Abstract
Despite over one hundred years of research, the duplication of the centrosome is a poorly understood process. Three recent papers--exploring three different kinases--may have provided the answer.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
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Review
MeSH terms
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Animals
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CDC2-CDC28 Kinases*
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Caenorhabditis elegans Proteins*
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Cell Cycle / physiology
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Centrosome / physiology*
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Cyclin E / metabolism
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Cyclin E / physiology
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Cyclin-Dependent Kinase 2
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Cyclin-Dependent Kinases / metabolism*
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Cyclin-Dependent Kinases / physiology
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Mitosis / physiology
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Nuclear Proteins / metabolism
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Nucleolus Organizer Region / metabolism
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Nucleophosmin
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Protein Kinases / genetics
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Protein Kinases / metabolism*
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Protein Kinases / physiology
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Protein Serine-Threonine Kinases / genetics
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Protein Serine-Threonine Kinases / metabolism*
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Protein Serine-Threonine Kinases / physiology
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Protein-Tyrosine Kinases / genetics
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Protein-Tyrosine Kinases / metabolism*
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Protein-Tyrosine Kinases / physiology
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Receptor Protein-Tyrosine Kinases / genetics
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Receptor Protein-Tyrosine Kinases / metabolism*
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Receptor Protein-Tyrosine Kinases / physiology
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Receptor, EphA1
Substances
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Caenorhabditis elegans Proteins
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Cyclin E
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Nuclear Proteins
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Nucleophosmin
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Protein Kinases
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Ttk protein, mouse
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zyg-1 protein, C elegans
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Protein-Tyrosine Kinases
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Receptor Protein-Tyrosine Kinases
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Receptor, EphA1
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Protein Serine-Threonine Kinases
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CDC2-CDC28 Kinases
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Cyclin-Dependent Kinase 2
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Cyclin-Dependent Kinases