Publications of Nils Brose

Wegmeyer, H.; Egea, J.; Rabe, N.; Gezelius, H.; Filosa, A.; Enjin, A.; Varoqueaux, F.; Deininger, K.; Schnütgen, F.; Brose, N. et al.; Klein, R.; Kullander, K.; Betz, A.: EphA4-Dependent axon guidance is mediated by the RacGAP alpha 2-chimaerin. Neuron 55 (5), pp. 756 - 767 (2007)

Wojcik, S. M.; Brose, N.: Regulation of membrane fusion in synaptic excitation-secretion coupling: Speed and accuracy matter. Neuron 55 (1), pp. 11 - 24 (2007)

Glynn, D.; Reim, K.; Brose, N.; Morton, A. J.: Depletion of Complexin II does not affect disease progression in a mouse model of Huntington's disease (HD); support for role for complexin II in behavioural pathology in a mouse model of HD. Brain Research Bulletin 72 (2-3), pp. 108 - 120 (2007)

Basu, J.; Betz, A.; Brose, N.; Rosenmund, C.: Munc13-1 C1 domain activation lowers the energy barrier for synaptic vesicle fusion. The Journal of Neuroscience 27 (5), pp. 1200 - 1210 (2007)

Brose, N.: Autismus - wenn Nervenzellen kontaktscheu sind. BIOspektrum 13, pp. 614 - 616 (2007)

Chubykin, A. A.; Atasoy, D.; Etherton, M. R.; Brose, N.; Kavalali, E. T.; Gibson, J. R.; Südhof, T. C.: Activity-dependent validation of excitatory versus inhibitory synapses by neuroligin-1 versus neuroligin-2. Neuron 54 (6), pp. 919 - 931 (2007)

Tordera, R. M.; Totterdell, S.; Wojcik, S. M.; Brose, N.; Elizalde, N.; Lasheras, B.; Del Rio, J.: Enhanced anxiety, depressive-like behaviour and impaired recognition memory in mice with reduced expression of the vesicular glutamate transporter 1 (VGLUT1). European Journal of Neuroscience 25 (1), pp. 281 - 290 (2007)

Dimova, K.; Kawabe, H.; Betz, A.; Brose, N.; Jahn, O.: Characterization of the Munc13-calmodulin interaction by photoaffinity labeling. Biochimica et Biophysica Acta: BBA 1763 (11), pp. 1256 - 1265 (2006)

Herzog, E.; Takamori, S.; Jahn, R.; Brose, N.; Wojcik, S. M.: Synaptic and vesicular co-localization of the glutamate transporters VGLUT1 and VGLUT2 in the mouse hippocampus. Journal of Neurochemistry 99 (3), pp. 1011 - 1018 (2006)

Speidel, D.; Lundquist, I.; Brose, N.; Rorsman, P.; Renstrom, E.: Glucagon hypersecretion underlies glucose intolerance in CAPS-deficient mice. Diabetologia 49, pp. 354 - 355 (2006)

Varoqueaux, F.; Aramuni, G.; Rawson, R. L.; Mohrmann, R.; Missler, M.; Gottmann, K.; Zhang, W.; Südhof, T. C.; Brose, N.: Neuroligins determine synapse maturation and function. Neuron 51 (6), pp. 741 - 754 (2006)

Andrews-Zwilling, Y. S.; Kawabe, H.; Reim, K.; Varoqueaux, F.; Brose, N.: Binding to Rab3A-interacting molecule RIM regulates the presynaptic recruitment of Munc13-1 and ubMunc13-2. Journal of Biological Chemistry 281 (28), pp. 19720 - 19731 (2006)

Kang, L. J.; He, Z.; Xu, P.; Fan, J.; Betz, A.; Brose, N.; Xu, T.: Munc13-1 is required for the sustained release of insulin from pancreatic β cells. Cell Metabolism 3 (6), pp. 463 - 468 (2006)

Kwan, E. P.; Xie, L.; Sheu, L.; Nolan, C. J.; Prentki, M.; Betz, A.; Brose, N.; Gaisano, H. Y.: Munc13-1 deficiency reduces insulin secretion and causes abnormal glucose tolerance. Diabetes 55 (5), pp. 1421 - 1429 (2006)

Vinatier, J.; Herzog, E.; Plamont, M.-A.; Wojcik, S. M.; Schmidt, A.; Brose, N.; Daviet, L.; El Mestikawy, S.; Giros, B.: Interaction between the vesicular glutamate transporter type 1 and endophilin A1, a protein essential for endocytosis. Journal of Neurochemistry 97 (4), pp. 1111 - 1125 (2006)

Wojcik, S. M.; Katsurabayashi, S.; Guillemin, I.; Friauf, E.; Rosenmund, C.; Brose, N.; Rhee, J.-S.: A shared vesicular carrier allows synaptic corelease of GABA and glycine. Neuron 50 (4), pp. 575 - 587 (2006)

Kalla, S.; Stern, M.; Basu, J.; Varoqueaux, F.; Reim, K.; Rosenmund, C.; Ziv, N. E.; Brose, N.: Molecular dynamics of a presynaptic active zone protein studied in Munc13-1-enhanced yellow fluorescent protein knock-in mutant mice. Journal of Neuroscience 26 (50), pp. 13054 - 13066 (2006)

Stevens, D. R.; Wu, Z.-X.; Matti, U.; Junge, H. J.; Schirra, C.; Becherer, U.; Wojcik, S. M.; Brose, N.; Rettig, J.: Identification of the minimal protein domain required for priming activity of Munc13-1. Current Biology 15 (24), pp. 2243 - 2248 (2005)

Gibson, H. E.; Reim, K.; Brose, N.; Morton, A. J.; Jones, S.: A similar impairment in CA3 mossy fibre LTP in the R6/2 mouse model of Huntington's disease and in the complexin II knockout mouse. European Journal of Neuroscience 22 (7), pp. 1701 - 1712 (2005)

Glynn, D.; Drew, C. J.; Reim, K.; Brose, N.; Morton, A. J.: Profound ataxia in complexin I knockout mice masks a complex phenotype that includes exploratory and habituation deficits. Human Molecular Genetics 14 (16), pp. 2369 - 2385 (2005)