The Y141C knockin mutation in RDS leads to complex phenotypes in the mouse

Insights into the mechanisms of macular degeneration associated with the R172W mutation in RDS

(2014) S. M. Conley et al.   HUMAN MOLECULAR GENETICS

S/MAR-containing DNA nanoparticles promote persistent RPE gene expression and improvement in RPE65-associated LCA

(2013) Adarsha Koirala et al.   HUMAN MOLECULAR GENETICS

Structural and Functional Analysis of the Native Peripherin-ROM1 Complex Isolated from Photoreceptor Cells

(2013) Brian M. Kevany et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Membrane curvature generation by a C-terminal amphipathic helix in peripherin-2/rds, a tetraspanin required for photoreceptor sensory cilium morphogenesis

(2013) N. Khattree et al.   JOURNAL OF CELL SCIENCE

A Single Valine Residue Plays an Essential Role in Peripherin/rds Targeting to Photoreceptor Outer Segments

(2013) Raquel Y. Salinas et al.   PLoS One

Defects in the Outer Limiting Membrane Are Associated with Rosette Development in the Nrl−/− Retina

(2012) Michael W. Stuck et al.   PLoS One

PATTERN DYSTROPHY WITH HIGH INTRAFAMILIAL VARIABILITY ASSOCIATED WITH Y141C MUTATION IN THE PERIPHERIN/RDS GENE AND SUCCESSFUL TREATMENT OF SUBFOVEAL CNV RELATED TO MULTIFOCAL PATTERN TYPE WITH ANTI-VEGF (RANIBIZUMAB) INTRAVITREAL INJECTIONS

(2012) Veronika Vaclavik et al.   RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES

Increased cone sensitivity to ABCA4 deficiency provides insight into macular vision loss in Stargardt's dystrophy

(2011) Shannon M. Conley et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

Structural and functional relationships between photoreceptor tetraspanins and other superfamily members

(2011) Shannon M. Conley et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Increased expression of multifunctional serine protease, HTRA1, in retinal pigment epithelium induces polypoidal choroidal vasculopathy in mice

(2011) A. Jones et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Biochemical Analysis of Phenotypic Diversity Associated with Mutations in Codon 244 of the Retinal Degeneration Slow Gene

(2010) Shannon M. Conley et al.   BIOCHEMISTRY

Differences in RDS trafficking, assembly and function in cones versus rods: insights from studies of C150S-RDS

(2010) Dibyendu Chakraborty et al.   HUMAN MOLECULAR GENETICS

A Partial Structural and Functional Rescue of a Retinitis Pigmentosa Model with Compacted DNA Nanoparticles

(2009) Xue Cai et al.   PLoS One

Outer Segment Oligomerization of Rds:  Evidence from Mouse Models and Subcellular Fractionation†

(2008) Dibyendu Chakraborty et al.   BIOCHEMISTRY

The spectrum of retinal dystrophies caused by mutations in the peripherin/RDS gene

(2008) Camiel J.F. Boon et al.   PROGRESS IN RETINAL AND EYE RESEARCH