Evidence map›Paper›PMID 38558491›Full record

ArticleClinical and experimental dental research2024

Impact of Sonic Hedgehog-dependent sphenoid bone defect on craniofacial growth.

Hélène Guyodo, Aurélie Rizzo, Farah Diab, Fanny Noury, Svetlana Mironov, Marie de Tayrac, Véronique David, Sylvie Odent, Christèle Dubourg, Valérie Dupé

Open access · goldAbstract read
In one paragraph

Article in Clinical and experimental dental research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 2 institutions in 1 country.

Hélène GuyodoUniv Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes)-UMR6290, Rennes, France.
Aurélie RizzoUniv Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes)-UMR6290, Rennes, France.
Farah DiabSorbonne Université, Institut National de la Santé et de la Recherche Médicale (INSERM), "Maladies génétiques d'expression pédiatrique", Paris, France.
Fanny NouryFaculté des Sciences Pharmaceutiques et Biologiques, Univ Rennes, INSERM, LTSI - UMR 1099, Rennes, France.
Svetlana MironovUniv Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes)-UMR6290, Rennes, France.
Marie de TayracUniv Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes)-UMR6290, Rennes, France.
Véronique DavidUniv Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes)-UMR6290, Rennes, France.
Sylvie OdentUniv Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes)-UMR6290, Rennes, France.
Christèle DubourgUniv Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes)-UMR6290, Rennes, France.
Valérie DupéUniv Rennes, CNRS, IGDR (Institut de Génétique et Développement de Rennes)-UMR6290, Rennes, France.ORCID 0000-0003-4859-0612
Centre National de la Recherche Scientifique · FRInserm · FR

Funding

CNRSInsermUniversité de Rennes
6 · The paper itself

Abstract

objectivesThe main objective of this study was to evaluate how an apparently minor anomaly of the sphenoid bone, observed in a haploinsufficient mouse model for Sonic Hedgehog (Shh), affects the growth of the adult craniofacial region. This study aims to provide valuable information to orthodontists when making decisions regarding individuals carrying SHH mutation. MATERIALS AND

methodsThe skulls of embryonic, juvenile and adult mice of two genotypes (Shh heterozygous and wild type) were examined and measured using landmark-based linear dimensions. Additionally, we analysed the clinical characteristics of a group of patients and their relatives with SHH gene mutations.

resultsIn the viable Shh

conclusionHaploinsufficiency of Shh leads to isolated craniofacial skeletal hypoplasia in adult mouse. This finding highlights the importance of radiographic monitoring of the skull base in all individuals with SHH gene mutations.

Indexed as

Hedgehog ProteinsHoloprosencephalyAdultAnimalsHumansMiceMice, Inbred C57BLMutationSphenoid BoneHedgehog ProteinsSHH protein, humanShh protein, mousebasisphenoid bonehypomorphic mouse modelintersphenoid synchondrosissonic hedgehog

Identifiers

PMID38558491
PMCPMC10982674
OpenAlexW4393389793

What OpenQuestion holds

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LicenceCC BY
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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.