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Exact(26)
Gelation times (ranging from 15 to 150 min) were significantly dependent on reagents' nature and concentration.
At baseline, the resting and stimulated salivary flow rates (g/5 min) were significantly greater in the control group than in the study group (p < 0.05).
As salinity decreased after simulated rainfall, haemolymph osmolality (after 60 min) and survival (after 180 min) were significantly lower than in control treatments.
The cortisol response in the protein condition (AUC = 37,024 ± 3518 nmol/L min) and in the fat condition (AUC = 35,977 ± 3562 nmol/L min) were significantly smaller when compared with the cortisol response in the carbohydrate condition (AUC = 47,310 ± 3667 nmol/L min) (p < 0.03), but did not differ from the control condition (AUC = 32,784 ± 1683 nmol/L min) (Fig. 1).
NF measurements taken at and after 20 min were significantly different from the size of NF obtained in EGE in the reperfused model (P < 0.001), and there was a similar, significant reduction in the NF at 25 min in the non-reperfused model (P < 0.001).
The maximal rate of LV pressure rise (dP/dt max) and LV pressure fall (dP/dt min) were significantly decreased in DM group (Fig. 1C & D, respectively).
Similar(34)
In both groups, Tsk after 30 min was significantly lower (ΔTsk~0.5 °C) than at rest (p<0.05).
Subsequently, there was a gradual decrease so that at 150 min the plasma cortisol concentration had returned to pre-stress levels and at 240 min was significantly lower from the concentration at 0 min (p <.05 Fisher's LSD).
In the HR group post-hoc analysis indicated that the plasma cortisol concentration at 60 min was significantly higher from the pre-stress levels at 30 min (p <.05 Newman-Keuls).
In addition, the ALP activity of hMSCs cultured on PD-PLLA (1.74 ± 0.14 nmine/DNA/30 min) was significantly higher than on PLLA (0.97 ± 0.07 nmine/DNA/30 min).
The release of dopamine in the PFC produced by handling stress (40 min) was significantly reduced in both enriched and control 24 months animals.
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