Sentence examples for mouse cells suggesting from inspiring English sources

Over-expressing KAT5 in cis did not downregulate RNASEH2C protein level in mouse cells, suggesting the newly evolved distal pA site in human was critical to mediate APA in RNASEH2C and ultimately reduced the protein level.

The results are similar to what we observed in mouse cells, suggesting that the significant role of IL-34 in osteoclast differentiation is not species-specific.

Furthermore, 23 out of the 38 proteins appeared to associate with telomeres both in human and mouse cells, suggesting that their activities on telomeres may be evolutionarily conserved (Supplementary Table 2).

The finding that TLR4 action correlates to the telomere length and associated chromosome instability in mouse cells suggests that telomeres are involved in broader immune functions beyond the protection of chromosomes.

Previous observations in human and mouse cells suggested that a gene could show MAE in one cell type but not another (Gimelbrant et al., 2005; Gimelbrant and Chess, 2006; Gimelbrant et al., 2007).

This comparison of human and mouse cells suggested that both telomere-independent and telomere-associated damage may be similarly involved in the signaling to induce cellular senescence and organismal aging [ 14].

Besides gastric cancer, Pre-miR-126 over-expression reduced the SOX2 protein level in mouse ES cells, suggesting that miR-126 may generally control SOX2 expression, at least in two species (human and mouse) and various cell lineages, including ES cells.

Peanut protein films did not support the attachment and growth of mouse fibroblast cells suggesting that peanut proteins were cytotoxic.

Meanwhile, Cbf-14-2 Cbf-14-2 Cbf-14-2els of hemolysis in sheep redisplayedelow (sRBCs) and neglevelse cytofoxicity against mouse spleen cells, suggesting low toxicity against mammalian cells.

After treatment of DT or DTmu for 14 days, we observed that the selective depletion of TAMs evidently inhibited the production of CCL20 by CMT93GFP mouse tumor cells, suggesting that TAMs are not only the major source of CCL20 but also distinctly contribute to the release of CCL20 from CRC cells in mice (Figure 5E).

Nec1i at higher concentrations inhibited necroptosis in mouse L929 cells, suggesting that Nec1i may target molecules other than RIP1.