Evidence map›Paper›PMID 33681195›Full record

ArticleFrontiers in cell and developmental biology2021

Loss of Ciliary Gene

Sandra Schneider, Rossella De Cegli, Jayapriya Nagarajan, Viola Kretschmer, Peter Andreas Matthiessen, Daniela Intartaglia, Nathan Hotaling, Marius Ueffing, Karsten Boldt, Ivan Conte and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  5. Role of Primary Cilia in the Eye.Advances in experimental medicine and biology · 2025
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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

11 authors at 5 institutions in 3 countries.

Sandra SchneiderFaculty of Biology, Institute of Molecular Physiology, Johannes Gutenberg-University, Mainz, Germany.
Rossella De CegliTelethon Institute of Genetics and Medicine, Pozzuoli, Italy.
Jayapriya NagarajanNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, United States.
Viola KretschmerFaculty of Biology, Institute of Molecular Physiology, Johannes Gutenberg-University, Mainz, Germany.
Peter Andreas MatthiessenFaculty of Biology, Institute of Molecular Physiology, Johannes Gutenberg-University, Mainz, Germany.
Daniela IntartagliaTelethon Institute of Genetics and Medicine, Pozzuoli, Italy.
Nathan HotalingNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, United States.
Marius UeffingMedical Bioanalytics, Institute for Ophthalmic Research, Eberhard-Karls University, Tübingen, Germany.
Karsten BoldtMedical Bioanalytics, Institute for Ophthalmic Research, Eberhard-Karls University, Tübingen, Germany.
Ivan ConteTelethon Institute of Genetics and Medicine, Pozzuoli, Italy.
Helen Louise May-SimeraFaculty of Biology, Institute of Molecular Physiology, Johannes Gutenberg-University, Mainz, Germany.
Johannes Gutenberg University Mainz · DENational Institutes of Health · USTelethon Institute Of Genetics And Medicine · ITUniversity of Tübingen · DEUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary cilia are sensory organelles vital for developmental and physiological processes. Their dysfunction causes a range of phenotypes including retinopathies. Although primary cilia have been described in the retinal pigment epithelium (RPE), little is known about their contribution to biological processes within this tissue. Ciliary proteins are increasingly being identified in non-ciliary locations and might carry out additional functions, disruption of which possibly contributes to pathology. The RPE is essential for maintaining photoreceptor cells and visual function. We demonstrate that upon loss of

Indexed as

ciliaciliopathyEpithelial-to-Mesenchym Transition (EMT)genetic diseasemolecular medicineretinal pigment epitheliumRPE

Identifiers

PMID33681195
PMCPMC7930748
OpenAlexW3131706391

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.