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produced by the filamentous fungi in solid state system have a determining role in degradation of oil seeds cell wall, leading to the release of most of the lipids (generally bound to proteins or to the polyglucides) enmeshed in cellular structures [23].
In young wild type seeds, cell separation was not observed, the cells remaining intact and of regular round and compact form.
In maturing seeds, cell separation in the AZ occurred immediately below the counter palisade layer in the hilum region with cell separation starting in the middle and developed outwards to the epidermis of the funicle.
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This acceleration was independent from the seeded cell type.
Then, step-by-step, each cell distinct from the seed cells is marked with the same optical properties as that of the nearest seed cell.
Larger amount of proteins accumulated in developing seed cell of LOCL while considerable higher amount of oil bodies deposited in developing seed cell of HOCL.
Different from seed cell, silique cell mainly consisted of nucleolus, vacuoles, and chloroplasts without oil bodies.
The area of starch grain in seed cell was larger than that in silique (Figure 3A).
Pore structures of scaffolds should facilitate cell seeding, cell penetration, and distribution in the scaffolds.
Unfortunately, most synthetic scaffolds lack the biological recognition motifs required for seeded cell interaction.
NSs exposed to the HMF maintained significantly higher proliferation rates (>10 times the seeding cell number) than those returned to the GMF condition (~5 times the seeding cell number) (P1, P = 0.0026; P2, P = 0.0457; P3, P = 0.0024; P4, P = 0.0007) (Fig. 2E).
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