2006
DOI: 10.1016/j.cellsig.2005.10.007
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Corrigendum to “M-CSF stimulated differentiation requires persistent MEK activity and MAPK phosporylation independent of Grb2–Sos association and phosphatidylinositol 3-kinase activity” [Cell. Signall. 17 (2005) 1352–1362]

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(2 citation statements)
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“…MEK inhibition converts M-CSF-R differentiation signal from macrophage to granulocyte pathway M-CSF-stimulated differentiation requires persistent mitogen-activated protein kinase (MAPK) kinase (MEK) activity (Gobert Gosse et al, 2005). M-CSF induced biphasic MAPK phosphorylation in EGERFms cells (Figure 5a), featuring the rapid and transient first wave, and late and persistent second wave, as previously described in a myeloid progenitor cell line (Bourgin et al, 2000).…”
Section: Eger-fms Cells Differentiated In Macrophages In Response To supporting
confidence: 60%
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“…MEK inhibition converts M-CSF-R differentiation signal from macrophage to granulocyte pathway M-CSF-stimulated differentiation requires persistent mitogen-activated protein kinase (MAPK) kinase (MEK) activity (Gobert Gosse et al, 2005). M-CSF induced biphasic MAPK phosphorylation in EGERFms cells (Figure 5a), featuring the rapid and transient first wave, and late and persistent second wave, as previously described in a myeloid progenitor cell line (Bourgin et al, 2000).…”
Section: Eger-fms Cells Differentiated In Macrophages In Response To supporting
confidence: 60%
“…Activation of the Ras to MAPK signaling pathway is essential for M-CSF-R differentiation signal (Gobert Gosse et al, 2005). In EGER-Fms cells, inhibition of MAPK activation not only prevented M-CSF-induced macrophage differentiation, but instead EGER-Fms cells differentiated into granulocytes, unveiling the latent granulocytic potential of EGER-Fms cells in addition to its macrophage potential.…”
Section: Discussionmentioning
confidence: 98%