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In dark conditions, the prothalli formed thick mats of rhizoids which had to be removed for visualization with scanning electron microscopy.
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The masking layer can be removed for better visualization.
Water molecules and Na+ counterions were removed for better visualization.
In Figure 5, the input node and all input-to-gene edges were removed for better visualization.
The 5′ UTR sequences of each gene were removed for a better visualization and comparison.
If greater visualization is necessary, a portion of the inferior spinous process can be removed.
Periodically, organoids were removed, under microscopic visualization, for propagation into new culture flasks or phenotypic and molecular analysis.
In the figures, the defect-free atoms in the workpiece are removed from the visualization.
The L4/5 nucleus pulposus was removed under direct visualization, and the L4/5 intervertebral space was cleaned.
For clarity and to facilitate interpretation, time points at 2, 4, and 8 hours were removed from further visualizations and analyses, and PCA was performed for all conditions at 0, 24 and 48 hours, as seen in Figure 4.
Inferred input-to-gene edges which were removed from Figure 5 for better visualization.
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