Small heat shock proteins in neurodegenerative diseases von Vendredy, Leen, Adriaenssens, Elias, Timmerman, Vincent

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Mitochondria-associated membranes as hubs for neurodegeneration von Krols, Michiel, van Isterdael, Gert, Asselbergh, Bob, Kremer, Anna, Lippens, Saskia, Timmerman, Vincent, Janssens, Sophie

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Genetics of Charcot-Marie-Tooth (CMT) Disease within the Frame of the Human Genome Project Success von Timmerman, Vincent, Strickland, Alleene V, Züchner, Stephan

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HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1–induced Charcot-Marie-Tooth disease von d'Ydewalle, Constantin, Krishnan, Jyothsna, Chiheb, Driss M, Van Damme, Philip, Irobi, Joy, Kozikowski, Alan P, Berghe, Pieter Vanden, Timmerman, Vincent, Robberecht, Wim, Van Den Bosch, Ludo

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Neuropathy-causing mutations in HSPB1 impair autophagy by disturbing the formation of SQSTM1/p62 bodies von Haidar, Mansour, Asselbergh, Bob, Adriaenssens, Elias, De Winter, Vicky, Timmermans, Jean-Pierre, Auer-Grumbach, Michaela, Juneja, Manisha, Timmerman, Vincent

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Animal models and therapeutic prospects for Charcot-Marie-Tooth disease von Bouhy, Delphine, Timmerman, Vincent

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A de novo gain-of-function mutation in SCN11A causes loss of pain perception von Leipold, Enrico, Liebmann, Lutz, Korenke, G Christoph, Heinrich, Theresa, Gießelmann, Sebastian, Baets, Jonathan, Ebbinghaus, Matthias, Goral, R Oliver, Stödberg, Tommy, Hennings, J Christopher, Bergmann, Markus, Altmüller, Janine, Thiele, Holger, Wetzel, Andrea, Nürnberg, Peter, Timmerman, Vincent, De Jonghe, Peter, Blum, Robert, Schaible, Hans-Georg, Weis, Joachim, Heinemann, Stefan H, Hübner, Christian A, Kurth, Ingo

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Autophagy as an Emerging Common Pathomechanism in Inherited Peripheral Neuropathies von Haidar, Mansour, Timmerman, Vincent

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Overlapping molecular pathological themes link Charcot–Marie–Tooth neuropathies and hereditary spastic paraplegias von Timmerman, Vincent, Clowes, Virginia E., Reid, Evan

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The neuroinflammatory role of Schwann cells in disease von Ydens, Elke, Lornet, Guillaume, Smits, Veerle, Goethals, Sofie, Timmerman, Vincent, Janssens, Sophie

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Altered interplay between endoplasmic reticulum and mitochondria in Charcot–Marie–Tooth type 2A neuropathy von Bernard-Marissal, Nathalie, van Hameren, Gerben, Juneja, Manisha, Pellegrino, Christophe, Louhivuori, Lauri, Bartesaghi, Luca, Rochat, Cylia, El Mansour, Omar, Médard, Jean-Jacques, Croisier, Marie, Maclachlan, Catherine, Poirot, Olivier, Uhlén, Per, Timmerman, Vincent, Tricaud, Nicolas, Schneider, Bernard L., Chrast, Roman

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Acute injury in the peripheral nervous system triggers an alternative macrophage response von Ydens, Elke, Cauwels, Anje, Asselbergh, Bob, Goethals, Sofie, Peeraer, Lieve, Lornet, Guillaume, Almeida-Souza, Leonardo, Van Ginderachter, Jo A, Timmerman, Vincent, Janssens, Sophie

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A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8 von Bouhy, Delphine, Juneja, Manisha, Katona, Istvan, Holmgren, Anne, Asselbergh, Bob, De Winter, Vicky, Hochepied, Tino, Goossens, Steven, Haigh, Jody J., Libert, Claude, Ceuterick-de Groote, Chantal, Irobi, Joy, Weis, Joachim, Timmerman, Vincent

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Sensory neuropathy-causing mutations in ATL3 affect ER-mitochondria contact sites and impair axonal mitochondrial distribution von Krols, Michiel, Asselbergh, Bob, De Rycke, Riet, De Winter, Vicky, Seyer, Alexandre, Müller, Franz-Josef, Kurth, Ingo, Bultynck, Geert, Timmerman, Vincent, Janssens, Sophie

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The hnRNP family: insights into their role in health and disease von Geuens, Thomas, Bouhy, Delphine, Timmerman, Vincent

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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A von Vance, Jeffery M, Züchner, Stephan, Mersiyanova, Irina V, Muglia, Maria, Bissar-Tadmouri, Nisrine, Rochelle, Julie, Dadali, Elena L, Zappia, Mario, Nelis, Eva, Patitucci, Alessandra, Senderek, Jan, Parman, Yesim, Evgrafov, Oleg, Jonghe, Peter De, Takahashi, Yuji, Tsuji, Shoij, Pericak-Vance, Margaret A, Quattrone, Aldo, Battologlu, Esra, Polyakov, Alexander V, Timmerman, Vincent, Schröder, J Michael

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Mutations in FAM134B , encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy von Gal, Andreas, Huebner, Antje K, Baets, Jonathan, De Jonghe, Peter, Soehendra, Désirée, Nürnberg, Gudrun, Rotthier, Annelies, Senderek, Jan, Kaether, Christoph, Hübner, Christian A, Hennings, J Christopher, Timmerman, Vincent, Farrell, Sandra A, Pamminger, Torsten, Kurth, Ingo, Topaloglu, Haluk, Nürnberg, Peter

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Tyrosyl-tRNA synthetase has a noncanonical function in actin bundling von Ermanoska, Biljana, Asselbergh, Bob, Morant, Laura, Petrovic-Erfurth, Maria-Luise, Hosseinibarkooie, Seyyedmohsen, Leitão-Gonçalves, Ricardo, Almeida-Souza, Leonardo, Bervoets, Sven, Sun, Litao, Lee, LaTasha, Atkinson, Derek, Khanghahi, Akram, Tournev, Ivaylo, Callaerts, Patrick, Verstreken, Patrik, Yang, Xiang-Lei, Wirth, Brunhilde, Rodal, Avital A., Timmerman, Vincent, Goode, Bruce L., Godenschwege, Tanja A., Jordanova, Albena

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Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1 von Capponi, Simona, Geuens, Thomas, Geroldi, Alessandro, Origone, Paola, Verdiani, Simonetta, Cichero, Elena, Adriaenssens, Elias, De Winter, Vicky, Bandettini di Poggio, Monica, Barberis, Marco, Chiò, Adriano, Fossa, Paola, Mandich, Paola, Bellone, Emilia, Timmerman, Vincent

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KIF1A, an Axonal Transporter of Synaptic Vesicles, Is Mutated in Hereditary Sensory and Autonomic Neuropathy Type 2 von Rivière, Jean-Baptiste, Ramalingam, Siriram, Lavastre, Valérie, Shekarabi, Masoud, Holbert, Sébastien, Lafontaine, Julie, Srour, Myriam, Merner, Nancy, Rochefort, Daniel, Hince, Pascale, Gaudet, Rébecca, Mes-Masson, Anne-Marie, Baets, Jonathan, Houlden, Henry, Brais, Bernard, Nicholson, Garth A., Van Esch, Hilde, Nafissi, Shahriar, De Jonghe, Peter, Reilly, Mary M., Timmerman, Vincent, Dion, Patrick A., Rouleau, Guy A.

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