Evidence map›Paper›PMID 16441561›Full record

ArticleJournal of anatomy2006

An in situ hybridization study of Runx2, Osterix, and Sox9 at the onset of condylar cartilage formation in fetal mouse mandible.

Shunichi Shibata, Naoto Suda, Shoichi Suzuki, Hiroki Fukuoka, Yasuo Yamashita

Open access · greenAbstract read
In one paragraph

Article in Journal of anatomy, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 12% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

  1. Pooled it
  2. Article
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  7. Toward zonally tailored scaffolds for osteochondral differentiation of synovial mesenchymal stem cells.Journal of biomedical materials research. Part B, Applied biomaterials · 2019
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  13. Continuous hydrostatic pressure induces differentiation phenomena in chondrocytes mediated by changes in polycystins, SOX9, and RUNX2.Journal of orofacial orthopedics = Fortschritte der Kieferorthopadie : Organ/official journal Deutsche Gesellschaft fur Kieferorthopadie · 2017
    Article
  14. Review
  15. Article
  16. Mandible and Tongue Development.Current topics in developmental biology · 2015
    Review
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  19. 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.

Shunichi ShibataMaxillofacial Anatomy, Department of Maxillofacial Biology, Tokyo Medical and Dental University, Japan. S.Shibata.mfa@tmd.ac.jp
Naoto Suda
Shoichi Suzuki
Hiroki Fukuoka
Yasuo Yamashita
Tokyo Medical and Dental University · JPNational Medical Research Center of Dentistry and Maxillofacial Surgery · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mandibular condylar cartilage is the principal secondary cartilage, differing from primary cartilage in its rapid differentiation from progenitor cells (preosteoblasts/skeletoblasts) to hypertrophic chondrocytes. The expression of three transcription factors related to bone and cartilage formation, namely Runx2, Osterix and Sox9, was investigated at the onset of mouse mandibular condylar cartilage formation by in situ hybridization. Messenger RNAs for these three molecules were expressed in the condylar anlage, consisting of preosteoblasts/skeletoblasts, at embryonic day (E)14. Hypertrophic chondrocytes appeared at E15 as soon as cartilage tissue appeared. Runx2 mRNA was expressed in the embryonic zone at the posterior position of the newly formed cartilage, in the bone collar and in the newly formed cartilage, but expression intensity in the newly formed cartilage was slightly weaker. Osterix mRNA was also expressed in the embryonic zone and in the bone collar, but was at markedly lower levels in the newly formed cartilage. Sox9 mRNA was continuously expressed from the embryonic zone to the newly formed cartilage. At this stage, Sox5 mRNA was expressed only in the newly formed cartilage. These results suggest that reduced expression of Osterix in combination with Sox9-Sox5 expression is important for the onset of condylar (secondary) cartilage formation.

Indexed as

AnimalsCartilage, ArticularCore Binding Factor Alpha 1 SubunitFemaleFetal DevelopmentHigh Mobility Group ProteinsIn Situ HybridizationMandibular CondyleMesodermMiceMice, Inbred ICRPregnancyRNA, MessengerRNA ProbesSOX9 Transcription FactorSp7 Transcription FactorCore Binding Factor Alpha 1 SubunitHigh Mobility Group ProteinsRNA, MessengerRNA ProbesSox9 protein, mouseSOX9 Transcription FactorSp7 protein, mouseSp7 Transcription FactorTranscription Factors

Identifiers

PMID16441561
PMCPMC2100199
OpenAlexW1993769414

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.