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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Neuro Oncol
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2020
Aiheet:
Atypical Teratoid/Rhabdoid Tumors
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7715320/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noaa222.012
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