ZFIN ID: ZDB-LAB-120215-1
Ben Odermatt Lab
PI/Director: Odermatt, Benjamin
Contact Person: Odermatt, Benjamin
Email: b.odermatt@uni-bonn.de
URL: http://www.anatomie.uni-bonn.de/forschung/odermatt-benjamin-prof-1
Address: CNS Myelin Research Group Anatomical Institute University of Bonn (Medical Faculty) Nussallee 10; Room O-11.2 53115 Bonn Germany
Country: Germany
Phone: ++49 228 739021
Fax: ++49 228 73992647
Line Designation: bn


GENOMIC FEATURES ORIGINATING FROM THIS LAB No data available


STATEMENT OF RESEARCH INTERESTS
Investigating Myelination in vivo
Investigating Nephric & Urogenital Development in vivo


LAB MEMBERS
Nagarajan, Bhuvaneswari Graduate Student


ZEBRAFISH PUBLICATIONS OF LAB MEMBERS
Rieke, J.M., Zhang, R., Braun, D., Yilmaz, Ö., Japp, A.S., Lopes, F.M., Pleschka, M., Hilger, A.C., Schneider, S., Newman, W.G., Beaman, G.M., Nordenskjöld, A., Ebert, A.K., Promm, M., Rösch, W.H., Stein, R., Hirsch, K., Schäfer, F.M., Schmiedeke, E., Boemers, T.M., Lacher, M., Kluth, D., Gosemann, J.H., Anderberg, M., Barker, G., Holmdahl, G., Läckgren, G., Keene, D., Cervellione, R.M., Giorgio, E., Di Grazia, M., Feitz, W.F.J., Marcelis, C.L.M., Van Rooij, I.A.L.M., Bökenkamp, A., Beckers, G.M.A., Keegan, C.E., Sharma, A., Dakal, T.C., Wittler, L., Grote, P., Zwink, N., Jenetzky, E., Brusco, A., Thiele, H., Ludwig, M., Schweizer, U., Woolf, A.S., Odermatt, B., Reutter, H. (2020) SLC20A1 Is Involved in Urinary Tract and Urorectal Development. Frontiers in cell and developmental biology. 8:567
Nagarajan, B., Harder, A., Japp, A., Häberlein, F., Mingardo, E., Kleinert, H., Yilmaz, Ö., Zoons, A., Rau, B., Christ, A., Kubitscheck, U., Eiberger, B., Sandhoff, R., Eckhardt, M., Hartmann, D., Odermatt, B. (2019) CNS myelin protein 36K regulates oligodendrocyte differentiation through Notch. Glia. 68(3):509-527
Kolvenbach, C.M., Dworschak, G.C., Frese, S., Japp, A.S., Schuster, P., Wenzlitschke, N., Yilmaz, Ö., Lopes, F.M., Pryalukhin, A., Schierbaum, L., van der Zanden, L.F.M., Kause, F., Schneider, R., Taranta-Janusz, K., Szczepańska, M., Pawlaczyk, K., Newman, W.G., Beaman, G.M., Stuart, H.M., Cervellione, R.M., Feitz, W.F.J., van Rooij, I.A.L.M., Schreuder, M.F., Steffens, M., Weber, S., Merz, W.M., Feldkötter, M., Hoppe, B., Thiele, H., Altmüller, J., Berg, C., Kristiansen, G., Ludwig, M., Reutter, H., Woolf, A.S., Hildebrandt, F., Grote, P., Zaniew, M., Odermatt, B., Hilger, A.C. (2019) Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction. American journal of human genetics. 104:994-1006
Yu, W.Q., El-Danaf, R.N., Okawa, H., Pacholec, J.M., Matti, U., Schwarz, K., Odermatt, B., Dunn, F.A., Lagnado, L., Schmitz, F., Huberman, A.D., Wong, R.O.L. (2018) Synaptic Convergence Patterns onto Retinal Ganglion Cells Are Preserved despite Topographic Variation in Pre- and Postsynaptic Territories. Cell Reports. 25:2017-2026.e3
Engerer, P., Suzuki, S.C., Yoshimatsu, T., Chapouton, P., Obeng, N., Odermatt, B., Williams, P.R., Misgeld, T., Godinho, L. (2017) Uncoupling of neurogenesis and differentiation during retinal development. The EMBO journal. 36(9):1134-1146
Ralser, D.J., Basmanav, F.B., Tafazzoli, A., Wititsuwannakul, J., Delker, S., Danda, S., Thiele, H., Wolf, S., Busch, M., Pulimood, S.A., Altmüller, J., Nürnberg, P., Lacombe, D., Hillen, U., Wenzel, J., Frank, J., Odermatt, B., Betz, R.C. (2017) Mutations in γ-secretase subunit-encoding PSENEN underlie Dowling-Degos disease associated with acne inversa. The Journal of Clinical Investigation. 127(4):1485-1490
Zhang, R., Knapp, M., Suzuki, K., Kajioka, D., Schmidt, J.M., Winkler, J., Yilmaz, Ö., Pleschka, M., Cao, J., Kockum, C.C., Barker, G., Holmdahl, G., Beaman, G., Keene, D., Woolf, A.S., Cervellione, R.M., Cheng, W., Wilkins, S., Gearhart, J.P., Sirchia, F., Di Grazia, M., Ebert, A.K., Rösch, W., Ellinger, J., Jenetzky, E., Zwink, N., Feitz, W.F., Marcelis, C., Schumacher, J., Martinón-Torres, F., Hibberd, M.L., Khor, C.C., Heilmann-Heimbach, S., Barth, S., Boyadjiev, S.A., Brusco, A., Ludwig, M., Newman, W., Nordenskjöld, A., Yamada, G., Odermatt, B., Reutter, H. (2017) ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development. Scientific Reports. 7:42170
Pelassa, I., Zhao, C., Pasche, M., Odermatt, B., Lagnado, L. (2014) Synaptic vesicles are "primed" for fast clathrin-mediated endocytosis at the ribbon synapse. Frontiers in molecular neuroscience. 7:91
Baden, T., Nikolaev, A., Esposti, F., Dreosti, E., Odermatt, B., Lagnado, L. (2014) A synaptic mechanism for temporal filtering of visual signals. PLoS Biology. 12:e1001972
Nikolaev, A., Leung, K.M., Odermatt, B., and Lagnado, L. (2013) Synaptic mechanisms of adaptation and sensitization in the retina. Nature Neuroscience. 16(7):934-41
Odermatt, B., Nikolaev, A., and Lagnado, L. (2012) Encoding of luminance and contrast by linear and nonlinear synapses in the retina. Neuron. 73(4):758-773
Hunter, P.R., Nikolaou, N., Odermatt, B., Williams, P.R., Drescher, U., and Meyer, M.P. (2011) Localization of cadm2a and cadm3 proteins during development of the zebrafish nervous system. The Journal of comparative neurology. 519(11):2252-70
Dorostkar, M.M., Dreosti, E., Odermatt, B., and Lagnado, L. (2010) Computational processing of optical measurements of neuronal and synaptic activity in networks. Journal of Neuroscience Methods. 188(1):141-150
Dreosti, E., Odermatt, B., Dorostkar, M.M., and Lagnado, L. (2009) A genetically encoded reporter of synaptic activity in vivo. Nature Methods. 6(12):883-889