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    • Loss of Pin1 function in the mouse causes phenotypes resembling cyclin D1-null phenotypes 

      Liou, Yih-Cherng; Ryo, Akihide; Huang, Han-Kuei; Lu, Pei-Jung; Bronson, Roderick; Fujimori, Fumihiro; Uchida, Takafumi; Hunter, Tony; Lu, Kun Ping (National Academy of Sciences, 2002)
      Phosphorylation of proteins on serine/threonine residues preceding proline is a key signaling mechanism. The conformation and function of a subset of these phosphorylated proteins is regulated by the prolyl isomerase Pin ...