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EMBO Molecular Medicine|April 29, 2024
GP64-pseudotyped lentiviral vectors target liver endothelial cells and correct hemophilia A miceMichela Milani, Cesare Canepari, Simone Assanelli, et al.Haematologica|May 30, 2020
Deciphering the Ets-1/2-mediated transcriptional regulation of F8 gene identifies a minimal F8 promoter for hemophilia A gene therapyRosella Famà, Ester Borroni, Simone Merlin, et al.Plos One|September 17, 2015
Human Cardiac Progenitor Spheroids Exhibit Enhanced Engraftment PotentialFrancesca Oltolina, Andrea Zamperone, Donato Colangelo, et al.Stem Cell Reports|November 13, 2018
Patient-Specific iPSC-Derived Endothelial Cells Provide Long-Term Phenotypic Correction of Hemophilia ACristina Olgasi, Maria Talmon, Simone Merlin, et al.Gene|May 20, 2014
Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan AnemiaAnna Aspesi, Elisa Pavesi, Elisa Robotti, et al.Molecular Therapy. Methods & Clinical Development|December 2, 2021
Efficient and safe correction of hemophilia A by lentiviral vector-transduced BOECs in an implantable deviceCristina Olgasi, Chiara Borsotti, Simone Merlin, et al.Journal of Hepatology|January 19, 2020
Thyroid hormone inhibits hepatocellular carcinoma progression via induction of differentiation and metabolic reprogrammingMarta Anna Kowalik, Elisabetta Puliga, Lavinia Cabras, et al.Pageof 4