Arama Sonuçları - Stephan Sonntag

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  1. 1
    Gating, permselectivity and pH‐dependent modulation of channels formed by connexin57, a major connexin of horizontal cells in the mouse retina

    Gating, permselectivity and pH‐dependent modulation of channels formed by connexin57, a major connexin of horizontal cells in the mouse retina Yazar: Nicolás Palacios‐Prado, Stephan Sonntag, Vytenis Arvydas Skeberdis, Klaus Willecke, Feliksas F. Bukauskas

    Baskı/Yayın Bilgisi 2009
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  2. 2
    The neuronal connexin36 interacts with and is phosphorylated by CaMKII in a way similar to CaMKII interaction with glutamate receptors

    The neuronal connexin36 interacts with and is phosphorylated by CaMKII in a way similar to CaMKII interaction with glutamate receptors Yazar: Cantas Alev, Stephanie Urschel, Stephan Sonntag, Georg Zoidl, Alfredo Fort, Thorsten Höher, Mamoru Matsubara, Klaus Willecke, David C. Spray, Rolf Dermietzel

    Baskı/Yayın Bilgisi 2008
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  3. 3
    Epigenetic regulation of promiscuous gene expression in thymic medullary epithelial cells

    Epigenetic regulation of promiscuous gene expression in thymic medullary epithelial cells Yazar: Lars‐Oliver Tykocinski, Anna Sinemus, Esmail Rezavandy, Yanina Weiland, David Baddeley, Christoph Cremer, Stephan Sonntag, Klaus Willecke, Jens Derbinski, Bruno Kyewski

    Baskı/Yayın Bilgisi 2010
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  4. 4
    The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice

    The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice Yazar: Melanie Schütz, Pietro Scimemi, Paromita Majumder, Romolo Daniele De Siati, Giulia Crispino, Laura Rodríguez, Mario Bortolozzi, Rosamaria Santarelli, Anke Seydel, Stephan Sonntag, Neil J. Ingham, Karen P. Steel, Klaus Willecke, Fabio Mammano

    Baskı/Yayın Bilgisi 2010
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  5. 5
    SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects

    SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects Yazar: Johanne Dubail, Céline Huber, Sandrine Chantepie, Stephan Sonntag, Beyhan Tüysüz, Ercan Mıhçı, Christopher T. Gordon, Elisabeth Steichen‐Gersdorf, Jeanne Amiel, Banu Nur, Irene Stolte‐Dijkstra, Albertien M. van Eerde, Koen L.I. van Gassen, Corstiaan C. Breugem, Alexander P.A. Stegmann, Caroline Lekszas, Reza Maroofian, Ehsan Ghayoor Karimiani, Arnaud Bruneel, Nathalie Seta, Arnold Münnich, Dulce Papy‐Garcia, Muriel De La Dure‐Molla, Valérie Cormier‐Daire

    Baskı/Yayın Bilgisi 2018
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