Somatic Mutations in the STK11/LKB1 Gene Are Uncommon in Rare Gynecological Tumor Types Associated with Peutz-Jegher's Syndrome
- 1 January 2000
- journal article
- research article
- Published by Elsevier in The American Journal of Pathology
- Vol. 156 (1) , 339-345
- https://doi.org/10.1016/s0002-9440(10)64735-9
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Germline and Somatic Mutations of the STK11/LKB1 Peutz-Jeghers Gene in Pancreatic and Biliary CancersThe American Journal of Pathology, 1999
- Somatic mutation of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanomaOncogene, 1999
- LKB1 Somatic Mutations in Sporadic TumorsThe American Journal of Pathology, 1999
- Genetic Pathways of Colorectal Carcinogenesis Rarely Involve thePTEN and LKB1 Genes Outside the Inherited Hamartoma SyndromesThe American Journal of Pathology, 1998
- Peutz-Jeghers syndrome is caused by mutations in a novel serine threoninekinaseNature Genetics, 1998
- Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3.Journal of Medical Genetics, 1998
- Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysisNature Genetics, 1997
- Disseminated Cervical Adenoma Malignum and Bilateral Ovarian Sex Cord Tumors with Annular Tubules Associated with Peutz-Jeghers SyndromeGynecologic Oncology, 1994
- Increased Risk of Cancer in the Peutz–Jeghers SyndromeNew England Journal of Medicine, 1987
- Ovarian Tumors Associated with the Peutz-Jeghers SyndromeAnnals of Surgery, 1970