Cargando…
MDM2 Amplification and PI3KCA Mutation in a Case of Sclerosing Rhabdomyosarcoma
A rare sclerosing variant of rhabdomyosarcoma characterized by prominent hyalinization and pseudovascular pattern has recently been described as a subtype biologically distinct from embryonal, alveolar, and pleomorphic forms. We present cytogenetic and molecular findings as well as experimental stud...
Autores principales: | Kikuchi, Ken, Wettach, George R., Ryan, Christopher W., Hung, Arthur, Hooper, Jody E., Beadling, Carol, Warrick, Andrea, Corless, Christopher L., Olson, Susan B., Keller, Charles, Mansoor, Atiya |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673319/ https://www.ncbi.nlm.nih.gov/pubmed/23766666 http://dx.doi.org/10.1155/2013/520858 |
Ejemplares similares
-
Functional impact and targetability of PI3KCA, GNAS, and PTEN mutations in a spindle cell rhabdomyosarcoma with MYOD1 L122R mutation
por: Choo, Florence, et al.
Publicado: (2022) -
Low Prevalence of TP53 Mutations and MDM2 Amplifications in Pediatric Rhabdomyosarcoma
por: Ognjanovic, Simona, et al.
Publicado: (2012) -
Pediatric Sclerosing Rhabdomyosarcomas: A Review
por: Kumar, Amandeep, et al.
Publicado: (2014) -
TBX2 represses PTEN in rhabdomyosarcoma and skeletal muscle
por: Zhu, Bo, et al.
Publicado: (2015) -
Preclinical rationale for entinostat in embryonal rhabdomyosarcoma
por: Bharathy, Narendra, et al.
Publicado: (2019)