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In confocal images of lumbar tissue stained for NeuN and NK1-R immunoreactivity (figure 3B G), NK1-R expression is characterized by appearance of an outline of NK1-R immunoreactivity surrounding NeuN immunoreactivity.
The inflammatory reaction is a fundamental component of the innate immune response, and its most proximal expression is characterized by the elaboration of proinflammatory cytokines – tumor necrosis factor (TNF -α and inTNF -αkin (IL)-1β.
Given the established role of CDC6 in the control of DNA replication initiation, we were interested in determining whether acute loss of CDC6 expression is characterized by an increase in DNA damage signaling with concomitant effects on cell cycle distribution and whether any such effects would be more apparent in RAS mutant cells.
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Figure 6C indicates that cell populations with enforced miR-26a expression were characterized by significantly increased numbers of cells arrested in G1, which is more than that of tumor cells treated with miR-NC containing PLGA nanocomplex or untreated control (Table 3).
The LPS-induced cytokine production and cell surface marker expression were characterized by flow cytometric analysis.
To study the two candidate genes for the development of NPC, mRNA expression was characterized by quantitative real-time PCR in 3 NPC cell lines, CNE2, SUNE1, and C666-1, in the immortalized normal nasopharyngeal epithelial cell line NP69, and in 11 primary NPC tissue samples with adjacent normal tissue.
Morphological changes caused by EGFP-MVaf1 expression were characterized by fluorescence microscopy, in Z-stack acquisition mode.
Enzyme expression was characterized by electrophoresis and immunoblotting as a function of time in culture and phenotypic differentiation.
Genes with lineage-specific patterns of differential expression were characterized by a high frequency of SNPs associated with TSSs.
However, the most anterior domain of AmphiSyn expression was characterized by a cluster of ventro-lateral nerve cells.
Levels of apoptotic markers, signaling molecules, and cell cycle regulators expression were characterized by Western blot analysis.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com