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The results of statistical analyses of EtG and EtS levels of urine initial and post-consumption 4th hour samples are given in Tables 7 and 8 for all beverages.
For 24 hour samples, the primary driver of gene expression profiles was geographic location, regardless of the treatment temperature at which they were raised.
The greatest number of DEGs that varied by location at control temperature were observed in the 24 hour samples (n = 294).
The right shift in the 2N peak becomes a shoulder in 7 hour and 9 hour samples and is indicative of cells in S phase of the cycle.
The 3 hour samples and the 24 hour samples clustered together respectively, indicating that there was more similarity at each time point between gene expression in the different samples that contained monocytes, than there was between the same sample types at different times.
This enables a more continuous view of embryonic development over the first two days because the 48 hour samples from Mexico used here are the same as those used in Voolstra et al. [27].
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This indicates that there are some small differences in concentrations by urine collection days which may be lost in our sampling approach of using 24-hour samples in the pregnancy period.
The results for 12- and 24-hour samples correlate for patients without proteinuria.
The urine volume, and total protein and creatinine levels were measured in the 8-, 12-, and 24-hour samples.
Conclusion: Total protein values for 8- and 12-hour urine samples correlate positively with values for 24-hour samples for patients with proteinuria.
Results: Significant correlation was found for all biochemistry parameters between 24-hour urine results and those obtained from 2-hour and 12-hour samples regardless of day or night sampling.
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