Výsledky vyhledávání - Ninnemann, Olaf
- Zobrazuji výsledky 1 - 9 z 9
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Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation Autor Issa, Lina, Mueller, Katrin, Seufert, Katja, Kraemer, Nadine, Rosenkotter, Henning, Ninnemann, Olaf, Buob, Michael, Kaindl, Angela M, Morris-Rosendahl, Deborah J
Vydáno 2013Text -
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Role of the Transmembrane Potential in the Membrane Proton Leak Autor Rupprecht, Anne, Sokolenko, Elena A., Beck, Valeri, Ninnemann, Olaf, Jaburek, Martin, Trimbuch, Thorsten, Klishin, Sergey S., Jezek, Petr, Skulachev, Vladimir P., Pohl, Elena E.
Vydáno 2010Text -
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Combined immunodeficiency develops with age in Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2) Autor von Bernuth, Horst, Ravindran, Ethiraj, Du, Hang, Fröhler, Sebastian, Strehl, Karoline, Krämer, Nadine, Issa-Jahns, Lina, Amulic, Borko, Ninnemann, Olaf, Xiao, Mei-Sheng, Eirich, Katharina, Kölsch, Uwe, Hauptmann, Kathrin, John, Rainer, Schindler, Detlev, Wahn, Volker, Chen, Wei, Kaindl, Angela M
Vydáno 2014Text -
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Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation Autor Ravindran, Ethiraj, Hu, Hao, Yuzwa, Scott A., Hernandez-Miranda, Luis R., Kraemer, Nadine, Ninnemann, Olaf, Musante, Luciana, Boltshauser, Eugen, Schindler, Detlev, Hübner, Angela, Reinecker, Hans-Christian, Ropers, Hans-Hilger, Birchmeier, Carmen, Miller, Freda D., Wienker, Thomas F., Hübner, Christoph, Kaindl, Angela M.
Vydáno 2017Text -
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Mutations in PTRH2 cause novel infantile-onset multisystem disease with intellectual disability, microcephaly, progressive ataxia, and muscle weakness Autor Hu, Hao, Matter, Michelle L, Issa-Jahns, Lina, Jijiwa, Mayumi, Kraemer, Nadine, Musante, Luciana, de la Vega, Michelle, Ninnemann, Olaf, Schindler, Detlev, Damatova, Natalia, Eirich, Katharina, Sifringer, Marco, Schrötter, Sandra, Eickholt, Britta J, van den Heuvel, Lambert, Casamina, Chanel, Stoltenburg-Didinger, Gisela, Ropers, Hans-Hilger, Wienker, Thomas F, Hübner, Christoph, Kaindl, Angela M
Vydáno 2014Text -
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Synaptic PRG-1 Modulates Excitatory Transmission via Lipid Phosphate-Mediated Signaling Autor Trimbuch, Thorsten, Beed, Prateep, Vogt, Johannes, Schuchmann, Sebastian, Maier, Nikolaus, Kintscher, Michael, Breustedt, Jörg, Schuelke, Markus, Streu, Nora, Kieselmann, Olga, Brunk, Irene, Laube, Gregor, Strauss, Ulf, Battefeld, Arne, Wende, Hagen, Birchmeier, Carmen, Wiese, Stefan, Sendtner, Michael, Kawabe, Hiroshi, Kishimoto-Suga, Mika, Brose, Nils, Baumgart, Jan, Geist, Beate, Aoki, Junken, Savaskan, Nic E., Bräuer, Anja U., Chun, Jerold, Ninnemann, Olaf, Schmitz, Dietmar, Nitsch, Robert
Vydáno 2009Text -
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Precise Somatotopic Thalamocortical Axon Guidance Depends on LPA-Mediated PRG-2/Radixin Signaling Autor Cheng, Jin, Sahani, Sadhna, Hausrat, Torben Johann, Yang, Jenq-Wei, Ji, Haichao, Schmarowski, Nikolai, Endle, Heiko, Liu, Xinfeng, Li, Yunbo, Böttche, Rahel, Radyushkin, Konstantin, Maric, Hans M., Hoerder-Suabedissen, Anna, Molnár, Zoltán, Prouvot, Pierre-Hugues, Trimbuch, Thorsten, Ninnemann, Olaf, Huai, Jisen, Fan, Wei, Visentin, Barbara, Sabbadini, Roger, Strømgaard, Kristian, Stroh, Albrecht, Luhmann, Heiko J., Kneussel, Matthias, Nitsch, Robert, Vogt, Johannes
Vydáno 2016Text