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1. NUMB as a Therapeutic Target for Melanoma

2. Overcoming Intrinsic Multidrug Resistance in Melanoma by Blocking the Mitochondrial Respiratory Chain of Slow-Cycling JARID1Bhigh Cells

3. Supplementary Figure S6 from Hypoxia Induces Phenotypic Plasticity and Therapy Resistance in Melanoma via the Tyrosine Kinase Receptors ROR1 and ROR2

4. Data from Hypoxia Induces Phenotypic Plasticity and Therapy Resistance in Melanoma via the Tyrosine Kinase Receptors ROR1 and ROR2

6. Supplementary Data Figure Legends from Hypoxia Induces Phenotypic Plasticity and Therapy Resistance in Melanoma via the Tyrosine Kinase Receptors ROR1 and ROR2

7. Supplementary Table 2 from Hypoxia Induces Phenotypic Plasticity and Therapy Resistance in Melanoma via the Tyrosine Kinase Receptors ROR1 and ROR2

8. Data from Neural Crest-Like Stem Cell Transcriptome Analysis Identifies LPAR1 in Melanoma Progression and Therapy Resistance

9. Table S5 from Neural Crest-Like Stem Cell Transcriptome Analysis Identifies LPAR1 in Melanoma Progression and Therapy Resistance

10. Supplementary Figures from Neural Crest-Like Stem Cell Transcriptome Analysis Identifies LPAR1 in Melanoma Progression and Therapy Resistance

13. Supplementary Figure S5 from The Novel SMAC Mimetic Birinapant Exhibits Potent Activity against Human Melanoma Cells

14. Data from Protein Signatures of NK Cell–Mediated Melanoma Killing Predict Response to Immunotherapies

15. Supplementary Table 2 from Brain Metastasis Cell Lines Panel: A Public Resource of Organotropic Cell Lines

16. Supplementary Figures from Protein Signatures of NK Cell–Mediated Melanoma Killing Predict Response to Immunotherapies

17. Supplementary Table S1 from The Novel SMAC Mimetic Birinapant Exhibits Potent Activity against Human Melanoma Cells

18. Figure S1 from Brain Metastasis Cell Lines Panel: A Public Resource of Organotropic Cell Lines

19. Supplementary Files 1-11 from Protein Signatures of NK Cell–Mediated Melanoma Killing Predict Response to Immunotherapies

20. Data from Brain Metastasis Cell Lines Panel: A Public Resource of Organotropic Cell Lines

21. Supplementary Table 1 from Brain Metastasis Cell Lines Panel: A Public Resource of Organotropic Cell Lines

22. 335 Analyses of severe immune-mediated toxicity in patients with advanced mCRPC treated with a PSMA-targeted armored CAR T-cells

23. MCU controls melanoma progression through a redox‐controlled phenotype switch

24. A distinct pattern of growth and RAC1 signaling in melanoma brain metastasis cells

26. Acquired Resistance to BRAF Inhibitors Mediated by a RAF Kinase Switch in Melanoma Can Be Overcome by Cotargeting MEK and IGF-1R/PI3K

27. Protein Signatures of NK Cell–Mediated Melanoma Killing Predict Response to Immunotherapies

28. Neural Crest-Like Stem Cell Transcriptome Analysis Identifies LPAR1 in Melanoma Progression and Therapy Resistance

29. Melanoma

31. Beyond structure, to survival: activation of stat3 by cadherin engagement

32. Differential effects of c-Ras upon transformation, adipocytic differentiation, and apoptosis mediated by the simian virus 40 large tumor antigen

34. Brain Metastasis Cell Lines Panel: A Public Resource of Organotropic Cell Lines

37. 52. BrMPANEL: A PUBLIC RESOURCE OF ORGANOTROPIC CELL LINES

42. Redox signals at the ER –mitochondria interface control melanoma progression

45. Hypoxia-activated prodrug enhances therapeutic effect of sunitinib in melanoma

46. A Comprehensive Patient-Derived Xenograft Collection Representing the Heterogeneity of Melanoma

48. The Soldier and the Animal: metaphor in maintenance of antiretroviral adherence in Ghana’s Eastern Region

49. Targeting Notch enhances the efficacy of ERK inhibitors in BRAF-V600E melanoma

50. Abstract A02: A novel orthotopic ovarian patient derived xenograft model platform to investigate novel therapies for BRCA deficient ovarian cancers

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