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Furthermore, we show that the DNA of different lengths can be differentiated through the measurement of scattering signals leading to possible new DNA sensor applications.
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The dopaminergic and GABAergic cells cannot be differentiated visually but may be differentiated through their pharmacological and physiological responses.
Our data show that ESC-derived c-Kit+/Sca-1-cells can be differentiated through a Klf4/β-catenin dependent pathway and are a suitable source of vascular progenitors for the creation of superior tissue-engineered vessels from decellularised scaffolds.
These subtypes can be differentiated through clinical features, ethnic background and neuropathological features.
However, most of these subtypes can only be differentiated through genetic tests.
ES cell lines were differentiated through EB differentiation and subjected to RNA FISH to detect Xist RNA.
Nodes are differentiated through different colors and labels.
Dairy creams were differentiated through their thicknesses and granularity properties.
mESCs were differentiated through embryoid body [15] formation (hanging droplet technique) as described [16].
iPSCs were differentiated through embryoid body (EB) formation in EB medium (DMEM supplemented with 15 % FBS, l-glutamine, nonessential amino acids, and β-mercaptoethanol).
For research studies and therapeutic applications, monocytes isolated from peripheral human blood can be differentiated into macrophages through the addition of the monocyte colony stimulating factor MCSF, and polarized to different macrophage phenotypes via the addition of specific cytokines [25] (Figure 5). Figure 5 Derivation of subsets of human macrophages from monocytes.
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