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http://www.ebi.ac.uk/ontology-lookup/?termId=MOD:00000
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http://purl.obolibrary.org/obo/BFO_0000066
http://purl.bioontology.org/ontology/MSH/D002460
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http://purl.obolibrary.org/obo/BFO_0000066
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TextLocation
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Results
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http://www.w3.org/2000/01/rdf-schema#label
p(HGNC:IGF1) -> p(HGNC:AKT1,pmod(P,S,473))
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http://resource.belframework.org/belframework/1.0/knowledge/small_corpus.bel
http://purl.org/dc/elements/1.1/description
Approximately 2000 hand curated statements drawn from 57 PubMeds.
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http://purl.org/dc/elements/1.1/rights
Copyright (c) 2011-2012, Selventa. All Rights Reserved.
http://resource.belframework.org/belframework/1.0/knowledge/small_corpus.bel
http://purl.org/dc/elements/1.1/title
BEL Framework Small Corpus Document
http://resource.belframework.org/belframework/1.0/knowledge/small_corpus.bel
http://purl.org/dc/terms/license
Creative Commons Attribution-Non-Commercial-ShareAlike 3.0 Unported License
http://resource.belframework.org/belframework/1.0/knowledge/small_corpus.bel
http://purl.org/pav/authoredBy
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http://purl.org/pav/version
1.6
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To determine whether PKA-induced PKB activation accounts for GSK-3 phosphorylation
after treatment with 8-Br-cAMP, forskolin, or isoproterenol, PKB phosphorylation
at serine 473 and threonine 308, which is crucial for activation of PKB (20),
was assessed. As expected, insulin and IGF-1 strongly stimulated phosphorylation
of PKB at serine 473 in NIH 3T3 or Rat1 cells (Fig. 2B). In contrast, 8-Br-cAMP,
forskolin, and isoproterenol did not significantly alter PKB phosphorylation
at serine 473 (Fig. 2B). Similar results were obtained with a threonine 308 phosphorylation-specific
antibody (data not shown).
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http://www.ncbi.nlm.nih.gov/pubmed/11035810
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support@belframework.org
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Selventa
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http://www.ncbi.nlm.nih.gov/pubmed/11035810
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http://purl.org/dc/terms/created
2014-07-03T14:29:34.691+02:00
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