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During the experiment, the cortical layer boundaries were identified from the infrared differential interference contrast (IR-DIC) images based on cell shape, size, and density.
In certain studies where the cells have a very distinctive shape, such us bacteria or yeast cells, the object separation could be done based on cell shape, removing the need for a nuclear marker and thus, the need for fluorescence altogether.
We also characterised adaxial epidermal cells of the flower perianth by SEM, finding that the petals and sepals each are divided into two distinct domains based on cell shape and size (Fig. 8b, c, e and f).
We also characterised adaxial epidermal cells of the flower perianth by SEM, finding that the petals and sepals each are divided into two distinct domains based on cell shape and size, while the labella had seven domains.
Scanning electron microscopy characterisation of adaxial epidermal cells of the flower perianth, showed that the petals and sepals each are divided into two distinct domains based on cell shape and size, while the labellum comprises seven domains.
A previous study with several species of orchid also described various cell types based on cell shape and size, but not in terms of domains within the petals, sepals or labella [ 29].
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As illustrated in Table 1, there are several microfluidic devices that have been developed for separation based on cell size, shape, and density, including inertial microfluidics and deterministic lateral displacement.
The infiltrating cells appear to be mostly neutrophils and macrophages (based on cell size and shape) although no detailed analysis was attempted.
One-day ligated glands contained large numbers of infiltrating inflammatory cells that were most prominent in the gland stroma but also present within the interstitial spaces between acini and ductal structures, and were mostly neutrophils and macrophages (based on cell size and shape).
Here, we define cell polarization based on cell morphology in which the cells become highly elongated (pilate ellipsoid), and we use quantitative metrics (roundness) to assess cell shape (below).
Based on characteristic cell shape, size and their relative locations, cochlear cells in the sensory epithelial, lateral wall and stria vascularis are clearly identifiable in this live tissue preparation (various cell types are marked in Fig. 1,A&B).
More suggestions(15)
based on particle shape
based on cell density
based on cell decomposition
based on cell morphology
based on cell aggregation
based on cell count
based on cell adhesion
based on cell elongation
based on cell replacement
based on cell overlapping
based on cell seeding
based on cell lineage
based on cell proliferation
based on cell body
based on cell radius
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