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The fractographic analysis on the blends with the above two types of morphologies provides experimental evidence for the suitability of our models for these morphologies that emphasize the roles of rubber particle spatial distribution and matrix ligament thickness.
NMSC was also divided into basal cell- and squamous-cell cancers, and separate analyses were performed for these morphologies (see Supplementary Materials).
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A comprehensive suite of morphology descriptors were evaluated for each of these morphologies using a recently developed graph based approach.
In addition to the 25 type 1 DA cells described above, a variety of other AP+ amacrine cell types were also found in this set of 120 retinas: 110 AII amacrine cells, four starburst amacrine cells, four large field amacrine cells, two "waterfall" amacrine cells, and two narrow field amacrine cells [see ref. 5 for examples of these morphologies].
Our main finding is that the aforementioned types of fluorine coverage are crucial for the morphology of these materials.
For the morphology on these scales, mesoscopic simulations such as the dynamic mean field density functional theory and dissipative particle dynamics are available as alternatives to atomistic simulations.
For the morphology on these scales, mesoscopic modeling techniques such as the dynamic mean field density functional theory (Mesodyn) and dissipative particle dynamics (DPD) are now available as effective simulation tools.
For the morphology on these scales, mesoscopic simulations such as the dynamic mean field density functional theory (Mesodyn) and dissipative particle dynamics (DPD) are available as alternatives to atomistic simulations.
Open image in new window Fig. 2 Time dependence of storage modulus (G′) and loss modulus (G″) of a Ch/Gp solution (2% chitosan & 8% Gp) and b Van/HPMCs-Ch/Gp) solution (2% chitosan, 8% Gp & 16% Van/Hpmcs at 37 °C, the gelling times for this hydrogels were a 13 min and b 8 min. Figure 3a, b shows the SEM results for the morphology of these hydrogels.
Therefore, an important question of current cell biology in conjunction with physics and mathematics is to elucidate the functional cause for these different membrane morphologies as well as how they are formed.
"So, it is very satisfying that the molecules have provided a positive test for the morphology".
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