Publications of Fritz Benseler

Andreae, H.; Curcio, M.; Owrang, D.; Esmaeelpour, S.; Jahnke, F.; Benseler, F.; Brose, N.; Vona, B.: Protocol for a minigene splice assay using the pET01 vector. STAR Protocols 6 (3), 103908 (2025)

Kowald, M.; Bachollet, S. P. J. T.; Benseler, F.; Steinecker, M.; Boll, M.; Kaushik, S.; Soykan, T.; Sun, S.; Birke, R.; Ilic, D. et al.; Brose, N.; Hoernberg, H.; Lehmann, M.; Rizzoli, S. O.; Broichhagen, B.; Lipstein, N.: Endogenous SNAP-Tagging of Munc13-1 for Monitoring Synapse Nanoarchitecture. JACS Au 5 (6), pp. 2475 - 2490 (2025)

Chen, H.; Monga, M.; Fang, Q.; Slitin, L.; Neef, J.; Chepurwar, S. S.; Netto, R. C. M.; Lezirovitz, K.; Tabith Jr, A.; Benseler, F. et al.; Brose, N.; Kusch, K.; Wichmann, C.; Strenzke, N.; Vona, B.; Preobraschenski, J.; Moser, T.: Ca²⁺ binding to the C₂E domain of otoferlin is required for hair cell exocytosis and hearing. Protein & Cell 15 (4), pp. 305 - 312 (2024)

Chen, H.; Fang, Q.; Benseler, F.; Brose, N.; Moser, T.: Probing the role of the C₂F domain of otoferlin. Frontiers in Molecular Neuroscience 16, 1299509 (2023)

Suk, T. R.; Tirard, M. T.; Fisk, Z. A.; Mitkovski, M.; Geertsma, H. M.; Parmasad, J.-L. A.; Heer, M. M.; Callaghan, S. M.; Benseler, F.; Brose, N. et al.; Tirard, M.; Rousseaux, M. W. C.: Characterizing the differential distribution and targets of Sumo1 and Sumo2 in the mouse brain. iScience 26 (4), 106350 (2023)

Maxeiner, S.; Benseler, F.; Brose, N.; Krasteva-Christ, G.: Of Humans and Gerbils— Independent Diversification of Neuroligin-4 Into X- and Y-Specific Genes in Primates and Rodents. Frontiers in Molecular Neuroscience 15, 838262 (2022)

Banerjee, A.; Imig, C.; Balakrishnan, K.; Kershberg, L.; Lipstein, N.; Uronen, R.-K.; Wang, J.; Cai, X.; Benseler, F.; Rhee, J. S. et al.; Cooper, B. H.; Liu, C.; Wojcik, S. M.; Brose, N.; Kaeser, P. S.: Molecular and functional architecture of striatal dopamine release sites. Neuron 110 (2), pp. 248 - 265.e9 (2022)

Segelcke, D.; Fischer, H. K.; Hütte, M.; Dennerlein, S.; Benseler, F.; Brose, N.; Pogatzki-Zahn, E. M.; Schmidt, M.: Tmem160 contributes to the establishment of discrete nerve injury-induced pain behaviors in male mice. Cell Reports 37 (12), 110152 (2021)

Chitirala, P.; Chang, H.-F.; Martzloff, P.; Harenberg, C.; Ravichandran, K.; Abdulreda, M. H.; Berggren, P.-O.; Krause, E.; Schirra, C.; Leinders-Zufall, T. et al.; Benseler, F.; Brose, N.; Rettig, J.: Studying the biology of cytotoxic T lymphocytes in vivo with a fluorescent granzyme B-mTFP knock-in mouse. eLife 9, e58065 (2020)

Maxeine, S.; Benseler, F.; Krasteva-Christ, G.; Brose, N.; Südhof, T. C.: Evolution of the Autism-Associated Neuroligin-4 Gene Reveals Broad Erosion of Pseudoautosomal Regions in Rodents. Molecular Biology and Evolution 37 (5), pp. 1243 - 1258 (2020)

Luo, L.; Ambrozkiewicz, M.; Benseler, F.; Chen, C.; Dumontier, E.; Falkner, S.; Furlanis, E.; Gomez, A. M.; Hoshina, N.; Huang, W.-H. et al.; Hutchison, M. A.; Itoh-Maruoka, Y.; Lavery, L. A.; Li, W.; Maruo, T.; Motohashi, J.; Pai, E. L.-L.; Pelkey, K. A.; Pereira, A.; Philips, T.; Sinclair, J. L.; Stogsdill, J. A.; Traunmüller, L.; Wang, J.; Wortel, J.; You, W.; Abumaria, N.; Beier, K. T.; Brose, N.; Burgess, H. A.; Cepko, C. L.; Cloutier, J.-F.; Eroglu, C.; Goebbels, S.; Kaeser, P. S.; Kay, J. N.; Lu, W.; Luo, L.; Mandai, K.; McBain, C. J.; Nave, K.-A.; Prado, M. A.M.; Prado, V. F.; Rothstein, J.; Rubenstein, J. L.R.; Saher, G.; Sakimura, K.; Sanes, J. R.; Scheiffele, P.; Takai, Y.; Umemori, H.; Verhage, M.; Yuzaki, M.; Zoghbi, H. Y.; Kawabe, H.; Craig, A. M.: Optimizing nervous system-specific gene targeting with Cre driver lines: prevalence of germline recombination and influencing factors. Neuron 106 (1), pp. 37 - 65.e5 (2020)

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), pp. 1565 - 1579 (2015)

Papiol, S.; Begemann, M.; Rosenberger, A.; Friedrichs, H.; Ribbe, K.; Grube, S.; Schwab, M. H.; Jahn, H.; Gunkel, S.; Benseler, F. et al.; Nave, K.-A.; Ehrenreich, H.: A phenotype-based genetic association study reveals the contribution of neuregulin1 gene variants to age of onset and positive symptom severity in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (3), pp. 340 - 345 (2011)

Grube, S.; Gerchen, M. F.; Adamcio, B.; Pardo, L. A.; Martin, S.; Malzahn, D.; Papiol, S.; Begemann, M.; Ribbe, K.; Friedrichs, H. et al.; Radyushkin, K. A.; Müller, M.; Benseler, F.; Riggert, J.; Falkai, P.; Bickeböller, H.; Nave, K.-A.; Brose, N.; Stühmer, W.; Ehrenreich, H.: A CAG repeat polymorphism of KCNN3 predicts SK3 channel function and cognitive performance in schizophrenia. Embo Molecular Medicine 3 (6), pp. 309 - 319 (2011)

Begemann, M.; Grube, S.; Papiol, S.; Malzahn, D.; Krampe, H.; Ribbe, K.; Friedrichs, H.; Radyushkin, K. A.; El-Kordi, A.; Benseler, F. et al.; Hannke, K.; Sperling, S.; Schwerdtfeger, D.; Thanhäuser, I.; Gerchen, M. F.; Ghorbani, M.; Gutwinski, S.; Hilmes, C.; Leppert, R.; Ronnenberg, A.; Sowislo, J.; Stawicki, S.; Stödtke, M.; Szuszies, C.; Reim, K.; Riggert, J.; Eckstein, F.; Falkai, P.; Bickeböller, H.; Nave, K.-A.; Brose, N.; Ehrenreich, H.: Modification of cognitive performance in schizophrenia by complexin 2 gene polymorphisms. Archives of General Psychiatry 67 (9), pp. 879 - 888 (2010)

Betz, A.; Okamoto, M.; Benseler, F.; Brose, N.: Direct Interaction of the Rat unc-13 Homologue Munc13-1 with the N Terminus of Syntaxin. Journal of Biological Chemistry 272 (4), pp. 2520 - 2526 (1997)

Telemenakis, I.; Benseler, F.; Stenius, K.; Südhof, T.; Brose, N.: Rat homologue of yeast sec7p. European Journal of Cell Biology 74 (2), pp. 143 - 149 (1997)