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Nature Communications|May 23, 2025
Enhancing the potency of in vivo lentiviral vector mediated gene therapy to hepatocytesCesare Canepari, Michela Milani, Chiara Simoni, et al.
Ecancermedicalscience|May 20, 2015
VIN usual type-from the past to the futureMario Preti, Sarah Igidbashian, Silvano Costa, 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.
EMBO Molecular Medicine|August 30, 2021
Myeloid cell-based delivery of IFN-γ reprograms the leukemia microenvironment and induces anti-tumoral immune responsesAdele Mucci, Gabriele Antonarelli, Carolina Caserta, et al.
Stem Cells Translational Medicine|February 14, 2017
Generation of Human Induced Pluripotent Stem Cell-Derived Bona Fide Neural Stem Cells for Ex Vivo Gene Therapy of Metachromatic LeukodystrophyVasco Meneghini, Giacomo Frati, Davide Sala, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 27, 2013
Cancer-initiating cells from colorectal cancer patients escape from T cell-mediated immunosurveillance in vitro through membrane-bound IL-4Andrea Volonté, Tiziano Di Tomaso, Michela Spinelli, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 6, 2008
Maturing dendritic cells depend on RAGE for in vivo homing to lymph nodesAngelo A Manfredi, Annalisa Capobianco, Antonio Esposito, et al.
Nature Medicine|May 30, 2018
Monocyte-derived IL-1 and IL-6 are differentially required for cytokine-release syndrome and neurotoxicity due to CAR T cellsMargherita Norelli, Barbara Camisa, Giulia Barbiera, et al.
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