Objetivo
The proposal focuses on synthetic gene delivery vectors designed for gene therapy. It aims at getting better understanding of one critical aspect of the mode of action of synthetic vectors; the mechanism by which vectors facilitate DNA entry into the cell. The proposal is of a fundamental nature, but its results may be applicable for the design of improved delivery systems.
Ámbito científico
Convocatoria de propuestas
Data not availableRégimen de financiación
RGI - Research grants (individual fellowships)Coordinador
67401 ILLKIRCH GRAFFENSTADEN
Francia