Publikationen von Michael W. Sereda

Prukop, T.; Epplen, D. B.; Nientiedt, T.; Wichert, S. P.; Fledrich, R.; Stassart, R. M.; Rossner, M. J.; Edgar, J. M.; Werner, H. B.; Nave, K.-A. et al.; Sereda, M. W.: Progesterone antagonist therapy in a Pelizaeus-Merzbacher mouse model. American Journal of Human Genetics 94, S. 533 - 546 (2014)

Tönges, L.; Günther, R.; Suhr, M.; Jansen, J.; Balck, A.; Saal, K.-A.; Barski, E.; Nientied, T.; Götz, A. A.; Koch, J.-C. et al.; Mueller, B. K.; Weishaupt, J. H.; Sereda, M. W.; Hanisch, U.-K.; Bähr, M.; Lingor, P.: Rho kinase inhibition modulates microglia activation and improves survival in a model of amyotrophic lateral sclerosis. GLIA 62 (2), S. 217 - 232 (2014)

Mannil, M.; Solari, A.; Leha, A.; Pelayo-Negro, A. L.; Berciano, J.; Schlotter-Weigel, B.; Walter, M. C.; Rautenstrauss, B.; Schnizer, T. J.; Schenone, A. et al.; Seeman, P.; Kadian, C.; Schreiber, O.; Angarita, N. G.; Fabrizi, G. M.; Gemignani, F.; Padua, L.; Santoro, L.; Quattrone, A.; Vita, G.; Calabrese, D.; CMT-TRIAAL/CMT-TRAUK Group; Young, P.; Laurà, M.; Haberlová, J.; Mazanec, R.; Paulus, W.; Beissbarth, T.; Shy, M. E.; Reilly, M. M.; Pareyson, D.; Sereda, M. W.: Selected items from the Charcot-Marie-Tooth (CMT) neuropathy score and secondary clinical outcome measures serve as sensitive clinical markers of disease severity in CMT1A patients. Neuromuscular Disorders 24, S. 1003 - 1017 (2014)

Stassart, R. M.; Fledrich, R.; Velanac, V.; Brinkmann, B. G.; Schwab, M. H.; Meijer, D.; Sereda, M. W.; Nave, K.-A.: A role for Schwann cell-derived neuregulin-1 in remyelination. Nature Neuroscience 16 (1), S. 48 - 54 (2013)

Fledrich, R.; Stassart, R. M.; Sereda, M. W.: Murine therapeutic models for Charcot-Marie-Tooth (CMT) disease. British Medical Bulletin 102, S. 89 - 113 (2012)

Goebbels, S.; Oltrogge, J.; Wolfer, S.; Wieser, G. L.; Nientiedt, T.; Pieper, A.; Ruhwedel, T.; Groszer, M.; Sereda, M. W.; Nave, K.-A.: Genetic disruption of Pten in a novel mouse model of tomaculous neuropathy. EMBO Molecular Medicine 4 (6), S. 486 - 499 (2012)

Fünfschilling, U.; Supplie, L. M.; Mahad, D.; Boretius, S.; Saab, A. S.; Edgar, J. M.; Brinkmann, B. G.; Kassmann, C. M.; Tzvetanova, I.; Möbius, W. et al.; Diaz, F.; Meijer, D.; Suter, U.; Hamprecht, B.; Sereda, M. W.; Moraes, C. T.; Frahm, J.; Goebbels, S.; Nave, K.-A.: Glycolytic oligodendrocytes maintain myelin and long-term axonal integrity. Nature 485 (7399), S. 517 - 521 (2012)

Makoukji, J.; Belle, M.; Meffre, D.; Stassart, R.; Grenier, J.; Shackleford, G. G.; Fledrich, R.; Fonte, C.; Branchu, J.; Goulard, M. et al.; de Waele, C.; Charbonnier, F.; Sereda, M. W.; Baulieu, E.-E.; Schumacher, M.; Bernard, S.; Massaad, C.: Lithium enhances remyelination of peripheral nerves. Proceedings of the National Academy of Sciences of USA 109 (10), S. 3973 - 3978 (2012)

Fledrich, R.; Schlotter-Weigel, B.; Schnizer, T. J.; Wichert, S. P.; Stassart, R. M.; Meyer zu Hörste, G.; Klink, A.; Weiss, B. G.; Haag, U.; Walter, M. C. et al.; Rautenstrauss, B.; Paulus, W.; Rossner, M. J.; Sereda, M. W.: A rat model of Charcot-Marie-Tooth disease 1A recapitulates disease variability and supplies biomarkers of axonal loss in patients. Brain 135 (1), S. 72 - 87 (2012)

Gess, B.; Röhr, D.; Fledrich, R.; Sereda, M. W.; Kleffner, I.; Humberg, A.; Nowitzki, J.; Strecker, J.-K.; Halfter, H.; Young, P.: Sodium-dependent vitamin C transporter 2 deficiency causes hypomyelination and extracellular matrix defects in the peripheral nervous system. Journal of Neuroscience 31 (47), S. 17180 - 17192 (2011)

Kassmann, C. M.; Quintes, S.; Rietdorf, J.; Möbius, W.; Sereda, M. W.; Nientiedt, T.; Saher, G.; Baes, M.; Nave, K.-A.: A role for myelin-associated peroxisomes in maintaining paranodal loops and axonal integrity. FEBS Letters 585, S. 2205 - 2211 (2011)

Meyer zu Hoerste, G.; Miesbach, T. A.; Müller, J. I.; Fledrich, R.; Stassart, R. M.; Kieseier, B. C.; Coleman, M. P.; Sereda, M. W.: The Wlds transgene reduces axon loss in a Charcot-Marie-Tooth disease 1A rat model and nicotinamide delays post-traumatic axonal degeneration. Neurobiology of Disease 42, S. 1 - 8 (2011)

Leal, A.; Huehne, K.; Bauer, F.; Sticht, H.; Berger, P.; Suter, U.; Morera, B.; Del Valle, G.; Lupski, J. R.; Ekici, A. et al.; Pasutto, F.; Endele, S.; Barrantes, R.; Berghoff, C.; Neundörfer, B.; Heuss, D.; Dorn, T.; Young, P.; Santolin, L.; Uhlmann, T.; Meisterernst, M.; Sereda, M.; Meyer zu Hörste, G.; Nave, K.-A.; Reis, A.; Rautenstrauss, B.: Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal models. Neurogenetics 10 (4), S. 275 - 287 (2009)

Schardt, A.; Brinkmann, B. G.; Mitkovski, M.; Sereda, M. W.; Werner, H. B.; Nave, K.-A.: The SNARE protein SNAP-29 interacts with the GTPase Rab3A: Implications for membrane trafficking in myelinating glia. Journal of Neuroscience Research 87, S. 3465 - 3479 (2009)

Merkler, D.; Klinker, F.; Jürgens, T.; Glaser, R.; Paulus, W.; Brinkmann, B. G.; Sereda, M. W.; Stadelmann-Nessler, C.; Guedes, R. C. A.; Brück, W. et al.; Liebetanz, D.: Propagation of spreading depression inversely correlates with cortical myelin content. Annals of Neurology 66, S. 355 - 365 (2009)

Brinkmann, B. G.; Agarwal, A.; Sereda, M. W.; Garratt, A. N.; Müller, T.; Wende, H.; Stassart, R. M.; Nawaz, S.; Humml, C.; Velanac, V. et al.; Radyushkin, K.; Goebbels, S.; Fischer, T. M.; Franklin, R. J.; Lai, C.; Ehrenreich, H.; Birchmeier, C.; Schwab, M. H.; Nave, K.-A.: Neuregulin-1/ErbB signaling serves distinct functions in myelination of the peripheral and central nervous system. Neuron 59, S. 581 - 595 (2008)

Wessig, C.; Jestaedt, L.; Sereda, M. W.; Bendszus, M.; Stoll, G.: Gadofluorine M-enhanced magnetic resonance nerve imaging: comparison between acute inflammatory and chronic degenerative demyelination in rats. Experimental Neurology 210, S. 137 - 143 (2008)

Nave, K.-A.; Sereda, M. W.; Ehrenreich, H.: Mechanisms of Disease: inherited demyelinating neuropathies - from basic to clinical research. Nature Clinical Practice Neurology 3 (8), S. 453 - 464 (2007)

Ivanova, N.; Claeys, K. G.; Deconinck, T.; Litvinenko, I.; Jordanova, A.; Auer-Grumbach, M.; Haberlova, J.; Löfgren, A.; Smeyers, G.; Nelis, E. et al.; Mercelis, R.; Plecko, B.; Priller, J.; Zamecnik, J.; Ceulemans, B.; Erichsen, A. K.; Björck, E.; Nicholson, G.; Sereda, M. W.; Seeman, P.; Kremensky, I.; Mitev, V.; De Jonghe, P.: Hereditary spastic paraplegia 3A associated with axonal neuropathy. Archives of Neurology 64 (5), S. 706 - 713 (2007)

Meyer zu Hörste, G.; Prukop, T.; Liebetanz, D.; Möbius, W.; Nave, K.-A.; Sereda, M. W.: Antiprogesterone therapy uncouples axonal loss from demyelination in a transgenic rat model of CMT1A neuropathy. Annals of Neurology 61 (1), S. 61 - 72 (2007)