Role of Inherited Defects of MYH in the Development of Sporadic Colorectal Cancer

Genes Chromosomes and Cancer

Volumn 40, Issue 1, 2004, Pages 1-9

  Kambara, Takeshi ^a,b   Whitehall, Vicki L J ^a   Spring, Kevin J ^a   Barker, Melissa A ^a   Arnold, Sven ^a   Wynter, Coral V A ^a   Matsubara, Nagahide ^b   Tanaka, Noriaki ^b   Young, Joanne P ^a   Leggett, Barbara A ^a   Jass, Jeremy R ^c  

^a Royal Brisbane and Womens Hospital Research Foundation   (Australia)

^b OKAYAMA UNIVERSITY   (Japan)

^c MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

APC PROTEIN; DNA;

AGED; ARTICLE; CHROMOSOME 1P; COLORECTAL CANCER; CONTROLLED STUDY; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; DNA REPAIR; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC POLYMORPHISM; GERM LINE; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; MICROSATELLITE INSTABILITY; MISMATCH REPAIR; NONSENSE MUTATION; ONCOGENE; ONCOGENE K RAS; ONCOGENE K RAS 2; ONCOGENE MYH; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISM; TUMOR SUPPRESSOR GENE;

ADENOMA; ADENOMATOUS POLYPOSIS COLI; AGE OF ONSET; AGED; COLORECTAL NEOPLASMS; DNA GLYCOSYLASES; FEMALE; GENES, APC; GENETIC PREDISPOSITION TO DISEASE; GERM-LINE MUTATION; HUMANS; LOSS OF HETEROZYGOSITY; MALE; PROTO-ONCOGENE PROTEINS; TRINUCLEOTIDE REPEAT EXPANSION;

EID: 11144355687     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/gcc.20011     Document Type: Article

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