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1. Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy

2. Author Correction: Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy

3. The Transcriptional Regulator Prdm1 Is Essential for the Early Development of the Sensory Whisker Follicle and Is Linked to the Beta-Catenin First Dermal Signal.

7. Inclusivity and diversity: Integrating international perspectives on stem cell challenges and potential

9. Standing the test of COVID-19: charting the new frontiers of medicine

15. Lancet Commission: Stem cells and regenerative medicine

28. Potency assays and biomarkers for cell-based advanced therapy medicinal products

29. No Identical “Mesenchymal Stem Cells” at Different Times and Sites: Human Committed Progenitors of Distinct Origin and Differentiation Potential Are Incorporated as Adventitial Cells in Microvessels

31. Pericyte–fibroblast transition promotes tumor growth and metastasis

32. Mesoangioblasts at 20: From the embryonic aorta to the patient bed

33. Mesoangioblasts at 20: From the embryonic aorta to the patient bed

34. Reversible immortalisation enables genetic correction of human muscle progenitors and engineering of next‐generation human artificial chromosomes for Duchenne muscular dystrophy

37. Mesoangioblasts at 20: From the embryonic aorta to the patient bed

41. Multi-stage bioengineering of a layered oesophagus with in vitro expanded muscle and epithelial adult progenitors

42. Optical Wireless Communication in an Avionics Test Facility for Spacecrafts

47. Intra‐arterial transplantation of HLA‐matched donor mesoangioblasts in Duchenne muscular dystrophy

49. In vivo generation of a mature and functional artificial skeletal muscle

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