Novel insights into FGD3, a putative GEF for Cdc42, that undergoes SCF<sup>FWD1/β‐TrCP</sup>‐mediated proteasomal degradation analogous to that of its homologue FGD1 but regulates cell morphology and motility differently from FGD1
Makio Hayakawa(Tokyo University of Pharmacy and Life Sciences), Masatoshi Kitagawa(Hamamatsu University School of Medicine)
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