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Human Gene Therapy|August 22, 2017
Lentiviral Vector Promoter is Decisive for Aberrant Transcript FormationSimone J Scholz, Raffaele Fronza, Cynthia C Bartholomä, et al.
European Journal of Immunology|December 17, 2013
Wiskott-Aldrich syndrome protein deficiency in natural killer and dendritic cells affects antitumor immunityMarco Catucci, Ivan Zanoni, Elena Draghici, et al.
Human Reproduction (Oxford, England)|June 1, 2018
Testicular microbiome in azoospermic men-first evidence of the impact of an altered microenvironmentMassimo Alfano, Roberto Ferrarese, Irene Locatelli, et al.
Nature Biotechnology|May 30, 2006
Hematopoietic stem cell gene transfer in a tumor-prone mouse model uncovers low genotoxicity of lentiviral vector integrationEugenio Montini, Daniela Cesana, Manfred Schmidt, et al.
The Journal of Clinical Investigation|March 25, 2009
The genotoxic potential of retroviral vectors is strongly modulated by vector design and integration site selection in a mouse model of HSC gene therapyEugenio Montini, Daniela Cesana, Manfred Schmidt, et al.
Nature Communications|September 10, 2017
HIV-1-mediated insertional activation of STAT5B and BACH2 trigger viral reservoir in T regulatory cellsDaniela Cesana, Francesca R Santoni de Sio, Laura Rudilosso, et al.
Blood|February 15, 2023
Intrathymic AAV delivery results in therapeutic site-specific integration at TCR loci in miceAndrea Calabria, Carlo Cipriani, Giulio Spinozzi, et al.
The Journal of Allergy and Clinical Immunology|September 13, 2019
Intrathymic adeno-associated virus gene transfer rapidly restores thymic function and long-term persistence of gene-corrected T cellsMarie Pouzolles, Alice Machado, Mickaël Guilbaud, et al.
Nature Methods|January 15, 2013
Lentiviral vector-based insertional mutagenesis identifies genes associated with liver cancerMarco Ranzani, Daniela Cesana, Cynthia C Bartholomae, et al.
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