Cone loss is delayed relative to rod loss during induced retinal degeneration in the diurnal cone-rich rodent Arvicanthis ansorgei von Boudard, D.L, Tanimoto, N, Huber, G, Beck, S.C, Seeliger, M.W, Hicks, D

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Induction of STAT3-related genes in fast degenerating cone photoreceptors of cpfl1 mice von Schaeferhoff, K, Michalakis, S, Tanimoto, N, Fischer, M. D, Becirovic, E, Beck, S. C, Huber, G, Rieger, N, Riess, O, Wissinger, B, Biel, M, Seeliger, M. W, Bonin, M

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Bone spicule pigment formation in retinitis pigmentosa: insights from a mouse model von Jaissle, Gesine B., May, Christian Albrecht, van de Pavert, Serge A., Wenzel, Andreas, Claes-May, Ellen, Gießl, Andreas, Szurman, Peter, Wolfrum, Uwe, Wijnholds, Jan, Fisher, M. D., Humphries, P., Seeliger, M. W.

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Synaptic vesicle alterations in rod photoreceptors of synaptophysin-deficient mice von Spiwoks-Becker, I, Vollrath, L, Seeliger, M.W, Jaissle, G, Eshkind, L.G, Leube, R.E

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Multifocal electroretinography in patients with Stargardt’s macular dystrophy von Kretschmann, U, Seeliger, M W, Ruether, K, Usui, T, Apfelstedt-Sylla, E, Zrenner, E

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Prevention of Photoreceptor Apoptosis by Activation of the Glucocorticoid Receptor von Wenzel, Andreas, Grimm, Christian, Seeliger, Mathias W, Jaissle, Gesine, Hafezi, Farhad, Kretschmer, Robert, Zrenner, Eberhart, Reme, Charlotte E

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Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis von Seeliger, MW, Biesalski, HK, Wissinger, B, Gollnick, H, Gielen, S, Frank, J, Beck, S, Zrenner, E

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Biochemical but not clinical vitamin A deficiency results from mutations in the gene for retinol binding protein von Biesalski, Hans K, Frank, Jürgen, Beck, Susanne C, Heinrich, Felix, Illek, Beate, Reifen, Ram, Gollnick, Harald, Seeliger, Mathias W, Wissinger, Bernd, Zrenner, Eberhart

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In vivo confocal imaging of the retina in animal models using scanning laser ophthalmoscopy von Seeliger, Mathias W., Beck, Susanne C., Pereyra-Muñoz, Naira, Dangel, Susann, Tsai, Jen-Yue, Luhmann, Ulrich F.O., van de Pavert, Serge A., Wijnholds, Jan, Samardzija, Marijana, Wenzel, Andreas, Zrenner, Eberhart, Narfström, Kristina, Fahl, Edda, Tanimoto, Naoyuki, Acar, Niyazi, Tonagel, Felix

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Long-term engraftment of systemically transplanted, gene-modified bone marrow-derived cells in the adult mouse retina von Boettcher, C, Ulbricht, E, Helmlinger, D, Mack, A F, Reichenbach, A, Wiedemann, P, Wagner, H-J, Seeliger, M W, Bringmann, A, Priller, J

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In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death von Samardzija, Marijana, Tanimoto, Naoyuki, Kostic, Corinne, Beck, Susanne, Oberhauser, Vitus, Joly, Sandrine, Thiersch, Markus, Fahl, Edda, Arsenijevic, Yvan, von Lintig, Johannes, Wenzel, Andreas, Seeliger, Mathias W., Grimm, Christian

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Genetic Disorders of Vision Revealed by a Behavioral Screen of 400 Essential Loci in Zebrafish von Neuhauss, Stephan C. F, Biehlmaier, Oliver, Seeliger, Mathias W, Das, Tilak, Kohler, Konrad, Harris, William A, Baier, Herwig

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Retinal degeneration modulates intracellular localization of CDC42 in photoreceptors von Heynen, S R, Tanimoto, N, Joly, S, Seeliger, M W, Samardzija, M, Grimm, C

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Implicit time topography of multifocal electroretinograms von Seeliger, MW, Kretschmann, UH, Apfelstedt-Sylla, E, Zrenner, E

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Inactivation of the Murine X-Linked Juvenile Retinoschisis Gene, Rs1h, Suggests a Role of Retinoschisin in Retinal Cell Layer Organization and Synaptic Structure von Bernhard H. F. Weber, Schrewe, Heinrich, Molday, Laurie L., Gehrig, Andrea, White, Karen L., Seeliger, Mathias W., Jaissle, Gesine B., Friedburg, Christoph, Tamm, Ernst, Molday, Robert S.

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New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis von Redmond, T. Michael, Zrenner, Eberhart, Wenzel, Andreas, Remé, Charlotte E, Jaissle, Gesine, Biel, Martin, Fariss, Robert N, Humphries, Peter, Ståhlberg, Fredrik, Grimm, Christian, Seeliger, Mathias W, Hofmann, Franz, Friedburg, Christoph, Guo, Hao

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Functional Assessment of the Regional Distribution of Disease in a Cat Model of Hereditary Retinal Degeneration von Seeliger, Mathias W, Narfstrom, Kristina

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Knockout of PARG110 confers resistance to cGMP-induced toxicity in mammalian photoreceptors von Sahaboglu, A, Tanimoto, N, Bolz, S, Garrido, M G, Ueffing, M, Seeliger, M W, Löwenheim, H, Ekström, P, Paquet-Durand, F

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Identification of Usher Syndrome Subtypes by ERG Implicit Time von Seeliger, Mathias W, Zrenner, Eberhart, Apfelstedt-Sylla, Eckart, Jaissle, Gesine B

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In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death von Samardzija, M., Tanimoto, N., Kostic, C., Beck, S., Oberhauser, V., Joly, S., Thiersch, M., Fahl, E., Arsenijevic, Y., von Lintig, J., Wenzel, A., Seeliger, M. W., Grimm, C.

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