Evidence map›Paper›PMID 28954202›Full record

ArticleJournal of dental research2018

Ciliopathy Protein Tmem107 Plays Multiple Roles in Craniofacial Development.

P Cela, M Hampl, N A Shylo, K J Christopher, M Kavkova, M Landova, T Zikmund, S D Weatherbee, J Kaiser, M Buchtova

Open access · greenAbstract read
In one paragraph

Article in Journal of dental research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

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  12. Transcriptome profiling in swine macrophages infected with African swine fever virus at single-cell resolution.Proceedings of the National Academy of Sciences of the United States of America · 2022
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  18. Mouse genetics reveals Barttin as a genetic modifier of Joubert syndrome.Proceedings of the National Academy of Sciences of the United States of America · 2020
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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

10 authors at 4 institutions in 2 countries.

P Cela1 Institute of Animal Physiology and Genetics, CAS, Brno, Czech Republic.
M Hampl1 Institute of Animal Physiology and Genetics, CAS, Brno, Czech Republic.
N A Shylo4 Department of Genetics, Yale University, School of Medicine, New Haven, CT, USA.
K J Christopher4 Department of Genetics, Yale University, School of Medicine, New Haven, CT, USA.
M Kavkova5 CEITEC-Central European Institute of Technology, Brno University of Technology, Brno, Czech Republic.
M Landova1 Institute of Animal Physiology and Genetics, CAS, Brno, Czech Republic.
T Zikmund5 CEITEC-Central European Institute of Technology, Brno University of Technology, Brno, Czech Republic.
S D Weatherbee4 Department of Genetics, Yale University, School of Medicine, New Haven, CT, USA.
J Kaiser5 CEITEC-Central European Institute of Technology, Brno University of Technology, Brno, Czech Republic.
M Buchtova1 Institute of Animal Physiology and Genetics, CAS, Brno, Czech Republic.
Central European Institute of Technology · CZYale University · USCzech Academy of Sciences, Institute of Animal Physiology and Genetics · CZMasaryk University · CZ

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007499 · NIGMS · YALE UNIVERSITY · PI CARLSON, JOHN R, REINKE, VALERIE J · 1985 to 2022
$13.9M
Skin Development Analysis in Mutant Mouse LinesR01AR059687 · NIAMS · YALE UNIVERSITY · PI WEATHERBEE, SCOTT DONALD · 2011 to 2015
$1.8M
NIAMS NIH HHS R01 AR059687NIGMS NIH HHS T32 GM007499
6 · The paper itself

Abstract

A broad spectrum of human diseases called ciliopathies is caused by defective primary cilia morphology or signal transduction. The primary cilium is a solitary organelle that responds to mechanical and chemical stimuli from extracellular and intracellular environments. Transmembrane protein 107 (TMEM107) is localized in the primary cilium and is enriched at the transition zone where it acts to regulate protein content of the cilium. Mutations in TMEM107 were previously connected with oral-facial-digital syndrome, Meckel-Gruber syndrome, and Joubert syndrome exhibiting a range of ciliopathic defects. Here, we analyze a role of Tmem107 in craniofacial development with special focus on palate formation, using mouse embryos with a complete knockout of Tmem107. Tmem107

Indexed as

AnimalsCiliaCleft LipCraniofacial AbnormalitiesFacial BonesMaxillofacial DevelopmentMembrane ProteinsMiceMice, KnockoutNeural Tube DefectsPalateSkullSOX Transcription FactorsMembrane ProteinsSOX Transcription FactorsTmem107 protein, mousecell signalingcraniofacial anomaliesgrowth/developmentmineralized tissue/developmentoral pathologyorofacial clefts

Identifiers

PMID28954202
PMCPMC5755812
OpenAlexW2756513945

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.