Evidence map›Paper›PMID 24135424›Full record

ReviewProgress in retinal and eye research2014

Molecular complexes that direct rhodopsin transport to primary cilia.

Jing Wang, Dusanka Deretic

Abstract readReview
In one paragraph

Review in Progress in retinal and eye research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
10.9field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

104 citing papers in PubMed, 149 citations in OpenAlex.

  1. Broadening horizons: Pathogenesis and therapeutics of renal ciliopathies.Journal of cell communication and signaling · 2026
    Review
  2. Review
  3. Review
  4. Ciliary Defects in Inherited Retinal Diseases.Advanced genetics (Hoboken, N.J.) · 2026
    Review
  5. Article
  6. A mutation inMolecular vision · 2026
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Complement Factor H and itsbioRxiv : the preprint server for biology · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. ZebrafishInternational journal of molecular sciences · 2025
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Contribution of intraflagellar transport to compartmentalization and maintenance of the photoreceptor cell.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article

44 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Jing WangDepartment of Surgery, Division of Ophthalmology, University of New Mexico, Albuquerque, NM 87131, USA.
Dusanka DereticDepartment of Surgery, Division of Ophthalmology, University of New Mexico, Albuquerque, NM 87131, USA; Department of Cell Biology and Physiology, University of New Mexico, Albuquerque, NM 87131, USA. Electronic address: dderetic@salud.unm.edu.
University of New Mexico · US

Funding

Rhodopsin Trafficking & Photoreceptor Membrane RenewalR01EY012421 · NEI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI DERETIC, DUSANKA DANIELLE · 1999 to 2023
$7.2M
NEI NIH HHS EY-12421NEI NIH HHS R01 EY012421
6 · The paper itself

Abstract

Rhodopsin is a key molecular constituent of photoreceptor cells, yet understanding of how it regulates photoreceptor membrane trafficking and biogenesis of light-sensing organelles, the rod outer segments (ROS) is only beginning to emerge. Recently identified sequence of well-orchestrated molecular interactions of rhodopsin with the functional networks of Arf and Rab GTPases at multiple stages of intracellular targeting fits well into the complex framework of the biogenesis and maintenance of primary cilia, of which the ROS is one example. This review will discuss the latest progress in dissecting the molecular complexes that coordinate rhodopsin incorporation into ciliary-targeted carriers with the recruitment and activation of membrane tethering complexes and regulators of fusion with the periciliary plasma membrane. In addition to revealing the fundamental principals of ciliary membrane renewal, recent advances also provide molecular insight into the ways by which disruptions of the exquisitely orchestrated interactions lead to cilia dysfunction and result in human retinal dystrophies and syndromic diseases that affect multiple organs, including the eyes.

Indexed as

AnimalsBiological TransportHumansMacromolecular SubstancesPhotoreceptor Connecting CiliumProtein TransportRhodopsinRod Cell Outer SegmentMacromolecular SubstancesRhodopsina conserved complex of BBS proteinsADRPArfsAutosomal Dominant Retinitis PigmentosaBardet-Biedl SyndromeBBSBBSomeCiliary Targeting SignalCiliumCTSDHADocosahexaenoic AcidGAPGC1GEFGTPase Activating ProteinGuanine Nucleotide Exchange FactorGuanylyl Cyclase 1IFTIntraflagellar TransportJBTSJoubert SyndromeMeckel SyndromeMicrotubule Organizing CenterMicrotubulesMKSMTMTOCNephronophthisisNPHPOCTOptical Coherence TomographyPLAProximity Ligation AssayRabsRetinitis Pigmentosa GTPase RegulatorRhodopsinRhodopsin Transport Carrier(s)RISRod Inner Segment(s)Rod Outer Segment(s)ROSRPGRRTC(s)SNARESoluble N-ethylmaleimide-sensitive Factor Attachment Protein ReceptorTGNTraffickingTrans-Golgi Network

Identifiers

PMID24135424
PMCPMC3883129
OpenAlexW2083287420

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.