Contributions in the domain of cancer research: Review¶Negative regulators of cyclin-dependent kinases and their roles in cancers
暂无分享,去创建一个
M.-H. Lee | H-Y Yang | M.-H. Lee | H.-Y. Yang
[1] G. Hannon,et al. A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4 , 1993, Nature.
[2] B. Amati,et al. Growth arrest by the cyclin‐dependent kinase inhibitor p27Kip1 is abrogated by c‐Myc. , 1996, The EMBO journal.
[3] W. Ansorge,et al. Direct induction of cyclin D2 by Myc contributes to cell cycle progression and sequestration of p27 , 1999, The EMBO journal.
[4] C. Turck,et al. Inhibition of CDK2 activity in vivo by an associated 20K regulatory subunit , 1993, Nature.
[5] L. Soucek,et al. Making decisions through Myc , 2001, FEBS letters.
[6] S. Okret,et al. p57Kip2, a glucocorticoid-induced inhibitor of cell cycle progression in HeLa cells. , 1999, Molecular endocrinology.
[7] D. Stokoe,et al. p27Kip1 is required for PTEN-induced G1 growth arrest. , 2001, Cancer Research.
[8] J. Nesland,et al. Protein expression of the cell-cycle inhibitor p27Kip1 in malignant melanoma: inverse correlation with disease-free survival. , 1998, The American journal of pathology.
[9] J. Massagué,et al. Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution. , 1995, Genes & development.
[10] J. Palazzo,et al. Inhibitor p27 in Epithelial Ovarian Cancer Frequent Loss of Expression of the Cyclin-dependent Kinase , 1999 .
[11] W. Gerald,et al. Cyclin-dependent kinase inhibitor p57KIP2 in soft tissue sarcomas and Wilms'tumors. , 1996, Cancer research.
[12] M. Loda,et al. Increased proteasome-dependent degradation of the cyclin-dependent kinase inhibitor p27 in aggressive colorectal carcinomas , 1997, Nature Medicine.
[13] J. Darnell,et al. The role of STATs in transcriptional control and their impact on cellular function , 2000, Oncogene.
[14] V. P. Collins,et al. Adenovirus-mediated overexpression of p15INK4B inhibits human glioma cell growth, induces replicative senescence, and inhibits telomerase activity similarly to p16INK4A. , 2000, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.
[15] I. Hampson,et al. Regulation of CDK4 activity by a novel CDK4-binding protein, p34(SEI-1). , 1999, Genes & development.
[16] J. Mestan,et al. Skp2 is oncogenic and overexpressed in human cancers , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[17] J. Jónasson,et al. Loss of heterozygosity at chromosome 1p in different solid human tumours: association with survival , 1999, British Journal of Cancer.
[18] T. Pandita,et al. High frequency of hypermethylation at the 14-3-3 sigma locus leads to gene silencing in breast cancer. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[19] H. S. Kim,et al. Mechanism for inactivation of the KIP family cyclin-dependent kinase inhibitor genes in gastric cancer cells. , 2000, Cancer research.
[20] Gregory J. Hannon,et al. pl5INK4B is a potentia| effector of TGF-β-induced cell cycle arrest , 1994, Nature.
[21] B. Wiedenmann,et al. A Novel Function for the Tumor Suppressor p16INK4a , 2000, The Journal of Cell Biology.
[22] K. Kinzler,et al. 14-3-3σ is required to prevent mitotic catastrophe after DNA damage , 1999, Nature.
[23] James M. Roberts,et al. The p21Cip1 and p27Kip1 CDK ‘inhibitors’ are essential activators of cyclin D‐dependent kinases in murine fibroblasts , 1999, The EMBO journal.
[24] R. Liang,et al. Methylation of p15 and p16 genes in acute promyelocytic leukemia: potential diagnostic and prognostic significance. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[25] M. Reiss,et al. Cloning of putative growth regulatory genes from primary human keratinocytes by subtractive hybridization. , 1995, Gene.
[26] Tony Hunter,et al. p27, a novel inhibitor of G1 cyclin-Cdk protein kinase activity, is related to p21 , 1994, Cell.
[27] A. Kumagai,et al. Positive Regulation of Wee 1 by Chk 1 and 14-3-3 Proteins , 2001 .
[28] K. Kinzler,et al. 14-3-3σ Is a p53-Regulated Inhibitor of G2/M Progression , 1997 .
[29] B. Amati. Integrating Myc and TGF-β signalling in cell-cycle control , 2001, Nature Cell Biology.
[30] S. Elledge,et al. p53-independent expression of p21Cip1 in muscle and other terminally differentiating cells , 1995, Science.
[31] James M. Roberts,et al. CDK inhibitors: positive and negative regulators of G1-phase progression. , 1999, Genes & development.
[32] S. Sakaki,et al. Restoration of wild-type p16 down-regulates vascular endothelial growth factor expression and inhibits angiogenesis in human gliomas. , 1999, Cancer research.
[33] F. McKeon,et al. Tyrosine kinases wee1 and mik1 as effectors of DNA replication checkpoint control. , 1996, Progress in cell cycle research.
[34] G. Peters,et al. Regulation of p16CDKN2 expression and its implications for cell immortalization and senescence , 1996, Molecular and cellular biology.
[35] H. Piwnica-Worms,et al. The human Myt1 kinase preferentially phosphorylates Cdc2 on threonine 14 and localizes to the endoplasmic reticulum and Golgi complex , 1997, Molecular and cellular biology.
[36] A. Cittadini,et al. Loss of p21Waf1 expression is a strong predictor of reduced survival in primary superficial bladder cancers. , 2000, Clinical cancer research : an official journal of the American Association for Cancer Research.
[37] Jong-Yeon Shin,et al. Mutation and expression of the p27KIP1 and p57KIP2 genes in human gastric cancer , 2000, Experimental & Molecular Medicine.
[38] A. Kumagai,et al. Positive regulation of Wee1 by Chk1 and 14-3-3 proteins. , 2001, Molecular biology of the cell.
[39] J. Trent,et al. WAF1, a potential mediator of p53 tumor suppression , 1993, Cell.
[40] Jianxiang,et al. In vivo gene therapy with p53 or p21 adenovirus for prostate cancer. , 1995, Cancer research.
[41] J. Lammers,et al. Forkhead Transcription Factor FKHR-L1 Modulates Cytokine-Dependent Transcriptional Regulation of p27KIP1 , 2000, Molecular and Cellular Biology.
[42] M. Hung,et al. Correlation of p27 protein expression with HER‐2/neu expression in breast cancer , 2001, Molecular carcinogenesis.
[43] Herman Yeger,et al. Decreased levels of the cell-cycle inhibitor p27Kip1 protein: Prognostic implications in primary breast cancer , 1997, Nature Medicine.
[44] David Beach,et al. p21 is a universal inhibitor of cyclin kinases , 1993, Nature.
[45] P. Beer-Romero,et al. Role of the ubiquitin-proteasome pathway in regulating abundance of the cyclin-dependent kinase inhibitor p27. , 1995, Science.
[46] S. Elledge,et al. Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome , 1997, Nature.
[47] P. Yaswen,et al. p57KIP2 expression and loss of heterozygosity during immortal conversion of cultured human mammary epithelial cells. , 1999, Cancer research.
[48] A. Sewing,et al. Cyclins D1 and D2 mediate Myc‐induced proliferation via sequestration of p27Kip1 and p21Cip1 , 1999, The EMBO journal.
[49] D. Coppola,et al. CEP1612, a dipeptidyl proteasome inhibitor, induces p21WAF1 and p27KIP1 expression and apoptosis and inhibits the growth of the human lung adenocarcinoma A-549 in nude mice. , 2001, Cancer research.
[50] I. Hoffmann,et al. Cell cycle regulation by the Cdc25 phosphatase family. , 2000, Progress in cell cycle research.
[51] M. Nistér,et al. Induction of senescence in human malignant glioma cells by p16INK4A , 1997, Oncogene.
[52] J. Massagué,et al. Defective repression of c-myc in breast cancer cells: A loss at the core of the transforming growth factor beta growth arrest program. , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[53] W. Schulz,et al. Decreased expression of p57KIP2mRNA in human bladder cancer , 2000, British Journal of Cancer.
[54] Xiao-Fan Wang,et al. Functional Analysis of the Transforming Growth Factor βResponsive Elements in the WAF1/Cip1/p21 Promoter (*) , 1995, The Journal of Biological Chemistry.
[55] Y. Liaw,et al. Aberrant transcripts of the cyclin-dependent kinase-associated protein phosphatase in hepatocellular carcinoma. , 2000, Cancer research.
[56] R. Fåhraeus,et al. The p16INK4a tumour suppressor protein inhibits αvβ3 integrin‐mediated cell spreading on vitronectin by blocking PKC‐dependent localization of αvβ3 to focal contacts , 1999 .
[57] A. Fattaey,et al. Myt1: a Wee1-type kinase that phosphorylates Cdc2 on residue Thr14. , 1997, Progress in cell cycle research.
[58] G. Peters,et al. Opposing effects of Ets and Id proteins on p16INK4a expression during cellular senescence , 2001, Nature.
[59] D. Alberts,et al. Amplification of 19q13.1-q13.2 sequences in ovarian cancer. G-band, FISH, and molecular studies. , 1996, Cancer genetics and cytogenetics.
[60] T. Ørntoft,et al. Proteome profiling of bladder squamous cell carcinomas: identification of markers that define their degree of differentiation. , 1997, Cancer research.
[61] A. Kamb,et al. Cell-cycle regulators and cancer. , 1995, Trends in genetics : TIG.
[62] Kathleen R. Cho,et al. Frequency of homozygous deletion at p16/CDKN2 in primary human tumours , 1995, Nature Genetics.
[63] S. Elledge,et al. The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases , 1993, Cell.
[64] Xin-Yuan Fu,et al. Cell Growth Arrest and Induction of Cyclin-Dependent Kinase Inhibitor p21WAF1/CIP1 Mediated by STAT1 , 1996, Science.
[65] O. Bachs,et al. The Protein SET Regulates the Inhibitory Effect of p21Cip1 on Cyclin E-Cyclin-dependent Kinase 2 Activity* , 1999, The Journal of Biological Chemistry.
[66] J. Bartek,et al. Aberrant p27Kip1 promoter methylation in malignant melanoma , 2000, Oncogene.
[67] Roger Brent,et al. C dil, a Human Gl and S Phase Protein Phosphatase That Associates with Cdk2 , 2003 .
[68] T. Kiyono,et al. Both Rb/p16INK4a inactivation and telomerase activity are required to immortalize human epithelial cells , 1998, Nature.
[69] J. Herman,et al. 5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers , 1995, Nature Medicine.
[70] J. R. Smith,et al. Cloning of senescent cell-derived inhibitors of DNA synthesis using an expression screen. , 1994, Experimental cell research.
[71] P. Elliott,et al. The proteasome inhibitor PS-341 inhibits growth, induces apoptosis, and overcomes drug resistance in human multiple myeloma cells. , 2001, Cancer research.
[72] K. Mimori,et al. p27 expression and gastric carcinoma , 1997, Nature Medicine.
[73] M. Kitagawa,et al. Targeted disruption of Skp2 results in accumulation of cyclin E and p27Kip1, polyploidy and centrosome overduplication , 2000, The EMBO journal.
[74] E. Nabel,et al. The p21 cyclin–dependent kinase inhibitor suppresses tumorigenicity in vivo , 1995, Nature Medicine.
[75] Jeffrey E. Green,et al. Suppression of mammary carcinoma growth in vitro and in vivo by inducible expression of the Cdk inhibitor p21 , 2001, Cancer Gene Therapy.
[76] M. Hung,et al. Cytoplasmic localization of p21Cip1/WAF1 by Akt-induced phosphorylation in HER-2/neu-overexpressing cells , 2001, Nature Cell Biology.
[77] R. Parsons,et al. PTEN: life as a tumor suppressor. , 2001, Experimental cell research.
[78] J. Herman,et al. p15(INK4B) CpG island methylation in primary acute leukemia is heterogeneous and suggests density as a critical factor for transcriptional silencing. , 1999, Blood.
[79] J. Herman,et al. Inactivation of the CDKN2/p16/MTS1 gene is frequently associated with aberrant DNA methylation in all common human cancers. , 1995, Cancer research.
[80] G. Hannon,et al. Chromosomal mapping of the genes for the human cell cycle proteins cyclin C (CCNC), cyclin E (CCNE), p21 (CDKN1) and KAP (CDKN3). , 1995, Cytogenetics and cell genetics.
[81] James M. Roberts,et al. Expression of cell-cycle regulators p27Kip1 and cyclin E, alone and in combination, correlate with survival in young breast cancer patients , 1997, Nature Medicine.
[82] R. Mamillapalli,et al. PTEN regulates the ubiquitin-dependent degradation of the CDK inhibitor p27KIP1 through the ubiquitin E3 ligase SCFSKP2 , 2001, Current Biology.
[83] C. Cordon-Cardo,et al. Distinct altered patterns of p27KIP1 gene expression in benign prostatic hyperplasia and prostatic carcinoma. , 1999, Journal of the National Cancer Institute.
[84] Stuart A. Aaronson,et al. Overexpression of Kinase-Associated Phosphatase (KAP) in Breast and Prostate Cancer and Inhibition of the Transformed Phenotype by Antisense KAP Expression , 2000, Molecular and Cellular Biology.
[85] G. Hannon,et al. Correlation of terminal cell cycle arrest of skeletal muscle with induction of p21 by MyoD , 1995, Science.
[86] K. Kinzler,et al. 14-3-3Sigma is required to prevent mitotic catastrophe after DNA damage. , 1999, Nature.
[87] James M. Roberts,et al. The murine gene p27Kip1 is haplo-insufficient for tumour suppression , 1998, Nature.
[88] E Ruoslahti,et al. Integrins and anoikis. , 1997, Current opinion in cell biology.
[89] R. DePinho,et al. Suppression of cell transformation by the cyclin-dependent kinase inhibitor p57KIP2 requires binding to proliferating cell nuclear antigen. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[90] J. Marshall,et al. The role of αv-integrins in tumour progression and metastasis , 1996 .
[91] N. Heisterkamp,et al. Quantitative measure of c-abl and p15 methylation in chronic myelogenous leukemia: biological implications. , 2000, Blood.
[92] R. Klausner,et al. The von Hippel-Lindau tumor suppressor gene is required for cell cycle exit upon serum withdrawal. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[93] R. Kratzke,et al. Gene therapy of established mesothelioma xenografts with recombinant p16INK4a adenovirus , 2000, Cancer Gene Therapy.
[94] Wilhelm Krek,et al. p45SKP2 promotes p27Kip1 degradation and induces S phase in quiescent cells , 1999, Nature Cell Biology.
[95] J. Kato,et al. Degradation of the cyclin-dependent-kinase inhibitor p27Kip1 is instigated by Jab1 , 1999, Nature.
[96] M. Hung,et al. Oncogenic Signals of HER-2/neu in Regulating the Stability of the Cyclin-dependent Kinase Inhibitor p27* , 2000, The Journal of Biological Chemistry.
[97] C. O'keefe,et al. Isolation and characterization of p19INK4d, a p16-related inhibitor specific to CDK6 and CDK4. , 1996, Molecular biology of the cell.
[98] M. Steiner,et al. Adenoviral vector containing wild-type p16 suppresses prostate cancer growth and prolongs survival by inducing cell senescence , 2000, Cancer Gene Therapy.
[99] U. Mansmann,et al. Differential gene expression in colon carcinoma cells and tissues detected with a cDNA array , 1999, International journal of cancer.
[100] James M. Roberts,et al. Cloning of p27 Kip1 , a cyclin-dependent kinase inhibitor and a potential mediator of extracellular antimitogenic signals , 1994, Cell.
[101] M. Roussel,et al. Novel INK4 proteins, p19 and p18, are specific inhibitors of the cyclin D-dependent kinases CDK4 and CDK6 , 1995, Molecular and cellular biology.
[102] E. Pérez-Payá,et al. Calmodulin Binds to p21Cip1 and Is Involved in the Regulation of Its Nuclear Localization* , 1999, The Journal of Biological Chemistry.
[103] R. Weksberg,et al. Expression of p57(KIP2) potently blocks the growth of human astrocytomas and induces cell senescence. , 2000, The American journal of pathology.
[104] Mong-Hong Lee,et al. Association of the Cyclin-dependent Kinases and 14-3-3 Sigma Negatively Regulates Cell Cycle Progression* , 2000, The Journal of Biological Chemistry.
[105] M. Skolnick,et al. A cell cycle regulator potentially involved in genesis of many tumor types. , 1994, Science.
[106] R. Hruban,et al. High‐resolution deletion mapping of chromosome arm 1p in pancreatic cancer identifies a major consensus region at 1p35 , 1999, Genes, chromosomes & cancer.
[107] M. Skolnick,et al. Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus , 1994, Nature Genetics.
[108] M. Cleary,et al. Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome. , 1999, Genes & development.
[109] S. Natsugoe,et al. p21 expression is a prognostic factor in patients with p53-negative gastric cancer. , 2000, Cancer letters.
[110] L. Hengst,et al. Effects of p21Cip1/Waf1 at Both the G1/S and the G2/M Cell Cycle Transitions: pRb Is a Critical Determinant in Blocking DNA Replication and in Preventing Endoreduplication , 1998, Molecular and Cellular Biology.
[111] M. Toyota,et al. Inactivation of the 14-3-3 sigma gene is associated with 5' CpG island hypermethylation in human cancers. , 2000, Cancer research.
[112] David O. Morgan,et al. Principles of CDK regulation , 1995, Nature.
[113] J. Massagué,et al. TGFβ influences Myc, Miz-1 and Smad to control the CDK inhibitor p15INK4b , 2001, Nature Cell Biology.
[114] I. Wong,et al. Aberrant p15 promoter methylation in adult and childhood acute leukemias of nearly all morphologic subtypes: potential prognostic implications. , 2000, Blood.
[115] W. Kaelin,et al. The von Hippel-Lindau tumor suppressor gene. , 2001, Experimental cell research.
[116] F. Sarkar,et al. Inhibition of tumor cell growth by p21WAF1 adenoviral gene transfer in lung cancer. , 1998, Cancer gene therapy.
[117] D. Sidransky,et al. p16(MTS-1/CDKN2/INK4a) in cancer progression. , 2001, Experimental cell research.
[118] A. Koff,et al. Cell-cycle inhibitors: three families united by a common cause. , 2000, Gene.
[119] Ling He,et al. Inhibition of the interferon-gamma/signal transducers and activators of transcription (STAT) pathway by hypermethylation at a STAT-binding site in the p21WAF1 promoter region. , 2000, Cancer research.
[120] S. Seeber,et al. Expression of p21WAF1 predicts outcome of esophageal cancer patients treated by surgery alone or by combined therapy modalities. , 1998, Clinical cancer research : an official journal of the American Association for Cancer Research.
[121] Q. Li,et al. Recombinant adenovirus expressing Von Hippel-Lindau-mediated cell cycle arrest is associated with the induction of cyclin-dependent kinase inhibitor p27Kip1. , 1998, Biochemical and biophysical research communications.
[122] 岩田 徳和. Frequent hypermethylation of CpG islands and loss of expression of the 14-3-3 σ gene in human hepatocellular carcinoma , 2001 .
[123] D. Carson,et al. Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers , 1994, Nature.
[124] M. Malumbres,et al. Cellular Response to Oncogenic Ras Involves Induction of the Cdk4 and Cdk6 Inhibitor p15INK4b , 2000, Molecular and Cellular Biology.
[125] S. Elledge,et al. p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene. , 1995, Genes & development.
[126] L. Reid,et al. Genomic organization of the human p57KIP2 gene and its analysis in the G401 Wilms' tumor assay. , 1996, Cancer research.
[127] M. Leibovitch,et al. Stabilization of MyoD by Direct Binding to p57Kip2 * , 2000, The Journal of Biological Chemistry.
[128] T. Coleman,et al. Myt1: A Membrane-Associated Inhibitory Kinase That Phosphorylates Cdc2 on Both Threonine-14 and Tyrosine-15 , 1995, Science.
[129] J. Roth,et al. Inhibition of esophageal cancer proliferation by adenovirally mediated delivery of p16INK4. , 1996, Cancer gene therapy.
[130] Esposito,et al. Prognostic role of the cyclin-dependent kinase inhibitor p27 in non-small cell lung cancer. , 1997, Cancer research.
[131] J. Xiang,et al. Adenovirus-mediated p16INK4 gene transfer significantly suppresses human breast cancer growth , 2000, Cancer Gene Therapy.
[132] J. Massagué,et al. Repression of p15INK4b expression by Myc through association with Miz-1 , 2001, Nature Cell Biology.
[133] A. Fattaey,et al. Human Myt1 Is a Cell Cycle-regulated Kinase That Inhibits Cdc2 but Not Cdk2 Activity* , 1997, The Journal of Biological Chemistry.
[134] Raymond White,et al. Characterization of colonic polyps by two‐dimensional gel electrophoresis , 1999, Electrophoresis.
[135] R. Medema,et al. AFX-like Forkhead transcription factors mediate cell-cycle regulation by Ras and PKB through p27kip1 , 2000, Nature.
[136] E. Dellambra,et al. Stratifin, a keratinocyte specific 14-3-3 protein, harbors a pleckstrin homology (PH) domain and enhances protein kinase C activity. , 1995, Journal of cell science.
[137] W Godolphin,et al. Studies of the HER-2/neu proto-oncogene in human breast and ovarian cancer. , 1989, Science.
[138] Michele Pagano,et al. SKP2 is required for ubiquitin-mediated degradation of the CDK inhibitor p27 , 1999, Nature Cell Biology.
[139] R. Medema,et al. p21waf1 can block cells at two points in the cell cycle, but does not interfere with processive DNA-replication or stress-activated kinases , 1998, Oncogene.
[140] M. Ivan,et al. The von Hippel-Lindau tumor suppressor protein. , 2001, Current opinion in genetics & development.
[141] Andrea C. Carrano,et al. SKP 2 is required for ubiquitin-mediated degradation of the CDK inhibitor p 27 , 1999 .
[142] A. Ferguson-Smith,et al. Increased IGF-II protein affects p57kip2 expression in vivo and in vitro: implications for Beckwith-Wiedemann syndrome. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[143] R. Kobayashi,et al. pl9 skp1 and p45 skp2 are essential elements of the cyclin A-CDK2 S phase kinase , 1995, Cell.
[144] D. W. Kim,et al. Repression of transcription of the p27Kip1 cyclin-dependent kinase inhibitor gene by c-Myc , 2001, Oncogene.
[145] N. Rhind,et al. Regulation of Mitotic Inhibitor Mik1 Helps to Enforce the DNA Damage Checkpoint , 2000, Molecular biology of the cell.
[146] Y. Fukushima,et al. An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome , 1996, Nature Genetics.
[147] K. Miyazono,et al. Smad-mediated Transcription Is Required for Transforming Growth Factor-β1-induced p57Kip2 Proteolysis in Osteoblastic Cells* , 2001, The Journal of Biological Chemistry.
[148] J. Gutterman,et al. Retardation of cell proliferation after expression of p202 accompanies an increase in p21(WAF1/CIP1). , 1999, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.
[149] M. Leibovitch,et al. p57Kip2 Stabilizes the MyoD Protein by Inhibiting Cyclin E-Cdk2 Kinase Activity in Growing Myoblasts , 1999, Molecular and Cellular Biology.
[150] E. Valverius,et al. Complementary DNA cloning of a novel epithelial cell marker protein, HME1, that may be down-regulated in neoplastic mammary cells. , 1992, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.
[151] S. Reed,et al. Nuclear Accumulation of p21Cip1 at the Onset of Mitosis: a Role at the G2/M-Phase Transition , 1998, Molecular and Cellular Biology.
[152] M. Barbacid,et al. Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development. , 1997, Genes & development.
[153] Hong Sun,et al. PTEN/MMAC1/TEP1 suppresses the tumorigenicity and induces G1 cell cycle arrest in human glioblastoma cells. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[154] S. R. Hann,et al. A role for transcriptional repression of p21CIP1 by c-Myc in overcoming transforming growth factor beta -induced cell-cycle arrest. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[155] M. Pagano,et al. Role of the F-box protein Skp2 in lymphomagenesis , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[156] D. Givol,et al. Induction of WAF1/CIP1 by a p53-independent pathway. , 1994, Cancer research.
[157] P. Lengyel,et al. p202, an Interferon-inducible Modulator of Transcription, Inhibits Transcriptional Activation by the p53 Tumor Suppressor Protein, and a Segment from the p53-binding Protein 1 That Binds to p202 Overcomes This Inhibition* , 1996, The Journal of Biological Chemistry.