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Multiple urine specimens for analyzing Na + K + Mg + Urea + Ca + phosphate + Creatinine + proteins and uric acid were obtained from 2-hour, 12-hour and 24-hour urine samples during day and night time, and results were compared with those obtained from the gold standard method (24-hour urine collection).
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Digital Image Correlation (DIC) and Electronic Speckle Pattern Interferometry ESPII) are two of the most common optical techniques used for analyzing specimens, prototypes, and real components subjected to mechanical deformation.
Improvements in sequencing technologies have evolved into new paradigms for analyzing tumor specimens; massively parallel screens can examine patient samples for potentially actionable targets.
In order to address the question of persisting spirochetes after therapy, highly sensitive direct detection methods for T. pallidum would be essential for analyzing patient specimens before and after treatment.
This technique is increasingly used in a preclinical setting as an in vitro imaging method for analyzing tissue specimens and as an in vivo imaging method for evaluating small animals [ 30, 31].
Similar tissue parts were sampled for all specimens and analyzed for C, N, and P tissue content.
Samples were archived in a controlled storage facility (Fisher Bioservice, Bishop's Stortford, UK) at −80°C for RBC and −20°C for all other specimens, and analyzed for this study in 2009 2010.
For the current analysis, blood specimens were analyzed for plasma CoQ10 and low-density lipoprotein (LDL) levels.
Immunolabeled specimens were analyzed for each antibody separately for a minimum of 10 individuals per developmental stage.
Outcome prediction was found to be highly similar for specimens analyzed in either the UAMS or Signal Genetics CLIA-certifiedd laboratories.
Urine specimens were analyzed for creatinine using a Beckman Synchron AS/ASTRA clinical analyzer (Beckman Instruments, Inc., Brea, CA) at the University of Minnesota Medical Center (Silva et al. 2004).
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