The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li–Fraumeni syndrome
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In the citing paper
“Germline TP53 mutations have been found in patients with Li–Fraumeni syndrome (LFS), an autosomal dominant cancer predisposition syndrome characterized by the early onset of a spectrum of childhood and adulthood cancers, including adrenocortical carcinomas, soft tissue sarcomas, osteosarcomas, brain tumors, and pre‐menopausal breast cancer [123, 124, 125].”
From The TP53 tumor suppressor gene: From molecular biology to clinical investigations (2025) · cites this paper as [124]
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Citations
Cites
The p53 proto-oncogene can act as a suppressor of transformation
Finlay, C. A., Hinds, P. W., & Levine, A. J. (1989) · Cell · doi:10.1016/0092-8674(89)90045-7 · Cited by 1,987
Cited by
p53 Mutations in Human Cancers
Hollstein, M., Sidransky, D., Vogelstein, B., & Harris, C. C. (1991) · Science · doi:10.1126/science.1905840 · Cited by 8,018
Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours
Donehower, L. A., Harvey, M., Slagle, B. L., McArthur, M. J., Montgomery, C. A., Butel, J. S., & Bradley, A. (1992) · Nature · doi:10.1038/356215a0 · Cited by 4,649
Kastan, M. B., Zhan, Q., El-Deiry, W. S., Carrier, F., Jacks, T., Walsh, W. V., Plunkett, B. S., Vogelstein, B., & Fornace, A. J. (1992) · Cell · doi:10.1016/0092-8674(92)90593-2 · Cited by 3,047
Malignant astrocytic glioma: genetics, biology, and paths to treatment
Furnari, F. B., Fenton, T., Bachoo, R. M., Mukasa, A., Stommel, J. M., Stegh, A., Hahn, W. C., Ligon, K. L., Louis, D. N., Brennan, C., et al. (2007) · Genes & Development · doi:10.1101/gad.1596707 · Cited by 2,316
The first 30 years of p53: growing ever more complex.
Levine, A. J., & Oren, M. (2009) · Nature Reviews Cancer · doi:10.1038/nrc2723 · Cited by 1,967
Metadata
- Authors
- Srivastava, S., Zou, Z., Pirollo, K., Blattner, W., & Chang, E. H.
- Venue
- Nature
- Published
- 1990-12
- Volume
- 348
- Issue
- 6303
- Pages
- 747-749
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2046780997
- Cited by
- 1,211
- References
- 1
- FWCI
- 34.85
- 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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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li–Fraumeni syndrome. https://app.cochat.ai/papers/10.1038/348747a0
- The paper
- Srivastava, S., Zou, Z., Pirollo, K., Blattner, W., & Chang, E. H. (1990). Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li–Fraumeni syndrome. Nature. https://doi.org/10.1038/348747a0
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.
