Familial gastrointestinal stromal tumours with germline mutation of the KIT gene

This publication has 16 references indexed in Scilit:

• Gain-of-Function Mutations of c- kit in Human Gastrointestinal Stromal Tumors
  Science, 1998
• Human Cancer Syndromes: Clues to the Origin and Nature of Cancer
  Science, 1997
• Somatic c-KIT activating mutation in urticaria pigmentosa and aggressive mastocytosis: establishment of clonality in a human mast cell neoplasm
  Nature Genetics, 1996
• Identification of a point mutation in the catalytic domain of the protooncogene c-kit in peripheral blood mononuclear cells of patients who have mastocytosis with an associated hematologic disorder.
  Proceedings of the National Academy of Sciences, 1995
• Leiomyosarcoma in leiomyomatosis of the small intestine
  Published by Oxford University Press (OUP) ,1994
• Ligand-independent activation of c-kit receptor tyrosine kinase in a murine mastocytoma cell line P-815 generated by a point mutation
  Blood, 1994
• Identification of mutations in the coding sequence of the proto-oncogene c-kit in a human mast cell leukemia cell line causing ligand-independent activation of c-kit product.
  Journal of Clinical Investigation, 1993
• ‘Cold SSCP’: a simple, rapid and non-radioactive method for optimized single-strand conformation polymorphism analyses
  Nucleic Acids Research, 1993
• A simple method for amplification of DNA from paraffin-embedded tissues
  Nucleic Acids Research, 1992
• Achalasia Due to Diffuse Esophageal Leiomyomatosis and Inherited as an Autosomal Dominant Disorder
  Gastroenterology, 1990