Resultados de procura - Simone Spinozzi

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  1. 1
    Identifying the Cardiac Dyad Proteome In Vivo by a BioID2 Knock-In Strategy

    Identifying the Cardiac Dyad Proteome In Vivo by a BioID2 Knock-In Strategy por Wei Feng, Canzhao Liu, Simone Spinozzi, Li Wang, Sylvia Μ. Evans, Ju Chen

    Publicado 2020
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  2. 2
    Parallel Lineage-Tracing Studies Establish Fibroblasts as the Prevailing In Vivo Adipocyte Progenitor

    Parallel Lineage-Tracing Studies Establish Fibroblasts as the Prevailing In Vivo Adipocyte Progenitor por Paola Cattaneo, Debanjan Mukherjee, Simone Spinozzi, Lunfeng Zhang, Veronica Larcher, William B. Stallcup, Hiroshi Kataoka, Ju Chen, Stefanie Dimmeler, Sylvia Μ. Evans, Nuno Guimarães‐Camboa

    Publicado 2020
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  3. 3
    Nexilin Is a New Component of Junctional Membrane Complexes Required for Cardiac T-Tubule Formation

    Nexilin Is a New Component of Junctional Membrane Complexes Required for Cardiac T-Tubule Formation por Canzhao Liu, Simone Spinozzi, Jiayu Chen, Xi Fang, Wei Feng, Guy Perkins, Paola Cattaneo, Nuno Guimarães‐Camboa, Nancy D. Dalton, Kirk L. Peterson, Tongbin Wu, Kunfu Ouyang, Xiang‐Dong Fu, Sylvia Μ. Evans, Ju Chen

    Publicado 2019
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  4. 4
    A Mutation in the<i>CASQ1</i>Gene Causes a Vacuolar Myopathy with Accumulation of Sarcoplasmic Reticulum Protein Aggregates

    A Mutation in the<i>CASQ1</i>Gene Causes a Vacuolar Myopathy with Accumulation of Sarcoplasmic Reticulum Protein Aggregates por Daniela Rossi, Bianca Vezzani, Lucia Galli, Cecilia Paolini, L. Toniolo, Enrico Pierantozzi, Simone Spinozzi, Virginia Barone, Elena Pegoraro, Luca Bello, Giovanna Cenacchi, Gaetano Vattemi, Giuliano Tomelleri, Giulia Ricci, Gabriele Siciliano, Feliciano Protasi, Carlo Reggiani, Vincenzo Sorrentino

    Publicado 2014
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  5. 5
    Cardiolipin Remodeling Defects Impair Mitochondrial Architecture and Function in a Murine Model of Barth Syndrome Cardiomyopathy

    Cardiolipin Remodeling Defects Impair Mitochondrial Architecture and Function in a Murine Model of Barth Syndrome Cardiomyopathy por Siting Zhu, Ze’e Chen, Mason Zhu, Ying Shen, Leonardo J. Leon, Liguo Chi, Simone Spinozzi, Changming Tan, Yusu Gu, Anh Nguyen, Yi Zhou, Wei Feng, Frédéric M. Vaz, Xiaohong Wang, Åsa B. Gustafsson, Sylvia Μ. Evans, Kunfu Ouyang, Xi Fang

    Publicado 2021
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  6. 6
    Identification and characterization of three novel mutations in the<i>CASQ1</i>gene in four patients with tubular aggregate myopathy

    Identification and characterization of three novel mutations in the<i>CASQ1</i>gene in four patients with tubular aggregate myopathy por Virginia Barone, Valeria Del Re, Alessandra Gamberucci, Valentina Polverino, Lucia Galli, Daniela Rossi, Elisa Costanzi, L. Toniolo, Gianna Berti, Alessandro Malandrini, Giulia Ricci, Gabriele Siciliano, Gaetano Vattemi, Giuliano Tomelleri, Enrico Pierantozzi, Simone Spinozzi, Nila Volpi, Rosella Fulceri, Roberto Battistutta, Carlo Reggiani, Vincenzo Sorrentino

    Publicado 2017
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