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Cell proliferation and morphology were tested and compared between two scaffolds using mouse osteoblastic cell line MC3T3-E1.
The polyimides consisting of interconnected nanosheets with a microflower-like morphology were tested as an NIB anode.
Multiple colonies of different morphology were tested from each tonsil sample.
Since the two trees were incongruent, the possible influences of the climate and interspecific competition on morphology were tested as follows.
Significant deviations from expected sex ratios or levels of abnormal adult and gonadal morphology were tested using the chi-square test.
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The mesocrystal structure and surface morphology are tested with the X-ray diffraction, scanning electron microscope and transmission electron microscope methods.
The sensitivity of optical coherence tomography images to sample morphology is tested by two methods.
In addition, based on the SAFE analysis results, the hypothesis that pyrethroids can affect neuronal branching morphology was tested in an in vitro model of cortical neuron development.
Osteoclast morphology was tested 3 days later, using a commercial tartrate-resistant acid phosphatase (TRAP) staining kit (Sigma) and imaged using a Leica DMI6000B inverted microscope, and the number of osteoclasts (defined as TRAP-positive cells with ≥3 nuclei) was counted manually.
For equivalent specific surfaces, these two membrane patterning morphologies were tested in fuel cell conditions with very low platinum loading (30 μg/cm2).
However, the kappa value was almost equal, at 0.23, when only ductal and lobular morphologies were tested.
More suggestions(15)
patterns were tested
morphology were considered
morphology were obtained
morphology were counted
morphology were seen
morphology were noted
morphology were recorded
morphology were reported
morphology were evaluated
morphology were prepared
morphology were used
morphology were compared
morphology were assessed
morphology were fabricated
morphology were picked
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