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Number of items: 6.

Samardzija, M; Caprara, C; Heynen, S R; Willcox DeParis, S; Meneau, I; Traber, G; Agca, C; von Lintig, J; Grimm, C (2014). A mouse model for studying cone photoreceptor pathologies. Investigative Ophthalmology & Visual Science [IOVS], 55(5):5304-5313.

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.

Fleisch, V C; Schonthaler, H B; von Lintig, J; Neuhauss, S C F (2008). Subfunctionalization of a retinoid-binding protein provides evidence for two parallel visual cycles in the cone-dominant zebrafish retina. Journal of Neuroscience, 28(33):8208-8216.

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.

Schonthaler, H B; Lampert, J M; Isken, A; Rinner, O; Mader, A; Gesemann, M; Oberhauser, V; Golczak, M; Biehlmaier, O; Palczewski, K; Neuhauss, S C F; von Lintig, J (2007). Evidence for RPE65-independent vision in the cone-dominated zebrafish retina. European Journal of Neuroscience, 26(7):1940-1949.

Schonthaler, H B; Lampert, J M; von Lintig, J; Schwarz, H; Geisler, R; Neuhauss, S C F (2005). A mutation in the silver gene leads to defects in melanosome biogenesis and alterations in the visual system in the zebrafish mutant fading vision. Developmental Biology, 284(2):421-436.

This list was generated on Wed Oct 18 04:54:12 2017 CEST.