Global network analysis in Schizosaccharomyces pombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease von Minnis, Christopher J., Townsend, StJohn, Petschnigg, Julia, Tinelli, Elisa, Bähler, Jürg, Russell, Claire, Mole, Sara E.

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De novo fatty acid synthesis by Schwann cells is essential for peripheral nervous system myelination von Montani, Laura, Pereira, Jorge A, Norrmén, Camilla, Pohl, Hartmut B F, Tinelli, Elisa, Trötzmüller, Martin, Figlia, Gianluca, Dimas, Penelope, von Niederhäusern, Belinda, Schwager, Rachel, Jessberger, Sebastian, Semenkovich, Clay F, Köfeler, Harald C, Suter, Ueli

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Schwann cells, but not Oligodendrocytes, Depend Strictly on Dynamin 2 Function von Gerber, Daniel, Ghidinelli, Monica, Tinelli, Elisa, Somandin, Christian, Gerber, Joanne, Pereira, Jorge A, Ommer, Andrea, Figlia, Gianluca, Miehe, Michaela, Nägeli, Lukas G, Suter, Vanessa, Tadini, Valentina, Sidiropoulos, Páris Nm, Wessig, Carsten, Toyka, Klaus V, Suter, Ueli

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Ablation of the UPR-Mediator CHOP Restores Motor Function and Reduces Demyelination in Charcot-Marie-Tooth 1B Mice von Pennuto, Maria, Tinelli, Elisa, Malaguti, MariaChiara, Del Carro, Ubaldo, D'Antonio, Maurizio, Ron, David, Quattrini, Angelo, Feltri, M. Laura, Wrabetz, Lawrence

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Author Correction: Global network analysis in Schizosaccharomyces pombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease von Minnis, Christopher J, Townsend, StJohn, Petschnigg, Julia, Tinelli, Elisa, Bähler, Jürg, Russell, Claire, Mole, Sara E

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Dynamin 2 mutations in Charcot―Marie―Tooth neuropathy highlight the importance of clathrin-mediated endocytosis in myelination von SIDIROPOULO, Páris N. M, MIEH, Michael, BOCK, Thomas, TINELLI, Elisa, OERTLI, Carole I, KUNER, Rohini, MEIJER, Dies, WOLLSCHEID, Bernd, NIEMANN, Axel, SUTER, Ueli

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MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B von Saporta, Mario A C, Shy, Brian R, Patzko, Agnes, Bai, Yunhong, Pennuto, Maria, Ferri, Cinzia, Tinelli, Elisa, Saveri, Paola, Kirschner, Dan, Crowther, Michelle, Southwood, Cherie, Wu, Xingyao, Gow, Alexander, Feltri, M Laura, Wrabetz, Lawrence, Shy, Michael E

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Muscle-specific function of the centronuclear myopathy and Charcot-Marie-Tooth neuropathy-associated dynamin 2 is required for proper lipid metabolism, mitochondria, muscle fibers,... von Tinelli, Elisa, Pereira, Jorge A, Suter, Ueli

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Author Correction: Global network analysis in Schizosaccharomycespombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease von Minnis, Christopher J., Townsend, StJohn, Petschnigg, Julia, Tinelli, Elisa, Bähler, Jürg, Russell, Claire, Mole, Sara E.

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NCLs and ER: A stressful relationship von Marotta, Davide, Tinelli, Elisa, Mole, Sara E.

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Antagonists of transient receptor potential-mucolipin 1: A new therapeutic strategy for cancer therapy von Mondini, Anna, Paina, Manuel, Ricci, Fernanda, Bessi, Matteo, Meini, Serena, Tinelli, Elisa, Liberati, Chiara, Catalani, Maria Pia, Rolland, Jean-Francois

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L’illusione della conoscenza nei Paradossi di Ortensio Lando von Tinelli, Elisa

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L’illusione della conoscenza nei Paradossi di Ortensio Lando von Elisa Tinelli

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L’illusione della conoscenza nei Paradossi di Ortensio Lando von Tinelli, Elisa

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Reuse of building components – Assessment system to support decisions in indoor re-layout interventions von Giancarlo Paganin, Cinzia Maria Luisa Talamo, Nazly Atta, Elisa Tinelli

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Global network analysis in Schizosaccharomyces pombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease (vol 11, 6332, 2021) von Minnis, Christopher J., Townsend, StJohn, Petschnigg, Julia, Tinelli, Elisa, Baehler, Juerg, Russell, Claire, Mole, Sara E.

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RENATO RICCO, Sulle tracce di Didone. Fra Età Classica e Rinascimento, l’evoluzione letteraria di un mito, Napoli, Guida Editori, 2015 von Elisa Tinelli

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Mice carrying an analogous heterozygous dynamin 2 K562E mutation that causes neuropathy in humans develop predominant characteristics of a primary myopathy von Pereira, Jorge A, Gerber, Joanne, Ghidinelli, Monica, Gerber, Daniel, Tortola, Luigi, Ommer, Andrea, Bachofner, Sven, Santarella, Francesco, Tinelli, Elisa, Lin, Shuo, Rüegg, Markus A, Kopf, Manfred, Toyka, Klaus V, Suter, Ueli

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Different Intracellular Pathomechanisms Produce Diverse Myelin Protein Zero Neuropathies in Transgenic Mice von Wrabetz, Lawrence, D'Antonio, Maurizio, Pennuto, Maria, Dati, Gabriele, Tinelli, Elisa, Fratta, Pietro, Previtali, Stefano, Imperiale, Daniele, Zielasek, Jurgen, Toyka, Klaus, Avila, Robin L, Kirschner, Daniel A, Messing, Albee, Feltri, M. Laura, Quattrini, Angelo

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P0S63del impedes the arrival of wild-type P0 glycoprotein to myelin in CMT1B mice von Fratta, Pietro, Saveri, Paola, Zambroni, Desiree, Ferri, Cinzia, Tinelli, Elisa, Messing, Albee, D'Antonio, Maurizio, Feltri, Maria Laura, Wrabetz, Lawrence

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