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Human Genetics|November 1, 1992
Deletions in exon 5 of the human rhodopsin gene causing a shift in the reading frame and autosomal dominant retinitis pigmentosaM Horn, P Humphries, M Kunisch, et al.
Plos One|May 5, 2012
Effects of combined ketamine/xylazine anesthesia on light induced retinal degeneration in ratsBlanca Arango-Gonzalez, Andreas Schatz, Sylvia Bolz, et al.
Experimental Eye Research|November 4, 2009
Neuroprotective effects of tempol on retinal ganglion cells in a partial optic nerve crush rat model with and without iron loadSebastian Thaler, Michal Fiedorowicz, Robert Rejdak, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 1, 2002
Studies on the feasibility of a subretinal visual prosthesis: data from Yucatan micropig and rabbitH N Schwahn, F Gekeler, K Kohler, et al.
Journal of Cardiovascular Electrophysiology|July 11, 2002
Characterization of paroxysmal and persistent atrial fibrillation in the human left atrium during initiation and sustained episodesGjin Ndrepepa, Martin R Karch, Michael A E Schneider, et al.
Herzschrittmachertherapie & Elektrophysiologie|September 25, 2007
[Use of the NavX navigation system in ablation of atrial fibrillation]H L Estner, G Hessling, A Luik, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 10, 2010
Neuroprotection by acetoacetate and β-hydroxybutyrate against NMDA-induced RGC damage in rat--possible involvement of kynurenic acidSebastian Thaler, Tomasz J Choragiewicz, Robert Rejdak, et al.
The New Phytologist|May 6, 2009
A functional analysis of the pyrimidine catabolic pathway in ArabidopsisRita Zrenner, Heike Riegler, Cathleen R Marquard, et al.
Plos One|July 19, 2011
Calpain and PARP activation during photoreceptor cell death in P23H and S334ter rhodopsin mutant ratsJasvir Kaur, Stine Mencl, Ayse Sahaboglu, et al.
Nature Genetics|July 14, 1998
Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channelS Kohl, T Marx, I Giddings, et al.
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