Insights into the molecular basis of human hereditary breast cancer from studies of the BRCA1 BRCT domain

Familial Cancer

Volumn 5, Issue 1, 2006, Pages 89-93

  Glover, J N Mark ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

Author keywords

BRCA1; BRCT; Breast cancer; DNA repair; M1775R; Missense variants; Phospho peptide interactions

Indexed keywords

BACH1 PROTEIN; BRCA1 PROTEIN; PHOSPHOTRANSFERASE; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; BINDING SITE; BREAST CANCER; CANCER INHIBITION; CANCER RISK; CANCER SCREENING; CARBOXY TERMINAL SEQUENCE; DNA DAMAGE; FAMILIAL CANCER; HUMAN; MISSENSE MUTATION; MOLECULAR RECOGNITION; ONCOGENE; PRIORITY JOURNAL; PROTEIN FOLDING; PROTEIN FUNCTION; PROTEIN MOTIF; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; REVIEW;

BRCA1 PROTEIN; BREAST NEOPLASMS; DNA REPAIR; DNA, NEOPLASM; FEMALE; GENE EXPRESSION REGULATION, NEOPLASTIC; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MOLECULAR BIOLOGY; MUTATION, MISSENSE; NEOPLASTIC SYNDROMES, HEREDITARY; SENSITIVITY AND SPECIFICITY;

EID: 33644879468     PISSN: 13899600     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10689-005-2579-z     Document Type: Review

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