Biblio

Author Title Type [ Year(Asc)]
Filters: Author is Morena, Francesco  [Clear All Filters]
2023
Guidotti G, Soccio M, Argentati C, Luzi F, Aluigi A, Torre L, Armentano I, Emiliani C, Morena F, Martino S, et al. Novel Nanostructured Scaffolds of Poly(butylene -1,4-cyclohexanedicarboxylate)-Based Copolymers with Tailored Hydrophilicity and Stiffness: Implication for Tissue Engineering Modeling. Nanomaterials (Basel). 2023;13(16).
2022
Perriello VMaria, Rotiroti MCaterina, Pisani I, Galimberti S, Alberti G, Pianigiani G, Ciaurro V, Marra A, Sabino M, Tini V, et al. IL3-zetakine combined with a CD33 costimulatory receptor as a Dual CAR approach for safer and selective targeting of AML. Blood Adv. 2022.
Argentati C, Dominici F, Morena F, Rallini M, Tortorella I, Ferrandez-Montero A, Pellegrino RMaria, Ferrari B, Emiliani C, Lieblich M, et al. Thermal treatment of magnesium particles in polylactic acid polymer films elicits the expression of osteogenic differentiation markers and lipidome profile remodeling in human adipose stem cells. Int J Biol Macromol. 2022.
2021
Mangiameli E, Cecchele A, Morena F, Sanvito F, Matafora V, Cattaneo A, Volpe LDella, Gnani D, Paulis M, Susani L, et al. Human iPSC-based neurodevelopmental models of globoid cell leukodystrophy uncover patient- and cell type-specific disease phenotypes. Stem Cell Reports. 2021.
2019
Ornaghi F, Sala D, Tedeschi F, Maffia MChiara, Bazzucchi M, Morena F, Valsecchi M, Aureli M, Martino S, Gritti A. Novel bicistronic lentiviral vectors correct β-Hexosaminidase deficiency in neural and hematopoietic stem cells and progeny: Implications for in vivo end ex vivo gene therapy of GM2 gangliosidosis. Neurobiol Dis. 2019:104667.
2016
Meneghini V, Frati G, Sala D, De Cicco S, Luciani M, Cavazzin C, Paulis M, Mentzen W, Morena F, Giannelli S, et al. Generation of Human Induced Pluripotent Stem Cell-Derived Bona Fide Neural Stem Cells for Ex Vivo Gene Therapy of Metachromatic Leukodystrophy. Stem Cells Transl Med. 2016.
Sessa M, Lorioli L, Fumagalli F, Acquati S, Redaelli D, Baldoli C, Canale S, Lopez ID, Morena F, Calabria A, et al. Lentiviral haemopoietic stem-cell gene therapy in early-onset metachromatic leukodystrophy: an ad-hoc analysis of a non-randomised, open-label, phase 1/2 trial. Lancet. 2016.
2015
Ungari S, Montepeloso A, Morena F, Cocchiarella F, Recchia A, Martino S, Gentner B, Naldini L, Biffi A. Design of a regulated lentiviral vector for hematopoietic stem cell gene therapy of globoid cell leukodystrophy. Mol Ther Methods Clin Dev. 2015;2:15038.