Items where Author is "Rinner, O."

Article

Schonthaler, H. B. and Fleisch, V. C. and Biehlmaier, O. and Makhankov, Y. and Rinner, O. and Bahadori, R. and Geisler, R. and Schwarz, H. and Neuhauss, S. C. F. and Dahm, R.. (2008) The zebrafish mutant lbk/vam6 resembles human multisystemic disorders caused by aberrant trafficking of endosomal vesicles. Development, 135 (2). pp. 387-399.

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

Bahadori, R. and Rinner, O. and Schonthaler, H. B. and Biehlmaier, O. and Makhankov, Y. V. and Rao, P. and Jagadeeswaran, P. and Neuhauss, S. C. F.. (2006) The Zebrafish fade out mutant: a novel genetic model for Hermansky-Pudlak syndrome. Investigative Ophthalmology & Visual Science, 47 (10). pp. 4523-4531.

Rinner, O. and Makhankov, Y. V. and Biehlmaier, O. and Neuhauss, S. C. F.. (2005) Knockdown of cone-specific kinase GRK7 in larval zebrafish leads to impaired cone response recovery and delayed dark adaptation. Neuron, 47 (2). pp. 231-242.