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The ionic concentrations observed are compared with corresponding "no sorption/desorption" concentration values determined theoretically.
In our proteome analysis we calculated statistical significance of protein abundance changes separately for each copper concentration (0.1, 0.75, 1.5 mM) at each time point (16, 22, 32 hr) relative to the corresponding no copper control, thus yielding growth stage specific proteome responses to increasing concentrations of Cu II) in the growth medium.
*Statistically different from corresponding "no pericyte" group, p<0.05.
The expected number of samples was 30 (or the corresponding no. of sows in herds with less than 30 sows).
Assortment was lower than in the corresponding no selection scenario, which resulted in frequency-dependent effects that act against the evolution of cooperation at small frequencies of cooperator.
Application of OFF for a total of 60 min resulted in a significant decrease in RANKL/OPG ratio compared to corresponding no flow controls at 1 Hz (3600 cycles) loading frequency only (p < 0.05).
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During the second stage, the strength and ductility of the specimens are examined after 2 and 7 days 'ageing' at room temperature and the results are compared with the corresponding no-age samples.
Furthermore, the corresponding no-tax economy will have the same product as the tax-economy (mathbf {p}_r^{*tau } R_mathrm{f}^*=mathbf {p}_r R_mathrm{f}), i.e., the same ratio (mathbf {p}_r^{*tau }/p_0^{*tau }=mathbf {p}_r/p_0).
Results show significantly lower soil bulk density (between 1.10 and 1.26 Mg m−3) in both tilled clear and black plastic-film mulched plots when compared to the corresponding no-till clear or black plastic-film mulched plots (1.40 1.45 Mg m−3).
L_{c} = sqrt {frac{{V_{text{ma}} }}{{mathop sum nolimits_{i = 1}^{s} frac{{A_{text{ma,i}} }}{{l_{text{ma,i}} }}}}} (4 where (s) is the number of the open faces to imbibition, (V_{text{ma}}) is the matrix bulk volume, (A_{text{ma}}) is the surface area open to flow in a given flow direction, and (l_{text{ma}}) the distance from the open surface to the corresponding no-flow boundary.
Each cDNA sample was run in triplicate, and the corresponding no-reverse transcriptase (RT) mRNA sample was included as a negative control.
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