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Although Ca2+ and action potential signals could not be measured simultaneously with this procedure, we were able to get insight into relation between Ca2+ and membrane potentials because, in most cases, muscle conditions were relatively stable for several minutes, which was longer than the period of determination of both signals.
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It was reported that changes in methylation states of several genes induced by exposure to antiandrogen vinclozolin during the period of sex determination are correlated with disease state in numerous organs of adult rats, including prostate [ 5, 59].
Other generic ciprofloxacin products were determined to be substandard products where their dissolution profile could not achieve 70% dissolution at 45 minutes or achieved 70% dissolution throughout the 1 hour period of the determination [ 30].
Blood was sampled at the start of the 2-h stable isotope infusion and every 10 min from −30 to 0 min (basal period) for determination of plasma glucose, insulin, and isotopic enrichment of glucose.
Readings were taken for the steady state period for determination of resting energy expenditure, and for a total of 30 min under these basal conditions for measurement of basal substrate respiratory quotient.
During cool PDO periods, coefficients of determination (r2) of cross-correlations between raw Φ t,40) and ENSO indices ranged from 0.45 and 0.59 with ENSO leading Φ t,40) by an average lag of 3.75 months, compared to 0.19 to 0.45 for the pre-whitened (autocorrelation removed) data.
Therefore, four fecal samples were collected from each rabbit during the study period for determination of fecal microbiota.
In our study, we used the kappa agreement method [ 13] and retrograde survival function to validate the optimal clearance period for determination of diabetes incidence from administrative data.
Blood was sampled at −180 min and every 10 min from −30 to 0 min (basal period) for determination of plasma glucose, insulin, C-peptide, FFA, and isotopic enrichment.
After an equilibration period of 60 min to ensure steady-state plasma exenatide concentrations, 61 urine will be collected by spontaneous voiding every 45 min for two time periods while blood will be collected before and after each collection period for determination of inulin and PAH.
Alamar blue is stable and nontoxic, so unlike other metabolic assays, it is possible to plate directly out of wells over long periods for determination of viable cell counts.
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