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Core pathway mutations induce de-differentiation of murine astrocytes into glioblastoma stem cells that are sensitive to radiation but resistant to temozolomide.
PubMed Full text in PMC Similar studies Analyze with GEO2R
Core pathway mutations induce de-differentiation of murine astrocytes into glioblastoma stem cells that are sensitive to radiation, but resistant to temozolomide
PubMed Full text in PMC Similar studies
Core pathway mutations induce de-differentiation of murine astrocytes into glioblastoma stem cells that are sensitive to radiation, but resistant to temozolomide (RNA-seq)
PubMed Full text in PMC Similar studies SRA Run Selector
Core pathway mutations induce de-differentiation of murine astrocytes into glioblastoma stem cells that are sensitive to radiation, but resistant to temozolomide (FAIRE-seq)
Oncogenic alterations in multiple core signaling pathways are required for glioblastoma pathogenesis in vitro and in vivo
Expression data from glioblastoma stem-like cells (GSCs) and astrocyte co-cultured GSCs
Quiescent glioblastoma cells shift to an epithelial-mesenchymal transition-like gene program
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Expression data from glioma cells exposed to interferon (IFN)-beta
Glioblastoma from a homogenous cohort of patients treated within clinical trial
Glioblastoma stem cell (GSC) clones survived 500uM Temozolomide (TMZ) treatment
Novel KDM1A inhibitors induce differentiation and apoptosis of glioma stem cells via unfolded protein response (UPR) pathway
Enriching glioma stem cells by intracranial implantation and developing clinically relevant model for therapeutic intervention
EGFR/FOXO3a/BIM signalling pathway determines chemosensitivity of BMP4-differentiated glioma stem cells to temozolomide
Expression data from glioblastoma stem cell clones (GSC)
Disulfiram when combined with copper enhances the therapeutic effects of temozolomide for the treatment of Glioblastoma
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RNA-sequencing WT vs SOCS3 knockout Glioblastoma stem-cells
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Patient-derived glioblastoma stem cells transcriptome regulation by CD109
Epigenetic determinants of self-renewal in glioblastoma [ATAC-seq]
PubMed Similar studies SRA Run Selector
MLL5 Orchestrates a Cancer Self-Renewal State by Repressing the Histone Variant H3.3 and Globally Reorganizing Chromatin [expression]
MLL5 orchestrates a cancer self-renewal state by repressing the histone variant H3.3 and globally reorganizing chromatin [methylation]
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