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The efficacy of CSMA/ECA in providing traffic differentiation is demonstrated in [21].
The need for a signal that instigates the behavioural change that leads to neural differentiation is demonstrated and potential mediators of this signal are explored through model analysis techniques.
Regarding P2X5 and TRPV4 no direct correlation between their expression and urothelial differentiation is demonstrated.
The typical morphology of the muscle cell culture during proliferation and differentiation is demonstrated in Figure 1.
The importance of MIS to male sexual differentiation is demonstrated by the morphological and endocrine sex reversal of fetal ovaries exposed to MIS [ 40].
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An integrative and quantitative approach for systematically studying the effects of changing the matrix environment on pluripotent cell viability and neuronal differentiation was demonstrated.
The importance of ERK for MSC differentiation was demonstrated by using the inhibitor of ERK activation, U0126, which completely suppressed osteogenesis of GH-stimulated MSCs on NSQ50.
A further differentiation was demonstrated by using other microsatellites [14], [22], [31].
The enlargement of MdMNs during soldier differentiation was demonstrated to be a common phenomenon over the termite lineages examined.
In addition, the appearance of enucleated cells following differentiation was demonstrated by flow cytometric analysis using SYTO85 staining (Figure S6).
The OC differentiation was demonstrated by the presence of multinucleated/TRAP positive cells from cancer patient and healthy control PBMCs (Fig. 1A C).
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