Browsing by Subject "Fabry disease"

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  • α-Galactosidase-A loaded-nanoliposomes with enhanced enzymatic activity and intracellular penetration
    Cabrera, Ingrid; Abasolo, Ibane; Corchero, José L.; Elizondo, Elisa; Rivera Gil, Pilar, 1976-; Moreno, Evelyn; Faraudo, Jordi; Sala, Santi; Bueno, Dolores; González Mira, Elisabet; Rivas, Merche; Melgarejo, Marta; Pulido, Daniel; Albericio, Fernando; Royo, Miriam; Villaverde, Antonio; García Parajó, María F.; Schwartz Jr, Simó; Ventosa, Nora; Veciana, Jaume (Wiley, 2016)
    Lysosomal storage disorders (LSD) are caused by lysosomal dysfunction usually as a consequence of deficiency of a single enzyme required for the metabolism of macromolecules, such as lipids, glycoproteins, and mucopolysaccharides. ...

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