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To establish a cellular basis for hyperfluorescent GA border zones, histologic autofluorescence (HAF) was measured at defined stages of RPE pathologic progression.
To find out whether increased IL-6 and TGF-β1 plasma levels after completion of RT originate from the tumour, IL-6 and TGF-β1 plasma concentrations measured at defined time-points during follow-up were plotted against the concurrently determined tumour responses of every patient (fig. 6).
To measure the effect of sera on cellular growth, total protein was measured at defined time points during culture in 6-well plates by the colorimetric method [ 37].
Then, the mice were injected intraperitoneally with glucose (2 g glucose per kg body weight), and blood glucose levels were measured at defined time points (15 min, 30 min, 45 min, 60 min, and 120 min).
The extent of migration (i.e., the distance from the cell column base to the tip of the outgrowth) was measured at defined positions with SPOT software (SPOT Imaging Solutions, a division of diagnostic instruments, Inc., Sterling Heights, MI, USA).
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The main objective of efficacy tests is to determine the number of surviving microorganisms after a specific contact time measured at a defined time point.
Cardiovascular variables and gas exchange data were measured at three defined points in time: 1 hour before the extubation (T1), continuously during the NIV trial (a mean value was calculated and expressed as T2), and at the end of the NIV trial with the patient in spontaneous breathing (T3).
Serum 25(OH)D3, 1α,25(OH)2D3, parathyroid hormone, C-reactive protein (CRP), and ionised calcium were measured at five defined timepoints: T1 - baseline, T2 - 5 minutes after onset of cardiopulmonary bypass (CPB) (time of maximal fluid effect), T3 - on return to the intensive care unit, T4 - 24 hrs after surgery and T5 - 5 days after surgery.
Seroconversion was measured at S2 and defined as a four-fold rise in HAI post-influenza vaccination compared to pre-vaccination or ≥40 if S1 was <10.
Traditional risk factors measured at baseline, as defined in the Framingham model, do not fully account for this increased risk [ 2].
Here we evaluate the use of an adapted microperimeter to measure visual function at defined retinal regions under scotopic conditions.
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