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Cytological studies were performed on salivary gland nuclei to compare the localization of the human proteins to their Drosophila counterparts (Fig. 1).
To do this, we performed a Q-FISH assay in metaphasic nuclei to compare the telomere length of group I G2 tert−/− progeny with that of the G2 progeny showing an abnormal phenotype (groups II and III) at 48 hpf.
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It would be of great interest to compare the nuclei in one or more Hexamitinae diplomonads (e.g.: Spironucleus, Hexamita or Trepomonas).
Apoptotic changes noted in the nuclei, such as chromatin degradation or condensation, were judged as markers of apoptosis, and counted to compare with nontreated controls.
Student's t test was used to compare differences in the mean number of Fos-ir nuclei/cell group between normal and labyrinthectomy control.
The latter may predominate in the SGZ with its high ratio of nuclei to blood vessels compared to other brain regions (Mazumdar et al., 2010).
After 24 hours of exposure to VAN 0.6, 3, and 6 mg/mL, apoptosis of RPTECs measured as nucleosomal DNA fragmentation and migration from nuclei to cytosol was quantified and compared with apoptosis under the same conditions but in the presence of cilastatin).
In Figure 4C, the normalized N CM with respect to T0 (∆NCM) was plotted, indicating the shift in β-catenin between the compartments due to the specific perturbations in time (i.e. a greater ∆NCM implies a shift of β-catenin levels to the nuclei compartment as compared to T0).
CaSki cells exhibited a lower whole-cell stiffness and a softer nuclei zone compared to the normal counterpart cells.
Treatment with Tat alone or in combination with morphine caused time-dependent increases in the percentage of cells expressing p65 (RelA) within their nuclei as compared to vehicle (control) or morphine-treated cells (Fig. 3 A).
TEM showed that M90T induced degenerative changes in submucosal neurons and nerve fibers such as cell shrinkage, axonal swelling, multilamellar cytoplasmic bodies and chromatin alterations of nuclei, as compared to control tissues (Figure 5A D).
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