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Moreover, both can differentiate into tissues of mesodermal and nonmesodermal origins.
Currently, ASCs have been shown to differentiate toward cells that are mesodermal and nonmesodermal in origin.
ADSCs have similar features to MSCs from other tissues such as a high proliferative rate and the potential to differentiate into diverse cell lineages of both mesodermal and nonmesodermal origin.
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Exogenous Xbra activity was also able to drive ectopic msgn1 transcription in mesodermal and, less frequently, nonmesodermal tissues (see asterisks in Figure 5C).
Furthermore, exposure of embryoid bodies (EB) to MBP increased expression of pluripotency-, proliferation- and nonmesodermal differentiation-related gene sets, which indicates inhibition of mesodermal differentiation.
They can proliferate extensively and have the ability to differentiate into endodermal, mesodermal, and ectodermal derivatives.
(G H) Spontaneous EB differentiation in vitro (G) and teratoma analysis in vivo (H) verify the differentiation potentials of iPSCs towards endodermal, mesodermal, and ectodermal tissues.
The feasibility of transforming embryonic endoderm into different cell types is tightly controlled by mesodermal and septum transversumal signalings during early embryonic development.
"Non-epithelial" kinase genes were associated with cytoskeleton organization, cell adhesion, mesodermal and epidermal development.
First, spherical cell EB aggregates were generated that contain ectodermal, mesodermal and endodermal derivatives (Primary Differentiation).
It acts in part by regulating the cohesion of mesodermal and endodermal (mesendodermal) progenitor cells [3].
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