Structural and functional phenotyping in the cone-specific photoreceptor function loss 1 (cpfl1) mouse mutant - a model of cone dystrophies. by Fischer, M, Tanimoto, N, Beck, S, Huber, G, Schaeferhoff, K, Michalakis, S, Riess, O, Wissinger, B, Biel, M, Bonin, M, Seeliger, M

In vivo analysis of cone survival in mice. by Beck, S, Schaeferhoff, K, Michalakis, S, Fischer, M, Huber, G, Rieger, N, Riess, O, Wissinger, B, Biel, M, Bonin, M, Seeliger, M, Tanimoto, N

Induction of STAT3-related genes in fast degenerating cone photoreceptors of cpfl1 mice. by Schaeferhoff, K, Michalakis, S, Tanimoto, N, Fischer, MD, Becirovic, E, Beck, S, Huber, G, Rieger, N, Riess, O, Wissinger, B, Biel, M, Seeliger, M, Bonin, M

Mutations in TOPORS cause autosomal dominant retinitis pigmentosa with perivascular retinal pigment epithelium atrophy. by Chakarova, C, Papaioannou, MG, Khanna, H, Lopez, I, Waseem, N, Shah, A, Theis, T, Friedman, J, Maubaret, C, Bujakowska, K, Veraitch, B, El-Aziz, A, Prescott, D, Parapuram, S, Bickmore, W, Munro, P, Gal, A, Hamel, C, Marigo, V, Ponting, C, Wissinger, B, Zrenner, E, Matter, K, Swaroop, A, Koenekoop, R