Evidence map›Paper›PMID 37863656›Full record

ArticleLife science alliance2023

Role of ciliopathy protein TMEM107 in eye development: insights from a mouse model and retinal organoid.

Marija Dubaic, Lucie Peskova, Marek Hampl, Kamila Weissova, Canan Celiker, Natalia A Shylo, Eva Hruba, Michaela Kavkova, Tomas Zikmund, Scott D Weatherbee and 3 more

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. A human-specificMolecular therapy. Nucleic acids · 2025
    Article
  5. Review
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

13 authors at 5 institutions in 2 countries.

Marija DubaicLaboratory of Molecular Morphogenesis, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, Brno, Czech Republic.
Lucie PeskovaDepartment of Histology and Embryology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Marek HamplLaboratory of Molecular Morphogenesis, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, Brno, Czech Republic.
Kamila WeissovaLaboratory of Molecular Morphogenesis, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, Brno, Czech Republic.ORCID https://orcid.org/0000-0002-3023-4751
Canan CelikerDepartment of Histology and Embryology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Natalia A ShyloDepartment of Genetics, Yale University, School of Medicine, New Haven, CT, USA.
Eva HrubaLaboratory of Molecular Morphogenesis, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, Brno, Czech Republic.
Michaela KavkovaCEITEC - Central European Institute of Technology, Brno University of Technology, Brno, Czech Republic.
Tomas ZikmundCEITEC - Central European Institute of Technology, Brno University of Technology, Brno, Czech Republic.
Scott D WeatherbeeDepartment of Genetics, Yale University, School of Medicine, New Haven, CT, USA.ORCID https://orcid.org/0000-0002-0915-1329
Jozef KaiserCEITEC - Central European Institute of Technology, Brno University of Technology, Brno, Czech Republic.
Tomas BartaLaboratory of Molecular Morphogenesis, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, Brno, Czech Republic tbarta@med.muni.cz.ORCID https://orcid.org/0000-0003-0703-066X
Marcela BuchtovaLaboratory of Molecular Morphogenesis, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, Brno, Czech Republic buchtova@iach.cz.ORCID https://orcid.org/0000-0002-0262-6774
Czech Academy of Sciences · CZBrno University of Technology · CZMasaryk University · CZFairfield University · USStowers Institute for Medical Research · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary cilia are cellular surface projections enriched in receptors and signaling molecules, acting as signaling hubs that respond to stimuli. Malfunctions in primary cilia have been linked to human diseases, including retinopathies and ocular defects. Here, we focus on TMEM107, a protein localized to the transition zone of primary cilia. TMEM107 mutations were found in patients with Joubert and Meckel-Gruber syndromes. A mouse model lacking

Indexed as

Ciliary Motility DisordersPolycystic Kidney DiseasesRetinitis PigmentosaAnimalsFemaleHumansMembrane ProteinsMicePregnancyRetinaMembrane ProteinsTMEM107 protein, humanTmem107 protein, mouse

Identifiers

PMID37863656
PMCPMC10589122
OpenAlexW4387805845

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.