Evidence map›Paper›PMID 37307827›Full record

ArticleAging and disease2024

ROR2-Related Skeletal Dysplasia Reveals Disrupted Chondrocyte Polarity through Modulation of BMP/TGF-β Signaling.

Yichen Yao, Xin Wang, Lichieh Lin, Xiaolei Zhang, Yan Wang

Open access · goldAbstract read
In one paragraph

Article in Aging and disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Loss of Stat3 in Prx1Advanced biology · 2025
    Article
  5. Review
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.

Yichen YaoHospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, China.
Xin WangDepartment of Medicine, Harvard Medical School, Boston, MA, USA.
Lichieh LinHospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, China.
Xiaolei ZhangDepartment of Stomatology, the Eighth Affiliated Hospital, Sun Yat-sen University, Shen Zhen, Guangdong, China.
Yan WangHospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, China.
Sun Yat-sen University · CNBrigham and Women's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic studies have shown that Robinow syndrome (RS), a rare skeletal dysplasia, is caused by ROR2 mutation. However, the cell origin and molecular mechanisms underlying this disease remain elusive. We established a conditional knockout system by crossing Prx1cre and Osxcre with Ror2

Indexed as

ChondrocytesCraniofacial AbnormalitiesDwarfismLimb Deformities, CongenitalOsteogenesisUrogenital AbnormalitiesAnimalsCell DifferentiationMiceOsteoblastsTransforming Growth Factor betaTransforming Growth Factor beta

Identifiers

PMID37307827
PMCPMC10796094
OpenAlexW4380422208

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.