490 results on '"Pollard, Steven"'
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2. Imaging extrachromosomal DNA (ecDNA) in cancer
3. RNA lipid nanoparticles as efficient in vivo CRISPR-Cas9 gene editing tool for therapeutic target validation in glioblastoma cancer stem cells
4. TAK1 inhibition leads to RIPK1-dependent apoptosis in immune-activated cancers
5. Autophagy supports PDGFRA-dependent brain tumor development by enhancing oncogenic signaling
6. The N-terminus of Stag1 is required to repress the 2C program by maintaining rRNA expression and nucleolar integrity
7. Elevated FOXG1 in glioblastoma stem cells cooperates with Wnt/β-catenin to induce exit from quiescence
8. Engineering Genetic Predisposition in Human Neuroepithelial Stem Cells Recapitulates Medulloblastoma Tumorigenesis
9. Myeloid cell interferon secretion restricts Zika flavivirus infection of developing and malignant human neural progenitor cells
10. Author Correction: The white matter is a pro-differentiative niche for glioblastoma
11. Benchmarking brain organoid recapitulation of fetal corticogenesis
12. Regional identity of human neural stem cells determines oncogenic responses to histone H3.3 mutants
13. Simultaneous disruption of PRC2 and enhancer function underlies histone H3.3-K27M oncogenic activity in human hindbrain neural stem cells
14. Glioblastomas acquire myeloid-affiliated transcriptional programs via epigenetic immunoediting to elicit immune evasion
15. Post-translational modification of SOX family proteins: Key biochemical targets in cancer?
16. The white matter is a pro-differentiative niche for glioblastoma
17. LRIG1 is a gatekeeper to exit from quiescence in adult neural stem cells
18. Inositol treatment inhibits medulloblastoma through suppression of epigenetic-driven metabolic adaptation
19. Reprogramming of Fibroblasts to Oligodendrocyte Progenitor-like Cells Using CRISPR/Cas9-Based Synthetic Transcription Factors
20. EGFR amplification and EGFRvIII predict and participate in TAT-Cx43266–283 antitumor response in preclinical glioblastoma models.
21. Author Reply to Peer Reviews of CDK12/CDK13 inhibition disrupts a transcriptional program critical for glioblastoma survival
22. Genome Editing in Human Neural Stem and Progenitor Cells
23. Neural G0: a quiescent‐like state found in neuroepithelial‐derived cells and glioma
24. Challenges to curing primary brain tumours
25. Accelerating glioblastoma drug discovery: Convergence of patient-derived models, genome editing and phenotypic screening
26. Transcriptional and epigenetic regulatory mechanisms in glioblastoma stem cells
27. Contributors
28. Synthetic Biology, Stem Cells, and Regenerative Medicine
29. Specific roles of laminins during vertebrate embryogenesis
30. A novel ILK/STAT3 pathway controls plasticity in a neural stem cell model of glioblastoma.
31. The tumour ecology of quiescence: Niches across scales of complexity
32. Corrigendum: Hierarchical reactivation of transcription during mitosis-to-G1 transition by Brn2 and Ascl1 in neural stem cells
33. A novel ILK/STAT3 pathway controls plasticity in a neural stem cell model of glioblastoma
34. Supplementary Figure 5 from Cancer-Specific Requirement for BUB1B/BUBR1 in Human Brain Tumor Isolates and Genetically Transformed Cells
35. Supplementary Figure 4 from Cancer-Specific Requirement for BUB1B/BUBR1 in Human Brain Tumor Isolates and Genetically Transformed Cells
36. Supplementary Figure 1 from Cancer-Specific Requirement for BUB1B/BUBR1 in Human Brain Tumor Isolates and Genetically Transformed Cells
37. Data from Cancer-Specific Requirement for BUB1B/BUBR1 in Human Brain Tumor Isolates and Genetically Transformed Cells
38. Supplementary Figure 7 from Cancer-Specific Requirement for BUB1B/BUBR1 in Human Brain Tumor Isolates and Genetically Transformed Cells
39. Supplementary Table 1 from Cancer-Specific Requirement for BUB1B/BUBR1 in Human Brain Tumor Isolates and Genetically Transformed Cells
40. Supplementary Figure 8 from Cancer-Specific Requirement for BUB1B/BUBR1 in Human Brain Tumor Isolates and Genetically Transformed Cells
41. Supplementary Figure 2 from Cancer-Specific Requirement for BUB1B/BUBR1 in Human Brain Tumor Isolates and Genetically Transformed Cells
42. Supplementary Figure 6 from Cancer-Specific Requirement for BUB1B/BUBR1 in Human Brain Tumor Isolates and Genetically Transformed Cells
43. Supplementary Figure 9 from Cancer-Specific Requirement for BUB1B/BUBR1 in Human Brain Tumor Isolates and Genetically Transformed Cells
44. Supplementary Figure 3 from Cancer-Specific Requirement for BUB1B/BUBR1 in Human Brain Tumor Isolates and Genetically Transformed Cells
45. Supplementary Methods from Cancer-Specific Requirement for BUB1B/BUBR1 in Human Brain Tumor Isolates and Genetically Transformed Cells
46. Supplementary Table 1 from The Tumor Suppressor CIC Directly Regulates MAPK Pathway Genes via Histone Deacetylation
47. Supplementary Table 3 from The Tumor Suppressor CIC Directly Regulates MAPK Pathway Genes via Histone Deacetylation
48. Supplementary Table 2 from The Tumor Suppressor CIC Directly Regulates MAPK Pathway Genes via Histone Deacetylation
49. Data from The Tumor Suppressor CIC Directly Regulates MAPK Pathway Genes via Histone Deacetylation
50. Figure S4 from The Tumor Suppressor CIC Directly Regulates MAPK Pathway Genes via Histone Deacetylation
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