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Blood and urine drug concentrations were collected from all 18 subjects at all six time points.
Samples for quantification of both protein levels and intracellular metabolite concentrations were collected from these continuous cultures as described below.
Urine specimens for analyses, including phthalate metabolites and creatinine concentrations, were collected from each participant during one of three daily examination periods (0830 1200, 1230 1600, or 1630 2000 hours) (Silva et al. 2004).
In addition, blood samples for determination of figitumumab concentrations were collected from patients enroled into the PK DDI cohort before dose in cycles 1 6 and 1 h after dose in cycle 4. Plasma concentrations of figitumumab were analysed by a validated ELISA as previously described (Haluska et al, 2007).
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In both the studies, blood samples for the determination of LIXI plasma concentration were collected from LIXI injection until 12 h thereafter.
Soil samples for determination of treatment responses of soil organic horizon C concentration were collected from all plots as described above and the depth of the soil organic horizon was measured.
To this end, an extensive databank covering wide ranges of temperature, pressure, and solvent concentration was collected from literature.
To increase the variability in colostral or serum IgG concentrations, samples were collected from more than one farm and or from 2 dairy breeds.
Hourly air pollution concentration data were collected from the Department of the Environment, automatic monitoring network during October and November 2012 for two monitoring sites (Abrasan and Farmandari sites) in Tabriz.
Tracer gas concentration data were collected from 17 sites, including parking places, streets, open areas, and high-rise buildings, in a dense urban environment in the Hamamatsu-cho Minato-ku area, Tokyo, Japan.
High-frequency atmospheric CO2 concentration data were collected from 35 towers located in the U.S. and Canada (Table S1).
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