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{ <http://www.tkuhn.ch/bel2nanopub/RAxC8TvBMQW5sjwFVKDjckOpGPt80IoGNr5JjxEbJyHwQ#_4> ?p ?o ?g. }
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Treatment of suspended G0-synchonized NIH 3T3 cells with PDGF resulted in the activation of ERK2 as determined by tyrosine phosphorylation and gel-shift. ERK2 activation was rapid and maximal at 10 min and transient.
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