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To accomplish this, the concentration gradient term ∂CL∂T was assumed to be constant for both (111)A and (111)B experiments.
We also show that the average bone porosity multiplied by the ratio of bound to mobile water may be constant for both normal and disuse bone groups.
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This maximum acceleration can be verified by experimental studies, however, since the objective of this study is to make a relative comparison between the intact and the ASR affected concrete, and this coefficient is constant for both models, it is believed that the exact value of accelerations do not hinder such a comparison.
As seen from (1) and (2), the ratio of τ max τ min is constant for both algorithms and is given by the eigenvalue spread (i.e., condition number), λ max λ min i.e., τ max τ min = λ max λ min. (3).
However, this increased fitness is constant for both types of pathways, and remains constant during the period in which the possible occurrence of a mutator mechanism is being considered.
Quintile break points were constant for both vaccine groups.
The underlying assumption of the analysis is that enrollment risk is constant for both bacteria (alone or in combination).
The rate of reaction was constant for both pregnant women and non-pregnant, female HCWs throughout the study period.
In contrast, in our experiment the physical size distance between digits was constant for both numerical distances.
Gene BR1035 of unknown function was used as internal reference for normalization, as its expression rate was constant for both strains in the experiments.
In this analysis, we assumed that the apparent rate of repositioning was constant for both substrates but that the number of translational positions was different for each substrate.
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CEO of Professional Science Editing for Scientists @ prosciediting.com