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Endo-meso transitional arrangements, as seen in the longitudinal section of the polyp, have ~28 linearly arranged attachment points that transition from endodermal (~50%% of points) to mesogleal (distal to proximal), and may be a misinterpretation of the cyclically transitional (as viewed in a single histological section) or cteniform endodermal arrangements.
Orthogonally-reticulate mesogleal arrangements, as seen in longitudinal section of the polyp, have rectangular-shaped lacunae arranged in contoured grids along the length of the marginal musculature such that the supporting mesoglea appears to be an orthogonal mesh (Fig. 1s t; Morphbank collection 851277; dimensions in Table 1).
We prepared three types of Si-ND arrangements, as seen in Figure 2: separated Si-NDs as a single QD, a 2D array of Si-NDs as a 2D QDSL, and a 3D array of Si-NDs as a 3D QDSL.
On a structural level, they differ in the methylene group packing arrangements as seen by wide angle X-ray diffraction experiments.
Linear mesogleal arrangements, as seen in longitudinal section of the polyp, have circular or elliptical lacunae that approximate a single, continuous, linear arrangement along the length of the marginal musculature (Fig. 1o p; Morphbank collection 851279; dimensions in Table 1).
Branchiform endodermal arrangements, as seen in longitudinal section of the polyp, have long gill-like mesogleal pleats supporting the distal 5 20 % of the length of the marginal musculature, transitioning abruptly to a cteniform-like morphology with relatively short and uniform mesogleal pleats through the remaining length (Fig. 1a b; Morphbank collection 851143; dimensions in Table 1).
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Adaptation can be in temporary arrangements, as was seen in the response to piracy off East Africa.
Duplications of entire domains result in tandem arrangements of the self-domain along the length of the protein in a beads-on-a-string arrangement as seen in cupredoxins and phospholipase D or result in discontinuous arrangements of the domain as in squalene hopene cyclase.
Although the interface appears to be stable, it cannot be excluded that DDR activation is accompanied by substantial changes in the ectodomain arrangement, as seen in the epidermal growth factor receptor, for instance [54].
The simplified mesogleal arrangement, as seen in published drawings of the longitudinal section of the polyp, have 7 17 circular or elliptical lacuna, arranged linearly, and may be an oversimplification of a known mesogleal or endodermal marginal muscle forms.
Nonetheless, as discussed in the next section, because hydrophobic interactions in the parallel Aβ16−22 organization are strong, they can overcome the electrostatic destabilization induced by flexible side-chains at the termini, leading to a parallel Aβ16−22 arrangement, as seen from Figure 8B.
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