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- W244934260 endingPage "151" @default.
- W244934260 startingPage "133" @default.
- W244934260 abstract "The regulation of cell cycle and proliferation has been extensively studied in the last few years and a consensus paradigm of cell cycle regulation has been developed (1). According to this paradigm, the master switch of the cell cycle is the Rb family of proteins. Proliferation is turned on by phosphorylation of these proteins by cyclin-dependent kinases (CDKS) (Fig. 1) (2). These kinases are activated by D-type cyclins (Dl, D2, and D3) and cyclin E, and inhibited by two families of CDK inhibitors (CKIs), the Ink (p16Ink4a, p15Ink4b, p18Ink4c, and pl9Ink4d) and Cip/Kip families (p2lCiPl, p27Kipt1, and p57Kipt2) (3,4)." @default.
- W244934260 created "2016-06-24" @default.
- W244934260 creator A5020635870 @default.
- W244934260 creator A5035389163 @default.
- W244934260 creator A5054111083 @default.
- W244934260 date "2003-01-01" @default.
- W244934260 modified "2023-10-17" @default.
- W244934260 title "Deregulation of Cell Cycle Progression by Oncogenic Transformation" @default.
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