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Now showing items 1-10 of 15
Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosxa 1 (RP1) gene
(Molecular Vision, 2003)
Morphological characterization of the retina of the CNGA3(-/-)Rho(-/-) mutant mouse lacking functional cones and rods
(Association for Research in Vision and Ophthalmology, 2004)
Influence of a quantitative trait locus on mouse chromosome 19 to the light-adapted electroretinogram.
(Association for Research in Vision and Ophthalmology, 2008)
Altered retinal microRNA expression profile in a mouse model of retinitis pigmentosa.
(BioMed Central, 2007)
On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention
(Nature Publishing Group, 2002)
Rod and cone contributions to horizontal cell light responses in the mouse retina.
(The Society for Neuroscience, 2008)
Synaptic plasticity in GNGA3-/- mice: Cone bipolar cells react up0onthe missing cone input and form ectopic synapses with rods
(The Society for Neuroscience, 2006)
Cone opsin mislocalization in Rpe65-/- mice: A defect that can be corrected by 11-cis retinal
(The Association for Research in Vision and Ophthalmology, Inc., 2005)