A novel missense germline mutation in exon 2 of the hMSH2 gene in a HNPCC family from Southern Italy

Cancer Letters

Volumn 223, Issue 2, 2005, Pages 285-291

  Baudi, Francesco ^a   Fersini, Giuseppina ^a   Lavecchia, Annamaria ^b   Terracciano, Rosa ^a   Leone, Francarlo ^b   Quaresima, Barbara ^a   Faniello, Maria C ^a   De Paola, Loredana ^a   Doldo, Patrizia ^a   Cuda, Giovanni ^a   Costanzo, Francesco ^a   Venuta, Salvatore ^a  

^a UNIVERSITY MAGNA GRAECIA OF CATANZARO   (Italy)

^b PUGLIESE CIACCIO HOSPITAL   (Italy)

Author keywords

HNPCC; Microsatellite instability (MSI); Mismatch repair (MMR); MSH2; Tumor infiltrating lymphocytes (TILs)

Indexed keywords

ADULT; AMINO ACID ANALYSIS; ARTICLE; CASE REPORT; COLORECTAL CARCINOMA; EXON; GENE EXPRESSION; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; HUMAN; HUMAN CELL; HUMAN TISSUE; ITALY; MICROSATELLITE INSTABILITY; MISMATCH REPAIR; MISSENSE MUTATION; PRIORITY JOURNAL; TUMOR ASSOCIATED LEUKOCYTE;

ADULT; BASE PAIR MISMATCH; CASE-CONTROL STUDIES; COLORECTAL NEOPLASMS; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; DNA MUTATIONAL ANALYSIS; DNA REPAIR; DNA REPAIR ENZYMES; DNA-BINDING PROTEINS; EXONS; FEMALE; GENE EXPRESSION REGULATION, NEOPLASTIC; GENETIC PREDISPOSITION TO DISEASE; GERM-LINE MUTATION; HUMANS; IMMUNOHISTOCHEMISTRY; ITALY; MALE; MICROSATELLITE REPEATS; MUTATION, MISSENSE; MUTS HOMOLOG 2 PROTEIN; PEDIGREE; PROTO-ONCOGENE PROTEINS;

EID: 21144445511     PISSN: 03043835     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.canlet.2004.09.051     Document Type: Article

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