acoustic data reveal that, in general, the solver predicts the peak sound levels well when the farfield is dominated by the in-duct target mode (the target mode being the one specified to the in-duct mode generator).
Similarly, using SrMPV mode, healthy young subjects had smaller deviations from the achieved symmetry ratio and, compared with the no vibration mode, the target symmetry ratio was approached well, as indicated by the p-values (p = 0.0065, 0.0823).
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Depending on the variable-rate strategy in Equation (34) of [8] and integrating the four transmission modes, the target transmission data rate R BPCU can be expressed as R = P ( A 0 ) ( 2 L ) R ~ 2 L + 1 + P ( A 1 ) R ~ 2 + P ( A 2, E ¯ ) 2 R ~ 5 + P ( A 2, E ) ( 2 L ) R ~ 2 L + 3. (B.19).
Modeling studies were carried out to further rationalize the NPSR binding mode of the target compounds.
Finally, molecular docking studies were performed to predict the possible binding mode of the target compounds.
Their binding mode with the target enzyme was clarified by molecular docking.
Selected ion monitoring mode determining the target ions of sitosterol (m/z 414, 396, 329, and 213) was applied for the quantification of this component.
The chromatography in the first dimension, operated in the heart-cutting mode, separates the target compound from the impurities by mass-triggered fractionation based on its molecular weight.
The cladding layer is assumed to be porous alumina (p-Al2O3) increasing the interaction of the surface plasmon mode and the target molecules.
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