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4. Learning and actioning general principles of cancer cell drug sensitivity

5. Exploring Regorafenib Responsiveness and Uncovering Molecular Mechanisms in Recurrent Glioblastoma Tumors Through Longitudinal In Vitro Sampling

7. NIMG-70. TRACKING CELLULAR SOCIAL BEHAVIOR OF PATIENT-DERIVED PRIMARY CELL LINES TO GATHER NEW INSIGHTS FOR BETTER STRATIFICATION OF GLIOBLASTOMA PATIENTS

8. EXTH-83. BIRC3 AS A PREDICTOR OF OUTCOME AND A NEW THERAPEUTIC TARGET IN TMZ RESISTANT GLIOBLASTOMA TUMORS

9. Exploring Regorafenib Responsiveness and Uncovering Molecular Mechanisms in Recurrent Glioblastoma Tumors through Longitudinal In Vitro Sampling.

10. P718: EPIGENOME PROFILING REVEALS ABERRANT DNA METHYLATION SIGNATURE IN GATA2 DEFICIENCY

11. Epigenome profiling reveals aberrant DNA methylation signature in GATA2 deficiency

13. Epigenome profiling reveals an aberrant DNA methylation signature in GATA2 deficiency

14. Monoallelic expression in melanoma

15. BIOM-35. A NEW PRECISION-MEDICINE APPROACH TO PREDICT TUMOR TREATMENT RESPONSE IDENTIFIES IN GLIOBLASTOMA A 17 GENE SIGNATURE PROGNOSTIC OF TMZ RESPONSE AND SURVIVAL WITH ROBUST PREDICTIVE VALUE

16. Metabolic-imaging of human glioblastoma live tumors: A new precision-medicine approach to predict tumor treatment response early

17. Chondroblastoma‐like osteosarcoma: a clinicopathological and molecular study of a rare osteosarcoma variant

18. Innovative Approach to Isolate and Characterize Glioblastoma Circulating Tumor Cells and Correlation with Tumor Mutational Status.

19. Identification of New Potential Prognostic and Predictive Markers in High-Grade Osteosarcoma Using Whole Exome Sequencing.

20. Serotonin depletion causes valproate-responsive manic-like condition and increased hippocampal neuroplasticity that are reversed by stress

24. Single-Cell Molecular Characterization to Partition the Human Glioblastoma Tumor Microenvironment Genetic Background

25. Single-cell molecular characterization to partition the human glioblastoma tumor microenvironment (TME) genetic background

28. Pathological Features and Molecular Phenotype of MMTV Like-Positive Feline Mammary Carcinomas

29. Liquid Biopsies from Pleural Effusions and Plasma from Patients with Malignant Pleural Mesothelioma: A Feasibility Study

30. Multiregional Sequencing of IDH-WT Glioblastoma Reveals High Genetic Heterogeneity and a Dynamic Evolutionary History

33. A human MMTV-like betaretrovirus linked to breast cancer has been present in humans at least since the copper age

34. Diffuse bone and soft tissue angiomatosis with GNAQ mutation

35. CXCL12α/SDF‐1 from perisynaptic Schwann cells promotes regeneration of injured motor axon terminals

36. MOESM2 of Monoallelic expression in melanoma

37. c-KIT receptor expression is strictly associated with the biological behaviour of thyroid nodules

39. Mouse mammary tumor virus (MMTV) - like exogenous sequences are associated with sporadic but not hereditary human breast carcinoma

40. ANKRD44 Gene Silencing: A Putative Role in Trastuzumab Resistance in Her2-Like Breast Cancer

41. Laser Capture Microdissection and RNA-Seq Analysis: High Sensitivity Approaches to Explain Histopathological Heterogeneity in Human Glioblastoma FFPE Archived Tissues

42. Molecular characterization of low grade and high grade bladder cancer

43. Mitochondrial enzyme GLUD2 plays a critical role in glioblastoma progression

44. Mouse mammary tumour virus-like env nucleotide and p14 signal peptide are present in feline mammary carcinomas, but not in neoplastic or dysplastic canine mammary lesions

45. Cancer astrocytes have a more conserved molecular status in long recurrence free survival (RFS) IDH1 wild-type glioblastoma patients: new emerging cancer players

46. Levels of miR-126 and miR-218 are elevated in ductal carcinoma in situ (DCIS) and inhibit malignant potential of DCIS derived cells

48. Whole-exome analysis in osteosarcoma to identify a personalized therapy

49. CXCL 12α/ SDF ‐1 from perisynaptic Schwann cells promotes regeneration of injured motor axon terminals

50. Exome analysis of a large family with familial isolated primary hyperparathyroidism (FIHP) and multiple cancers

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