Quantitative analysis of residual folding and DNA binding in mutant p53 core domain: definition of mutant states for rescue in cancer therapy.
The tumour suppressor p53 is mutated in half of all human cancers, most frequently with missense substitutions in its core domain. We present a new assessment of the mutation database based on quantitative folding and DNA-binding studies of the isolated core domain. Our data identify five distinct m...
Principais autores: | Bullock, A, Henckel, J, Fersht, A |
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Formato: | Journal article |
Idioma: | English |
Publicado em: |
2000
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