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For example, a previously described SLP-76-Nck-WASp complex may control actin reorganization independent of Rho-protein involvement [6], [15], [16].
These findings show that the Rac1 NFκB pathway may control actin organization.
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These data suggest that Sch9 may indirectly controls actin dynamics.
These results provide the first report of an outwardly rectifying Cl- channel in neocortical astrocytes and demonstrate how changes in cell shape and cytoskeletal actin may control Cl- conductance in these cells.
With this in mind, it is interesting that the actin regulators profilin and coronin are also likely palmitoylated (Kang et al., 2008), suggesting that palmitoylation may control multiple aspects of spine-specific actin regulation.
These data suggest that iron may control the interaction of TvACTN3 with actin or RNA possible by causing conformational changes by switching functions depending on the iron concentration but without modifying the amount of protein.
Conserved Arps likely participate in vesicular transport and gene expression, while apicomplexan-specific ALPs may control unique biological traits such as actin-based gliding motility.
The elegant platelet: signals controlling actin assembly.
Now the bacteria may inject actin into eukaryotes to disrupt their cells.
Profilin, actin-depolymerizing factor, a spectrin-like protein, villin and fimbrin have been detected which control apical actin polymerization and regulate the dynamic remodeling of the actin arrangement.
Cytoplasmic actin dynamics are tightly controlled by numerous actin-binding proteins, but regulation of nuclear actin has remained unclear.
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