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We further establish a precise link between the rate problem and Shannon Kolmogorov's entropy of X.
We further establish the conservation of TADs between polytene and diploid cells of Drosophila.
We further establish that chemically induced cytoskeletal disruption is accompanied by reduced cellular stiffness and viscosity.
We further establish properties of optimal solutions and indicate how these are related with the classical results on adverse selection.
We further establish a kinetic model to predict the ORR activity of these single-atom dispersed catalysts.
We further establish a quantitative version of the characterization of the weak Banach Saks property of a set using uniform weak convergence and ℓ1-spreading models.
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As enzyme costs are particularly difficult to estimate due to their strong dependence on the reactor temperature, we further established a model-based procedure for characterizing the biocatalyst in terms of operational stability and activation as a function of the reactor operating temperature.
Together with the Cre-LoxP system, we further established conditional targeted insertion system for lncRNA expression manipulation for the first time, which was valuable for lncRNA functional analysis.
To facilitate interaction and collaborative learning, we further established a discussion forum wherein users could participate in real-time discussions when they were on site with their smartphones.
While this finding is not entirely new or surprising, we further established a robust connection between intrinsic motivation and L2 listening strategy use, with the more intrinsically motivated students reporting increased self-regulated learning behavior.
We further established that congruency effects for the center two locations persisted throughout the experiment and were not driven by similar response mappings between the size and contrast single-dimension tasks (see Additional file 2 for details).
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