ATRT-13. DIFFERENT CELLS OF ORIGIN PAVE THE WAY FOR MOLECULAR HETEROGENEITY IN RHABDOID TUMORS

Rhabdoid tumors (RT) are rare but highly aggressive pediatric neoplasms. These tumors carry homozygous loss-of-function alterations of SMARCB1 in almost all cases with an otherwise low mutational load. RT arise at different intracranial (ATRT) as well as extracranial (MRT) anatomical sites. Three ma...

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Detalles Bibliográficos
Autores principales: Graf, Monika, Interlandi, Marta, Moreno, Natalia, Holdhof, Dörthe, Melcher, Viktoria, Kastrati, Dennis, zu Hörste, Gerd Meyer, Dugas, Martin, Frühwald, Michael C, Albert, Thomas K, Schüller, Ulrich, Kerl, Kornelius
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Atypical Teratoid/Rhabdoid Tumors
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715320/
http://dx.doi.org/10.1093/neuonc/noaa222.012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715320/
http://dx.doi.org/10.1093/neuonc/noaa222.012

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