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The response was considered correct when the stimulus presented in the exclusion trials was selected.
As a result of such stringent screening criteria, a highly-selective subset (21 total trials: aquatic = 5 jumps, amphibious = 4 jumps, terrestrial = 12 jumps) of the 68 recorded trials was selected for detailed analysis.
To distinguish between post-error effects caused by regression towards the mean from "pure" error-induced RT slowing, a subset of correct trials was selected that matched the erroneous trials in terms of reaction time and total number (see [27] for a similar procedure).
Per condition, the mean RT over three trials was selected for statistical analysis.
Anacetrapib, a CETP inhibitor (IC50 = 13 nM) that recently proceeded to phase III clinical trials, was selected as template for ligand-based pharmacophore elucidation [8].
If a survey participant had completed fewer than 4 trials, the highest peak force from the warm-up trials was selected.
Similar(53)
Following the selection criteria, eight clinical trials were selected, of which five were randomized controlled trials.
Individuals from GXR trials were selected if they matched inclusion/exclusion criteria from selected ATX trials; selected GXR IPD were then re-weighted to match the published ATX trial mean baseline characteristics and placebo outcomes.
The structurally diverse D3 and D4 antagonists above preclinical trials were selected to map common structural features of highly selective and efficacious antagonists.
In all, 118 lesions from 30 patients enrolled in these clinical trials were selected by a radiologist (L.H.S) according to RECIST 1.0 for the target lesion selection.
Fourteen controlled trials were selected.
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