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UnknownEstrogen-related receptor β activation and isoform shifting by cdc2-like kinase inhibition restricts migration and intracranial tumor growth in glioblastoma.
Not available
S-EPMC6894094 | biostudies-literature
UnknownAlkylpurine-DNA-N-glycosylase confers resistance to temozolomide in xenograft models of glioblastoma multiforme and is associated with poor survival in patients.
Not available
S-EPMC3248301 | biostudies-literature
UnknownCell migration simulator-based biomarkers for glioblastoma.
Not available
S-EPMC11600334 | biostudies-literature
UnknownDecreased affinity for efflux transporters increases brain penetrance and molecular targeting of a PI3K/mTOR inhibitor in a mouse model of glioblastoma.
Not available
S-EPMC4588756 | biostudies-literature
UnknownInsR/IGF1R Pathway Mediates Resistance to EGFR Inhibitors in Glioblastoma.
Not available
S-EPMC4818693 | biostudies-literature
UnknownWWP2 is an E3 ubiquitin ligase for PTEN.
Not available
S-EPMC3926303 | biostudies-literature
UnknownBrain Distribution of a Panel of Epidermal Growth Factor Receptor Inhibitors Using Cassette Dosing in Wild-Type and Abcb1/Abcg2-Deficient Mice.
Not available
S-EPMC6408736 | biostudies-literature
UnknownTargeting glioblastoma tumor hyaluronan to enhance therapeutic interventions that regulate metabolic cell properties.
Not available
S-EPMC12002556 | biostudies-literature
ProteomicsATM Inhibition Exploits Checkpoint Defects and ATM-Dependent Double Strand Break Repair in TP53-Mutant Glioblastoma
Determining the balance between DNA double strand break repair (DSBR) pathways is essential for understanding treatment response in cancer. We report a novel method for simultaneously measuring non-homologous end joining (NHEJ), homologous recombination (HR), and microhomology-mediated end joining (...
ORGANISM(S): Homo sapiens (Human) 
2024-03-08 | PXD047837 | Pride
Dna double strand break repair Tp53-mutant glioblastoma Atm inhibition 
ProteomicsQuantitative analysis of tyrosine phosphorylation from FFPE tissues reveals patient specific signaling networks
The aim of this study was to characterize tyrosine phosphorylation from FFPE tissues. Global phosphoproteomics, global proteomics and tyrosine phosphorylation were measured using quantitative LC-MS/MS based on TMT labeling.
ORGANISM(S): Homo sapiens (Human) 
2021-09-09 | PXD020284 | Pride
Lc-ms/ms Phosphotyrosine Ffpe Afatinib 
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