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5. CDK2 is a target for retinoic acid-mediated growth inhibition in MCF-7 human breast cancer cells. Teixeira C, Pratt MA. Mol Endocrinol; 1997 Aug 18; 11(9):1191-202. PubMed ID: 9259311 [Abstract] [Full Text] [Related]
6. Mechanisms of cyclin-dependent kinase inactivation by progestins. Musgrove EA, Swarbrick A, Lee CS, Cornish AL, Sutherland RL. Mol Cell Biol; 1998 Apr 18; 18(4):1812-25. PubMed ID: 9528753 [Abstract] [Full Text] [Related]
7. Lovastatin mediated G1 arrest in normal and tumor breast cells is through inhibition of CDK2 activity and redistribution of p21 and p27, independent of p53. Rao S, Lowe M, Herliczek TW, Keyomarsi K. Oncogene; 1998 Nov 05; 17(18):2393-402. PubMed ID: 9811471 [Abstract] [Full Text] [Related]
8. Involvement of p21 and p27 in the regulation of CDK activity and cell cycle progression in the regenerating liver. Albrecht JH, Poon RY, Ahonen CL, Rieland BM, Deng C, Crary GS. Oncogene; 1998 Apr 23; 16(16):2141-50. PubMed ID: 9572495 [Abstract] [Full Text] [Related]
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18. A pure estrogen antagonist inhibits cyclin E-Cdk2 activity in MCF-7 breast cancer cells and induces accumulation of p130-E2F4 complexes characteristic of quiescence. Carroll JS, Prall OW, Musgrove EA, Sutherland RL. J Biol Chem; 2000 Dec 08; 275(49):38221-9. PubMed ID: 10991938 [Abstract] [Full Text] [Related]