New genes emerging for colorectal cancer predisposition

World Journal of Gastroenterology

Volumn 20, Issue 8, 2014, Pages 1961-1971

  Esteban Jurado, Clara ^a   Garre, Pilar ^h   Vila, Maria ^c   Lozano, Juan José ^c   Pristoupilova, Anna ^d   Beltrán, Sergi ^d   Abulí, Anna ^a,b   Muñoz, Jenifer ^a   Balaguer, Francesc ^a   Ocaña, Teresa ^a   Castells, Antoni ^a   Piqué, Josep M ^a   Carracedo, Angel ^e,f   Ruiz Ponte, Clara ^e   Bessa, Xavier ^b   Andreu, Montserrat ^b   Bujanda, Luis ^g   Caldés, Trinidad ^h   Castellví Bel, Sergi ^a  

^a UNIVERSITY OF BARCELONA   (Spain)

^b UNIVERSITAT POMPEU FABRA   (Spain)

^c INSTITUTO DE SALUD CARLOS III   (Spain)

^d National Institute of Bioinformatics   (Spain)

^e UNIVERSITY OF SANTIAGO DE COMPOSTELA   (Spain)

^f KING ABDULAZIZ UNIVERSITY   (Saudi Arabia)

^g UNIVERSITY OF THE BASQUE COUNTRY UPV EHU   (Spain)

^h HOSPITAL CLÍNICO SAN CARLOS   (Spain)

Author keywords

Colorectal neoplasm; Genetic predisposition to disease; Genetic variant; Genotypephenotype correlation; Next generation sequencing; Single nucleotide polymorphism

Indexed keywords

PHOSPHATIDYLINOSITOL 3 KINASE; TRANSFORMING GROWTH FACTOR BETA RECEPTOR;

ADENOMATOUS POLYP; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; BMP4 GENE; CDH1 GENE; COLORECTAL CANCER; COWDEN SYNDROME; DNA SEQUENCE; ENG GENE; EPHB2 GENE; FAMILIAL COLON POLYPOSIS; GALNT12 GENE; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETIC VARIABILITY; HEREDITARY COLORECTAL CANCER; HEREDITARY NONPOLYPOSIS COLORECTAL CANCER; HUMAN; JUVENILE POLYPOSIS; LINKAGE ANALYSIS; MISMATCH REPAIR; PEUTZ JEGHERS SYNDROME; POLD1 GENE; POLE GENE; RISK FACTOR; WNT SIGNALING PATHWAY; ADENOMATOUS POLYPOSIS COLI; COLORECTAL NEOPLASMS; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; ENVIRONMENT; GENETICS; GEOGRAPHY; GERMLINE MUTATION; HUMAN GENOME; INCIDENCE; SINGLE NUCLEOTIDE POLYMORPHISM;

ADENOMATOUS POLYPOSIS COLI; COLORECTAL NEOPLASMS; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; ENVIRONMENT; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOME, HUMAN; GEOGRAPHY; GERM-LINE MUTATION; HUMANS; INCIDENCE; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS; SEQUENCE ANALYSIS, DNA;

EID: 84894593463     PISSN: 10079327     EISSN: 22192840     Source Type: Journal    
DOI: 10.3748/wjg.v20.i8.1961     Document Type: Article

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