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The conducted experiments confirmed the significance of two out of three analyzed at this stage factors, i.e. glycerol and urea, to the investigated process.
Only control group tumors will be analyzed at this stage to assess when to terminate all animals in the experiment.
For example, Aβ plaque loads can increase exponentially during the first stages of plaque deposition, and spurious drug effects may be seen in animals analyzed at this stage unless control and treatment groups are age-matched to within days of one another.
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The likely turnout is very difficult to predict or even analyze at this stage.
Since neutral lipid accumulation starts at the end of exponential growth phase and reaches its highest level in the stationary phase [3], wild type and mutant cells were analyzed at this growth stage.
Each imputed data set was analyzed individually at this stage, but the reported values are means across the 30 imputed data sets.
Mice were analyzed at end stage, defined as approximately 3 months of age or when tumors reached >1.5 cm diameter.
BC mouse models were analyzed at end stage, defined as tumors reaching 1.5 cm, the animal experienced >15% weight loss, or other absolute survival event.
PDAC mouse models were analyzed at end stage, defined as tumors reaching 1.0 cm, the animal experienced >15% weight loss, or other absolute survival event.
The structural evolution from ZnO through Cu(OH 2 and metallic Cu to Cu2O phase was analyzed at each stage with X-ray diffraction and X-ray absorption spectra.
KPC experiments were performed with mice of mixed genders and mice were analyzed at end stage, defined as approximately 6 months of age or when tumors reached 1.0 cm, the animal experienced >15% weight loss, or other absolute survival event.
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