Identification of a rare polymorphism in the human TP53 promoter

Cancer Genetics and Cytogenetics

Volumn 135, Issue 2, 2002, Pages 165-172

  Attwooll, Claire L ^a   McGown, Gail ^a   Thorncroft, Mary ^a   Stewart, Fiona J ^b   Birch, Jillian M ^c   Varley, Jennifer M ^a  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

^b BELFAST CITY HOSPITAL   (United Kingdom)

^c ROYAL MANCHESTER CHILDREN S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CONTROLLED STUDY; DNA POLYMORPHISM; FAMILIAL CANCER; GENE DELETION; GENE EXPRESSION; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; HUMAN; HUMAN CELL; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; PROMOTER REGION; STATISTICAL SIGNIFICANCE; WILD TYPE;

BASE PAIR MISMATCH; DNA MUTATIONAL ANALYSIS; ELECTROPHORETIC MOBILITY SHIFT ASSAY; FEMALE; GENE EXPRESSION REGULATION; GENES, P53; HUMANS; LI-FRAUMENI SYNDROME; MALE; PEDIGREE; POLYMORPHISM, GENETIC; PROMOTER REGIONS (GENETICS); REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; TUMOR CELLS, CULTURED;

EID: 0036075712     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(01)00649-5     Document Type: Article

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