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These results indicate that the differential sensitivity at growth stages can be clearly shown when stages are well defined in the timing treatments and the stress is quantified at growth stages based on the same duration of salinization.
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In this paper, we perform statistical studies of the features of the wave-likesubstorm auroral arcs and magnetic disturbances in the plasma sheet by examining substorm dipolarization events observed by THEMIS satellites during 2008 2009 which are defined in the substorm timing table provided by UCLA (http://www.igpp.ucla.edu/themis/events/).
2002 will be defined in the first instance by the timing and magnitude of the recession.
The timing behavior of the EDCA mechanism defined in the IEEE 802.11e standard is analyzed.
The timing of AKI and albumin administration were not defined in the study.
The timing of the image acquisition (before, during or after treatment delivery) was not defined in the protocol.
As shown in Figure S7B and C, after division of each mother cell, the v-cell underwent cell division at 9.8±1.9 h (group A) or 12.0±0.7 h (group B), while the h-cell differentiated into heterocyst at 10.8±2.4 h (group A) or 12.5±2.3 h (group B). Figure S7D shows normalized data so that time 0 and 1 are defined as the timing of cell division in each mother cell and each v-cell, respectively.
Our main explanatory variables included sex, age at starting treatment, medication, "duration" defined as the timing of measurement in days since the start of treatment, coded as 0, 1, 2, or 3, with 0 indicating "baseline", i.e., ≤ time 0, and 1, 2, and 3 indicating ">0, ≤3 months", ">3, ≤6 months", and ">6, ≤12 months" since the start of treatment, respectively.
Our main explanatory variables included sex, age at start of treatment, diagnosis of DM, and "duration" defined as the timing of measurement in days since the start of treatment as follows; baseline (within 3 months before start of treatment), 0~3 M (>0, ≤3 months), 3~6 (>3, ≤6 months), 6~9M (>6, ≤9 months) and 9~12 M (>9, ≤12 months).
These triggers also need to be considered in defining the timing of human pharmaceutical ADME assessments.
We use stated preference data to compare the valuation of travel time variability under a structural model where trip-timing preferences are defined in terms of time-dependent utility rates, the "slope model", against its reduced-form model.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com