Sentence examples for cellular outputs from inspiring English sources

The cellular outputs were analyzed according to the defrosting techniques, according to the method used in flow cytometry: single-platform (SP) versus double-platform (DP), or the product nature, i.e. in total blood or miniaturized.

It has been proposed that the activation of different signal transduction cascades downstream of Wnt/Fz leads to different cellular outputs.

Most brain regions, as well as the sog, were labeled with the same intensity, suggesting that there are no spatially separated cellular outputs in these regions (Figure 2J and 2K).

It is, however, difficult to assess which factors in this cascade are crucial in controlling these differential cellular outputs because signal transduction mechanisms are inherently complex and highly nonlinear, and thus quantitative molecular interactions in the network can not be understood from structural pathway maps alone.

These findings thus demonstrated that LSC with different maturation status and cellular outputs exist in mice.

The addition of other cellular outputs can be another factor in favor of using this approach.

Scattered arrows indicate no/low cellular output along the respective cellular lineage.

We review recent work combining theory and experiments that show how cellular output can be modulated by tuning the dynamical features of input pulses.

Besides the fluid dynamics of the system, which is quite well-characterised33,34 well-characterised33,34e of toe signalling environment requires a combuildion of cellular output ofullgnalling molecules including the respicturey the cells tofthe change to thisignallingenvironment

Consistent with the functional cellular output (Fig. 3a h), the 1038 genes normally activated by SCL (upregulated in WT versus Scl−/− cells) were associated with haematopoietic/endothelial differentiation, as revealed by Gene Ontology (GO) terms and GSEA analyses (Fig. 4b, examples of genes in Fig. 4c).

Biosensors — genetically encoded components that actuate a cellular output in response to a change in metabolite concentration — are therefore a promising tool for rapid and high-throughput evaluation of candidate pathway variants.