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Volumn 61, Issue 4, 2001, Pages 1741-1746
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Mechanism of functional inactivation of a Li-Fraumeni syndrome p53 that has a mutation outside of the DNA-binding domain
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Author keywords
[No Author keywords available]
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Indexed keywords
KARYOPHERIN;
MUTANT PROTEIN;
PROTEIN P53;
APOPTOSIS;
ARTICLE;
CONTROLLED STUDY;
DNA BINDING;
DNA DAMAGE;
FAMILIAL CANCER;
GENE CONSTRUCT;
GENE INACTIVATION;
GENE MUTATION;
GROWTH INHIBITION;
HUMAN;
HUMAN CELL;
MALIGNANT TRANSFORMATION;
NUCLEAR IMPORT;
PRIORITY JOURNAL;
PROTEIN DEGRADATION;
PROTEIN DOMAIN;
PROTEIN FUNCTION;
PROTEIN LOCALIZATION;
TRANSACTIVATION;
3T3 CELLS;
ANIMALS;
APOPTOSIS;
CELL DIVISION;
CYTOPLASM;
DNA;
DNA DAMAGE;
EXONS;
GENE EXPRESSION REGULATION;
GENE SILENCING;
GENES, P53;
HUMANS;
LI-FRAUMENI SYNDROME;
MICE;
MUTATION;
NUCLEAR PROTEINS;
PROTEIN STRUCTURE, TERTIARY;
PROTO-ONCOGENE PROTEINS;
PROTO-ONCOGENE PROTEINS C-MDM2;
RATS;
TRANS-ACTIVATION (GENETICS);
TRANSFECTION;
TUMOR SUPPRESSOR PROTEIN P53;
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EID: 0035866340
PISSN: 00085472
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (19)
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References (12)
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