Sentence examples for both doses exhibited a from inspiring English sources

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The extracts, at both doses, exhibited a significant (p < 0.05 - < 0.01) dose-dependent antinociceptive activity in hot plate and tail immersion test.

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The analyses of the mean step-down latency values for each group in the T1 period revealed that the CE-treated rats, at both doses, exhibited an increase in mean latency compared to the CS group (P < 0.0001), Tween® group (P < 0.0001) and Diazepam (P < 0.0001).

Following vaccination, both vaccine doses exhibited an acceptable safety profile with minimal injection site and systemic reactions.

Additionally, from PNDs 15 20 the mice exposed repeatedly to CPO at all three doses exhibited a dose-related transient hyperkinesis in the 20-min period following CPO administration, suggesting possible effects on catecholaminergic neurotransmission.

High doses of these antioxidants resulted in a decrease in GJIC activity, whereas rats exposed to low doses exhibited an increase in GJIC (Krutovskikh et al. 1997).

Drug plasma concentration and dose exhibited a strong linear relationship.

In comparison, unconjugated AMT at the matching subcutaneous dose exhibited a similar time to maximum concentration of 30 minutes, but the elimination half-life increased significantly (~140 minutes).

Moreover, patients treated with a lower daily dose of corticosteroids (≤ 80 mg methylpredisolone or equivalent dose) exhibited a similar mortality rate compared with those treated with higher daily dose (9/30 vs. 8/22, p = 0.854).

The data generated in separate experiments using 20 mg kg−1 twice-weekly or as a loading dose (followed by 10 mg kg−1 as a maintenance dose) exhibited a similar efficacy profile (Tumour Growth inhibition (TGI) values of 52% versus 55%).

Our results demonstrate that in contrast to high-dose PCB-77 dosing in vivo, lower doses exhibit an opposite effect to increase body weight.

The suspension dose exhibited an extended absorption profile with a T max of 2 h and a C max of 0.024 μg/mL, consistent with solubility/dissolution rate-limited absorption.

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