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A trafficking defect with intracellular accumulation of pro-sucrase-isomaltase in the Golgi apparatus was found to be responsible [1].
To summarize, a new kind of continuous-flow EC apparatus was found to be cost-effective and feasible in this work.
The apparatus was found to be an invaluable supplement to the theory taught in the classroom, and in particular in the areas of microprocessor programming and interfacing, areas that are traditionally foreign to Mechanical Engineering students.
A 1911 1913 survey found the light in good shape, though the apparatus was found out of date and needing replacement.
Similar to the results observed previously with TbCentrin2 [6], TbCentrin4 [10] and TbMORN1 [12], the single Golgi apparatus was found adjacent to the anterior half of the TbLRRP1-labeled bi-lobed structure.
In cases where the contact between the CTL and the cell body of virally infected astrocyte was so close as to exclude cellular cytoplasm from this contact, the Golgi apparatus was found displaced to one site of the contact (Figure 3, Category 4).
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The apparatus is found to ensure a consistent temperature among the samples in equilibrium, meeting the experimental requirements for samples of molalities less than 0.05 mol · kg−1.
In contrast, in the 420 probe sets with higher expression among the seven homozygotes for c.1521_1523delCTT in CFTR, which carry two rare EHF alleles, genes that specifically take part in the glycosylation of biopolymers and genes that are assigned to the Golgi apparatus were found to be enriched by DAVID (Supplementary Table 4).
However, components of the flagellar apparatus were found in L. enzymogenes C3; the 22 genes coding for a flagellar apparatus (including basal body, hook and regulatory genes) are also conserved in the genomes of L. capsici 55 and L. gummosus 3.2.11 (Additional file 3: Table S14).
We previously showed that fluorescent dextrans endocytosed from blood at the BLM first appear in punctate vesicles just under the BLM and then rapidly traffic, presumably on microtubules, to the pericanalicular region where endosomes, lysosomes and elements of the Golgi Apparatus are found [ 17].
The cumulative release profile of individual pellet using the 400-DS dissolution apparatus 7 was found to be more precise at distinguishing differences in the applied coat quality.
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