Spectrum of FGFR3 Mutations in Multiple Intraindividual Seborrheic Keratoses
- 1 August 2007
- journal article
- Published by Elsevier BV in Journal of Investigative Dermatology
- Vol. 127 (8), 1883-1885
- https://doi.org/10.1038/sj.jid.5700804
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- FGFR3 Mutations in Benign Skin TumorsCell Cycle, 2006
- High Frequency of FGFR3 Mutations in Adenoid Seborrheic KeratosesJournal of Investigative Dermatology, 2006
- Mosaicism of activatingFGFR3 mutations in human skin causes epidermal neviJCI Insight, 2006
- PIK3CA Mutations Are an Early Genetic Alteration Associated with FGFR3 Mutations in Superficial Papillary Bladder TumorsCancer Research, 2006
- A Simple and Fast Method for the Simultaneous Detection of Nine Fibroblast Growth Factor Receptor 3 Mutations in Bladder Cancer and Voided UrineClinical Cancer Research, 2005
- Activating mutations of the tyrosine kinase receptor FGFR3 are associated with benign skin tumors in mice and humansHuman Molecular Genetics, 2005
- Seborrheic keratosis in the Korean males: causative role of sunlightPhotodermatology, Photoimmunology & Photomedicine, 2003
- Craniosynostosis: genes and mechanismsHuman Molecular Genetics, 1997
- The prevalence of seborrhoeic keratoses in an Australian population: does exposure to sunlight play a part in their frequency?British Journal of Dermatology, 1997
- Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasiaNature Genetics, 1996