Evidence map›Paper›PMID 20404140›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

Uncoupling of growth plate maturation and bone formation in mice lacking both Schnurri-2 and Schnurri-3.

Dallas C Jones, Michelle N Schweitzer, Marc Wein, Kirsten Sigrist, Tsuyoshi Takagi, Shunsuke Ishii, Laurie H Glimcher

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. 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
1.5field-weighted citation impact, top 18% 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, 23 citations in OpenAlex.

  1. Trial
  2. Engineering a targeted and safe bone anabolic gene therapy to treat osteoporosis in alveolar bone loss.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  3. Article
  4. Review
  5. WNT-modulating gene silencers as a gene therapy for osteoporosis, bone fracture, and critical-sized bone defects.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  6. Article
  7. Article
  8. Inactivation of Nell-1 in Chondrocytes Significantly Impedes Appendicular Skeletogenesis.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  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

7 authors at 2 institutions in 1 country.

Dallas C JonesDepartment of Immunology and Infectious Disease, Harvard School of Public Health, Boston, MA 02115, USA. djones@hsph.harvard.edu
Michelle N Schweitzer
Marc Wein
Kirsten Sigrist
Tsuyoshi Takagi
Shunsuke Ishii
Laurie H Glimcher
Harvard University · USRagon Institute of MGH, MIT and Harvard · US

Funding

Novel Regulators of Bone FormationR01HD055601 · NICHD · WEILL MEDICAL COLL OF CORNELL UNIV · PI GLIMCHER, LAURIE HOLLIS · 2008 to 2012
$1.4M
Novel Regulators of Osteoblast DifferentiationK99AR055668 · NIAMS · HARVARD SCHOOL OF PUBLIC HEALTH · PI JONES, DALLAS C. · 2008 to 2009
$179k
NIAMS NIH HHS K99 AR055668NIAMS NIH HHS K99AR055668NICHD NIH HHS HD055601NICHD NIH HHS R01 HD055601
6 · The paper itself

Abstract

Formation and remodeling of the skeleton relies on precise temporal and spatial regulation of genes expressed in cartilage and bone cells. Debilitating diseases of the skeletal system occur when mutations arise that disrupt these intricate genetic regulatory programs. Here, we report that mice bearing parallel null mutations in the adapter proteins Schnurri2 (Shn2) and Schnurri3 (Shn3) exhibit defects in patterning of the axial skeleton during embryogenesis. Postnatally, these compound mutant mice develop a unique osteochondrodysplasia. The deletion of Shn2 and Shn3 impairs growth plate maturation during endochondral ossification but simultaneously results in massively elevated trabecular bone formation. Hence, growth plate maturation and bone formation can be uncoupled under certain circumstances. These unexpected findings demonstrate that both unique and redundant functions reside in the Schnurri protein family that are required for proper skeletal patterning and remodeling.

Indexed as

OsteogenesisAnimalsBone DensityDNA-Binding ProteinsGene DosageGene Expression Regulation, DevelopmentalGrowth PlateMiceMice, KnockoutOsteochondrodysplasiasPhenotypeDNA-Binding ProteinsHivep2 protein, mouseSchnurri-3 protein, mouse

Identifiers

PMID20404140
PMCPMC2889532
OpenAlexW2127745370

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.