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In order to allow for the mice to adapt to the control diet, their diet was changed from normal to the control AIN-93M diet 3 4 days prior to the experiment.
We allowed the mice to adapt to their new environment for 2 weeks before experimentation.
Each exposure was preceded by a period (~10 min) that allowed the mice to adapt to the plethysmograph to reach a stable level of breathing.
Each pair of mice was placed together in a cage for 1 month to allow the mice to adapt to each other [ 10, 11].
Izumo, Pejchal et al. found that the lost synchrony could be partially restored by training the mice to adapt to cycles of light and dark and feeding schedules.
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In response, Pink1−/− mice appear to adapt the expression levels of critical genes controlling innate immune responses, perhaps to mitigate inflammation and inflammation-induced neuronal damage (see also below).
Reversal learning requires behavioral flexibility: the mice need to adapt their previously learned behavior to stop pressing the old active lever and begin pressing the new active lever for food reward.
Therefore, the WAT of FSP27 deficient mice appear to adapt certain features similar to those found in BAT.
It is also possible that the absence of myogenin allowed mice to better adapt to long-term exercise-induced training.
For light-adapted pure cone ERG measurements, mice were allowed to adapt to light with an intensity of 72.7 cd/m2 for 20 min. ERG measurements were obtained by measuring the average response following 50 light flashes at a frequency of 1 Hz.
The writer says, for example, that "white-footed mice are evolving to adapt to urban stress".
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