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Number of items: 8.

Cachafeiro, M; Bemelmans, A P; Samardzija, M; Afanasieva, T; Pournaras, J A; Grimm, C; Kostic, C; Philippe, S; Wenzel, A; Arsenijevic, Y (2013). Hyperactivation of retina by light in mice leads to photoreceptor cell death mediated by VEGF and retinal pigment epithelium permeability. Cell Death and Disease, 4:e781.

Kostic, C; Crippa, S V; Pignat, V; Bemelmans, A P; Samardzija, M; Grimm, C; Wenzel, A; Arsenijevic, Y (2011). Gene therapy regenerates protein expression in cone photoreceptors in Rpe65R91W/R91W mice. PLoS ONE, 6(2):e16588.

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.

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.

Joly, S; Samardzija, M; Wenzel, A; Thiersch, M; Grimm, C (2009). Nonessential role of beta3 and beta5 integrin subunits for efficient clearance of cellular debris after light-induced photoreceptor degeneration. Investigative Ophthalmology and Visual Science, 50(3):1423-1432.

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.

Thiersch, M; Raffelsberger, W; Frigg, E; Samardzija, M; Wenzel, A; Poch, O; Grimm, C (2008). Analysis of the retinal gene expression profile after hypoxic preconditioning identifies candidate genes for neuroprotection. BMC Genomics, 9:73.

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.

This list was generated on Sat Jul 22 21:18:55 2017 CEST.