Liu, Ji; Kipreos, Edward T. (2000). “Evolution of Cyclin-Dependent Kinases (CDKs) and CDK-Activating Kinases (CAKs): Differential Conservation of CAKs in Yeast and Metazoa”. Molecular Biology and Evolution17 (7): 1061–74. doi:10.1093/oxfordjournals.molbev.a026387. PMID10889219.
“Beyond the cell cycle: a new role for Cdk6 in differentiation”. Journal of Cellular Biochemistry97 (3): 485–93. (Feb 2006). doi:10.1002/jcb.20712. PMID16294322.
Bartek, J; Lukas, J (2001). “Mammalian G1- and S-Phase Checkpoints in Response to DNA Damage”. Current Opinion in Cell Biology13 (6): 738–47. doi:10.1016/s0955-0674(00)00280-5. PMID11698191.
“Accumulation of high levels of the p53 and p130 growth-suppressing proteins in cell lines stably over-expressing cyclin-dependent kinase 6 (cdk6)”. Oncogene20 (23): 2889–99. (May 2001). doi:10.1038/sj.onc.1204396. PMID11420701.
Hussain, Muhammad S (2013). “CDK6 Associates with the Centrosome during Mitosis and Is Mutated in a Large Pakistani Family with Primary Microcephaly”. Human Molecular Genetics22 (25): 5199–5214. doi:10.1093/hmg/ddt374. PMID23918663.
LaBaer, J (1997). “New Functional Activities for the p21 Family of CDK Inhibitors”. Genes & Development11 (7): 847–62. doi:10.1101/gad.11.7.847. PMID9106657.
“The N-terminal peptide of the Kaposi's sarcoma-associated herpesvirus (KSHV)-cyclin determines substrate specificity”. The Journal of Biological Chemistry280 (12): 11165–74. (Mar 2005). doi:10.1074/jbc.M408887200. PMID15664993.
“Tumour selective targeting of cell cycle kinases for cancer treatment”. Current Opinion in Pharmacology13 (4): 529–35. (Aug 2013). doi:10.1016/j.coph.2013.03.012. PMID23597425.
“Knockdown of CDK6 enhances glioma sensitivity to chemotherapy”. Oncology Reports28 (3): 909–14. (Sep 2012). doi:10.3892/or.2012.1884. PMID22736304.
“Cyclin D1-dependent kinase activity in murine development and mammary tumorigenesis”. Cancer Cell9 (1): 13–22. (Jan 2006). doi:10.1016/j.ccr.2005.12.019. PMID16413468.
“Inhibition of pRb phosphorylation and cell-cycle progression by a 20-residue peptide derived from p16CDKN2/INK4A”. Current Biology6 (1): 84–91. (Jan 1996). doi:10.1016/s0960-9822(02)00425-6. PMID8805225.
“Structural basis for inhibition of the cyclin-dependent kinase Cdk6 by the tumour suppressor p16INK4a”. Nature395 (6699): 237–43. (Sep 1998). doi:10.1038/26155. PMID9751050.
“Dephosphorylation of human cyclin-dependent kinases by protein phosphatase type 2C alpha and beta 2 isoforms”. The Journal of Biological Chemistry275 (44): 34744–9. (Nov 2000). doi:10.1074/jbc.M006210200. PMID10934208.
Liu, Ji; Kipreos, Edward T. (2000). “Evolution of Cyclin-Dependent Kinases (CDKs) and CDK-Activating Kinases (CAKs): Differential Conservation of CAKs in Yeast and Metazoa”. Molecular Biology and Evolution17 (7): 1061–74. doi:10.1093/oxfordjournals.molbev.a026387. PMID10889219.
“Beyond the cell cycle: a new role for Cdk6 in differentiation”. Journal of Cellular Biochemistry97 (3): 485–93. (Feb 2006). doi:10.1002/jcb.20712. PMID16294322.
Bartek, J; Lukas, J (2001). “Mammalian G1- and S-Phase Checkpoints in Response to DNA Damage”. Current Opinion in Cell Biology13 (6): 738–47. doi:10.1016/s0955-0674(00)00280-5. PMID11698191.
“Accumulation of high levels of the p53 and p130 growth-suppressing proteins in cell lines stably over-expressing cyclin-dependent kinase 6 (cdk6)”. Oncogene20 (23): 2889–99. (May 2001). doi:10.1038/sj.onc.1204396. PMID11420701.
Hussain, Muhammad S (2013). “CDK6 Associates with the Centrosome during Mitosis and Is Mutated in a Large Pakistani Family with Primary Microcephaly”. Human Molecular Genetics22 (25): 5199–5214. doi:10.1093/hmg/ddt374. PMID23918663.
LaBaer, J (1997). “New Functional Activities for the p21 Family of CDK Inhibitors”. Genes & Development11 (7): 847–62. doi:10.1101/gad.11.7.847. PMID9106657.
“The N-terminal peptide of the Kaposi's sarcoma-associated herpesvirus (KSHV)-cyclin determines substrate specificity”. The Journal of Biological Chemistry280 (12): 11165–74. (Mar 2005). doi:10.1074/jbc.M408887200. PMID15664993.
“Tumour selective targeting of cell cycle kinases for cancer treatment”. Current Opinion in Pharmacology13 (4): 529–35. (Aug 2013). doi:10.1016/j.coph.2013.03.012. PMID23597425.
“Knockdown of CDK6 enhances glioma sensitivity to chemotherapy”. Oncology Reports28 (3): 909–14. (Sep 2012). doi:10.3892/or.2012.1884. PMID22736304.
“Cyclin D1-dependent kinase activity in murine development and mammary tumorigenesis”. Cancer Cell9 (1): 13–22. (Jan 2006). doi:10.1016/j.ccr.2005.12.019. PMID16413468.
“Inhibition of pRb phosphorylation and cell-cycle progression by a 20-residue peptide derived from p16CDKN2/INK4A”. Current Biology6 (1): 84–91. (Jan 1996). doi:10.1016/s0960-9822(02)00425-6. PMID8805225.
“Structural basis for inhibition of the cyclin-dependent kinase Cdk6 by the tumour suppressor p16INK4a”. Nature395 (6699): 237–43. (Sep 1998). doi:10.1038/26155. PMID9751050.
“Dephosphorylation of human cyclin-dependent kinases by protein phosphatase type 2C alpha and beta 2 isoforms”. The Journal of Biological Chemistry275 (44): 34744–9. (Nov 2000). doi:10.1074/jbc.M006210200. PMID10934208.