Publications of Hauke B. Werner

Dere, E.; Winkler, D.; Ritter, C.; Ronnenberg, A.; Poggi, G.; Patzig, J.; Gernert, M.; Müller, C.; Nave, K.-A.; Ehrenreich, H. et al.; Werner, H. B.: Gpm6b deficiency impairs sensorimotor gating and modulates the behavioral response to a 5-HT2A/C receptor agonist. Behavioural Brain Research 277, pp. 254 - 263 (2015)

Nave, K.-A.; Werner, H. B.: Myelination of the Nervous System: Mechanisms and Functions. Annual Review of Cell and Developmental Biology 30, pp. 503 - 533 (2014)

Muneer, Z.; Wiesinger, C.; Voigtländer, T.; Werner, H. B.; Berger, J.; Forss-Petter, S.: Abcd2 is a strong modifier of the metabolic impairments in peritoneal macrophages of Abcd1-deficient mice. PLoS One 9 (9), e108655 (2014)

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. The American Journal of Human Genetics 94 (4), pp. 533 - 546 (2014)

Mostowy, S.; Bi, E.; Füchtbauer, E.-M.; Goryachev, A. B.; Montagna, C.; Nagata, K.-i.; Trimble, W. S.; Werner, H. B.; Yao, X.; Zieger, B. et al.; Spiliotis, E. T.: Highlight: The 5th international workshop on septin biology. Biological Chemistry 395 (2), pp. 119 - 121 (2014)

Patzig, J.; Dworschak, M. S.; Martens, A.-K.; Werner, H. B.: Septins in the glial cells of the nervous system. Biological Chemistry 395 (2), pp. 143 - 149 (2014)

Werner, H. B.: Do we have to reconsider the evolutionary emergence of myelin? Frontiers in Cellular Neuroscience 7, 217 (2013)

Monasterio-Schrader, P. d.; Patzig, J.; Möbius, W.; Barrette, B.; Wagner, T. L.; Kusch, K.; Edgar, J. M.; Brophy, P. J.; Werner, H. B.: Uncoupling of neuroinflammation from axonal degeneration in mice lacking the myelin protein tetraspanin-2. Glia 61 (11), pp. 1832 - 1847 (2013)

Nawaz, S.; Schweitzer, J.; Jahn, O.; Werner, H. B.: Molecular evolution of myelin basic protein, an abundant structural myelin component. Glia 61 (8), pp. 1364 - 1377 (2013)

El-Kordi, A.; Kästner, A.; Grube, S.; Klugmann, M.; Begemann, M.; Sperling, S.; Hammerschmidt, K.; Hammer, C.; Stepniak, B.; Patzig, J. et al.; Monasterio-Schrader, P. d.; Strenzke, N.; Flügge, G.; Werner, H. B.; Pawlak, R.; Nave, K.-A.; Ehrenreich, H.: A single gene defect causing claustrophobia. Translational Psychiatry 3, e254 (2013)

Werner, H. B.; Krämer-Albers, E.-M.; Strenzke, N.; Saher, G.; Tenzer, S.; Ohno-Iwashita, Y.; Monasterio-Schrader, P. d.; Möbius, W.; Moser, T.; Griffiths, I. R. et al.; Nave, K.-A.: A critical role for the cholesterol-associated proteolipids PLP and M6B in myelination of the central nervous system. Glia 61 (4), pp. 567 - 586 (2013)

Jahn, O.; Tenzer, S.; Werner, H. B.: Proteomanalyse des Myelins, der Isolierschicht der Nerven. Biospektrum 19 (3), pp. 263 - 265 (2013)

Monasterio-Schrader, P. d.; Jahn, O.; Tenzer, S.; Wichert, S. P.; Patzig, J.; Werner, H. B.: Systematic approaches to central nervous system myelin. Cellular and Molecular Life Sciences 69 (17), pp. 2879 - 2894 (2012)

Gazzerro, E.; Baldassari, S.; Giacomini, C.; Musante, V.; Fruscione, F.; La Padula, V.; Biancheri, R.; Scarfi, S.; Prada, V.; Sotgia, F. et al.; Duncan, I. D.; Zara, F.; Werner, H. B.; Lisanti, M. P.; Nobbio, L.; Corradi, A.; Minetti, C.: Hyccin, the molecule mutated in the leukodystrophy hypomyelination and congenital cataract (HCC), is a neuronal protein. PLoS One 7 (3), e32180 (2012)

Patzig, J.; Jahn, O.; Tenzer, S.; Wichert, S. P.; De Monasterio-Schrader, P.; Rosfa, S.; Kuharev, J.; Yan, K.; Bormuth, I.; Bremer, J. et al.; Aguzzi, A.; Orfaniotou, F.; Hesse, D.; Schwab, M. H.; Möbius, W.; Nave, K.-A.; Werner, H. B.: Quantitative and integrative proteome analysis of peripheral nerve myelin identifies novel myelin proteins and candidate neuropathy loci. The Journal of Neuroscience 31 (45), pp. 16369 - 16386 (2011)

Brendel, C.; Belakhov, V.; Werner, H.; Wegener, E.; Gärtner, J.; Nudelman, I.; Baasov, T.; Huppke, P.: Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model. Journal of Molecular Medicine 89, pp. 389 - 398 (2011)

Werner, H. B.; Jahn, O.: Myelin matters: proteomic insights into white matter disorders. Expert Review of Proteomics 7 (2), pp. 159 - 164 (2010)

Edgar, J. M.; McLaughlin, M.; Werner, H. B.; McCulloch, M. C.; Barrie, J. A.; Brown, A.; Faichney, A. B.; Snaidero, N.; Nave, K.-A.; Griffiths, I. R.: Early ultrastructural defects of axons and axon-glia junctions in mice lacking expression of Cnp1. Glia 57 (16), pp. 1815 - 1824 (2009)

Jahn, O.; Tenzer, S.; Werner, H. B.: Myelin Proteomics: Molecular Anatomy of an Insulating Sheath. Molecular Neurobiology 40 (1), pp. 55 - 72 (2009)

Möbius, W.; Patzig, J.; Nave, K.-A.; Werner, H. B.: Phylogeny of proteolipid proteins: divergence, constraints, and the evolution of novel functions in myelination and neuroprotection. Neuron Glia Biology 4 (2), pp. 111 - 127 (2009)