Role of inherited defects ofMYH in the development of sporadic colorectal cancer
- 26 February 2004
- journal article
- research article
- Published by Wiley in Genes, Chromosomes and Cancer
- Vol. 40 (1) , 1-9
- https://doi.org/10.1002/gcc.20011
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Proportion and Phenotype of MYH-Associated Colorectal Neoplasia in a Population-Based Series of Finnish Colorectal Cancer PatientsThe American Journal of Pathology, 2003
- Exposing the MYtH about base excision repair and human inherited diseaseHuman Molecular Genetics, 2003
- Germline Mutations but Not Somatic Changes at the MYH Locus Contribute to the Pathogenesis of Unselected Colorectal CancersThe American Journal of Pathology, 2003
- Does a family history of cancer increase the risk of occurrence, growth, and recurrence of colorectal adenomas?Gut, 2003
- Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumorsNature Genetics, 2002
- Clonal karyotypic abnormalities in colorectal adenomas: Clues to the early genetic events in the adenoma‐carcinoma sequenceGenes, Chromosomes and Cancer, 1994
- Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancerNature, 1994
- The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancerCell, 1993
- Clues to the Pathogenesis of Familial Colorectal CancerScience, 1993
- A genetic model for colorectal tumorigenesisCell, 1990