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This research did not involve human subjects, human material, human data, animals, or plants.
Trapping is also commonly used to generate MR data: animals may be trapped once, given unique markings, and re-sighted or re-trapped on subsequent occasions.
After collection of treadmill data, animals were sacrificed and EDL muscles were harvested, flash-frozen in liquid nitrogen and stored at −80°C.
In the previously published data animals were dosed with the appropriate vehicle or vortioxetine at 0.001, 0.01, 0.1, 1, 3 or 10 mg·kg−1; escitalopram at 0.16, 0.49 or 1.6 mg·kg−1; duloxetine at 1 or 10 mg·kg−1; flesinoxan at 2.5 mg·kg−1; ondansetron at 0.3 mg·kg−1; or SB269970 at 10 mg·kg−1 (du Jardin et al., 2013; Pehrson et al., 2013).
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In contrast to the new data, animal studies do suggest the existence of the mu-opioid receptor in the trigeminocervical complex [53].
In the statistical analysis of the data, animal was the experimental or measurement unit.
In addition to observations from clinical data, animal experiments have investigated the relationship between tumor hypoxia and cancer progression.
Data from animals immunized with control liposomes (black) and soluble gp41-MinTT protein (grey) are included.
No human health effects have been discovered, but E.P.A. officials' concerns were raised by recent toxicological data in animals.
Baseline data between animals of experimental groups were not different.
Physiological data for animals that completed the study are presented in Table 1.
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