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Because expression of Foxp3 has been reported in lung epithelial cells and some tumor cell lines [17] [19], we co-stained lung tissues or lymph nodes for Foxp3 and CD3 expression, and confirmed that expression of Foxp3 was observed in CD3+ cells but not epithelial cells (Fig. S1a e).
Figure 4A illustrates that HIV replication was significantly inhibited in these cell lines, and confirmed that expression of the GBV-C NS5A 152–167 peptide and the S158E peptide inhibited HIV significantly more than the vector control, scrambled peptide, and both S158G and S158A peptides (p<0.001 days 3 through 6).
We also examined glomerular expression of NDST and confirmed that expression was decreased in the ZF group compared with ZL group and that ARB treatment increased NDST expression (data not shown).
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The authors note that many ASD candidate genes, including Cntnap2, Nrxn1 and Cntn4, are exceptionally long and confirm that expression of several ASD candidate genes is reduced by topoisomerase inhibition.
In fact, the presence of those few cells showing EGFP in the nuclei and absence of HcRed in cytoplasm improves discrimination between activated and non-activated transduced cells and furthermore confirms that expression of HcRed is not leaky.
The entire procedure was repeated using Caucasian gene and miRNA datasets to identify clusters validated in the corresponding Chinese datasets, i.e., 43/54 (80%) gene clusters and 24/24 (100%) miRNA clusters (Fig. S1A and B and Table S4), confirming that expression of pivotal transcriptional features in breast cancer is basically alike in Chinese and Caucasian samples.
Consistently, API5 depletion increased viral polymerase activity and viral titers, further confirming that expression of antiapoptotic protein API5 is detrimental for viral replication and propagation.
Here, we confirm that expression of mRNA encoding MCP-1 is elevated in bacterially infected murine bone tissue.
Therefore, our results increase the understanding of the molecular basis of human cervical cancer and confirm that aberrant expression of miRNA genes may be important for the pathogenesis of this human neoplasia by controlling or fine-tunning gene expression.
This result replicates our previous finding and confirms that BDNF expression in the DG increases after exposure to the small separation under exactly the same conditions in which we performed the memory experiments.
Collectively these findings suggest that 14-3-3σ 14-3-3σ 14-3-3σ a tumay suppressor and confunctiont 14-3-3 gene expression cas be regulatumory p53.
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