Evidence map›Paper›PMID 28360863›Full record

ArticleFrontiers in physiology2017

Differences in Oral Structure and Tissue Interactions during Mouse vs. Human Palatogenesis: Implications for the Translation of Findings from Mice.

Kai Yu, Mei Deng, Theresa Naluai-Cecchini, Ian A Glass, Timothy C Cox

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2017. 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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  7. Immortalization of patient-derived lip cells for establishing 3D lip models.Frontiers in cell and developmental biology · 2024
    Article
  8. Article
  9. Single cell sequencing of the mouse anterior palate reveals mesenchymal heterogeneity.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
    Article
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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

5 authors at 2 institutions in 2 countries.

Kai YuDepartment of Pediatrics, Division of Craniofacial Medicine, University of WashingtonSeattle, WA, USA; Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research InstituteSeattle, WA, USA.
Mei DengBirth Defects Research Laboratory, Department of Pediatrics, University of Washington Seattle, WA, USA.
Theresa Naluai-CecchiniBirth Defects Research Laboratory, Department of Pediatrics, University of Washington Seattle, WA, USA.
Ian A GlassBirth Defects Research Laboratory, Department of Pediatrics, University of Washington Seattle, WA, USA.
Timothy C CoxDepartment of Pediatrics, Division of Craniofacial Medicine, University of WashingtonSeattle, WA, USA; Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research InstituteSeattle, WA, USA; Department of Anatomy and Developmental Biology, Monash UniversityClayton, VIC, Australia.
University of Washington · USSeattle Children's Hospital · US

Funding

LABORATORY OF DEVELOPMENTAL BIOLOGYR24HD000836 · NICHD · UNIVERSITY OF WASHINGTON · PI Ian Amos Glass · 1995 to 2026
$16.9M
Intellectual and Developmental Disabilities Research CenterU54HD083091 · NICHD · UNIVERSITY OF WASHINGTON · PI DOHERTY, DANIEL · 2014 to 2019
$7.9M
Genetic and developmental pathways causing midface hypoplasiaR01DE022561 · NIDCR · SEATTLE CHILDREN'S HOSPITAL · PI COX, TIMOTHY CHILTON · 2012 to 2016
$3.3M
The Role of Hyaluronic Acid in Regulating Palate Morphogenesis During Secondary Palate ClosureR03DE025077 · NIDCR · SEATTLE CHILDREN'S HOSPITAL · PI YU, KAI · 2016 to 2017
$289k
NICHD NIH HHS R24 HD000836NICHD NIH HHS U54 HD083091NIDCR NIH HHS R01 DE022561NIDCR NIH HHS R03 DE025077
6 · The paper itself

Abstract

Clefting of the secondary palate is one of the most common human birth defects and results from failure of the palatal shelves to fuse during embryonic development. Palatogenesis is traditionally considered to be a highly conserved developmental process among mammalian species. However, cleft palate phenotypes in humans are considerably more variable than those seen in mice, the most common animal model for studying palatal development and pathogenesis of cleft palate. In this investigation, we utilized macroscopic observations, histology and 3D imaging techniques to directly compare palate morphology and the oral-nasal cavity during palate closure in mouse embryos and human conceptuses. We showed that mouse and human palates display distinct morphologies attributable to the structural differences of the oral-nasal cavity. We further showed that the palatal shelves interact differently with the primary palate and nasal septum in the hard palate region and with pharyngeal walls in the soft palate region during palate closure in mice and humans. Knowledge of these morphological differences is important for improved translation of findings in mouse models of human cleft lip/palate and, as such, should ultimately enhance our understanding of human palatal morphogenesis and the pathogenesis of cleft lip/palate in humans.

Indexed as

cleft palatehard palatehuman developmentmouse modelsnasal septumpalatogenesissoft palateuvula

Identifiers

PMID28360863
PMCPMC5350148
OpenAlexW2603202727

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.