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Number of items: 17.

Fischer, M D; Huber, G; Paquet-Durand, F; Humphries, P; Redmond, T M; Grimm, C; Seeliger, M W (2012). In Vivo Assessment of Rodent Retinal Structure Using Spectral Domain Optical Coherence Tomography. In: LaVail, M M; Ash, J D; Anderson, R G; Hollyfileld, J G; Grimm, C. Retinal Degenerative Diseases. New York: Springer, 489-494.

Egger, A; Samardzija, M; Sothilingam, V; Tanimoto, N; Lange, C; Salatino, S; Fang, L; Garcia-Garrido, M; Beck, S; Okoniewski, M J; Neutzner, A; Seeliger, M W; Grimm, C; Handschin, C (2012). PGC-1a determines light damage susceptibility of the murine retina. PLoS ONE, 7(2):e31272.

Lange, C; Heynen, S R; Tanimoto, N; Thiersch, M; Le, Y Z; Meneau, I; Seeliger, M W; Samardzija, M; Caprara, C; Grimm, C (2011). Normoxic activation of hypoxia-inducible factors in photoreceptors provides transient protection against light-induced retinal degeneration. Investigative Ophthalmology and Visual Science, 52(8):5872-5880.

Heynen, S R; Tanimoto, N; Joly, S; Seeliger, M W; Samardzija, M; Grimm, C (2011). Retinal degeneration modulates intracellular localization of CDC42 in photoreceptors. Molecular Vision, 17:2934-2946.

Huber, G; Heynen, S; Imsand, C; vom Hagen, F; Muehlfriedel, R; Tanimoto, N; Feng, Y; Hammes, H P; Grimm, C; Peichl, L; Seeliger, M W; Beck, S C (2010). Novel rodent models for macular research. PLoS ONE, 5(10):e13403.

Huber, G; Beck, S C; Grimm, C; Sahaboglu-Tekgoz, A; Paquet-Durand, F; Wenzel, A; Humphries, P; Redmond, T M; Seeliger, M W; Fischer, D (2009). Spectral domain optical coherence tomography in mouse models of retinal degeneration. Investigative Ophthalmology and Visual Science, 50(12):5888-5995.

Joly, S; Francke, M; Ulbricht, E; Beck, S; Seeliger, M W; Hirrlinger, P; Hirrlinger, J; Lang, K S; Zinkernagel, M; Odermatt, B; Samardzija, M; Reichenbach, A; Grimm, C; Remé, C E (2009). Cooperative phagocytes: resident microglia and bone marrow immigrants remove dead photoreceptors in retinal lesions. American Journal of Pathology, 174(6):2310-2323.

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 (2009). In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death. Human Molecular Genetics, 18(7):1266-1275.

Fischer, M D; Huber, G; Beck, S C; Tanimoto, N; Muehlfriedel, R; Fahl, E; Grimm, C; Wenzel, A; Remé, C E; van de Pavert, S A; Wijnholds, J; Pacal, M; Bremner, R; Seeliger, M W (2009). Noninvasive, in vivo assessment of mouse retinal structure using optical coherence tomography. PLoS ONE, 4(10):e7507.

Dumelin, C E; Trüssel, S; Buller, F; Trachsel, E; Bootz, F; Zhang, Y; Mannocci, L; Beck, S C; Drumea-Mirancea, M; Seeliger, M W; Baltes, C; Müggler, T; Kranz, F; Rudin, M; Melkko, S; Scheuermann, J; Neri, D (2008). A portable albumin binder from a DNA-encoded chemical library. Angewandte Chemie Internationale Edition, 47(17):3196-3201.

Fahl, E; Gassmann, M; Grimm, C; Seeliger, M W (2008). Oxygen supply and retinal function: insights from a transgenic animal model. In: Anderson, R E. Recent Advances in Retinal Degeneration. New York: Springer, 171-177.

Samardzija, M; von Lintig, J; Tanimoto, N; Oberhauser, V; Thiersch, M; Remé, C E; Seeliger, M W; Grimm, C; Wenzel, A (2008). R91W mutation in Rpe65 leads to milder early-onset retinal dystrophy due to the generation of low levels of 11-cis-retinal. Human Molecular Genetics, 17(2):281-292.

Schild, A; Isenmann, S; Tanimoto, N; Tonagel, F; Seeliger, M W; Ittner, L M; Kretz, A; Ogris, E; Götz, J (2006). Impaired development of the Harderian gland in mutant protein phosphatase 2A transgenic mice. Mechanisms of Development, 123(5):362-371.

Bahadori, R; Huber, M; Rinner, O; Seeliger, M W; Geiger-Rudolph, S; Geisler, R; Neuhauss, S C F (2003). Retinal function and morphology in two zebrafish models of oculo-renal syndromes. European Journal of Neuroscience, 18(6):1377-1386.

Neuhauss, S C F; Seeliger, M W; Schepp, C P; Biehlmaier, O (2003). Retinal defects in the zebrafish bleached mutant. Documenta Ophthalmologica, 107(1):71-78.

Seeliger, M W; Rilk, A; Neuhauss, S C F (2002). Ganzfeld ERG in zebrafish larvae. Documenta Ophthalmologica, 104(1):57-68.

Neuhauss, S C F; Biehlmaier, O; Seeliger, M W; Das, T; Kohler, K; Harris, W A; Baier, H (1999). Genetic disorders of vision revealed by a behavioral screen of 400 essential loci in zebrafish. Journal of Neuroscience, 19(19):8603-8615.

This list was generated on Thu Sep 21 02:06:17 2017 CEST.