The C-terminal domain of the Cdc2 inhibitory kinase Myt1 interacts with Cdc2 complexes and is required for inhibition of G(2)/M progression

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Articles by Wells, N. J.

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				C. Seidl, M. Port, K.-P. Gilbertz, A. Morgenstern, F. Bruchertseifer, M. Schwaiger, B. Roper, R. Senekowitsch-Schmidtke, and M. Abend 213Bi-induced death of HSC45-M2 gastric cancer cells is characterized by G2 arrest and up-regulation of genes known to prevent apoptosis but induce necrosis and mitotic catastrophe Mol. Cancer Ther., August 1, 2007; 6(8): 2346 - 2359. [Abstract] [Full Text] [PDF]

				B. A. Bryan, O. F. Dyson, and S. M. Akula Identifying cellular genes crucial for the reactivation of Kaposi's sarcoma-associated herpesvirus latency. J. Gen. Virol., March 1, 2006; 87(Pt 3): 519 - 529. [Abstract] [Full Text] [PDF]

				Z. Jin, E. M. Homola, P. Goldbach, Y. Choi, J. A. Brill, and S. D. Campbell Drosophila Myt1 is a Cdk1 inhibitory kinase that regulates multiple aspects of cell cycle behavior during gametogenesis Development, September 15, 2005; 132(18): 4075 - 4085. [Abstract] [Full Text] [PDF]

				I.-M. Kim, S. Ramakrishna, G. A. Gusarova, H. M. Yoder, R. H. Costa, and V. V. Kalinichenko The Forkhead Box M1 Transcription Factor Is Essential for Embryonic Development of Pulmonary Vasculature J. Biol. Chem., June 10, 2005; 280(23): 22278 - 22286. [Abstract] [Full Text] [PDF]

				A.-C. Goulet, M. Chigbrow, P. Frisk, and M. A. Nelson Selenomethionine induces sustained ERK phosphorylation leading to cell-cycle arrest in human colon cancer cells Carcinogenesis, January 1, 2005; 26(1): 109 - 117. [Abstract] [Full Text] [PDF]

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				M. L. Major, R. Lepe, and R. H. Costa Forkhead Box M1B Transcriptional Activity Requires Binding of Cdk-Cyclin Complexes for Phosphorylation-Dependent Recruitment of p300/CBP Coactivators Mol. Cell. Biol., April 1, 2004; 24(7): 2649 - 2661. [Abstract] [Full Text] [PDF]

				N. Watanabe, H. Arai, Y. Nishihara, M. Taniguchi, N. Watanabe, T. Hunter, and H. Osada M-phase kinases induce phospho-dependent ubiquitination of somatic Wee1 by SCF{beta}-TrCP PNAS, March 30, 2004; 101(13): 4419 - 4424. [Abstract] [Full Text] [PDF]

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				J. P. H. Chow, W. Y. Siu, H. T. B. Ho, K. H. T. Ma, C. C. Ho, and R. Y. C. Poon Differential Contribution of Inhibitory Phosphorylation of CDC2 and CDK2 for Unperturbed Cell Cycle Control and DNA Integrity Checkpoints J. Biol. Chem., October 17, 2003; 278(42): 40815 - 40828. [Abstract] [Full Text] [PDF]

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				A. Ryo, Y.-C. Liou, K. P. Lu, and G. Wulf Prolyl isomerase Pin1: a catalyst for oncogenesis and a potential therapeutic target in cancer J. Cell Sci., March 1, 2003; 116(5): 773 - 783. [Abstract] [Full Text] [PDF]

				H.-k. Huang, S. L. Forsburg, U. P. John, M. J. O'Connell, and T. Hunter Isolation and characterization of the Pin1/Ess1p homologue in Schizosaccharomyces pombe J. Cell Sci., March 12, 2002; 114(20): 3779 - 3788. [Abstract] [Full Text] [PDF]

				S. T. Lamitina and S. W. L'Hernault Dominant mutations in the Caenorhabditis elegans Myt1 ortholog wee-1.3 reveal a novel domain that controls M-phase entry during spermatogenesis Development, January 11, 2002; 129(21): 5009 - 5018. [Abstract] [Full Text] [PDF]

				C. J. Rothblum-Oviatt, C. E. Ryan, and H. Piwnica-Worms 14-3-3 Binding Regulates Catalytic Activity of Human Wee1 Kinase Cell Growth Differ., December 1, 2001; 12(12): 581 - 589. [Abstract] [Full Text] [PDF]

				J. R. Thorpe, S. J. Morley, and S. L. Rulten Utilizing the Peptidyl-Prolyl Cis-Trans Isomerase Pin1 as a Probe of Its Phosphorylated Target Proteins: Examples of Binding to Nuclear Proteins in a Human Kidney Cell Line and to Tau in Alzheimer's Diseased Brain J. Histochem. Cytochem., January 1, 2001; 49(1): 97 - 108. [Abstract] [Full Text]