Works by WILLECKE, Klaus


Results: 104
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    Expression patterns of connexin genes in mouse retina.

    Published in:
    Journal of Comparative Neurology, 2000, v. 425, n. 2, p. 193, doi. 10.1002/1096-9861(20000918)425:2<193::AID-CNE3>3.0.CO;2-N
    By:
    • Güldenagel, Martin;
    • Söhl, Goran;
    • Plum, Achim;
    • Traub, Otto;
    • Teubner, Barbara;
    • Weiler, Reto;
    • Willecke, Klaus
    Publication type:
    Article
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    Eliminating Glutamatergic Input onto Horizontal Cells Changes the Dynamic Range and Receptive Field Organization of Mouse Retinal Ganglion Cells.

    Published in:
    Journal of Neuroscience, 2018, v. 38, n. 8, p. 2015, doi. 10.1523/JNEUROSCI.0141-17.2018
    By:
    • Ströh, Sebastian;
    • Puller, Christian;
    • Swirski, Sebastian;
    • Hölzel, Maj-Britt;
    • van der Linde, Lea I. S.;
    • Segelken, Jasmin;
    • Schultz, Konrad;
    • Block, Christoph;
    • Monyer, Hannah;
    • Willecke, Klaus;
    • Weiler, Reto;
    • Greschner, Martin;
    • Janssen-Bienhold, Ulrike;
    • Dedek, Karin
    Publication type:
    Article
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    Engraftment of connexin 43-expressing cells prevents post-infarct arrhythmia.

    Published in:
    Nature, 2007, v. 450, n. 7171, p. 819, doi. 10.1038/nature06321
    By:
    • Roell, Wilhelm;
    • Lewalter, Thorsten;
    • Sasse, Philipp;
    • Tallini, Yvonne N.;
    • Bum-Rak Choi;
    • Breitbach, Martin;
    • Doran, Robert;
    • Becher, Ulrich M.;
    • Seong-Min Hwang;
    • Bostani, Toktam;
    • von Maltzahn, Julia;
    • Hofmann, Andreas;
    • Reining, Shaun;
    • Eiberger, Britta;
    • Gabris, Bethann;
    • Pfeifer, Alexander;
    • Welz, Armin;
    • Willecke, Klaus;
    • Salama, Guy;
    • Schrickel, Jan W.
    Publication type:
    Article
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    A Central Role of Connexin 43 in Hypoxic Preconditioning.

    Published in:
    Journal of Neuroscience, 2008, v. 28, n. 3, p. 681, doi. 10.1523/JNEUROSCI.3827-07.2008
    By:
    • Lin, Jane H.-C.;
    • Nanhong Lou;
    • Ning Kang;
    • Takano, Takahiro;
    • Furong Hu;
    • Xiaoning Han;
    • Qiwu Xu;
    • Lovatt, Ditte;
    • Torres, Arnulfo;
    • Willecke, Klaus;
    • Jay Yang;
    • Jian Kang;
    • Nedergaard, Maiken
    Publication type:
    Article
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    Deformation of Network Connectivity in the Inferior Olive of Connexin 36-Deficient Mice Is Compensated by Morphological and Electrophysiological Changes at the Single Neuron Level.

    Published in:
    Journal of Neuroscience, 2003, v. 23, n. 11, p. 4700, doi. 10.1523/JNEUROSCI.23-11-04700.2003
    By:
    • De Zeeuw, Chris I.;
    • Chorev, Edilzh;
    • Derov, Anna;
    • Manor, Yait;
    • Van Der Giessen, Ruben S.;
    • De Jeu, Marcel T.;
    • Hoogenraad, Casper C.;
    • Bijman, Jan;
    • Ruigrok, Tom J. H.;
    • French, Pim;
    • Jaarsma, Dick;
    • Kistler, Werner M.;
    • Meier, Carola;
    • Petrasch-Parwez, Eilsabeth;
    • Dermietzel, Rolf;
    • Sohl, Goran;
    • Gueldenagel, Martin;
    • Willecke, Klaus;
    • Yaorm, Yosi
    Publication type:
    Article
    21

    Connexin 47 (Cx47)-Deficient Mice with Enhanced Green Fluorescent Protein Reporter Gene Reveal Predominant Oligodendrocytic Expression of Cx47 and Display Vacuolized Myelin in the CNS.

    Published in:
    Journal of Neuroscience, 2003, v. 23, n. 11, p. 4549, doi. 10.1523/JNEUROSCI.23-11-04549.2003
    By:
    • Odermatt, Benjamin;
    • Wellershaus, kerstin;
    • Wallraff, Anke;
    • Seifert, Gerald;
    • Degen, Joachim;
    • Euwens, Carsten;
    • Fuss, Babette;
    • Bussow, Heinrich;
    • Schilling, Karl;
    • Steinhauser, Christian;
    • Willecke, Klaus
    Publication type:
    Article
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    Role of astroglial connexin30 in hippocampal gap junction coupling.

    Published in:
    Glia (0894-1491), 2011, v. 59, n. 3, p. 511, doi. 10.1002/glia.21120
    By:
    • Gosejacob, Dominic;
    • Dublin, Pavel;
    • Bedner, Peter;
    • Hüttmann, Kerstin;
    • Zhang, Jiong;
    • Tress, Oliver;
    • Willecke, Klaus;
    • Pfrieger, Frank;
    • Steinhäuser, Christian;
    • Theis, Martin
    Publication type:
    Article
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    The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans.

    Published in:
    Human Molecular Genetics, 2008, v. 17, n. 4, p. 539, doi. 10.1093/hmg/ddm329
    By:
    • Dobrowolski, Radoslaw;
    • Sasse, Philipp;
    • Schrickel, Jan W.;
    • Watkins, Marcus;
    • Kim, Jung-Sun;
    • Rackauskas, Mindaugas;
    • Troatz, Clemens;
    • Ghanem, Alexander;
    • Tiemann, Klaus;
    • Degen, Joachim;
    • Bukauskas, Feliksas F.;
    • Civitelli, Roberto;
    • Lewalter, Thorsten;
    • Fleischmann, Bernd K.;
    • Willecke, Klaus
    Publication type:
    Article
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