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Number of items: 9.

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; Caprara, C; Tanimoto, N; Beck, S; Huber, G; Samardzija, M; Seeliger, M; Grimm, C (2011). Retina-specific activation of a sustained hypoxia-like response leads to severe retinal degeneration and loss of vision. Neurobiology of Disease, 41(1):119-130.

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.

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.

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.

This list was generated on Sun Nov 19 12:05:05 2017 CET.