Barrett's esophagus in the patients with familial adenomatous polyposis

Familial Cancer

Volumn 13, Issue 2, 2014, Pages 213-217

  Gatalica, Zoran ^a,b   Chen, Mingkui ^a   Snyder, Carrie ^a   Mittal, Sumeet ^a   Lynch, Henry T ^a  

^a CREIGHTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b CARIS LIFE SCIENCES   (United States)

Author keywords

APC mutations; Barrett's esophagus; Familial adenomatous polyposis coli

Indexed keywords

APC PROTEIN; BETA CATENIN; CYCLIN D1; TRANSCRIPTION FACTOR CDX2; UVOMORULIN; APC PROTEIN, HUMAN; CADHERIN;

ARTICLE; BARRETT ESOPHAGUS; CLINICAL ARTICLE; COLON; CONTROLLED STUDY; DISEASE ASSOCIATION; DUODENUM; FAMILIAL COLON POLYPOSIS; FEMALE; GENE LOCUS; GENE MUTATION; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; MALE; NONSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; STOMACH; WNT SIGNALING PATHWAY; ADULT; AGED; BIOPSY; CASE CONTROL STUDY; CHEMISTRY; COLON POLYPOSIS; COMPLICATION; ESOPHAGUS; GASTROINTESTINAL ENDOSCOPY; GENE DELETION; GENETIC PREDISPOSITION; GENETICS; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY; TUMOR SUPPRESSOR GENE; YOUNG ADULT;

ADENOMATOUS POLYPOSIS COLI; ADENOMATOUS POLYPOSIS COLI PROTEIN; ADULT; AGED; BARRETT ESOPHAGUS; BASE SEQUENCE; BETA CATENIN; BIOPSY; CADHERINS; CASE-CONTROL STUDIES; CYCLIN D1; ENDOSCOPY, GASTROINTESTINAL; ESOPHAGUS; FEMALE; GENES, APC; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MUTATION; SEQUENCE DELETION; WNT SIGNALING PATHWAY; YOUNG ADULT;

EID: 84903308549     PISSN: 13899600     EISSN: 15737292     Source Type: Journal    
DOI: 10.1007/s10689-013-9638-7     Document Type: Article

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