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In a previous article using this same census-based sample, we reported that mtDNA lineages were 61.3% Native American, 27.2% African, and 11.5% European [29].
To provide evidence of the construct validity of the SF-36 in this study sample, we reported the differences in SF-36 scores by known-groups.
Recently with a combined SALZA and OCTO-Twin sample, we reported that higher body mass index (BMI) measured in 1963 predicted both later AD and later VaD (Hassing et al. 2009).
Due to the distribution of our sample, we reported data as medians with ranges for continuous variables using the Kruskal-Wallis test and the Mann-Whitney test for the STSS and SMART-COP scores, respectively.
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For each individual in the sample we report results for: Two binary "event" variables.
For each sample, we report the percentage values corresponding to the addition of early and late apoptosis.
Due to the complexity of the model and the nature of our sample we report significance tests derived by bootstrapped standard errors with 10,000 replications.
In this large-scale cohort of 11,986 diabetic HD patients (69,764 samples), we reported new HbA1c and BG equation models that are at least as good or better than previous equations.
Because many of the filters we visited were still in use (for these, all that is known is that the lifespan is greater than the current duration of use at the time of sampling), we reported the median lifespan (10 years), which is robust to censoring.
However, in a previous study comprising 28 breast cancer samples, we reported that hCAP18/LL-37 hCAP18/LL-37ted in breast cancer cells wash a correlation between hCAP18 protein levels and tupregulated, whereas in normal mammary tissue it was produced at a low level [ 17].
Using paired samples, we report two very important and translationally significant results.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com