Evidence map›Paper›PMID 41550718›Full record

ArticleiScience2026

Identification of skeletal muscle stem cell adhesion motifs using spot-synthesis-based peptide arrays.

Elizabeth Leblanc, Svenja C Schüler, Yuguo Liu, Léa Théroux, Emmeran Le Moal, Marc-André Bonin, Pierre-Luc Boudreault, C Florian Bentzinger

Abstract read
In one paragraph

Article in iScience, 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

8 authors.

Elizabeth LeblancDépartement de Pharmacologie-Physiologie, Institut de Pharmacologie de Sherbrooke, Centre de Recherche Du Centre Hospitalier Universitaire de Sherbrooke, Faculté de Médecine et des Sciences de La Santé, Université de Sherbrooke, Sherbrooke, QC, Canada.
Svenja C SchülerDépartement de Pharmacologie-Physiologie, Institut de Pharmacologie de Sherbrooke, Centre de Recherche Du Centre Hospitalier Universitaire de Sherbrooke, Faculté de Médecine et des Sciences de La Santé, Université de Sherbrooke, Sherbrooke, QC, Canada.
Yuguo LiuDépartement de Pharmacologie-Physiologie, Institut de Pharmacologie de Sherbrooke, Centre de Recherche Du Centre Hospitalier Universitaire de Sherbrooke, Faculté de Médecine et des Sciences de La Santé, Université de Sherbrooke, Sherbrooke, QC, Canada.
Léa ThérouxDépartement de Pharmacologie-Physiologie, Institut de Pharmacologie de Sherbrooke, Centre de Recherche Du Centre Hospitalier Universitaire de Sherbrooke, Faculté de Médecine et des Sciences de La Santé, Université de Sherbrooke, Sherbrooke, QC, Canada.
Emmeran Le MoalDépartement de Pharmacologie-Physiologie, Institut de Pharmacologie de Sherbrooke, Centre de Recherche Du Centre Hospitalier Universitaire de Sherbrooke, Faculté de Médecine et des Sciences de La Santé, Université de Sherbrooke, Sherbrooke, QC, Canada.
Marc-André BoninDépartement de Pharmacologie-Physiologie, Institut de Pharmacologie de Sherbrooke, Centre de Recherche Du Centre Hospitalier Universitaire de Sherbrooke, Faculté de Médecine et des Sciences de La Santé, Université de Sherbrooke, Sherbrooke, QC, Canada.
Pierre-Luc BoudreaultDépartement de Pharmacologie-Physiologie, Institut de Pharmacologie de Sherbrooke, Centre de Recherche Du Centre Hospitalier Universitaire de Sherbrooke, Faculté de Médecine et des Sciences de La Santé, Université de Sherbrooke, Sherbrooke, QC, Canada.
C Florian BentzingerDépartement de Pharmacologie-Physiologie, Institut de Pharmacologie de Sherbrooke, Centre de Recherche Du Centre Hospitalier Universitaire de Sherbrooke, Faculté de Médecine et des Sciences de La Santé, Université de Sherbrooke, Sherbrooke, QC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Altered interactions with the extracellular matrix (ECM) represent a root cause of skeletal muscle stem cell (MuSC) dysfunction in aging and disease, underscoring the therapeutic potential of targeting adhesion receptors. Here, we describe the development of an approach for the medium-throughput screening of bioactive ECM-derived adhesion motifs using peptide arrays generated by highly parallel SPOT synthesis. Based on a library of ∼50 peptide sequences originating from ECM proteins, we identified several candidate motifs that robustly enhance the adhesion of MuSC-derived cells. We demonstrate that these peptide motifs can improve the

Indexed as

BiotechnologyCell biology

Identifiers

PMID41550718
PMCPMC12808901

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Registered trials

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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.