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Genetically targeted adenovirus vector directed to CD40-expressing cells.
Targeting of adenovirus via genetic modification of the viral capsid combined with a protein bridge.
Enhanced gene transfer to mouse dendritic cells using adenoviral vectors coated with a novel adapter molecule.
High efficiency transduction of dendritic cells by adenoviral vectors targeted to DC-SIGN.
VB-111 for cancer.
Phase I dose-escalation study of VB-111, an antiangiogenic virotherapy, in patients with advanced solid tumors.