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Approximately 61,000 statements.
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Copyright (c) 2011-2012, Selventa. All rights reserved.
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RESULTS: Here we identify SKAR as a novel and specific binding partner and substrate of S6K1 but not S6K2. We find that serines 383 and 385 of human SKAR are insulin-stimulated and rapamycin-sensitive S6K1 phosphorylation sites.
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2014-07-03T14:30:27.278+02:00
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