20 results on '"Neises, Laura"'
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2. Serine metabolism is crucial for cGAS-STING signaling and viral defense control in the gut
3. GAP43-dependent mitochondria transfer from astrocytes enhances glioblastoma tumorigenicity
4. Mitochondria preserve an autarkic one-carbon cycle to confer growth-independent cancer cell migration and metastasis
5. CNSC-15. MITOCHONDRIA TRANSFER VIA GLIOMA-ASTROCYTE NETWORK MICROTUBES REPROGRAMS TUMOR CELLS FOR ENHANCED TUMORIGENICITY
6. Formate promotes invasion and metastasis in reliance on lipid metabolism
7. Formate Promotes Invasion and Metastasis by Activating Fatty Acid Synthesis and Matrix Metalloproteinases
8. PKM2 diverts glycolytic flux in dependence on mitochondrial one-carbon cycle
9. Metabolic plasticity of serine metabolism is crucial for cGAS/STING-signalling and innate immune response to viral infections in the gut
10. Mitochondrial One-Carbon Flux has a Growth-Independent Role in Promoting Breast Cancer Metastasis
11. Ascorbate kills breast cancer cells by rewiring metabolism via redox imbalance and energy crisis
12. Ascorbate kills breast cancer cells by rewiring metabolism via redox imbalance and energy crisis
13. Mitochondria preserve an autarkic one-carbon cycle to confer growth-independent cancer cell migration and metastasis
14. FSMP-09. FORMATE PROMOTES CANCER CELL INVASION AND METASTASIS VIA CALCIUM SIGNALING
15. Ascorbate kills breast cancer cells by rewiring metabolism via redox imbalance and energy crisis
16. Metabolic Potential of Cancer Cells in Context of the Metastatic Cascade
17. A Bioorthogonal Click Chemistry Toolbox for Targeted Synthesis of Branched and Well‐Defined Protein–Protein Conjugates
18. A Bioorthogonal Click Chemistry Toolbox for Targeted Synthesis of Branched and Well-Defined Protein-Protein Conjugates
19. Protocol using ex vivomouse brain slice culture mimicking in vivoconditions to study tumor growth and cell motility of glioblastoma cells
20. Protocol using ex vivo mouse brain slice culture mimicking in vivo conditions to study tumor growth and cell motility of glioblastoma cells.
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