Retina ciliopathies: From genes to mechanisms and treatment
Arl3 and RP2 mediated assembly and traffic of membrane associated cilia proteins
Molecular assemblies that control rhodopsin transport to the cilia
Transport and localization of signaling proteins in ciliated cells
The prenyl-binding protein PrBP/δ: A chaperone participating in intracellular trafficking
Uncoordinated (UNC)119: Coordinating the trafficking of myristoylated proteins
Kinesin-2 family motors in the unusual photoreceptor cilium
Analysis of KIF17 distal tip trafficking in zebrafish cone photoreceptors
Kinesin-2 motors transport IFT-particles, dyneins and tubulin subunits to the tips of Caenorhabditis elegans sensory cilia: Relevance to vision research?
The expression of whirlin and Cav1.3α1 is mutually independent in photoreceptors
Fundus autofluorescence and optical coherence tomography in relation to visual function in Usher syndrome type 1 and 2
Combination of retinitis pigmentosa and hearing loss caused by a novel mutation in PRPH2 and a known mutation in GJB2: Importance for differential diagnosis of Usher syndrome
Phenotypic expression of Bardet–Biedl syndrome in patients homozygous for the common M390R mutation in the BBS1 gene
Senior–Løken syndrome: A syndromic form of retinal dystrophy associated with nephronophthisis
Evidence of a role of inositol polyphosphate 5-phosphatase INPP5E in cilia formation in zebrafish
From quantitative protein complex analysis to disease mechanism
Ciliary signaling cascades in photoreceptors
Current mutation discovery approaches in Retinitis Pigmentosa