Canlyniadau Chwilio - Monica Cardone

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  1. 1
    Correction of Hunter syndrome in the MPSII mouse model by AAV2/8-mediated gene delivery

    Correction of Hunter syndrome in the MPSII mouse model by AAV2/8-mediated gene delivery gan Monica Cardone, Vinicia Assunta Polito, Stefano Pepe, Linda Männ, Alessandra d’Azzo, Alberto Auricchio, Andrea Ballabio, Maria Pia Cosma

    Cyhoeddwyd 2006
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  2. 2
    The Pharmacological Chaperone N-butyldeoxynojirimycin Enhances Enzyme Replacement Therapy in Pompe Disease Fibroblasts

    The Pharmacological Chaperone N-butyldeoxynojirimycin Enhances Enzyme Replacement Therapy in Pompe Disease Fibroblasts gan Caterina Porto, Monica Cardone, Federica Fontana, Barbara Rossi, Maria Rosaria Tuzzi, Antonietta Tarallo, Maria Vittoria Barone, Generoso Andria, Giancarlo Parenti

    Cyhoeddwyd 2009
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  3. 3
    Abnormal mannose-6-phosphate receptor trafficking impairs recombinant alpha-glucosidase uptake in Pompe disease fibroblasts

    Abnormal mannose-6-phosphate receptor trafficking impairs recombinant alpha-glucosidase uptake in Pompe disease fibroblasts gan Monica Cardone, Caterina Porto, Antonietta Tarallo, Mariella Vicinanza, Barbara Rossi, Elena Polishchuk, Francesca Donaudy, Generoso Andria, Maria Antonietta De Matteis, Giancarlo Parenti

    Cyhoeddwyd 2008
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  4. 4
    Transcription factor EB (TFEB) is a new therapeutic target for Pompe disease

    Transcription factor EB (TFEB) is a new therapeutic target for Pompe disease gan Carmine Spampanato, Erin Feeney, Lishu Li, Monica Cardone, Jeong‐A Lim, Fabio Annunziata, Hossein Zare, Roman Polishchuk, Rosa Puertollano, Giancarlo Parenti, Andrea Ballabio, Nina Raben

    Cyhoeddwyd 2013
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  5. 5
    ETV7 is an essential component of a rapamycin-insensitive mTOR complex in cancer

    ETV7 is an essential component of a rapamycin-insensitive mTOR complex in cancer gan Franklin C. Harwood, Ramon I. Klein Geltink, Brendan P. O’Hara, Monica Cardone, Laura J. Janke, David Finkelstein, Igor Entin, Leena Paul, Peter J. Houghton, Gerard C. Grosveld

    Cyhoeddwyd 2018
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