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The mice were maintained in controlled environment with food and water ad libitum.
The experiment conducted over a three-month period revealed that transcriptomic differences were maintained in controlled conditions.
The pots were maintained in controlled chambers at 24±2°C, 60% relative humidity, with a 16-h light/8-h dark regimen.
We characterized photoperiod-regulated proteins in the PT, using tissues collected from castrate male sheep maintained in controlled light-dark cycles, following exposure to LP or SP conditions.
Adults were given 10% sugar solution and maintained in controlled conditions at 27°C, 80% relative humidity, and a 12/12-hour 12/12-hourphotoperioday/night
Animals received standard rat food and water ad libitum, and were maintained in controlled 12-h light/12-h dark cycle (6AM/6PM) and 20-25°C 20-25°Ctemperatureions.
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Also, no probiotic treatment was maintained in control group.
We found that the fEPSP amplitude, in slices maintained in control medium (aCSF), was reduced by 30% with respect to baseline values (before Rot exposure), while the fEPSP amplitude of slices pretreated with 3 nM α-syn was reduced by 60% compared to baseline.
Undifferentiated hMSCs were maintained in control medium.
The same test conditions were maintained in controls containing Asc and either SOD1 or ctDNA.
This association was maintained in control subjects and all groups of diabetic patients for CNBD.
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