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1 ed C6 cell cultures contained high levels of appican and was a significantly better substrate for the
3 rt that rat C6 glioma cells transfected with appican displayed a dramatic change in their phenotypic
5 Together, these data suggest that secreted appican incorporates into ECM and promotes adhesion of n
7 er the same conditions, however, <20% of the appican-transfected C6 cells were dissociated from their
12 ed from their substrate, suggesting that the appican-transfected glia cells attach more avidly to the
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