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Exact(6)
Block copolymers prepared from isocyanate-terminated polybutadiene (NCOPBER) resulted in cured transparent epoxy networks with no discernible phase-separated morphology, as indicated by scanning electron microscopy.
This reproducibility spans across SN-MP (increase in SN-MP does not change the reproducibility of the measurement), even though the alveolar morphology, as indicated in the findings of aim 1, changes.
CGNs incubated under normoxic conditions were healthy and retained normal morphology, as indicated by large size, phase brightness and intact processes.
After 48 h of p32 siRNA, significant changes in the ER morphology as indicated by calnexin staining were observed with a higher number of punctate ER structures compared with tubule structures.
Healthy fibrin fibres show individual fibres (Fig. 2b) while fibrin fibres in diabetes have thickened masses of fibres with a netted morphology as indicated Fig. 2e, giving the appearance of dense-matted net.
In contrast, CT45 down-regulated cells revealed an altered morphology as indicated by changes in the cell shape (e.g. upper panels, ß-actin staining) and the organization of the microtubule network (middle panels, ß-tubulin staining) which appeared more diffuse and unorganized in siRNA-treated cells.
Similar(54)
The modification using acid did not change the surface morphology of zeolite as indicated in Fig. 2.
To examine cell death morphology, cells were treated as indicated in 12-well plates or 35-mm glass bottom dishes for image capture.
The roles of its individual Gα subunits, however, appear to be quite distinct with respect to developmental morphology and cellular differentiation as indicated by the phenotypes of gene disruption or overexpression mutants.
The eIF2αA/A MEFs ceased proliferating in early passages and displayed an enlarged, flattened morphology characteristic of senescent cells as indicated by increased staining for senescence associated β-galactosidase (SA-βGal) (Fig. 1B).
At 48 h post IR, crypt size and cell counts were decreased in mice of both genotypes; however, at 72 h after IR, Fus1+/+, but not Fus1−/− jejuna revealed regenerating crypts, as indicated by morphology.
Related(16)
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morphologically as indicated
morphology as compared
morphology as observed
morphology as shown
morphology as found
morphology as visualized
morphology as investigated
morphology as described
morphology as presented
morphology as revealed
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