Evidence map›Paper›PMID 31961320›Full record

ArticleeLife2020

Tgfβ signaling is critical for maintenance of the tendon cell fate.

Guak-Kim Tan, Brian A Pryce, Anna Stabio, John V Brigande, ChaoJie Wang, Zheng Xia, Sara F Tufa, Douglas R Keene, Ronen Schweitzer

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
11.6field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 89 citations in OpenAlex.

  1. Review
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  11. A role for TGFβ signaling in Gli1+ tendon and enthesis cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  12. Article
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  14. Lack of skeletal muscle contraction disrupts fibrous tissue morphogenesis in the developing murine knee.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2023
    Article
  15. PAI-1 mediates TGF-β1-induced myofibroblast activation in tenocytes via mTOR signaling.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2023
    Article
  16. 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

9 authors at 2 institutions in 1 country.

Guak-Kim TanResearch Division, Shriners Hospital for Children, Portland, United States.
Brian A PryceResearch Division, Shriners Hospital for Children, Portland, United States.
Anna StabioResearch Division, Shriners Hospital for Children, Portland, United States.
John V BrigandeOregon Hearing Research Center, Oregon Health & Science University, Portland, United States.
ChaoJie WangComputational Biology Program, Oregon Health & Science University, Portland, United States.
Zheng XiaComputational Biology Program, Oregon Health & Science University, Portland, United States.
Sara F TufaResearch Division, Shriners Hospital for Children, Portland, United States.
Douglas R KeeneResearch Division, Shriners Hospital for Children, Portland, United States.
Ronen SchweitzerResearch Division, Shriners Hospital for Children, Portland, United States.ORCID 0000-0002-7425-5028
Shriners Hospitals for Children - Portland · USOregon Health & Science University · US

Funding

Transcriptional regulation of tendon differentiation and matrix formationR01AR055973 · NIAMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI SCHWEITZER, RONEN · 2010 to 2014
$1.7M
Fetal Pharmacotherapy for Congenital DeafnessR01DC014160 · NIDCD · OREGON HEALTH & SCIENCE UNIVERSITY · PI BRIGANDE, JOHN VINCENT · 2014 to 2018
$1.6M
Maintenance and Regulation of Tendon and Ligament Maturation by TGFbeta SignalingR01AR067211 · NIAMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI SCHWEITZER, RONEN · 2016 to 2020
$1.5M
NIAMS NIH HHS R01 AR055973NIAMS NIH HHS R01 AR067211NIDCD NIH HHS R01 DC014160Shriners Hospitals for Children SHC 5410-POR-14
6 · The paper itself

Abstract

Studies of cell fate focus on specification, but little is known about maintenance of the differentiated state. In this study, we find that the mouse tendon cell fate requires continuous maintenance in vivo and identify an essential role for TGFβ signaling in maintenance of the tendon cell fate. To examine the role of TGFβ signaling in tenocyte function the TGFβ type II receptor (

Indexed as

AnimalsCell DedifferentiationCell LineageGene Expression RegulationMiceMutationReceptor, Transforming Growth Factor-beta Type IISignal TransductionStem CellsTendonsTenocytesTransforming Growth Factor betaReceptor, Transforming Growth Factor-beta Type IITransforming Growth Factor betacell biologycell fatededifferentiationdevelopmental biologymouseScleraxistendontendon degenerationTGF-beta signaling

Identifiers

PMID31961320
PMCPMC7025861
OpenAlexW3002549370

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.