Torthaí cuardaigh - Anke Seydel

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  1. 1
    Neuroblastoma treatment in the post-genomic era

    Neuroblastoma treatment in the post-genomic era de réir Maria Rosaria Esposito, Sanja Aveic, Anke Seydel, Gian Paolo Tonini

    Foilsithe / Cruthaithe 2017
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    Revisão
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  2. 2
    Oxidative Damage and Autophagy in the Human Trabecular Meshwork as Related with Ageing

    Oxidative Damage and Autophagy in the Human Trabecular Meshwork as Related with Ageing de réir Alessandra Pulliero, Anke Seydel, Anna Camoirano, Sergio Claudio Saccà, Marco Sandri, Alberto Izzotti

    Foilsithe / Cruthaithe 2014
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    Artigo
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  3. 3
    Combating autophagy is a strategy to increase cytotoxic effects of novel ALK inhibitor entrectinib in neuroblastoma cells

    Combating autophagy is a strategy to increase cytotoxic effects of novel ALK inhibitor entrectinib in neuroblastoma cells de réir Sanja Aveic, Marcella Pantile, Anke Seydel, Maria Rosaria Esposito, Carlo Zanon, Gary Li, Gian Paolo Tonini

    Foilsithe / Cruthaithe 2015
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    Artigo
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  4. 4
    ATP release through connexin hemichannels and gap junction transfer of second messengers propagate Ca <sup>2+</sup> signals across the inner ear

    ATP release through connexin hemichannels and gap junction transfer of second messengers propagate Ca <sup>2+</sup> signals across the inner ear de réir Fabio Anselmi, Victor H. Hernández, Giulia Crispino, Anke Seydel, Saida Ortolano, Stephen D. Roper, Nicoletta Kessaris, William D. Richardson, Gesa Rickheit, Mikhail A Filippov, Hannah Monyer, Fabio Mammano

    Foilsithe / Cruthaithe 2008
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    Artigo
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  5. 5
    Regulation of autophagy and the ubiquitin–proteasome system by the FoxO transcriptional network during muscle atrophy

    Regulation of autophagy and the ubiquitin–proteasome system by the FoxO transcriptional network during muscle atrophy de réir Giulia Milan, Vanina Romanello, Francesca Pescatore, Andrea Armani, Ji-Hye Paik, Laura Frasson, Anke Seydel, Jinghui Zhao, Reimar Abraham, Alfred L. Goldberg, Bert Blaauw, Ronald A. DePinho, Marco Sandri

    Foilsithe / Cruthaithe 2015
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    Artigo
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  6. 6
    The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice

    The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice de réir Melanie Schütz, Pietro Scimemi, Paromita Majumder, Romolo Daniele De Siati, Giulia Crispino, Laura Rodríguez, Mario Bortolozzi, Rosamaria Santarelli, Anke Seydel, Stephan Sonntag, Neil J. Ingham, Karen P. Steel, Klaus Willecke, Fabio Mammano

    Foilsithe / Cruthaithe 2010
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    Artigo
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