نتائج البحث - Odermatt, Benjamin

Encoding of Luminance and Contrast by Linear and Nonlinear Synapses in the Retina حسب Odermatt, Benjamin, Nikolaev, Anton, Lagnado, Leon

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The oligodendroglial precursor cell line Oli-neu represents a cell culture system to examine functional expression of the mouse gap junction gene connexin29 (Cx29) حسب Söhl, Goran, Hombach, Sonja, Degen, Joachim, Odermatt, Benjamin

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Clathrin-mediated endocytosis: the physiological mechanism of vesicle retrieval at hippocampal synapses حسب Granseth, Björn, Odermatt, Benjamin, Royle, Stephen J, Lagnado, Leon

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Computational processing of optical measurements of neuronal and synaptic activity in networks حسب Dorostkar, Mario M., Dreosti, Elena, Odermatt, Benjamin, Lagnado, Leon

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A genetically-encoded reporter of synaptic activity in vivo حسب Dreosti, Elena, Odermatt, Benjamin, Dorostkar, Mario M., Lagnado, Leon

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Synaptic mechanisms of adaptation and sensitization in the retina حسب Nikolaev, Anton, Leung, Kin-Mei, Odermatt, Benjamin, Lagnado, Leon

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Imaging pHluorin-based probes at hippocampal synapses حسب Royle, Stephen J., Granseth, Björn, Odermatt, Benjamin, Derevier, Aude, Lagnado, Leon

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Synaptic vesicles are “primed” for fast clathrin-mediated endocytosis at the ribbon synapse حسب Pelassa, Ilaria, Zhao, CongJian, Pasche, Mathias, Odermatt, Benjamin, Lagnado, Leon

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A Synaptic Mechanism for Temporal Filtering of Visual Signals حسب Baden, Tom, Nikolaev, Anton, Esposti, Federico, Dreosti, Elena, Odermatt, Benjamin, Lagnado, Leon

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Uncoupling of neurogenesis and differentiation during retinal development حسب Engerer, Peter, Suzuki, Sachihiro C, Yoshimatsu, Takeshi, Chapouton, Prisca, Obeng, Nancy, Odermatt, Benjamin, Williams, Philip R, Misgeld, Thomas, Godinho, Leanne

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Connexin 47 (Cx47)-Deficient Mice with Enhanced Green Fluorescent Protein Reporter Gene Reveal Predominant Oligodendrocytic Expression of Cx47 and Display Vacuolized Myelin in the... حسب Odermatt, Benjamin, Wellershaus, Kerstin, Wallraff, Anke, Seifert, Gerald, Degen, Joachim, Euwens, Carsten, Fuss, Babette, Büssow, Heinrich, Schilling, Karl, Steinhäuser, Christian, Willecke, Klaus

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Dynamic assembly of ribbon synapses and circuit maintenance in a vertebrate sensory system حسب Okawa, Haruhisa, Yu, Wan-Qing, Matti, Ulf, Schwarz, Karin, Odermatt, Benjamin, Zhong, Haining, Tsukamoto, Yoshihiko, Lagnado, Leon, Rieke, Fred, Schmitz, Frank, Wong, Rachel O. L.

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Functional Expression of the New Gap Junction Gene Connexin47 Transcribed in Mouse Brain and Spinal Cord Neurons حسب Teubner, Barbara, Odermatt, Benjamin, Güldenagel, Martin, Söhl, Goran, Degen, Joachim, Bukauskas, Feliksas F., Kronengold, Jack, Verselis, Vytas K., Jung, Yong Tae, Kozak, Christine A., Schilling, Karl, Willecke, Klaus

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Synaptic Convergence Patterns onto Retinal Ganglion Cells Are Preserved despite Topographic Variation in Pre- and Postsynaptic Territories حسب Yu, Wan-Qing, El-Danaf, Rana N., Okawa, Haruhisa, Pacholec, Justin M., Matti, Ulf, Schwarz, Karin, Odermatt, Benjamin, Dunn, Felice A., Lagnado, Leon, Schmitz, Frank, Huberman, Andrew D., Wong, Rachel O.L.

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Molecular basis for the distinct functions of redox-active and FeS-transfering glutaredoxins حسب Trnka, Daniel, Engelke, Anna D., Gellert, Manuela, Moseler, Anna, Hossain, Md Faruq, Lindenberg, Tobias T., Pedroletti, Luca, Odermatt, Benjamin, de Souza, João V., Bronowska, Agnieszka K., Dick, Tobias P., Mühlenhoff, Uli, Meyer, Andreas J., Berndt, Carsten, Lillig, Christopher Horst

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Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa حسب Ralser, Damian J., Basmanav, F. Buket Ü., Tafazzoli, Aylar, Wititsuwannakul, Jade, Delker, Sarah, Danda, Sumita, Thiele, Holger, Wolf, Sabrina, Busch, Michélle, Pulimood, Susanne A., Altmüller, Janine, Nürnberg, Peter, Lacombe, Didier, Hillen, Uwe, Wenzel, Jörg, Frank, Jorge, Odermatt, Benjamin, Betz, Regina C.

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Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism حسب Wilms, Christina, Lepka, Klaudia, Häberlein, Felix, Edwards, Steven, Felsberg, Jörg, Pudelko, Linda, Lindenberg, Tobias T., Poschmann, Gereon, Qin, Nan, Volbracht, Katrin, Prozorovski, Tim, Meuth, Sven G., Kahlert, Ulf D., Remke, Marc, Aktas, Orhan, Reifenberger, Guido, Bräutigam, Lars, Odermatt, Benjamin, Berndt, Carsten

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ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development حسب Zhang, Rong, Knapp, Michael, Suzuki, Kentaro, Kajioka, Daiki, Schmidt, Johanna M., Winkler, Jonas, Yilmaz, Öznur, Pleschka, Michael, Cao, Jia, Kockum, Christina Clementson, Barker, Gillian, Holmdahl, Gundela, Beaman, Glenda, Keene, David, Woolf, Adrian S., Cervellione, Raimondo M., Cheng, Wei, Wilkins, Simon, Gearhart, John P., Sirchia, Fabio, Di Grazia, Massimo, Ebert, Anne-Karolin, Rösch, Wolfgang, Ellinger, Jörg, Jenetzky, Ekkehart, Zwink, Nadine, Feitz, Wout F., Marcelis, Carlo, Schumacher, Johannes, Martinón-Torres, Federico, Hibberd, Martin Lloyd, Khor, Chiea Chuen, Heilmann-Heimbach, Stefanie, Barth, Sandra, Boyadjiev, Simeon A., Brusco, Alfredo, Ludwig, Michael, Newman, William, Nordenskjöld, Agneta, Yamada, Gen, Odermatt, Benjamin, Reutter, Heiko

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Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction حسب Kolvenbach, Caroline M., Dworschak, Gabriel C., Frese, Sandra, Japp, Anna S., Schuster, Peggy, Wenzlitschke, Nina, Yilmaz, Öznur, Lopes, Filipa M., Pryalukhin, Alexey, Schierbaum, Luca, van der Zanden, Loes F.M., Kause, Franziska, Schneider, Ronen, Taranta-Janusz, Katarzyna, Szczepańska, Maria, Pawlaczyk, Krzysztof, Newman, William G., Beaman, Glenda M., Stuart, Helen M., Cervellione, Raimondo M., Feitz, Wouter F.J., van Rooij, Iris A.L.M., Schreuder, Michiel F., Steffens, Martijn, Weber, Stefanie, Merz, Waltraut M., Feldkötter, Markus, Hoppe, Bernd, Thiele, Holger, Altmüller, Janine, Berg, Christoph, Kristiansen, Glen, Ludwig, Michael, Reutter, Heiko, Woolf, Adrian S., Hildebrandt, Friedhelm, Grote, Phillip, Zaniew, Marcin, Odermatt, Benjamin, Hilger, Alina C.

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SLC20A1 Is Involved in Urinary Tract and Urorectal Development حسب Rieke, Johanna Magdalena, Zhang, Rong, Braun, Doreen, Yilmaz, Öznur, Japp, Anna S., Lopes, Filipa M., Pleschka, Michael, Hilger, Alina C., Schneider, Sophia, Newman, William G., Beaman, Glenda M., Nordenskjöld, Agneta, Ebert, Anne-Karoline, Promm, Martin, Rösch, Wolfgang H., Stein, Raimund, Hirsch, Karin, Schäfer, Frank-Mattias, Schmiedeke, Eberhard, Boemers, Thomas M., Lacher, Martin, Kluth, Dietrich, Gosemann, Jan-Hendrik, Anderberg, Magnus, Barker, Gillian, Holmdahl, Gundela, Läckgren, Göran, Keene, David, Cervellione, Raimondo M., Giorgio, Elisa, Di Grazia, Massimo, Feitz, Wouter F. J., Marcelis, Carlo L. M., Van Rooij, Iris A. L. M., Bökenkamp, Arend, Beckers, Goedele M. A., Keegan, Catherine E., Sharma, Amit, Dakal, Tikam Chand, Wittler, Lars, Grote, Phillip, Zwink, Nadine, Jenetzky, Ekkehart, Brusco, Alfredo, Thiele, Holger, Ludwig, Michael, Schweizer, Ulrich, Woolf, Adrian S., Odermatt, Benjamin, Reutter, Heiko

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