Long-term in vivo imaging of fibrillar tau in the retina of P301S transgenic mice
Schön, Christian, Hoffmann, Nadine A, Ochs, Simon M, Burgold, Steffen, Filser, Severin, Steinbach, Sonja, Seeliger, Mathias W, Arzberger, Thomas, Goedert, Michel, Kretzschmar, Hans A, Schmidt, Boris, Herms, Jochen
Published in PloS one (31.12.2012)
Published in PloS one (31.12.2012)
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Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia
Kohl, Susanne, Zobor, Ditta, Chiang, Wei-Chieh, Weisschuh, Nicole, Staller, Jennifer, Menendez, Irene Gonzalez, Chang, Stanley, Beck, Susanne C, Garrido, Marina Garcia, Sothilingam, Vithiyanjali, Seeliger, Mathias W, Stanzial, Franco, Benedicenti, Francesco, Inzana, Francesca, Héon, Elise, Vincent, Ajoy, Beis, Jill, Strom, Tim M, Rudolph, Günther, Roosing, Susanne, Hollander, Anneke I den, Cremers, Frans P M, Lopez, Irma, Ren, Huanan, Moore, Anthony T, Webster, Andrew R, Michaelides, Michel, Koenekoop, Robert K, Zrenner, Eberhart, Kaufman, Randal J, Tsang, Stephen H, Wissinger, Bernd, Lin, Jonathan H
Published in Nature genetics (01.07.2015)
Published in Nature genetics (01.07.2015)
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Journal Article
The Mongolian gerbil as an advanced model to study cone system physiology
Günter, Alexander, Belhadj, Soumaya, Seeliger, Mathias W, Mühlfriedel, Regine
Published in Frontiers in cellular neuroscience (25.01.2024)
Published in Frontiers in cellular neuroscience (25.01.2024)
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Mural Serum Response Factor (SRF) Deficiency Provides Insights into Retinal Vascular Functionality and Development
Günter, Alexander, Sothilingam, Vithiyanjali, Orlich, Michael M., Nordheim, Alfred, Seeliger, Mathias W., Mühlfriedel, Regine
Published in International journal of molecular sciences (01.08.2023)
Published in International journal of molecular sciences (01.08.2023)
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Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach
Petersen-Jones, Simon M, Occelli, Laurence M, Winkler, Paige A, Lee, Winston, Sparrow, Janet R, Tsukikawa, Mai, Boye, Sanford L, Chiodo, Vince, Capasso, Jenina E, Becirovic, Elvir, Schön, Christian, Seeliger, Mathias W, Levin, Alex V, Michalakis, Stylianos, Hauswirth, William W, Tsang, Stephen H
Published in The Journal of clinical investigation (02.01.2018)
Published in The Journal of clinical investigation (02.01.2018)
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Relevance of Exocytotic Glutamate Release from Retinal Glia
Slezak, Michal, Grosche, Antje, Niemiec, Aurore, Tanimoto, Naoyuki, Pannicke, Thomas, Münch, Thomas A., Crocker, Britni, Isope, Philippe, Härtig, Wolfgang, Beck, Susanne C., Huber, Gesine, Ferracci, Geraldine, Perraut, Martine, Reber, Michael, Miehe, Monique, Demais, Valérie, Lévêque, Christian, Metzger, Daniel, Szklarczyk, Klaudia, Przewlocki, Ryszard, Seeliger, Mathias W., Sage-Ciocca, Dominique, Hirrlinger, Johannes, Reichenbach, Andreas, Reibel, Sophie, Pfrieger, Frank W.
Published in Neuron (Cambridge, Mass.) (10.05.2012)
Published in Neuron (Cambridge, Mass.) (10.05.2012)
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Spectral Domain Optical Coherence Tomography in Mouse Models of Retinal Degeneration
Huber, Gesine, Beck, Susanne C, Grimm, Christian, Sahaboglu-Tekgoz, Ayse, Paquet-Durand, Francois, Wenzel, Andreas, Humphries, Peter, Redmond, T. Michael, Seeliger, Mathias W, Fischer, M. Dominik
Published in Investigative ophthalmology & visual science (01.12.2009)
Published in Investigative ophthalmology & visual science (01.12.2009)
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Journal Article
Restoration of Cone Vision in the CNGA3−/− Mouse Model of Congenital Complete Lack of Cone Photoreceptor Function
Michalakis, Stylianos, Mühlfriedel, Regine, Tanimoto, Naoyuki, Krishnamoorthy, Vidhyasankar, Koch, Susanne, Fischer, M Dominik, Becirovic, Elvir, Bai, Lin, Huber, Gesine, Beck, Susanne C, Fahl, Edda, Büning, Hildegard, Paquet-Durand, François, Zong, Xiangang, Gollisch, Tim, Biel, Martin, Seeliger, Mathias W
Published in Molecular therapy (01.12.2010)
Published in Molecular therapy (01.12.2010)
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Targeted ablation of CRB1 and CRB2 in retinal progenitor cells mimics Leber congenital amaurosis
Pellissier, Lucie P, Alves, Celso Henrique, Quinn, Peter M, Vos, Rogier M, Tanimoto, Naoyuki, Lundvig, Ditte M S, Dudok, Jacobus J, Hooibrink, Berend, Richard, Fabrice, Beck, Susanne C, Huber, Gesine, Sothilingam, Vithiyanjali, Garcia Garrido, Marina, Le Bivic, André, Seeliger, Mathias W, Wijnholds, Jan
Published in PLoS genetics (01.12.2013)
Published in PLoS genetics (01.12.2013)
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T-type voltage-gated channels, Na+/Ca2+-exchanger, and calpain-2 promote photoreceptor cell death in inherited retinal degeneration
Yan, Jie, Wang, Lan, Yang, Qian-Lu, Yang, Qian-Xi, He, Xinyi, Dong, Yujie, Hu, Zhulin, Seeliger, Mathias W., Jiao, Kangwei, Paquet-Durand, François
Published in Cell communication and signaling (01.02.2024)
Published in Cell communication and signaling (01.02.2024)
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Journal Article
Endothelial SRF/MRTF ablation causes vascular disease phenotypes in murine retinae
Weinl, Christine, Riehle, Heidemarie, Park, Dongjeong, Stritt, Christine, Beck, Susanne, Huber, Gesine, Wolburg, Hartwig, Olson, Eric N, Seeliger, Mathias W, Adams, Ralf H, Nordheim, Alfred
Published in The Journal of clinical investigation (01.05.2013)
Published in The Journal of clinical investigation (01.05.2013)
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Journal Article
Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene
Alves, Celso Henrique, Sanz, Alicia Sanz, Park, Bokyung, Pellissier, Lucie P, Tanimoto, Naoyuki, Beck, Susanne C, Huber, Gesine, Murtaza, Mariyam, Richard, Fabrice, Sridevi Gurubaran, Iswariyaraja, Garcia Garrido, Marina, Levelt, Christiaan N, Rashbass, Penny, Le Bivic, André, Seeliger, Mathias W, Wijnholds, Jan
Published in Human molecular genetics (01.01.2013)
Published in Human molecular genetics (01.01.2013)
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Journal Article
A key role for cyclic nucleotide gated (CNG) channels in cGMP-related retinitis pigmentosa
Paquet-Durand, François, Beck, Susanne, Michalakis, Stylianos, Goldmann, Tobias, Huber, Gesine, Mühlfriedel, Regine, Trifunović, Dragana, Fischer, M Dominik, Fahl, Edda, Duetsch, Gabriele, Becirovic, Elvir, Wolfrum, Uwe, van Veen, Theo, Biel, Martin, Tanimoto, Naoyuki, Seeliger, Mathias W
Published in Human molecular genetics (01.03.2011)
Published in Human molecular genetics (01.03.2011)
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Journal Article
CRB2 acts as a modifying factor of CRB1-related retinal dystrophies in mice
Pellissier, Lucie P, Lundvig, Ditte M S, Tanimoto, Naoyuki, Klooster, Jan, Vos, Rogier M, Richard, Fabrice, Sothilingam, Vithiyanjali, Garcia Garrido, Marina, Le Bivic, André, Seeliger, Mathias W, Wijnholds, Jan
Published in Human molecular genetics (15.07.2014)
Published in Human molecular genetics (15.07.2014)
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Towards a quantitative OCT image analysis
Garcia Garrido, Marina, Beck, Susanne C, Mühlfriedel, Regine, Julien, Sylvie, Schraermeyer, Ulrich, Seeliger, Mathias W
Published in PloS one (13.06.2014)
Published in PloS one (13.06.2014)
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Journal Article
Targeted ablation of Crb2 in photoreceptor cells induces retinitis pigmentosa
Alves, Celso Henrique, Pellissier, Lucie P, Vos, Rogier M, Garcia Garrido, Marina, Sothilingam, Vithiyanjali, Seide, Christina, Beck, Susanne C, Klooster, Jan, Furukawa, Takahisa, Flannery, John G, Verhaagen, Joost, Seeliger, Mathias W, Wijnholds, Jan
Published in Human molecular genetics (01.07.2014)
Published in Human molecular genetics (01.07.2014)
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Journal Article
Constitutive overexpression of Norrin activates Wnt/β-catenin and endothelin-2 signaling to protect photoreceptors from light damage
Braunger, Barbara M, Ohlmann, Andreas, Koch, Marcus, Tanimoto, Naoyuki, Volz, Cornelia, Yang, Ying, Bösl, Michael R, Cvekl, Ales, Jägle, Herbert, Seeliger, Mathias W, Tamm, Ernst R
Published in Neurobiology of disease (01.02.2013)
Published in Neurobiology of disease (01.02.2013)
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