Evidence map›Paper›PMID 26250517›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2015

Mesenchymal fibroblast growth factor receptor signaling regulates palatal shelf elevation during secondary palate formation.

Kai Yu, Kannan Karuppaiah, David M Ornitz

Abstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Cleft Palate in Apert Syndrome.Journal of developmental biology · 2022
    Review
  5. Review
  6. The Evaluation ofChildren (Basel, Switzerland) · 2022
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Genetic tools for identifying and manipulating fibroblasts in the mouse.Differentiation; research in biological diversity · 2016
    Review
  13. Article
  14. Article
  15. 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

3 authors at 2 institutions in 1 country.

Kai YuDivision of Craniofacial Medicine, Department of Pediatrics, University of Washington and Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.
Kannan KaruppaiahDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, Missouri.
David M OrnitzDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, Missouri.
Washington University in St. Louis · USSeattle Children's Hospital · US

Funding

FGFs in skeletal development, vasculogenesis and repairR01HD049808 · NICHD · WASHINGTON UNIVERSITY · PI ORNITZ, DAVID M · 2006 to 2016
$2.9M
NICHD NIH HHS HD049808NICHD NIH HHS R01 HD049808
6 · The paper itself

Abstract

backgroundPalatal shelf elevation is an essential morphogenetic process during secondary palate closure and failure or delay of palatal shelf elevation is a common cause of cleft palate, one of the most common birth defects in humans. Here, we studied the role of mesenchymal fibroblast growth factor receptor (FGFR) signaling during palate development by conditional inactivation of Fgfrs using a mesenchyme-specific Dermo1-Cre driver.

resultsWe showed that Fgfr1 is expressed throughout the palatal mesenchyme and Fgfr2 is expressed in the medial aspect of the posterior palatal mesenchyme overlapping with Fgfr1. Mesenchyme-specific disruption of Fgfr1 and Fgfr2 affected palatal shelf elevation and resulted in cleft palate. We further showed that both Fgfr1 and Fgfr2 are expressed in mesenchymal tissues of the mandibular process but display distinct expression patterns. Loss of mesenchymal FGFR signaling reduced mandibular ossification and lower jaw growth resulting in abnormal tongue insertion in the oral-nasal cavity.

conclusionsWe propose a model to explain how redundant Fgfr1 and Fgfr2 expression in the palatal and mandibular mesenchyme regulates shelf medial wall protrusion and growth of the mandible to coordinate the craniofacial tissue movements that are required for palatal shelf elevation.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsCleft PalateGenotypeIn Situ HybridizationMandibleMesodermMiceMice, Inbred C57BLMice, KnockoutMorphogenesisPalatePhenotypeReceptor, Fibroblast Growth Factor, Type 1Receptor, Fibroblast Growth Factor, Type 2Signal TransductionFgfr1 protein, mouseFgfr2 protein, mouseReceptor, Fibroblast Growth Factor, Type 1Receptor, Fibroblast Growth Factor, Type 2cleft palateconditional gene knockoutFGFR gene expressionmandible developmentpalatal shelf elevationsecondary palate development

Identifiers

PMID26250517
PMCPMC4619180
OpenAlexW2138051521

What OpenQuestion holds

Textmetadata
LicenceTDM
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.