Myogenin, AP2β, NOS-1 and HMGA2 are surrogate markers of fusion status in rhabdomyosarcoma

Pediatric rhabdomyosarcoma (RMS) is traditionally classified by histologic appearance into alveolar (ARMS) and embryonal (ERMS) subtypes. The majority of ARMS contain a PAX3-FOXO1 or PAX7-FOXO1 gene fusion, but about 20% do not. Intergroup Rhabdomyosarcoma Study (IRS) Stage and group-matched ARMS ty...

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Main Authors: Rudzinski, Erin R., Anderson, James R., Lyden, Elizabeth R., Bridge, Julia A., Barr, Frederic G., Gastier-Foster, Julie M., Bachmeyer, Karen, Skapek, Stephen X., Hawkins, Douglas S., Teot, Lisa A., Parham, David M.
Formáid: Artigo
Teanga:Inglês
Foilsithe: 2014
Ábhair:
Article
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4010390/
https://ncbi.nlm.nih.gov/pubmed/24618610
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/PAS.0000000000000195
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