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pHH3+insulin+ (with punctuated pattern) cells were counted as β-cells at G2 phase.
Controlled 3D Cell Pattern: Cells were patterned on the 3D matrices into discrete zones.
Without showing any systematic pattern, cells were seen to actively weave their way through the ordered network of immobile Sertoli cells, over a range of approximately 20 150 μm within a single day.
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The percentage of mostly nuclear (N > C), even distribution (N = C), or mostly cytoplasmic (N < C) of Smurf2GFP pattern cells was calculated based images of 40 cells at each data point.
Unexpectedly, CTCF binding patterns in normal cells were remarkably different from those in immortal cells.
Both the test pattern and H-pattern cells are analyzed using intensity-dependent photoluminescence imaging (Suns-PL), and the H-pattern cells are additionally probed at each busbar to monitor their open-circuit voltage (via Suns-Voc measurements).
During growth and patterning, cells are specified by both quantitative and directional information.
In all pattern widths, cells were highly aligned, with maximum cell and nuclear elongation occurring for the 10 μm pattern width.
However, despite this abnormality, the results of replication pattern in H9 cells were comparable with that observed in H7 cells.
25 Alterations of the cellular ganglioside pattern in NEU3‐overexpressing HScellsells were analyzed by thin‐layer chromatography.
In the solid pattern, the myoepithelial cells were diffusely positive for ABCG2.
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