Role of Plk2 ( Snk ) in Mouse Development and Cell Proliferation
Author:
Affiliation:
1. Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138
2. Centre de Recherche en Cancérologie de l'Université Laval, L'Hôtel-Dieu de Québec, CHUQ, Québec, Canada G1R 2J6
Abstract
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Link
https://journals.asm.org/doi/pdf/10.1128/MCB.23.19.6936-6943.2003
Reference59 articles.
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2. Carmena, M., M. G. Riparbelli, G. Minestrini, A. M. Tavares, R. Adams, G. Callaini, and D. M. Glover. 1998. Drosophila polo kinase is required for cytokinesis. J. Cell Biol. 143 : 659-671.
3. Charron, J., B. A. Malynn, P. Fisher, V. Stewart, L. Jeannotte, S. P. Goff, E. J. Robertson, and F. W. Alt. 1992. Embryonic lethality in mice homozygous for a targeted disruption of the N-myc gene. Genes Dev. 6 : 2248-2257.
4. Chase, D., Y. Feng, B. Hanshew, J. A. Winkles, D. L. Longo, and D. K. Ferris. 1998. Expression and phosphorylation of fibroblast-growth-factor-inducible kinase (Fnk) during cell-cycle progression. Biochem. J. 333 : 655-660.
5. Conn, C. W., R. F. Hennigan, W. Dai, Y. Sanchez, and P. J. Stambrook. 2000. Incomplete cytokinesis and induction of apoptosis by overexpression of the mammalian polo-like kinase, Plk3. Cancer Res. 60 : 6826-6831.
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