Familial gastrointestinal stromal tumor with hyperpigmentation: Association with a germline mutation of the c-kit gene
- 1 January 2001
- journal article
- case report
- Published by Elsevier BV in Gastroenterology
- Vol. 120 (1), 210-215
- https://doi.org/10.1053/gast.2001.20880
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Mutations of c-kit JM domain are found in a minority of human gastrointestinal stromal tumorsOncogene, 1999
- Mutations in Exon 11 of c-Kit Occur Preferentially in Malignant versus Benign Gastrointestinal Stromal Tumors and Do Not Occur in Leiomyomas or LeiomyosarcomasThe American Journal of Pathology, 1999
- Gain-of-Function Mutations of c- kit in Human Gastrointestinal Stromal TumorsScience, 1998
- Gastrointestinal Stromal Tumors—Value of CD34 Antigen in their Identification and Separation from True Leiomyomas and SchwannomasThe American Journal of Surgical Pathology, 1995
- W/kit gene required for interstitial cells of Cajal and for intestinal pacemaker activityNature, 1995
- Leiomyosarcoma in leiomyomatosis of the small intestinePublished by Oxford University Press (OUP) ,1994
- Stem cell factor is encoded at the SI locus of the mouse and is the ligand for the c-kit tyrosine kinase receptorCell, 1990
- A new acute transforming feline retrovirus and relationship of its oncogene v-kit with the protein kinase gene familyNature, 1986
- Hyperpigmentation of skin and nails in a patient with intestinal leiomyosarcomaDigestive Diseases and Sciences, 1985
- Gastric stromal tumors Reappraisal of histogenesisThe American Journal of Surgical Pathology, 1983