Showing 1 - 5 results of 5 for search 'Roberta De Zio', query time: 0.02s Refine Results
  1. 1
    Role of Nuclear Lamin A/C in the Regulation of Nav1.5 Channel and Microtubules: Lesson From the Pathogenic Lamin A/C Variant Q517X

    Role of Nuclear Lamin A/C in the Regulation of Nav1.5 Channel and Microtubules: Lesson From the Pathogenic Lamin A/C Variant Q517X by Roberta De Zio, Giusy Pietrafesa, Serena Milano, Giuseppe Procino, Manuela Bramerio, Martino Pepe, Cinzia Forleo, Stefano Favale, Maria Svelto, Andrea Gerbino, Monica Carmosino

    Published 2022-06-01
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  2. 2
    Targeting unfolded protein response reverts ER stress and ER Ca2+ homeostasis in cardiomyocytes expressing the pathogenic variant of Lamin A/C R321X

    Targeting unfolded protein response reverts ER stress and ER Ca2+ homeostasis in cardiomyocytes expressing the pathogenic variant of Lamin A/C R321X by Giusy Pietrafesa, Roberta De Zio, Simona Ida Scorza, Maria Francesca Armentano, Martino Pepe, Cinzia Forleo, Giuseppe Procino, Andrea Gerbino, Maria Svelto, Monica Carmosino

    Published 2023-05-01
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  3. 3
    TRPML1-Induced Lysosomal Ca<sup>2+</sup> Signals Activate AQP2 Translocation and Water Flux in Renal Collecting Duct Cells

    TRPML1-Induced Lysosomal Ca<sup>2+</sup> Signals Activate AQP2 Translocation and Water Flux in Renal Collecting Duct Cells by Simona Ida Scorza, Serena Milano, Ilenia Saponara, Maira Certini, Roberta De Zio, Maria Grazia Mola, Giuseppe Procino, Monica Carmosino, Francesco Moccia, Maria Svelto, Andrea Gerbino

    Published 2023-01-01
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  4. 4
    Functional Characterization of a Novel Truncating Mutation in Lamin A/C Gene in a Family with a Severe Cardiomyopathy with Conduction Defects

    Functional Characterization of a Novel Truncating Mutation in Lamin A/C Gene in a Family with a Severe Cardiomyopathy with Conduction Defects by Andrea Gerbino, Irene Bottillo, Serena Milano, Martina Lipari, Roberta De Zio, Silvia Morlino, Maria Grazia Mola, Giuseppe Procino, Federica Re, Elisabetta Zachara, Paola Grammatico, Maria Svelto, Monica Carmosino

    Published 2017-12-01
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  5. 5
    DP71 and SERCA2 alteration in human neurons of a Duchenne muscular dystrophy patient

    DP71 and SERCA2 alteration in human neurons of a Duchenne muscular dystrophy patient by Simona Ruggieri, Luigi Viggiano, Tiziana Annese, Carmela Rubolino, Andrea Gerbino, Roberta De Zio, Patrizia Corsi, Roberto Tamma, Domenico Ribatti, Mariella Errede, Francesca Operto, Lucia Margari, Nicoletta Resta, Silvia Di Tommaso, Jessica Rosati, Maria Trojano, Beatrice Nico

    Published 2019-01-01
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