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3. Legal and Regulatory Challenges for Emerging Regenerative Medicine Solutions for Diabetes

7. Legal and Regulatory Challenges for Emerging Regenerative Medicine Solutions for Diabetes

8. CD14+/CD31+ monocytes expanded by UM171 correct hemophilia A in zebrafish upon lentiviral gene transfer of factor VIII

9. Factor VIII promotes angiogenesis and vessel stability regulating extracellular matrix proteins

11. Liver-directed lentiviral gene therapy corrects hemophilia A mice and achieves normal-range factor VIII activity in non-human primates

14. Efficacy of rehabilitation interventions on functioning in patients with hemophilic arthropathy: A systematic review with meta-analysis.

16. DNA base editing corrects common hemophilia A mutations and restores factor VIII expression in in vitroand ex vivomodels

19. Pleckstrin-2 is essential for erythropoiesis in β-thalassemic mice, reducing apoptosis and enhancing enucleation

25. Boosting intracellular sodium selectively kills hepatocarcinoma cells and induces hepatocellular carcinoma tumor shrinkage in mice

26. A tryptophan metabolite prevents depletion of circulating endothelial progenitor cells in systemic low-grade inflammation

31. Data from Genetic Ablation of Cav1 Differentially Affects Melanoma Tumor Growth and Metastasis in Mice: Role of Cav1 in Shh Heterotypic Signaling and Transendothelial Migration

32. Supplementary Figure Legend from Genetic Ablation of Cav1 Differentially Affects Melanoma Tumor Growth and Metastasis in Mice: Role of Cav1 in Shh Heterotypic Signaling and Transendothelial Migration

33. Supplementary Figure 1 from Genetic Ablation of Cav1 Differentially Affects Melanoma Tumor Growth and Metastasis in Mice: Role of Cav1 in Shh Heterotypic Signaling and Transendothelial Migration

34. Therapeutic potential of fetal liver cells transplantation in hemophilia A mice

36. A sustainable one-pot method to transform seashell waste calcium carbonate to osteoinductive hydroxyapatite micro-nanoparticles

38. Liver gene therapy with intein-mediated F8 trans-splicing corrects mouse haemophilia A

41. Transplantation of fetal liver hemato/vascular cells in newborn mice for correction of hemophilia A (HA)

44. Macrophage Reprogramming via the Modulation of Unfolded Protein Response with siRNA-Loaded Magnetic Nanoparticles in a TAM-like Experimental Model.

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