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{ <http://www.tkuhn.ch/bel2nanopub/RAlGFx-J14sgqoJMK_8RcbNDJETbXKMghJSY5gupzgaU4#_6> ?p ?o ?g. }
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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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