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In fact, the final outcome could be influenced by variables related to the product, such as dose, cell content, activation method and storage procedures, as well as application modality and concomitant procedures [38].
With a high dose cell immunization, highly protective immunities were generated by both CMT.TAP1/B7.1 and CMT.B7.1/p cells.
At this dose, cell viability is approximately 75%.
At this dose cell viability decreased only by 20% (see Figure 1A).
Applying a 0.6 J cm−2 light dose, cell viability decreased to 50%.
At every light dose, cell survival was significantly lower for the cells extracted after 24 h (P<0.05).
Similar(50)
These unique GC-mediated unique molecular effects are likely time, dose, cell-type, and cell-lineage dependent.
Consequently, the higher the ultraviolet B (UVB) dose cells receive, the more likely is that they suffer an irreparable damage and activate apoptosis.
At fixed incubation times and laser irradiation doses, cell viability significantly differed with photosensitizer concentrations.
At fixed photosensitizer concentrations and laser irradiation doses, cell viability was significantly affected by the incubation time.
The protective response in the epidermis was represented by two major GO terms observed for gene sets identified for both irradiation doses: cell differentiation and the inflammatory response.
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