Evidence map›Paper›PMID 23567335›Full record

ReviewSmall GTPases

Crosstalk of Arf and Rab GTPases en route to cilia.

Dusanka Deretic

Open access · hybridAbstract readReview
In one paragraph

Review in Small GTPases. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

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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

1 author at 1 institution in 1 country.

Dusanka DereticDepartment of Surgery, Division of Ophthalmology, University of New Mexico, Albuquerque, NM, USA. 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

Small GTPases are versatile temporal and spatial regulators of virtually all cellular processes including signal transduction, cytoskeleton dynamics and membrane trafficking. They function as molecular switches, aided by a multitude of regulatory and effector proteins that link them into functional networks. A picture is beginning to emerge whereupon scaffold proteins with many functional domains perform the regulatory and effector functions, thus allowing the ordered recruitment and activation of small GTPases. This leads to the formation of scaffolding patches that coordinate cargo concentration and capture, with the recruitment and activation of the membrane tethering complexes and fusion regulators. This review will focus on the crosstalk of Arf and Rab GTPases at the Golgi complex and the scaffolds that facilitate their activation during trafficking of sensory receptors to primary cilia. The evolutionary conservation of the GTPase cascades in ciliogenesis and yeast budding will be discussed.

Indexed as

ADP-Ribosylation FactorsAnimalsCiliaGolgi ApparatusHumansProtein Transportrab GTP-Binding ProteinsADP-Ribosylation Factorsrab GTP-Binding ProteinsArf GTPasesciliumGolgimembrane traffickingRab GTPases

Identifiers

PMID23567335
PMCPMC3747259
OpenAlexW2053068636

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.