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Transcriptome analyses showed that 11,328 of the oligonucleotides demonstrated expression in at least one tissue.
The initial profiling of organs or cells for IL-33 mRNA demonstrated expression in purified dendritic cells, epithelial cells, activated macrophages and, interestingly, high expression in stomach, lung, brain and skin tissues [4], all sites that are rich in mast cells.
The proposed NC marker gene T, demonstrated expression in both NP and NC cells, but expression was significantly higher in NC cells (P < 0.0001).
Immunolocalization of PROKR1 demonstrated expression in term myometrium, predominantly in smooth muscle cells, confirming what we previously observed in nonpregnant myometrium.
While PM normal tissues demonstrated expression in less than 20% of constituent cells, PM degenerate tissues demonstrated increases in the proportion of immunopositive cells with increasing stage of degeneration; however, this did not reach significance at any point.
Nevertheless, by adulthood the NR2F2- lacZ animals demonstrated expression in the anterior hypothalamic nuclei, as well as the basomedial amygdalar nuclei, results that correlated with those obtained for the ABA, and GENSAT datasets.
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We demonstrate expression in Drosophila PRCs as an efficient and inexpensive tool for the large scale production of functional eukaryotic MPs.
We predict KIR3DL0 to encode a functional molecule in all primates by demonstrating expression in human, chimpanzee and rhesus monkey.
Lastly, immunohistochemistry for pSTAT3 was performed using a feline OSCC tissue microarray, demonstrating expression in 48%% of samples tested.
The branching pattern seen for Ldhb demonstrates expression in the primary bronchi, pulmonary bronchi and terminal bronchioles, with expression not detected in alveolar ducts, alveoli and blood vessels for this gene (Fig. 4B).
In situ hybridization demonstrated expression of ASHH2 in the endosperm as well as in the developing embryo (Figure 2C).
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