Evidence map›Paper›PMID 29084951›Full record

ArticleNature communications2017

Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb development.

Pedro Vallecillo-García, Mickael Orgeur, Sophie Vom Hofe-Schneider, Jürgen Stumm, Verena Kappert, Daniel M Ibrahim, Stefan T Börno, Shinichiro Hayashi, Frédéric Relaix, Katrin Hildebrandt and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

70 citing papers in PubMed, 133 citations in OpenAlex.

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10 more citing papers are in PubMed but not listed here.

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

17 authors at 6 institutions in 2 countries.

Pedro Vallecillo-GarcíaInstitute for Chemistry and Biochemistry, Freie Universität Berlin, D-14195, Berlin, Germany.ORCID http://orcid.org/0000-0001-6833-5972
Mickael OrgeurInstitute for Chemistry and Biochemistry, Freie Universität Berlin, D-14195, Berlin, Germany.
Sophie Vom Hofe-SchneiderInstitute for Chemistry and Biochemistry, Freie Universität Berlin, D-14195, Berlin, Germany.ORCID http://orcid.org/0000-0003-4874-6971
Jürgen StummInstitute for Chemistry and Biochemistry, Freie Universität Berlin, D-14195, Berlin, Germany.
Verena KappertInstitute for Chemistry and Biochemistry, Freie Universität Berlin, D-14195, Berlin, Germany.
Daniel M IbrahimMax Planck Institute for Molecular Genetics, D-14195, Berlin, Germany.ORCID http://orcid.org/0000-0002-0019-3354
Stefan T BörnoMax Planck Institute for Molecular Genetics, D-14195, Berlin, Germany.
Shinichiro HayashiInserm, IMRB U955-E10, F-94000, Créteil, France.
Frédéric RelaixInserm, IMRB U955-E10, F-94000, Créteil, France.
Katrin HildebrandtInstitute for Biochemistry, University of Cologne, D-50931, Cologne, Germany.
Gerhard SengleInstitute for Biochemistry, University of Cologne, D-50931, Cologne, Germany.
Manuel KochInstitute for Biochemistry, University of Cologne, D-50931, Cologne, Germany.ORCID http://orcid.org/0000-0002-2962-7814
Bernd TimmermannMax Planck Institute for Molecular Genetics, D-14195, Berlin, Germany.
Giovanna MarazziStem Cells and Regenerative Medicine, ICAN-UMRS 1166, Université de Pierre et Marie Curie, Sorbonne Universités, F-75634, Paris, France.
David A SassoonStem Cells and Regenerative Medicine, ICAN-UMRS 1166, Université de Pierre et Marie Curie, Sorbonne Universités, F-75634, Paris, France.
Delphine DuprezSorbonne Universités, UPMC Univ Paris 06, CNRS UMR7622, IBPS-Developmental Biology Laboratory, F-75005, Paris, France.ORCID http://orcid.org/0000-0003-0248-7417
Sigmar StrickerInstitute for Chemistry and Biochemistry, Freie Universität Berlin, D-14195, Berlin, Germany. sigmar.stricker@fu-berlin.de.ORCID http://orcid.org/0000-0002-7174-5363
Max Planck Institute for Molecular Genetics · DEUniversity of Cologne · DECentre National de la Recherche Scientifique · FRInserm · FRSorbonne Université · FRFreie Universität Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibro-adipogenic progenitors (FAPs) are an interstitial cell population in adult skeletal muscle that support muscle regeneration. During development, interstitial muscle connective tissue (MCT) cells support proper muscle patterning, however the underlying molecular mechanisms are not well understood and it remains unclear whether adult FAPs and embryonic MCT cells share a common lineage. We show here that mouse embryonic limb MCT cells expressing the transcription factor Osr1, differentiate into fibrogenic and adipogenic cells in vivo and in vitro defining an embryonic FAP-like population. Genetic lineage tracing shows that developmental Osr1

Indexed as

Muscle DevelopmentAgingAnimalsBody PatterningConnective TissueEmbryo, MammalianExtracellular Matrix ProteinsExtremitiesGene Expression RegulationMiceMyoblastsSignal TransductionTranscription Factor 4Transcription FactorsExtracellular Matrix ProteinsOsr1 protein, mouseTcf4 protein, mouseTranscription Factor 4Transcription Factors

Identifiers

PMID29084951
PMCPMC5662571
OpenAlexW2766765760

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.