Evidence map›Paper›PMID 23560812›Full record

ReviewThe FEBS journal2013

Recent progress in satellite cell/myoblast engraftment -- relevance for therapy.

Deborah Briggs, Jennifer E Morgan

Open access · hybridAbstract readReview
In one paragraph

Review in The FEBS journal, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 89 citations in OpenAlex.

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  13. Stem cell therapy for muscular dystrophies.The Journal of clinical investigation · 2020
    Review
  14. 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

2 authors at 1 institution in 1 country.

Deborah BriggsThe Dubowitz Neuromuscular Centre, UCL Institute of Child Health, London, UK.
Jennifer E Morgan
University College London · GB

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council MR/K000608/1Wellcome Trust
6 · The paper itself

Abstract

There is currently no cure for muscular dystrophies, although several promising strategies are in basic and clinical research. One such strategy is cell transplantation with satellite cells (or their myoblast progeny) to repair damaged muscle and provide dystrophin protein with the aim of preventing subsequent myofibre degeneration and repopulating the stem cell niche for future use. The present review aims to cover recent advances in satellite cell/myoblast therapy and to discuss the challenges that remain for it to become a realistic therapy.

Indexed as

AnimalsGraft SurvivalHumansMuscular DystrophiesMyoblastsSatellite Cells, Skeletal Musclecell therapyDuchenne muscular dystrophymdx mousemuscular dystrophymyoblastssatellite cellsskeletal muscle regeneration

Identifiers

PMID23560812
PMCPMC3795440
OpenAlexW2043100917

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.