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All rights reserved. http://resource.belframework.org/belframework/20131211/knowledge/large_corpus.bel http://purl.org/dc/elements/1.1/title BEL Framework Large Corpus Document http://resource.belframework.org/belframework/20131211/knowledge/large_corpus.bel http://purl.org/pav/authoredBy http://www.tkuhn.ch/bel2nanopub/RA3sfii7OrJ0wKVQVN3TSHjXVgN9Z055me5no4r2F2y3A#_8 http://resource.belframework.org/belframework/20131211/knowledge/large_corpus.bel http://purl.org/pav/version 20131211 http://www.tkuhn.ch/bel2nanopub/RA3sfii7OrJ0wKVQVN3TSHjXVgN9Z055me5no4r2F2y3A#_7 http://www.w3.org/ns/prov#value from full text - However, after introduction of theWTMdm2 into these cells, a strong and rapid (5 min.) phosphorylation of both ERK1p42 and ERK2p44occurred. Upon stimulation with serum instead of IGF-1, phosphorylation of ERKs increased strongly in both mock and Mdm2-transfected Mdm2 KO cells (Fig. 4A, right panel) but was stabilized by Mdm2. This suggests that serum-induced ERK activation mediated by other growth factor receptor pathways is not dependent on Mdm2. 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