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1. The importance of considering competing risks in recurrence analysis of intracranial meningioma.

3. In situ brain tumor detection using a Raman spectroscopy system—results of a multicenter study

4. Metastatic breast cancer cells are metabolically reprogrammed to maintain redox homeostasis during metastasis

5. Author Correction: SMARCA4/2 loss inhibits chemotherapy-induced apoptosis by restricting IP3R3-mediated Ca2+ flux to mitochondria

6. Evolution of chromosome-arm aberrations in breast cancer through genetic network rewiring

8. Relation between mismatch repair status, chemoresponse, survival and anatomic location in gastroesophageal adenocarcinoma

9. Single-cell spatial immune landscapes of primary and metastatic brain tumours

10. 1 A novel CARD9-deficiency mouse model recapitulates chronic CNS candidiasis and identifies defective monocytic-cell responses in immunopathogenesis

11. Author Correction: [11C]Martinostat PET analysis reveals reduced HDAC I availability in Alzheimer’s disease

12. [11C]Martinostat PET analysis reveals reduced HDAC I availability in Alzheimer’s disease

14. Quantification of [11C]ABP688 binding in human brain using cerebellum as reference region: biological interpretation and limitations

15. Neutrophil oxidative stress mediates obesity-associated vascular dysfunction and metastatic transmigration

16. Invasive growth of brain metastases is linked to CHI3L1 release from pSTAT3-positive astrocytes.

19. SMARCA4/2 loss inhibits chemotherapy-induced apoptosis by restricting IP3R3-mediated Ca2+ flux to mitochondria

20. A Young Man with Memory and Walking Difficulties

21. The Fungal Exopolysaccharide Galactosaminogalactan Mediates Virulence by Enhancing Resistance to Neutrophil Extracellular Traps.

23. Cryo-EM structure of Alzheimer’s disease tau filaments with PET ligand MK-6240

25. Spatially distinct tumor immune microenvironments stratify triple-negative breast cancers

26. Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy

27. In Situ Brain Tumor Detection Using the Raman Spectroscopy Sentry System – Results of a Multicenter Study

28. MoS2-Plasmonic Nanocavities for Raman Spectra of Single Extracellular Vesicles Reveal Molecular Progression in Glioblastoma

29. The Use of Tau PET to Stage Alzheimer Disease According to the Braak Staging Framework

30. Evolution of chromosome arm aberrations in breast cancer through genetic network rewiring

32. Author Correction: Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy

33. CDK4/6 inhibitors target SMARCA4-determined cyclin D1 deficiency in hypercalcemic small cell carcinoma of the ovary

34. SMARCA4 loss is synthetic lethal with CDK4/6 inhibition in non-small cell lung cancer

35. Abstract 69: Minimally invasive brain metastases are characterized by elevated immune cell infiltrate

37. Table S2 from eIF4A Inhibitors Suppress Cell-Cycle Feedback Response and Acquired Resistance to CDK4/6 Inhibition in Cancer

38. Supplemental Figure 3 from Elevated V–ATPase Activity Following PTEN Loss Is Required for Enhanced Oncogenic Signaling in Breast Cancer

42. Data from Elevated V–ATPase Activity Following PTEN Loss Is Required for Enhanced Oncogenic Signaling in Breast Cancer

43. Supplemental Table 2 from Elevated V–ATPase Activity Following PTEN Loss Is Required for Enhanced Oncogenic Signaling in Breast Cancer

44. Supplemental Figure Legends 1-3 from Elevated V–ATPase Activity Following PTEN Loss Is Required for Enhanced Oncogenic Signaling in Breast Cancer

45. Supplemental Figures 1 - 10 from eIF4A Inhibitors Suppress Cell-Cycle Feedback Response and Acquired Resistance to CDK4/6 Inhibition in Cancer

47. Supplemental Table 3 from Elevated V–ATPase Activity Following PTEN Loss Is Required for Enhanced Oncogenic Signaling in Breast Cancer

48. Data from eIF4A Inhibitors Suppress Cell-Cycle Feedback Response and Acquired Resistance to CDK4/6 Inhibition in Cancer

50. Supplemental Figure 2 from Elevated V–ATPase Activity Following PTEN Loss Is Required for Enhanced Oncogenic Signaling in Breast Cancer

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