Evidence map›Paper›PMID 29464516›Full record

ArticleJournal of molecular neuroscience : MN2018

Quantitative Comparison of Primary Cilia Marker Expression and Length in the Mouse Brain.

Éva Sipos, Sámuel Komoly, Péter Ács

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Article in Journal of molecular neuroscience : MN, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

44 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
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  3. Review
  4. The nociceptor primary cilium.Brain : a journal of neurology · 2026
    Review
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  6. Article
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  16. Parkinsonism Sac domain mutation in Synaptojanin-1 affects ciliary properties in iPSC-derived dopaminergic neurons.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  17. Article
  18. Uncovering cilia function in glial development.Annals of human genetics · 2024
    Review
  19. Article
  20. Article
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

3 authors at 1 institution in 1 country.

Éva SiposDepartment of Neurology, Faculty of Medicine, University of Pécs, Rét utca 2, Pécs, 7623, Hungary. eve.sipos@gmail.com.ORCID http://orcid.org/0000-0002-8168-2271
Sámuel KomolyDepartment of Neurology, Faculty of Medicine, University of Pécs, Rét utca 2, Pécs, 7623, Hungary.
Péter ÁcsDepartment of Neurology, Faculty of Medicine, University of Pécs, Rét utca 2, Pécs, 7623, Hungary.
University of Pecs · HU

Funding

University of Pécs KA-2015-09
6 · The paper itself

Abstract

Primary cilia are small, special cellular organelles that provide important sensory and signaling functions during the development of mammalian organs and coordination of postnatal cellular processes. Dysfunction of primary cilia are thought to be the main cause of ciliopathies, a group of genetic disorders characterized by overlapping developmental defects and prominent neurodevelopmental features. Although, disrupted cilia-linked signaling pathways have been implicated in the regulation of numerous neuronal functions, the precise role of primary cilia in the brain are still unknown. Importantly, studies of recent years have highlighted that different functions of primary cilia are reflected by their diverse morphology and unique signaling components localized in the ciliary membrane. In the present study, we conducted a comparative analysis of the expression pattern, distribution and length of adenylyl cyclase 3, somatostatin receptor 3, and ADP-ribosylation factor-like protein 13B expressing primary cilia in the mouse brain. We show that cilia of neurons and astrocytes display a well characterized distribution and ciliary marker arrangements. Moreover, quantitative comparison of their length, density and occurrence rate revealed that primary cilia exhibit region-specific alternations. In summary, our study provides a comprehensive overview of the cellular organization and morphological traits of primary cilia in regions of the physiological adult mouse brain.

Indexed as

Adenylyl CyclasesADP-Ribosylation FactorsAnimalsAstrocytesBrainCiliaMaleMiceMice, Inbred C57BLNeuronsReceptors, Somatostatinadenylate cyclase 3Adenylyl CyclasesADP-Ribosylation FactorsArl13b protein, mouseReceptors, Somatostatinsomatostatin receptor 3CNSDistributionLengthPrimary cilia marker expression

Identifiers

PMID29464516
OpenAlexW2789417502

What OpenQuestion holds

Textmetadata
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.