A germline missense mutation R337C in exon 10 of the human p53 gene.

Luca JW; Strong LC; Hansen MF

doi:10.1002/humu.1380110121

A germline missense mutation R337C in exon 10 of the human p53 gene.

Luca JW ¹,

Strong LC ,

Hansen MF

Affiliations

1. Department of Molecular Genetics, University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.
Authors
Luca JW¹
(1 author)

Human Mutation, 01 Jan 1998, Suppl 1:S58-61
https://doi.org/10.1002/humu.1380110121 PMID: 9452042

Abstract

No abstract provided.

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Read article at publisher's site: https://doi.org/10.1002/humu.1380110121

References

Articles referenced by this article (15)

p53 gene mutation: software and database.
Beroud C, Verdier F, Soussi T
Nucleic Acids Res, (1):147-150 1996
MED: 8594565
Familial cancer syndromes and clusters.
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Br Med Bull, (3):624-639 1994
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Mutations in the p53 tumor suppressor gene: clues to cancer etiology and molecular pathogenesis.
Greenblatt MS, Bennett WP, Hollstein M, Harris CC
Cancer Res, (18):4855-4878 1994
MED: 8069852
Somatic point mutations in the p53 gene of human tumors and cell lines: updated compilation.
Hollstein M, Shomer B, Greenblatt M, Soussi T, Hovig E, Montesano R, Harris CC
Nucleic Acids Res, (1):141-146 1996
MED: 8594564
Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome?
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A cancer family syndrome in twenty-four kindreds.
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Cancer Res, (18):5358-5362 1988
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Detection of p53 gene mutations in human brain tumors by single-strand conformation polymorphism analysis of polymerase chain reaction products.
Mashiyama S, Murakami Y, Yoshimoto T, Sekiya T, Hayashi K
Oncogene, (8):1313-1318 1991
MED: 1886708
A simple salting out procedure for extracting DNA from human nucleated cells.
Miller SA, Dykes DD, Polesky HF
Nucleic Acids Res, (3):1215 1988
MED: 3344216
Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.
Orita M, Iwahana H, Kanazawa H, Hayashi K, Sekiya T
Proc Natl Acad Sci U S A, (8):2766-2770 1989
MED: 2565038
Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction.
Orita M, Suzuki Y, Sekiya T, Hayashi K
Genomics, (4):874-879 1989
MED: 2687159

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Proteins in UniProt

Cellular tumor antigen p53(UniProt - P04637)

GlyGen is an international glycobioinformatics knowledgebase funded by The National Institutes of Health to facilitate glycoscience research by integrating diverse kinds of information, including glycomics, genomics, proteomics (and glycoproteomics), cell biology, developmental biology and biochemistry.

https://www.glygen.org/publication/MED/9452042

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Funders who supported this work.

NCI NIH HHS (2)

Grant ID: CA 38929
2 publications
Grant ID: CA 53318
4 publications

Search life-sciences literature (45,103,589 articles, preprints and more)

A germline missense mutation R337C in exon 10 of the human p53 gene.

Affiliations

Authors

Abstract

Full text links

References

p53 gene mutation: software and database.

Familial cancer syndromes and clusters.

Mutations in the p53 tumor suppressor gene: clues to cancer etiology and molecular pathogenesis.

Somatic point mutations in the p53 gene of human tumors and cell lines: updated compilation.

Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome?

A cancer family syndrome in twenty-four kindreds.

Detection of p53 gene mutations in human brain tumors by single-strand conformation polymorphism analysis of polymerase chain reaction products.

A simple salting out procedure for extracting DNA from human nucleated cells.

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction.

Citations & impact

Impact metrics

Citations of article over time

Smart citations by scite.ai
Explore citation contexts and check if this article has been supported or disputed.
https://scite.ai/reports/10.1002/humu.1380110121

Article citations

Li-Fraumeni-associated pancreatic neuroendocrine tumour and XAF1 p.Glu134Ter risk modifier variant.

The first pancreatic neuroendocrine tumor in Li-Fraumeni syndrome: a case report.

An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma.

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Proteins in UniProt

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NCI NIH HHS (2)

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Search life-sciences literature (45,103,589 articles, preprints and more)

A germline missense mutation R337C in exon 10 of the human p53 gene.

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Funding

NCI NIH HHS (2)﻿

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NCI NIH HHS (2)