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http://purl.obolibrary.org/obo/RO_0002204
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Approximately 61,000 statements.
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BEL Framework Large Corpus Document
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In summary, we have found the following: (i) beta-arrestin-1 can alter insulin signaling by inhibiting insulin-induced proteasomal degradation of IRS-1; (ii) beta-arrestin-1 decreases the rate of ubiquitination of IRS-1 by competitively binding to endogenous Mdm2, an E3 ligase that can ubiquitinate IRS-1; (iii) dephosphorylation of S412 on beta-arrestin and the amino terminus of beta-arrestin-1 are required for this effect of beta-arrestin on IRS-1 degradation; and (iv) inhibition of beta-arrestin-1 leads to enhanced IRS-1 degradation and accentuated cellular insulin resistance.
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Selventa
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http://www.w3.org/ns/prov#wasDerivedFrom
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2014-07-03T14:30:28.204+02:00
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