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Article

Characterization of the oligomerization defects of two p53 mutants found in families with Li–Fraumeni and Li–Fraumeni-like syndrome

6 Aug 1998

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9704931
DOI: 10.1038/sj.onc.1202062

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Related research

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Characterization of the oligomerization defects of two p53 mutants found in families with Li–Fraumeni and Li–Fraumeni-like syndromePMID 9704931Read ↗

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The Status of p53 Oligomeric and Aggregation States in CancerSemantic proximity Read ↗

p53 oligomerization status modulates cell fate decisions between growth, arrest and apoptosisSemantic proximity Read ↗

Detection of 11 germline inactivating TP53 mutations and absence of TP63 andHCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndromeSemantic proximity Read ↗

Effects of tumor-associated mutations in the p53 tetramerization domain on oligomerization state and transcriptional activity.Semantic proximity Read ↗

Linkage studies in a Li-Fraumeni family with increased expression of p53 protein but no germline mutation in p53Semantic proximity Read ↗

The role of tetramerization in p53 function.Semantic proximity Read ↗

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