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Publications by Seeliger, M W

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Number of items: 6.


Reinhard, J, Messias, A, Dietz, K, Mackeben, M, Lakmann, R, Scholl, H P, Apfelstedt-Sylla, E, Weber, Bernhard H. F. , Seeliger, M W, Zrenner, E and Trauzettel-Klosinski, S (2007) Quantifying fixation in patients with Stargardt disease. Vision Research 47 (15), pp. 2076-2085. Fulltext not available.


Molday, L L, Min, S H, Seeliger, M W, Wu, W W, Dinculescu, A, Timmers, A M, Janssen, A, Tonagel, F, Hudl, K, Weber, Bernhard H. F. , Hauswirth, W W and Molday, R S (2006) Disease mechanisms and gene therapy in a mouse model for x-linked retinoschisis. Advances in experimental medicine and biology 572, pp. 283-289. Fulltext not available.


Min, S H, Molday, L L, Seeliger, M W, Dinculescu, A, Timmers, A M, Janssen, A, Tonagel, F, Tanimoto, N, Weber, Bernhard H. F. , Molday, R S and Hauswirth, W W (2005) Prolonged recovery of retinal structure/function after gene therapy in an Rs1h-deficient mouse model of X-linked juvenile retinoschisis. Molecular Therapy 12 (4), pp. 644-651.


Seeliger, M W, Weber, Bernhard H. F. , Besch, D, Zrenner, E, Schrewe, H and Mayser, H (2003) mfERG waveform characteristics in the RS1h mouse model featuring a `negative' ERG. Documenta Ophthalmologica 107 (1), pp. 37-44. Fulltext not available.


Weber, Bernhard H. F. , Lin, B, White, K, Kohler, K, Soboleva, G, Herterich, S, Seeliger, M W, Jaissle, G B, Grimm, C, Reme, C, Wenzel, A, Asan, E and Schrewe, H (2002) A mouse model for Sorsby fundus dystrophy. Investigative ophthalmology and visual science 43 (8), pp. 2732-2740.

Weber, Bernhard H. F. , Schrewe, H, Molday, L L, Gehrig, A, White, K L, Seeliger, M W, Jaissle, G B, Friedburg, C, Tamm, E and Molday, R S (2002) Inactivation of the murine X-linked juvenile retinoschisis gene, Rs1h, suggests a role of retinoschisin in retinal cell layer organization and synaptic structure. Proceedings of the National Academy of Sciences of the United States of America : PNAS 99 (9), pp. 6222-6227.

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