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{ <http://www.tkuhn.ch/bel2nanopub/RAttLbFdBB20AoDGnOUVgeEWCIbpopIG6S8Jg_HOr2dFw#_5> ?p ?o ?g. }
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Importantly, mACTN2 not only served as a primary coactivator for androgen receptor, estrogen receptor and thyroid receptor activities, but also acted synergistically with GRIP1 to enhance these nuclear receptor (NR) functions.
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