A foretaste for pediatric glioblastoma therapy: targeting the NF-kB pathway with DHMEQ
Author:
Funder
FAPESP
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00381-023-05878-4.pdf
Reference50 articles.
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2. Sturm D, Witt H, Hovestadt V et al (2012) Hotspot mutations in H3F3A and IDH1 define distinct epigenetic and biological subgroups of glioblastoma. Cancer Cell 22:425–437. https://doi.org/10.1016/j.ccr.2012.08.024
3. Faury D, Nantel A, Dunn SE et al (2007) Molecular profiling identifies prognostic subgroups of pediatric glioblastoma and shows increased YB-1 expression in tumors. J Clin Oncol 25:1196–1208. https://doi.org/10.1200/JCO.2006.07.8626
4. Phillips HS, Kharbanda S, Chen R et al (2006) Molecular subclasses of high-grade glioma predict prognosis, delineate a pattern of disease progression, and resemble stages in neurogenesis. Cancer Cell 9:157–173. https://doi.org/10.1016/j.ccr.2006.02.019
5. DeSisto J, Donson A, Flannery P et al (2017) HGG-17. Pediatric radiation-induced glioblastoma: transcriptomic and drug screening analysis of primary patient samples. Neuro Oncol 19:iv26–iv26. https://doi.org/10.1093/neuonc/nox083.106
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