Evidence map›Paper›PMID 42748246›Full record

ArticleScience advances2026

PAX3-SIX2 muscle stem cell heterogeneity drives muscle-specific repair dynamics diversification.

Virginia Zoglio, Sarah Chebouti, Fayez Issa, Théo Massard, Benjamin Polin, Sylvie Manin, Pascal Maire, Dawon Choi, Indigo T C Chan, Tom H Cheung and 2 more

Abstract read
In one paragraph

Article in Science advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Virginia ZoglioUniversité Paris-Est Créteil, INSERM, U955 IMRB, F-94010 Créteil, France.ORCID 0009-0006-5585-4232
Sarah CheboutiUniversité Paris-Est Créteil, INSERM, U955 IMRB, F-94010 Créteil, France.
Fayez IssaUniversité Paris-Est Créteil, INSERM, U955 IMRB, F-94010 Créteil, France.
Théo MassardUniversité Paris-Est Créteil, INSERM, U955 IMRB, F-94010 Créteil, France.
Benjamin PolinUniversité Paris-Est Créteil, INSERM, U955 IMRB, F-94010 Créteil, France.
Sylvie ManinUniversité Paris-Est Créteil, INSERM, U955 IMRB, F-94010 Créteil, France.
Pascal MaireUniversité de Paris Cité, Institut Cochin, INSERM, CNRS, Paris, France.ORCID 0000-0001-7795-0029
Dawon ChoiDivision of Life Science, Center for Stem Cell Research, HKUST-Nan Fung Life Sciences Joint Laboratory, State Key Laboratory of Nervous System Disorders, Daniel and Mayce Yu Molecular Neuroscience Center, The Hong Kong University of Science and Technology, Hong Kong, China.ORCID 0009-0009-0457-1410
Indigo T C ChanDivision of Life Science, Center for Stem Cell Research, HKUST-Nan Fung Life Sciences Joint Laboratory, State Key Laboratory of Nervous System Disorders, Daniel and Mayce Yu Molecular Neuroscience Center, The Hong Kong University of Science and Technology, Hong Kong, China.ORCID 0009-0008-5954-3284
Tom H CheungDivision of Life Science, Center for Stem Cell Research, HKUST-Nan Fung Life Sciences Joint Laboratory, State Key Laboratory of Nervous System Disorders, Daniel and Mayce Yu Molecular Neuroscience Center, The Hong Kong University of Science and Technology, Hong Kong, China.ORCID 0000-0003-0796-5406
Joana Esteves de LimaUniversité Paris-Est Créteil, INSERM, U955 IMRB, F-94010 Créteil, France.ORCID 0000-0002-5497-5669
Frederic RelaixUniversité Paris-Est Créteil, INSERM, U955 IMRB, F-94010 Créteil, France.ORCID 0000-0003-1270-1472

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human body contains around 640 distinct muscles, each capable of regeneration following injury through the action of muscle-specific stem cells (MuSCs), that express the transcription factor PAX7. Its paralog, PAX3, a master regulator of embryonic myogenesis, is selectively expressed in a subset of adult quiescent MuSCs. The proportion of PAX3-pos MuSCs varies across muscles. By combining lineage tracing and skeletal muscle injury, we demonstrate that PAX3 drives MuSC diversity and muscle-specific regeneration rates. PAX3-expressing MuSCs display enhanced proliferation and differentiation capacities, enabling a faster response following injury, whereas loss of PAX3 leads to proliferation arrest and cell death. Single-cell RNA-sequencing analyses revealed the specific expression of

Indexed as

Homeodomain ProteinsMuscle, SkeletalPAX3 Transcription FactorRegenerationStem CellsAnimalsCell DifferentiationCell ProliferationMiceMuscle DevelopmentMyoblastsTranscription FactorsHomeodomain ProteinsPax3 protein, mousePAX3 Transcription FactorSix2 protein, mouseTranscription Factors

Identifiers

PMID42748246
PMCPMC13580566

What Socratic 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 Socratic graph.