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We therefore plugged the observed values into a Michaelis Menten-type equation that approxiMichaelis Menten-type thequationacthat sites, e.g., for the 3PG oxidapproximateson: The results predicompetitionar 2HG production forxes in MDA-MB-468 and Bthese respectwoely, active and 15% of the 3PG oxidation (i.e., sitese.g.osynthetic forx).
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Based on this successful step, the method was then used for the quantitative determination of these two active ingredients in three pharmaceutical brands marketed in the Democratic Republic of Congo.
This is consistent with current functional models for eukaryotic DNA polymerases, which alternate between polymerizing and editing modes, as determined by competition between these two active sites for the 3′ end of the DNA.
Average aerial application rates for these three active ingredients were estimated at 3.3 kg ha-1, 7.0 kg ha-1 and 1.8 kg ha-1, respectively.
Both genetic and biochemical investigations demonstrate an unequal functional contribution among these six active sites for DNA unwinding [ 16, 19, 22– 22]).
In addition, engagement scores were significantly higher for the two active embodied groups.
Engagement scores were significantly higher for the two active high embodied groups as well.
In the latter case, separate dissolution curves for the two active components were obtained.
One-year follow-up results for the three active therapies will be presented later.
Figure 8 presents the normalized results of tweet Content for the four active Tweeters.
Respondents' preferences varied amongst the scenarios for the four active treatments and all the life-sustaining treatments.
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CEO of Professional Science Editing for Scientists @ prosciediting.com