Evidence map›Paper›PMID 32019766›Full record

ArticleLife science alliance2020

Metabolic reprogramming of fibro/adipogenic progenitors facilitates muscle regeneration.

Alessio Reggio, Marco Rosina, Natalie Krahmer, Alessandro Palma, Lucia Lisa Petrilli, Giuliano Maiolatesi, Giorgia Massacci, Illari Salvatori, Cristiana Valle, Stefano Testa and 5 more

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 57 citations in OpenAlex.

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  10. PdgfrαGenes & diseases · 2025
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  15. Article
  16. MuSCs and IPCs: roles in skeletal muscle homeostasis, aging and injury.Cellular and molecular life sciences : CMLS · 2024
    Review
  17. Review
  18. 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

15 authors at 4 institutions in 2 countries.

Alessio ReggioDepartment of Biology, University of Rome Tor Vergata, Rome, Italy.ORCID 0000-0001-5333-7502
Marco RosinaDepartment of Biology, University of Rome Tor Vergata, Rome, Italy.ORCID 0000-0003-0952-1710
Natalie KrahmerDepartment Proteomics and Signal Transduction, Max-Planck Institute of Biochemistry, Martinsried, Germany.
Alessandro PalmaDepartment of Biology, University of Rome Tor Vergata, Rome, Italy.ORCID 0000-0003-1300-5479
Lucia Lisa PetrilliDepartment of Biology, University of Rome Tor Vergata, Rome, Italy.ORCID 0000-0001-6453-3031
Giuliano MaiolatesiDepartment of Biology, University of Rome Tor Vergata, Rome, Italy.
Giorgia MassacciDepartment of Biology, University of Rome Tor Vergata, Rome, Italy.ORCID 0000-0003-3223-6547
Illari SalvatoriFondazione Santa Lucia Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome, Italy.ORCID 0000-0001-9700-1269
Cristiana ValleFondazione Santa Lucia Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome, Italy.ORCID 0000-0002-0914-6511
Stefano TestaDepartment of Biology, University of Rome Tor Vergata, Rome, Italy.
Cesare GargioliDepartment of Biology, University of Rome Tor Vergata, Rome, Italy.ORCID 0000-0003-1742-3969
Claudia FuocoDepartment of Biology, University of Rome Tor Vergata, Rome, Italy.ORCID 0000-0001-8372-305X
Luisa CastagnoliDepartment of Biology, University of Rome Tor Vergata, Rome, Italy castagnoli@uniroma2.it.
Gianni CesareniDepartment of Biology, University of Rome Tor Vergata, Rome, Italy cesareni@uniroma2.it.ORCID 0000-0002-9528-6018
Francesca SaccoDepartment of Biology, University of Rome Tor Vergata, Rome, Italy francesca.sacco@uniroma2.it.ORCID 0000-0001-5586-9529
University of Rome Tor Vergata · ITFondazione Santa Lucia · ITIstituto di Farmacologia Traslazionale · ITMax Planck Institute of Biochemistry · DE

Funding

European Research Council 322749
6 · The paper itself

Abstract

In Duchenne muscular dystrophy (DMD), the absence of the dystrophin protein causes a variety of poorly understood secondary effects. Notably, muscle fibers of dystrophic individuals are characterized by mitochondrial dysfunctions, as revealed by a reduced ATP production rate and by defective oxidative phosphorylation. Here, we show that in a mouse model of DMD (

Indexed as

AdipogenesisAnimalsCell DifferentiationCells, CulturedDiet, High-FatDisease Models, AnimalDystrophinMaleMiceMice, Inbred C57BLMice, Inbred mdxMuscle Fibers, SkeletalMuscle, SkeletalMuscular Dystrophy, DuchenneMyoblastsProteomicsDystrophin

Identifiers

PMID32019766
PMCPMC7003708
OpenAlexW3005137977

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.