Publikationen

Wüstefeld, L.; Winkler, D.; Janc, O. A.; Hassouna, I.; Ronnenberg, A.; Ostmeier, K.; Müller, M.; Brose, N.; Ehrenreich, H.; Wojcik, S. M.: Selective expression of a constitutively active erythropoietin receptor in GABAergic neurons alters hippocampal network properties without affecting cognition. Journal of Neurochemistry 136 (4), S. 698 - 705 (2015)

Man, K.-n. M.; Imig, C.; Walter, A. M.; Pinheiro, P. S.; Stevens, D. R.; Rettig, J.; Sørensen, J. B.; Cooper, B. H.; Brose, N.; Wojcik, S. M.: Identification of a Munc13-sensitive step in chromaffin cell large dense-core vesicle exocytosis. eLife, 10635 (2015)

Rahman, J.; Besser, S.; Schnell, C.; Eulenburg, V.; Hirrlinger, J.; Wojcik, S. M.; Hülsmann, S.: Genetic ablation of VIAAT in glycinergic neurons causes a severe respiratory phenotype and perinatal death. Brain Structure & Function 220, S. 2835 - 2849 (2015)

Daniel, J. A.; Chau, N.; Abdel-Hamid, M. K.; Hu, L.; von Kleist, L.; Whiting, A.; Krishnan, S.; Maamary, P.; Joseph, S. R.; Simpson, F. et al.; Haucke, V.; McCluskey, A.; Robinson, P. J.: Phenothiazine-derived antipsychotic drugs inhibit dynamin and clathrin-mediated endocytosis. Traffic 16 (6), S. 635 - 654 (2015)

Chang, S.; Reim, K.; Pedersen, M.; Neher, E.; Brose, N.; Taschenberger, H.: Complexin stabilizes newly primed synaptic vesicles and prevents their premature fusion at the mouse calyx of held synapse. Journal of Neuroscience 35 (21), S. 8272 - 8290 (2015)

Ambrozkiewicz, M.; Kawabe, H.: HECT-type E3 ubiquitin ligases in nerve cell development and synapse physiology. FEBS Letters 589 (14 ), S. 1635 - 1643 (2015)

Schotten, S.; Meijer, M.; Walter, A. M.; Huson, V.; Mamer, L.; Kalogreades, L.; ter Veer, M.; Ruiter, M.; Brose, N.; Rosenmund, C. et al.; Sørensen, J. B.; Verhage, M.; Cornelisse, L. N.: Additive effects on the energy barrier for synaptic vesicle fusion cause supralinear effects on the vesicle fusion rate. eLife, 10.7554/eLife.09036 (2015)

Netrakanti, P. R.; Cooper, B. H.; Dere, E.; Poggi, G.; Winkler, D.; Brose, N.; Ehrenreich, H.: Fast cerebellar reflex circuitry requires synaptic vesicle priming by Munc13-3. Cerebellum 14, S. 264 - 283 (2015)

Hammer, M.; Krüger-Burg, D. D.; Tuffy, L.; Cooper, B. H.; Taschenberger, H.; Goswami, S. P.; Ehrenreich, H.; Jonas, P.; Varoqueaux, F.; Rhee, J. et al.; Brose, N.: Perturbed hippocampal synaptic inhibition and γ-oscillations in a neuroligin-4 knockout mouse model of autism. Cell Reports 13 (3), S. 516 - 523 (2015)

Jedlicka, P.; Vnencak, M.; Krueger, D. D.; Jungenitz, T.; Brose, N.; Schwarzacher, S. W.: Neuroligin-1 regulates excitatory synaptic transmission, LTP and EPSP-spike coupling in the dentate gyrus in vivo. Brain Structure and Function 220 (1), S. 47 - 58 (2015)

Jung, S.; Oshima-Takago, T.; Chakrabarti, R.; Wong, A. B.; Jing, Z.; Yamanbaeva, G.; Picher, M. M.; Wojcik, S. M.; Göttfert, F.; Predoehl, F. et al.; Michel, K.; Hell, S. W.; Schoch, S.; Strenzke, N.; Wichmann, C.; Moser, T.: Rab3-interacting molecules 2α and 2β promote the abundance of voltage-gated Caν1.3 Ca²⁺ channels at hair cell active zones. Proceedings of the National Academy of Sciences of the United States of America 112 (24), S. E3141 - E3149 (2015)

Kilimann, M. W.; Oldfors, A.: Glycogen pathways in disease: new developments in a classical field of medical genetics. Journal of Inherited Metabolic Disease 38 (3), S. 483 - 487 (2015)

Lipina, T. V.; Prasad, T.; Yokomaku, D.; Luo, L.; Connor, S. A.; Kawabe, H.; Wang, Y. T.; Brose, N.; Roder, J. C.; Craig, A. M.: Cognitive deficits in Calsyntenin-2 deficient mice associated with reduced GABAergic transmission. Neuropsychopharmacology 41, S. 802 - 810 (2015)

Nawaz, S.; Sánchez, P.; Schmitt, S.; Snaidero, N.; Mitkovski, M.; Velte, C.; Brückner, B. R.; Alexopoulos, I. K.; Czopka, T.; Jung, S. et al.; Rhee, J.; Janshoff, A.; Witke, W.; Schaap, I. A. T.; Lyons, D. A.; Simons, M.: Actin filament turnover drives leading edge growth during myelin sheath formation in the central nervous system. Developmental Cell 34 (2), S. 139 - 151 (2015)

Ott, C.; Martens, H.; Hassouna, I.; Oliveira, B.; Erck, C.; Zafeiriou, M.-P.; Peteri, U.-K.; Hesse, D.; Gerhart, S.; Altas, B. et al.; Kolbow, T.; Stadler, H.; Kawabe, H.; Zimmermann, W.-H.; Nave, K.-A.; Schulz-Schaeffer, W.; Jahn, O.; Ehrenreich, H.: Widespread expression of erythropoietin receptor in brain and its induction by injury. Molecular Medicine 21, S. 803 - 815 (2015)

Papadopoulos, T.; Schemm, R.; Grubmüller, H.; Brose, N.: Lipid binding defects and perturbed synaptogenic activity of a collybistin R290H mutant that causes epilepsy and intellectual disability. Journal of Biological Chemistry 290 (13), S. 8256 - 8270 (2015)

Stepniak, B.; Kästner, A.; Poggi, G.; Mitjans, M.; Begemann, M.; Hartmann, A.; Van der Auwera, S.; Sananbenesi, F.; Krueger-Burg, D.; Matuszko, G. et al.; Brosi, C.; Homuth, G.; Völzke, H.; Benseler, F.; Bagni, C.; Fischer, U.; Dityatev, A.; Grabe, H.-J.; Rujescu, D.; Fischer, A.; Ehrenreich, H.: Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes. EMBO molecular medicine 7 (12), S. 1565 - 1579 (2015)

Vogl, C.; Cooper, B. H.; Neef, J.; Wojcik, S. M.; Reim, K.; Reisinger, E.; Brose, N.; Rhee, J.-S.; Moser, T.; Wichmann, C.: Unconventional molecular regulation of synaptic vesicle replenishment in cochlear inner hair cells. Journal of Cell Science 128 (4), S. 638 - 644 (2015)