Genetic steps in the development of squamous cell carcinoma of the esophagus

This publication has 22 references indexed in Scilit:

• The type of somatic mutation at APC in familial adenomatous polyposis is determined by the site of the germline mutation: a new facet to Knudson's 'two-hit' hypothesis
  Nature Medicine, 1999
• Cytoplasmic ?-catenin in esophageal cancers
  International Journal of Cancer, 1999
• Aberrant methylation of p16INK4a and deletion of p15INK4b are frequent events in human esophageal cancer in Linxian, China
  Carcinogenesis: Integrative Cancer Research, 1999
• Distinct regions of frequent loss of heterozygosity of chromosome 5p and 5q in human esophageal cancer
  International Journal of Cancer, 1998
• Loss of heterozygosity in sporadic oesophageal tumors in the tylosis oesophageal cancer (TOC) gene region of chromosome 17q
  Oncogene, 1998
• Tylosis esophageal cancer locus on chromosome 17q25.1 is commonly deleted in sporadic human esophageal cancer
  Gastroenterology, 1998
• The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
  Cell, 1993
• Altered expression of the cyclin D1 and retinoblastoma genes in human esophageal cancer.
  Proceedings of the National Academy of Sciences, 1993
• A genetic model for colorectal tumorigenesis
  Cell, 1990
• Amplification of the EGF receptor and c‐myc genes in human esophageal cancers
  International Journal of Cancer, 1988