The DOI matches its Crossref record; 84 of the 84 references it cites were found in a registry or an index.
Cyclin‐dependent protein kinases: Key regulators of the eukaryotic cell cycle
Abstract
Passage through the cell cycle requires the successive activation of different cyclin‐dependent protein kinases (CDKs). These enzymes are controlled by transient associations with cyclin regulatory subunits, binding of inhibitory polypeptides and reversible phosphorylation reactions. To promote progression towards DNA replication, CDK/cyclin complexes phosphorylate proteins required for the activation of genes involved in DNA synthesis, as well as components of the DNA replication machinery. Subsequently, a different set of CDK/cyclin complexes triggers the phosphorylation of numerous proteins to promote the profound structural reorganizations that accompany the entry of cells into mitosis. At present, much research is focused on elucidating the links between CDK/cyclin complexes and signal transduction pathways controlling cell growth, differentiation and death. In future, a better understanding of the cell cycle machinery and its deregulation during oncogenesis may provide novel opportunities for the diagnostic and therapeutic management of cancer and other proliferation‐related diseases.
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A cell cycle regulator potentially involved in genesis of many tumor types
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Cited by
Hershko, A., & Ciechanover, A. (1998) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.67.1.425 · Cited by 8,840
Sherr, C. J. (1996) · Science · doi:10.1126/science.274.5293.1672 · Cited by 5,379
Mitotic phosphorylation of dynamin-related GTPase Drp1 participates in mitochondrial fission.
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Pathways of apoptotic and non-apoptotic death in tumour cells
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Metadata
- Authors
- Nigg, E. A.
- Venue
- BioEssays
- Publisher
- Wiley
- Published
- 1995-06
- Volume
- 17
- Issue
- 6
- Pages
- 471-480
- ISSN
- 0265-9247 (ISSN-L)
- 1521-1878
- OpenAlex
- W2018537155
- Cited by
- 932
- References
- 84
- FWCI
- 5.79
- Type
- journal article
- Language
- en
- Open access
- closed
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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