Wilms tumour as a possible early manifestation of hereditary leiomyomatosis and renal cell cancer?
- 1 March 2009
- journal article
- case report
- Published by Oxford University Press (OUP) in British Journal of Dermatology
- Vol. 160 (3) , 707-709
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Wilms tumor genetics: Mutations in WT1, WTX, and CTNNB1 account for only about one‐third of tumorsGenes, Chromosomes and Cancer, 2008
- Renal abnormalities and their developmental originNature Reviews Genetics, 2007
- Conventional renal cancer in a patient with fumarate hydratase mutationHuman Pathology, 2007
- Diffuse and segmental variants of cutaneous leiomyomatosis: novel mutations in the fumarate hydratase gene and review of the literatureExperimental Dermatology, 2006
- HIF overexpression correlates with biallelic loss of fumarate hydratase in renal cancer: Novel role of fumarate in regulation of HIF stabilityCancer Cell, 2005
- Mutations in the Fumarate Hydratase Gene Cause Hereditary Leiomyomatosis and Renal Cell Cancer in Families in North AmericaThe American Journal of Human Genetics, 2003
- Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiencyHuman Molecular Genetics, 2003
- Oxygen‐regulated expression of the Wilms’ tumor suppressor Wt1 involves hypoxia‐inducible factor‐1 (HIF‐1)The FASEB Journal, 2003
- Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancerNature Genetics, 2002
- Coexpression of hypoxia-inducible factor 1-alpha and vascular endothelial growth factor in Wilms' tumorJournal of Pediatric Surgery, 2000