| P50 | author | Dusanka Deretic | Q89620494 |
| P2093 | author name string | Jing Wang | |
| P2860 | cites work | An ARL3-UNC119-RP2 GTPase cycle targets myristoylated NPHP3 to the primary cilium | Q24297497 |
| | Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways | Q24302034 |
| | Nephrocystins and MKS proteins interact with IFT particle and facilitate transport of selected ciliary cargos | Q24304173 |
| | UNC119 is required for G protein trafficking in sensory neurons | Q24305723 |
| | CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium | Q24310530 |
| | A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis | Q24311615 |
| | Functional dissection of Rab GTPases involved in primary cilium formation | Q24321757 |
| | The conserved Bardet-Biedl syndrome proteins assemble a coat that traffics membrane proteins to cilia | Q24337528 |
| | Primary cilia membrane assembly is initiated by Rab11 and transport protein particle II (TRAPPII) complex-dependent trafficking of Rabin8 to the centrosome | Q24338514 |
| | CP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary disease | Q24568058 |
| | Scrutinizing ciliopathies by unraveling ciliary interaction networks | Q27025614 |
| | Crystal structure of rhodopsin: A G protein-coupled receptor | Q27625972 |
| | BAR domains as sensors of membrane curvature: the amphiphysin BAR structure | Q27642663 |
| | Rhodopsin C terminus, the site of mutations causing retinal disease, regulates trafficking by binding to ADP-ribosylation factor 4 (ARF4). | Q27919673 |
| | Vertebrate Smoothened functions at the primary cilium | Q27919682 |
| | A BAR domain in the N terminus of the Arf GAP ASAP1 affects membrane structure and trafficking of epidermal growth factor receptor | Q27919688 |
| | Polycystin-2 traffics to cilia independently of polycystin-1 by using an N-terminal RVxP motif | Q27919692 |
| | Ciliary targeting of olfactory CNG channels requires the CNGB1b subunit and the kinesin-2 motor protein, KIF17. | Q27919701 |
| | Elipsa is an early determinant of ciliogenesis that links the IFT particle to membrane-associated small GTPase Rab8. | Q27919719 |
| | Sequential interactions with Sec23 control the direction of vesicle traffic | Q27929972 |
| | Arf GTPase-activating protein ASAP1 interacts with Rab11 effector FIP3 and regulates pericentrosomal localization of transferrin receptor-positive recycling endosome | Q27967622 |
| | Autoinhibition of Arf GTPase-activating protein activity by the BAR domain in ASAP1 | Q27967632 |
| | Ciliary targeting motif VxPx directs assembly of a trafficking module through Arf4. | Q27967640 |
| | Different roles for KIF17 and kinesin II in photoreceptor development and maintenance | Q27967646 |
| | Intraflagellar transport and the sensory outer segment of vertebrate photoreceptors | Q37167508 |
| | Regulation of sorting and post-Golgi trafficking of rhodopsin by its C-terminal sequence QVS(A)PA. | Q37478322 |
| | Photoreceptor IFT complexes containing chaperones, guanylyl cyclase 1 and rhodopsin. | Q39223997 |
| | Rab11-FIP3 binds dynein light intermediate chain 2 and its overexpression fragments the Golgi complex | Q39730359 |
| | Identification of ciliary localization sequences within the third intracellular loop of G protein-coupled receptors | Q40015719 |
| | Fine structure of a periciliary ridge complex of frog retinal rod cells revealed by ultrahigh resolution scanning electron microscopy. | Q41390141 |
| | Characterization of rhodopsin mis-sorting and constitutive activation in a transgenic rat model of retinitis pigmentosa. | Q41734306 |
| | A molecular network for de novo generation of the apical surface and lumen | Q42116509 |
| | Disease progression in patients with dominant retinitis pigmentosa and rhodopsin mutations | Q44119130 |
| | The carboxyl-terminal domain is essential for rhodopsin transport in rod photoreceptors | Q44955188 |
| | rab8 in retinal photoreceptors may participate in rhodopsin transport and in rod outer segment disk morphogenesis | Q49165645 |
| | Vesicular transport of newly synthesized opsin from the Golgi apparatus toward the rod outer segment. Ultrastructural immunocytochemical and autoradiographic evidence in Xenopus retinas | Q69974905 |
| | Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. Online | Q77214675 |
| | Syntaxin 3 and SNAP-25 pairing, regulated by omega-3 docosahexaenoic acid, controls the delivery of rhodopsin for the biogenesis of cilia-derived sensory organelles, the rod outer segments | Q27967650 |
| | Trafficking to the ciliary membrane: how to get across the periciliary diffusion barrier? | Q27967655 |
| | Coordination of Rab8 and Rab11 in primary ciliogenesis | Q27967674 |
| | A septin diffusion barrier at the base of the primary cilium maintains ciliary membrane protein distribution | Q28000024 |
| | A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition | Q28000057 |
| | A conserved signal and GTPase complex are required for the ciliary transport of polycystin-1. | Q28000060 |
| | A ciliopathy complex at the transition zone protects the cilia as a privileged membrane domain | Q28000085 |
| | Identification and characterization of a family of Rab11-interacting proteins | Q28211889 |
| | Interaction of retinitis pigmentosa GTPase regulator (RPGR) with RAB8A GTPase: implications for cilia dysfunction and photoreceptor degeneration | Q28287923 |
| | Tulp1 is involved in specific photoreceptor protein transport pathways | Q28507721 |
| | IFT20 is required for opsin trafficking and photoreceptor outer segment development | Q28593972 |
| | When cilia go bad: cilia defects and ciliopathies | Q29547198 |
| | The vertebrate primary cilium in development, homeostasis, and disease | Q29614609 |
| | CEP290 tethers flagellar transition zone microtubules to the membrane and regulates flagellar protein content. | Q29614822 |
| | Bi-directional protein transport between the ER and Golgi | Q29615233 |
| | The intraflagellar transport protein, IFT88, is essential for vertebrate photoreceptor assembly and maintenance | Q29620386 |
| | Kinetic analysis of GTP hydrolysis catalysed by the Arf1-GTP-ASAP1 complex | Q30159561 |
| | A primer on vesicle budding | Q33603151 |
| | The cytoplasmic tail of fibrocystin contains a ciliary targeting sequence | Q33616456 |
| | Mutant rab8 Impairs docking and fusion of rhodopsin-bearing post-Golgi membranes and causes cell death of transgenic Xenopus rods | Q33944067 |
| | Evolution: On a bender--BARs, ESCRTs, COPs, and finally getting your coat | Q34027290 |
| | Dysfunction of heterotrimeric kinesin-2 in rod photoreceptor cells and the role of opsin mislocalization in rapid cell death. | Q34360933 |
| | Beyond counting photons: trials and trends in vertebrate visual transduction | Q34465227 |
| | FAPP2, cilium formation, and compartmentalization of the apical membrane in polarized Madin-Darby canine kidney (MDCK) cells. | Q34583202 |
| | Phosphoinositides, ezrin/moesin, and rac1 regulate fusion of rhodopsin transport carriers in retinal photoreceptors | Q34786622 |
| | Arfophilins are dual Arf/Rab 11 binding proteins that regulate recycling endosome distribution and are related to Drosophila nuclear fallout | Q35161159 |
| | Arf GAPs: multifunctional proteins that regulate membrane traffic and actin remodelling | Q35622152 |
| | ARF family G proteins and their regulators: roles in membrane transport, development and disease. | Q35632439 |
| | Steric volume exclusion sets soluble protein concentrations in photoreceptor sensory cilia | Q35657676 |
| | Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segments | Q35947581 |
| | Identification of an outer segment targeting signal in the COOH terminus of rhodopsin using transgenic Xenopus laevis | Q36293695 |
| | Arf GAPs and membrane traffic | Q36428818 |
| | Bardet-Biedl syndrome: an emerging pathomechanism of intracellular transport. | Q36565794 |
| | Light-driven translocation of signaling proteins in vertebrate photoreceptors | Q36601427 |
| | Coats, tethers, Rabs, and SNAREs work together to mediate the intracellular destination of a transport vesicle | Q36815404 |
| P304 | page(s) | 5-10 | |
| P577 | publication date | 2012-08-07 | |
| P1433 | published in | Vision Research | Q1307852 |
| P1476 | title | Molecular assemblies that control rhodopsin transport to the cilia | |
| P478 | volume | 75 | |