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Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 19, 2013
[Effects of transcorneal electrical stimulation in patients with Stargardt's disease]T Röck, A Schatz, L Naycheva, et al.Cell Death & Disease|December 6, 2014
DNA methylation and differential gene regulation in photoreceptor cell deathP Farinelli, A Perera, B Arango-Gonzalez, et al.Ophthalmic Research|January 1, 1997
The development of subretinal microphotodiodes for replacement of degenerated photoreceptorsE Zrenner, K D Miliczek, V P Gabel, et al.American Journal of Human Genetics|June 1, 1992
Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencingJ A van den Hurk, T J van de Pol, C M Molloy, et al.Investigative Ophthalmology & Visual Science|November 30, 2000
Genetics and phenotypes of RPE65 mutations in inherited retinal degenerationD A Thompson, P Gyürüs, L L Fleischer, et al.Nature Genetics|August 31, 2001
New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosisM W Seeliger, C Grimm, F Ståhlberg, et al.Nature Genetics|July 14, 1998
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindnessT M Strom, G Nyakatura, E Apfelstedt-Sylla, et al.Nano Letters|November 19, 2024
Solid-State Nanopores for Spatially Resolved Chemical NeuromodulationF Vacca, F Galluzzi, M Blanco-Formoso, et al.Human Molecular Genetics|June 1, 1997
Mouse choroideremia gene mutation causes photoreceptor cell degeneration and is not transmitted through the female germlineJ A van den Hurk, W Hendriks, D J van de Pol, et al.Nature Genetics|May 1, 1996
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)A Meindl, K Dry, K Herrmann, et al.Pageof 30