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Viruses|August 28, 2021
Designing Lentiviral Vectors for Gene Therapy of Genetic DiseasesValentina Poletti, Fulvio MavilioHuman Gene Therapy|September 12, 2018
Gene Therapy for HemoglobinopathiesMarina Cavazzana, Fulvio MavilioMolecular Therapy. Methods & Clinical Development|November 22, 2017
Interactions between Retroviruses and the Host Cell GenomeValentina Poletti, Fulvio MavilioStem Cells and Development|May 5, 2026
Hematopoietic Stem Cell-Based Cell and Gene Therapy Beyond Monogenic DiseasesMasayuki Kai, Fulvio MavilioNature|March 4, 2015
Nuclear architecture dictates HIV-1 integration site selectionBruna Marini, Attila Kertesz-Farkas, Hashim Ali, et al.Hematology/Oncology Clinics of North America|September 13, 2017
Gene Therapy Approaches to HemoglobinopathiesGiuliana Ferrari, Marina Cavazzana, Fulvio MavilioHuman Gene Therapy|January 22, 2013
Mechanisms of retroviral integration and mutagenesisAlessia Cavazza, Arianna Moiani, Fulvio MavilioMolecular Therapy : the Journal of the American Society of Gene Therapy|March 19, 2009
Transcriptional enhancers induce insertional gene deregulation independently from the vector type and designGiulietta Maruggi, Simona Porcellini, Giulia Facchini, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|June 14, 2013
Targeted gene addition in human epithelial stem cells by zinc-finger nuclease-mediated homologous recombinationAndrea Coluccio, Francesca Miselli, Angelo Lombardo, et al.Blood|May 18, 2007
Hot spots of retroviral integration in human CD34+ hematopoietic cellsClaudia Cattoglio, Giulia Facchini, Daniela Sartori, et al.Pageof 13