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Fig. 4 Hysteresis loops (after corrected for paramagnetism) of three selected samples.
After corrected for differences in protein stability, the C434A and C417A, C474A mutant proteins had a 60%and90%0% reduction in 55Fe binding, respectively (Fig. 6D).
Plasma volumes were measured and the changes in hematocrit were, after corrected for the fluid gain and loss, used to estimate global plasma extravasation.
Uptake of 2-deoxy-[3H]glucose in heart, soleus muscle, and epididymal fat was detected in perchloric acid extracts after corrected for label in the extracellular space as determined by the [14C] counts for sucrose.
Results obtained on 150 subjects with normal, intermediate, and deficient G6PD phenotypes show that, although differences exist between the aforementioned characteristics in capillary and venous blood, these do not impact on the quantitative assessment of G6PD activity after corrected for hemoglobin concentration or red blood cell count.
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However, after correcting for multiple testing (Bonferroni correction with 36 comparisons), these results became nonsignificant.
ANOVA was applied to evaluate the tested hypothesis, after correcting for multiple comparisons (Tukey correction).
This association of minimal sclerosis remains strongly significant even after correcting for multiple comparisons (Bonferroni correction).
This remains true after correcting for multiple comparisons using the Bonferroni correction.
After correcting for incompleteness, the individual XLFs are statistically consistent with a single power-law.
After correcting for the effect of size, shape complexity, isolation, and matrix properties remained significant.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com