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It can be concluded that cells of melanoglial origin can easily be obtained from hair follicle bulge explants.
Thus, taking intracellular particle agglomeration into account, it can be concluded that cells accumulated three- to eightfold higher numbers of the 25 nm particles compared with the 85 nm particles.
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Finally, it can be concluded that cell fate depends on a combination of different important elements juxtaposing with each other (Irani et al. 2013; Adams 2002).
It could, therefore, be concluded that cell seeding plays a positive role in strengthening a tissue engineered construct, and cell type has a significant influence on the extent of this improvement.
Therefore, it can be concluded that cell concentration, unfrozen fraction size and vitrification are important parameters for both the frozen and the dried states, a conclusion that was confirmed in the present study.
It can be concluded that cell viability did not appear to be affected by the kind of the substrate.
Thus, it can be concluded that cell survival conferred by CX3CR1 constitutes its pro-atherogenic potential, rather than cell recruitment (Landsman et al, 2009).
From this study, it can be concluded that cell culture PCV1 can replicate efficiently and produce pathology in the lungs of porcine foetuses inoculated at 55 days of foetal life.
From the final experiment result, it was concluded that cells can be effectively positioned in a desired region across a microfluidic channel using hydrodynamic forces brought about by a series of continuously changing herringbone structures.
It is concluded that cells from some experimental tumours have the capacity to activate Coagulation Factor X directly.
Additionally it was concluded that cell viability could recover post-transfection with these DBPs, which were less toxic than the commercially available transfection reagent Lipofectamine® 2000.
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