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We additionally probe C3H8 conversion and C3H6 selectivity between 850 °C and 1100 °C as a function of membrane area, fiber length, and He flow rate.
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For control purposes, we additionally probed retention of the 16 triplets that were already used for estimating baseline performance, and found that in most subjects recall rate for these items at retrieval was indeed close to 100%, indicating a ceiling effect.
As shown in Supporting Information Table 1, we observed significant differences in several of the agonist KA values in the presence of VU0155094 or VU0422288; additionally, probe dependence for this effect was noted.
Additionally, probe 4 could also be applied to monitor hydrazine in living cells by biological imaging.
Additionally, probe 1 could detect ClO− quantitatively in the range of 0 120 μM with the detection limit of 4 μM.
Additionally, probe 1 is cell membrane permeable and can be used for cellular imaging of endogenous CE2 in living cells.
Additionally, probe sets coding for glycolytic enzymes showed induced expression levels.
Additionally, probe time and watts in VO2max presented a large ES and HR at ventilatory threshold, a moderate ES.
Additionally, probe sets for putative nodulin (or nodulin-like) genes were identified using known nodulin protein sequences (E-value < 10-10) in the public database.
Additionally, probe classification by CpG enrichment classes and to a lesser extent gene feature groups resulted in distinct patterns of DNAm.
Additionally, probe tone frequencies near to CF cannot provide any useful test of the hypothesis that the frequency of the probe tone affects the tuning of suppression (they should sit near the origin in Fig. 3A).
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