Affiliation: Stanford University
- Mos mediates the mitotic activation of p42 MAPK in Xenopus egg extractsJianbo Yue
Department of Molecular Pharmacology, Stanford University, Stanford, CA 94305 5174, USA
Curr Biol 14:1581-6. 2004..Taken together, these data demonstrate that Mos is responsible for the mitotic activation of the p42 MAPK pathway in Xenopus egg extracts...
- B-Raf and C-Raf are required for Ras-stimulated p42 MAP kinase activation in Xenopus egg extractsJ Yue
Department of Molecular Pharmacology, Stanford University, CA 94305 5174, USA
Oncogene 25:3307-15. 2006..These data indicate that two upstream stimuli, active Ras and active Cdc2, utilize different MAPKKKs to activate MEK1 and p42 MAPK...
- Mechanistic studies of the mitotic activation of MosJianbo Yue
Stanford University School of Medicine, Department of Molecular Pharmacology, CCSR Room 3155, Stanford, CA 94305 5174, USA
Mol Cell Biol 26:5300-9. 2006..Our work suggests that Ser 105 dephosphorylation represents a novel mechanism for reorienting helix alphaC...
- Requirement of TGF-beta receptor-dependent activation of c-Jun N-terminal kinases (JNKs)/stress-activated protein kinases (Sapks) for TGF-beta up-regulation of the urokinase-type plasminogen activator receptorJianbo Yue
Department of Pharmacology, Pennsylvania State University College of Medicine, Hershey 17033, USA
J Cell Physiol 199:284-92. 2004..Our results also indicate that the type II TGF-beta receptor (RII) is required for TGF-beta activation of JNK1 and the resulting up-regulation of uPAR expression...