Evidence map›Paper›PMID 25158185›Full record

ArticleConnective tissue research2014

Critical role of Bmpr1a in mandibular condyle growth.

Junjun Jing, Robert J Hinton, Yuji Mishina, Ying Liu, Xuedong Zhou, Jian Q Feng

Abstract read
In one paragraph

Article in Connective tissue research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.1field-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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Bone or Tooth dentin: The TGF-β signaling is the key.International journal of biological sciences · 2024
    Article
  6. Article
  7. [Latest Research Findings on the Regulation of Bone Homeostasis by ALK3].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2022
    Review
  8. Review
  9. An ECHO of Cartilage:Frontiers in bioengineering and biotechnology · 2021
    Article
  10. ScxBone · 2021
    Article
  11. Article
  12. IFT20 is required for the maintenance of cartilaginous matrix in condylar cartilage.Biochemical and biophysical research communications · 2019
    Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. 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

6 authors at 3 institutions in 2 countries.

Junjun JingDepartment of Biomedical Sciences, Texas A&M Baylor College of Dentistry , Dallas, TX , USA .
Robert J Hinton
Yuji Mishina
Ying Liu
Xuedong Zhou
Jian Q Feng
Sichuan University · CNState Key Laboratory of Oral DiseasesUniversity of Michigan–Ann Arbor · US

Funding

DMP1 Mutations: Defects in OdontogenesisR01DE018486 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI FENG, JIAN Q. · 2008 to 2012
$1.7M
Tooth Root Formation: An Emerging Signaling PathwayR56DE022789 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI FENG, JIAN Q. · 2013 to 2013
$291k
NIDCR NIH HHS DE018486NIDCR NIH HHS R01 DE018486NIDCR NIH HHS R56 DE022789NIDCR NIH HHS R56DE022789
6 · The paper itself

Abstract

The importance of Bone Morphogenetic Proteins (BMPs) in the regulation of cell fate, differentiation and proliferation in the growth plate is well-known. However, in secondary cartilages (such as that in the temporomandibular joint) that grow by proliferation of prechondrocytes and differ in their pattern of growth, the role of BMPs is largely unexplored. To examine this question, we ablated Bmpr1a in the condylar cartilage of neonatal mice and assessed the consequences for mandibular condyle growth and organization at intervals over the ensuing 4 weeks. Bmpr1a deficiency caused significant chondrodysplasia and almost eliminated the chondrocytic phenotype in the TMJ. Expression of Sox9, collagen II, proteoglycan were all greatly reduced, and cell proliferation as detected by BrdU was almost non-existent in the knockout mice. Primary bone spongiosa formation was also disturbed and was accompanied by reduced Osterix expression. These findings strongly suggest that Bmpr1a is critical for the development and growth of the mandibular condyle via its effect on proliferation of prechondroblasts and chondrocyte differentiation.

Indexed as

AnimalsBone Morphogenetic Protein Receptors, Type ICartilageCell DifferentiationChondrogenesisGene Expression Regulation, DevelopmentalGrowth PlateMandibular CondyleMiceMice, KnockoutTemporomandibular JointBmpr1a protein, mouseBone Morphogenetic Protein Receptors, Type IBmpr1acondylar cartilageendochondral ossificationmandibular condyle

Identifiers

PMID25158185
PMCPMC4638146
OpenAlexW1986625894

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.