The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
The codon 72 polymorphic variants of p53 have markedly different apoptotic potential
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In the citing paper
“The TADs are followed by a PRD (AA residues 62–94) that includes five PXXP (P: proline; X: any AA) motifs.15 This region plays a critical role in promoting cell cycle arrest and p53-associated death.24,25”
From p53: from understanding its structure to advances in therapeutic targeting (2026) · cites this paper as [25]
In the citing paper
“The proline-rich region linking the TAD to DBD is required for p53 to induce cell cycle arrest and apoptosis.278,279”
From Targeting p53 pathways: mechanisms, structures, and advances in therapy (2023) · cites this paper as [278]
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Citations
Cites
Mice Lacking p21CIP1/WAF1 undergo normal development, but are defective in G1 checkpoint control
Deng, C., Zhang, P., Wade Harper, J., Elledge, S. J., & Leder, P. (1995) · Cell · doi:10.1016/0092-8674(95)90039-x · Cited by 2,113
Proteolytic Cleavage of the mdm2 Oncoprotein during Apoptosis
Chen, L., Marechal, V., Moreau, J., Levine, A. J., & Chen, J. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.36.22966 · Cited by 121
Cited by
Fridman, J. S., & Lowe, S. W. (2003) · Oncogene · doi:10.1038/sj.onc.1207116 · Cited by 1,401
Targeting p53 pathways: mechanisms, structures, and advances in therapy
Wang, H., Guo, M., Wei, H., & Chen, Y. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01347-1 · Cited by 1,016
TP53 mutations in human cancers: Functional selection and impact on cancer prognosis and outcomes
Petitjean, A., Achatz, M. I. W., Borresen-Dale, A. L., Hainaut, P., & Olivier, M. (2007) · Oncogene · doi:10.1038/sj.onc.1210302 · Cited by 884
Transcription-independent pro-apoptotic functions of p53
Moll, U. M., Wolff, S., Speidel, D., & Deppert, W. (2005) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2005.09.007 · Cited by 468
A Small Molecule Inhibitor of Inducible Heat Shock Protein 70
Leu, J. I.-J., Pimkina, J., Frank, A., Murphy, M. E., & George, D. L. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.09.023 · Cited by 441
Self-citation
Metadata
- Authors
- Dumont, P., Leu, J. I.-J., Della Pietra, A. C., George, D. L., & Murphy, M.
- Venue
- Nature Genetics
- Published
- 2003-02-03
- Volume
- 33
- Issue
- 3
- Pages
- 357-365
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2075230059
- Cited by
- 1,273
- References
- 2
- FWCI
- 29.06
- Type
- journal article
- Language
- en
- Open access
- closed
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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Cite CoChat for the checks on this page, and the paper for its own findings.
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- CoChat. (2026). Citation check: The codon 72 polymorphic variants of p53 have markedly different apoptotic potential. https://app.cochat.ai/papers/10.1038/ng1093
- The paper
- Dumont, P., Leu, J. I.-J., Della Pietra, A. C., George, D. L., & Murphy, M. (2003). The codon 72 polymorphic variants of p53 have markedly different apoptotic potential. Nature Genetics. https://doi.org/10.1038/ng1093
Data sources
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).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
