Works matching AU D'Antonio, Maurizio

Results: 39
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    Polyglutamine-Expanded Androgen Receptor Alteration of Skeletal Muscle Homeostasis and Myonuclear Aggregation Are Affected by Sex, Age and Muscle Metabolism.

    Published in:
    Cells (2073-4409), 2020, v. 9, n. 2, p. 325, doi. 10.3390/cells9020325
    By:
    • Chivet, Mathilde;
    • Marchioretti, Caterina;
    • Pirazzini, Marco;
    • Piol, Diana;
    • Scaramuzzino, Chiara;
    • Polanco, Maria Josè;
    • Romanello, Vanina;
    • Zuccaro, Emanuela;
    • Parodi, Sara;
    • D'Antonio, Maurizio;
    • Rinaldi, Carlo;
    • Sambataro, Fabio;
    • Pegoraro, Elena;
    • Soraru, Gianni;
    • Pandey, Udai Bhan;
    • Sandri, Marco;
    • Basso, Manuela;
    • Pennuto, Maria
    Publication type:
    Article
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    Nerve pathology in animal models of neuropathies.

    Published in:
    Journal of the Peripheral Nervous System, 2021, v. 26, p. S61, doi. 10.1111/jns.12463
    By:
    • Carozzi, Valentina Alda;
    • Bolino, Alessandra;
    • D'Antonio, Maurizio;
    • Quattrini, Angelo;
    • Cavaletti, Guido
    Publication type:
    Article
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    novel mouse model of CMT1B identifies hyperglycosylation as a new pathogenetic mechanism.

    Published in:
    Human Molecular Genetics, 2022, v. 31, n. 24, p. 4255, doi. 10.1093/hmg/ddac170
    By:
    • Veneri, Francesca A;
    • Prada, Valeria;
    • Mastrangelo, Rosa;
    • Ferri, Cinzia;
    • Nobbio, Lucilla;
    • Passalacqua, Mario;
    • Milanesi, Maria;
    • Bianchi, Francesca;
    • Carro, Ubaldo Del;
    • Vallat, Jean-Michel;
    • Duong, Phu;
    • Svaren, John;
    • Schenone, Angelo;
    • Grandis, Marina;
    • D'Antonio, Maurizio
    Publication type:
    Article
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    Pathophysiology of Allergic Rhinitis.

    Published in:
    International Archives of Allergy & Immunology, 1996, v. 110, n. 3, p. 207, doi. 10.1159/000237289
    By:
    • Bousquet, Jean;
    • Vignola, Antonio Maurizio;
    • Campbell, Alison M.;
    • Michel, François-Bernard
    Publication type:
    Article
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    Clinical and Biological Heterogeneity in Children with Moderate Asthma.

    Published in:
    American Journal of Respiratory & Critical Care Medicine, 2003, v. 167, n. 11, p. 1490, doi. 10.1164/rccm.200206-549OC
    By:
    • La Grutta, Stefania;
    • Gagliardo, Rosalia;
    • Mirabella, Franco;
    • Pajno, Giovanni Battista;
    • Bonsignore, Giovanni;
    • Bousquet, Jean;
    • Bellia, Vincenzo;
    • Vignola, Antonio Maurizio
    Publication type:
    Article
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    A new mouse model of Charcot-Marie-Tooth 2J neuropathy replicates human axonopathy and suggest alteration in axo-glia communication.

    Published in:
    PLoS Genetics, 2022, v. 18, n. 11, p. 1, doi. 10.1371/journal.pgen.1010477
    By:
    • Shackleford, Ghjuvan'Ghjacumu;
    • Marziali, Leandro N.;
    • Sasaki, Yo;
    • Claessens, Anke;
    • Ferri, Cinzia;
    • Weinstock, Nadav I.;
    • Rossor, Alexander M.;
    • Silvestri, Nicholas J.;
    • Wilson, Emma R.;
    • Hurley, Edward;
    • Kidd, Grahame J.;
    • Manohar, Senthilvelan;
    • Ding, Dalian;
    • Salvi, Richard J.;
    • Feltri, M. Laura;
    • D'Antonio, Maurizio;
    • Wrabetz, Lawrence
    Publication type:
    Article
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    Treatment with IFB-088 Improves Neuropathy in CMT1A and CMT1B Mice.

    Published in:
    Molecular Neurobiology, 2022, v. 59, n. 7, p. 4159, doi. 10.1007/s12035-022-02838-y
    By:
    • Bai, Yunhong;
    • Treins, Caroline;
    • Volpi, Vera G.;
    • Scapin, Cristina;
    • Ferri, Cinzia;
    • Mastrangelo, Rosa;
    • Touvier, Thierry;
    • Florio, Francesca;
    • Bianchi, Francesca;
    • Del Carro, Ubaldo;
    • Baas, Frank F.;
    • Wang, David;
    • Miniou, Pierre;
    • Guedat, Philippe;
    • Shy, Michael E.;
    • D'Antonio, Maurizio
    Publication type:
    Article
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    HDAC1/2-Dependent P0 Expression Maintains Paranodal and Nodal Integrity Independently of Myelin Stability through Interactions with Neurofascins.

    Published in:
    PLoS Biology, 2015, v. 13, n. 9, p. 1, doi. 10.1371/journal.pbio.1002258
    By:
    • Brügger, Valérie;
    • Engler, Stefanie;
    • Pereira, Jorge A.;
    • Ruff, Sophie;
    • Horn, Michael;
    • Welzl, Hans;
    • Münger, Emmanuelle;
    • Vaquié, Adrien;
    • Sidiropoulos, Páris N. M.;
    • Egger, Boris;
    • Yotovski, Peter;
    • Filgueira, Luis;
    • Somandin, Christian;
    • Lühmann, Tessa C.;
    • D’Antonio, Maurizio;
    • Yamaguchi, Teppei;
    • Matthias, Patrick;
    • Suter, Ueli;
    • Jacob, Claire
    Publication type:
    Article
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    Unraveling gene expression profiles in peripheral motor nerve from amyotrophic lateral sclerosis patients: insights into pathogenesis.

    Published in:
    Scientific Reports, 2016, p. 39297, doi. 10.1038/srep39297
    By:
    • Riva, Nilo;
    • Clarelli, Ferdinando;
    • Domi, Teuta;
    • Cerri, Federica;
    • Gallia, Francesca;
    • Trimarco, Amelia;
    • Brambilla, Paola;
    • Lunetta, Christian;
    • Lazzerini, Alberto;
    • Lauria, Giuseppe;
    • Taveggia, Carla;
    • Iannaccone, Sandro;
    • Nobile-Orazio, Eduardo;
    • Comi, Giancarlo;
    • D'Antonio, Maurizio;
    • Martinelli-Boneschi, Filippo;
    • Quattrini, Angelo
    Publication type:
    Article
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    Corrigendum: Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy.

    Published in:
    Human Molecular Genetics, 2019, v. 28, n. 13, p. 2282, doi. 10.1093/hmg/ddz037
    By:
    • Belin, Sophie;
    • Ornaghi, Francesca;
    • Shackleford, Ghjuvan'Ghjacumu;
    • Wang, Jie;
    • Scapin, Cristina;
    • Lopez-Anido, Camila;
    • Silvestri, Nicholas;
    • Robertson, Neil;
    • Williamson, Courtney;
    • Ishii, Akihiro;
    • Taveggia, Carla;
    • Svaren, John;
    • Bansal, Rashmi;
    • Schwab, Markus H;
    • Nave, Klaus;
    • Fratta, Pietro;
    • D'Antonio, Maurizio;
    • Poitelon, Yannick;
    • Feltri, M Laura;
    • Wrabetz, Lawrence
    Publication type:
    Article
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    Corrigendum: Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy.

    Published in:
    Human Molecular Genetics, 2019, v. 28, n. 10, p. 1752, doi. 10.1093/hmg/ddz021
    By:
    • Belin, Sophie;
    • Ornaghi, Francesca;
    • Shackleford, Ghjuvan'Ghjacumu;
    • Wang, Jie;
    • Scapin, Cristina;
    • Lopez-Anido, Camila;
    • Silvestri, Nicholas;
    • Robertson, Neil;
    • Williamson, Courtney;
    • Ishii, Akihiro;
    • Taveggia, Carla;
    • Svaren, John;
    • Bansal, Rashmi;
    • Schwab, Markus H;
    • Nave, Klaus;
    • Fratta, Pietro;
    • D'Antonio, Maurizio;
    • Poitelon, Yannick;
    • Feltri, M Laura;
    • Wrabetz, Lawrence
    Publication type:
    Article
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    Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy.

    Published in:
    Human Molecular Genetics, 2019, v. 28, n. 8, p. 1260, doi. 10.1093/hmg/ddy420
    By:
    • Belin, Sophie;
    • Ornaghi, Francesca;
    • Shackleford, Ghjuvan'Ghjacumu;
    • Wang, Jie;
    • Scapin, Cristina;
    • Lopez-Anido, Camila;
    • Silvestri, Nicholas;
    • Robertson, Neil;
    • Williamson, Courtney;
    • Ishii, Akihiro;
    • Taveggia, Carla;
    • Svaren, John;
    • Bansal, Rashmi;
    • Schwab, Markus H;
    • Nave, Klaus;
    • Fratta, Pietro;
    • D'Antonio, Maurizio;
    • Poitelon, Yannick;
    • Feltri, M Laura;
    • Wrabetz, Lawrence
    Publication type:
    Article
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    Enhanced axonal neuregulin-1 type-III signaling ameliorates neurophysiology and hypomyelination in a Charcot–Marie–Tooth type 1B mouse model.

    Published in:
    Human Molecular Genetics, 2019, v. 28, n. 6, p. 992, doi. 10.1093/hmg/ddy411
    By:
    • Scapin, Cristina;
    • Ferri, Cinzia;
    • Pettinato, Emanuela;
    • Zambroni, Desiree;
    • Bianchi, Francesca;
    • Carro, Ubaldo Del;
    • Belin, Sophie;
    • Caruso, Donatella;
    • Mitro, Nico;
    • Pellegatta, Marta;
    • Taveggia, Carla;
    • Schwab, Markus H;
    • Nave, Klaus-Armin;
    • Feltri, M Laura;
    • Wrabetz, Lawrence;
    • D'Antonio, Maurizio
    Publication type:
    Article
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    Loss of Fig4 in both Schwann cells and motor neurons contributes to CMT4J neuropathy.

    Published in:
    Human Molecular Genetics, 2015, v. 24, n. 2, p. 383, doi. 10.1093/hmg/ddu451
    By:
    • Vaccari, Ilaria;
    • Carbone, Antonietta;
    • Previtali, Stefano Carlo;
    • Mironova, Yevgeniya A.;
    • Alberizzi, Valeria;
    • Noseda, Roberta;
    • Rivellini, Cristina;
    • Bianchi, Francesca;
    • Del Carro, Ubaldo;
    • D'Antonio, Maurizio;
    • Lenk, Guy M.;
    • Wrabetz, Lawrence;
    • Giger, Roman J.;
    • Meisler, Miriam H.;
    • Bolino, Alessandra
    Publication type:
    Article
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