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The same test conditions were maintained in controls containing Asc and either SOD1 or ctDNA.
Rapid pacing of the cells induced a decrease in NADH fluorescence, an indirect indicator of respiratory chain activity, whereas this was maintained in controls.
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Also, no probiotic treatment was maintained in control group.
Undifferentiated hMSCs were maintained in control medium.
This association was maintained in control subjects and all groups of diabetic patients for CNBD.
Fish were maintained in control water conditions as described earlier (Table S1).
The mice were maintained in controlled environment with food and water ad libitum.
The one exception was SMOC2, which is normally expressed in differentiated P0 and P1 cells maintained in control medium.
The pots were maintained in controlled chambers at 24±2°C, 60% relative humidity, with a 16-h light/8-h dark regimen.
The experiment conducted over a three-month period revealed that transcriptomic differences were maintained in controlled conditions.
Afterwards all samples were either maintained in control medium or replaced with chondrogenic or osteogenic medium for 28 days.
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