Pages that link to "Q34341141"
Jump to navigation
Jump to search
The following pages link to Differences in RDS trafficking, assembly and function in cones versus rods: insights from studies of C150S-RDS (Q34341141):
Displaying 30 items.
- Photoreceptor Sensory Cilium: Traversing the Ciliary Gate (Q26778955) (← links)
- Structural and functional relationships between photoreceptor tetraspanins and other superfamily members (Q28742243) (← links)
- Insights into the mechanisms of macular degeneration associated with the R172W mutation in RDS. (Q33649255) (← links)
- Initiation of rod outer segment disc formation requires RDS. (Q33712465) (← links)
- Rim formation is not a prerequisite for distribution of cone photoreceptor outer segment proteins. (Q33913251) (← links)
- Fundus autofluorescence and photoreceptor cell rosettes in mouse models (Q34166719) (← links)
- Defects in the outer limiting membrane are associated with rosette development in the Nrl-/- retina (Q34199858) (← links)
- Gene therapy for PRPH2-associated ocular disease: challenges and prospects (Q34400262) (← links)
- The Y141C knockin mutation in RDS leads to complex phenotypes in the mouse (Q34463210) (← links)
- Overexpression of retinal degeneration slow (RDS) protein adversely affects rods in the rd7 model of enhanced S-cone syndrome (Q34708558) (← links)
- SNAREs Interact with Retinal Degeneration Slow and Rod Outer Segment Membrane Protein-1 during Conventional and Unconventional Outer Segment Targeting (Q35788032) (← links)
- Nanoparticle-mediated gene transfer specific to retinal pigment epithelial cells (Q35876917) (← links)
- Increased cone sensitivity to ABCA4 deficiency provides insight into macular vision loss in Stargardt's dystrophy (Q35957421) (← links)
- Retinal Degeneration Slow (RDS) Glycosylation Plays a Role in Cone Function and in the Regulation of RDS·ROM-1 Protein Complex Formation (Q36282945) (← links)
- Varying the GARP2-to-RDS Ratio Leads to Defects in Rim Formation and Rod and Cone Function. (Q36425001) (← links)
- Retinal angiogenesis in the Ins2(Akita) mouse model of diabetic retinopathy (Q36571714) (← links)
- Role of RDS and Rhodopsin in Cngb1-Related Retinal Degeneration (Q36648914) (← links)
- S/MAR-containing DNA nanoparticles promote persistent RPE gene expression and improvement in RPE65-associated LCA (Q36709143) (← links)
- PRPH2/RDS and ROM-1: Historical context, current views and future considerations (Q36829127) (← links)
- Structural characterization of the second intra-discal loop of the photoreceptor tetraspanin RDS (Q36839752) (← links)
- Rom1 converts Y141C-Prph2-associated pattern dystrophy to retinitis pigmentosa (Q39039992) (← links)
- The K153Del PRPH2 mutation differentially impacts photoreceptor structure and function (Q39732823) (← links)
- Loss of HCN1 enhances disease progression in mouse models of CNG channel-linked retinitis pigmentosa and achromatopsia (Q40994703) (← links)
- Overexpression of ROM-1 in the Cone-Dominant Retina (Q51834333) (← links)
- Prph2 initiates outer segment morphogenesis but maturation requires Prph2/Rom1 oligomerization (Q57283997) (← links)
- Oligomerization of Prph2 and Rom1 is essential for photoreceptor outer segment formation (Q57463077) (← links)
- Structural but Not Functional Alterations in Cones in the Absence of the Retinal Disease Protein Retinitis Pigmentosa 2 (RP2) in a Cone-Only Retina (Q64071564) (← links)
- Mislocalization of Oligomerization-Incompetent RDS is Associated with Mislocalization of Cone Opsins and Cone Transducin (Q83064729) (← links)
- The Interplay between Peripherin 2 Complex Formation and Degenerative Retinal Diseases (Q90662445) (← links)
- Genotype-phenotype associations in a large PRPH2-related retinopathy cohort (Q96344591) (← links)