Evidence map›Paper›PMID 30089464›Full record

ArticleBMC genetics2018

Skeletal muscle in aged mice reveals extensive transformation of muscle gene expression.

I-Hsuan Lin, Junn-Liang Chang, Kate Hua, Wan-Chen Huang, Ming-Ta Hsu, Yi-Fan Chen

Abstract read
In one paragraph

Article in BMC genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing 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

49 citing papers in PubMed.

  1. Review
  2. Article
  3. Improved Sphincter Muscle Regeneration by Myoblasts fromMedical sciences (Basel, Switzerland) · 2026
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  5. Review
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  19. The Molecular Role of Polyamines in Age-Related Diseases: An Update.International journal of molecular sciences · 2023
    Review
  20. Article
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

6 authors.

I-Hsuan LinVYM Genome Research Center, National Yang-Ming University, Taipei, 112, Taiwan.
Junn-Liang ChangDepartment of Pathology & Laboratory Medicine, Taoyuan Armed Forces General Hospital, Taoyuan, 325, Taiwan.
Kate HuaVYM Genome Research Center, National Yang-Ming University, Taipei, 112, Taiwan.
Wan-Chen HuangThe Ph.D. Program for Translational Medicine, College of Medical Science and Technology, Taipei Medical University, No.250, Wu-Hsing Street, Taipei, 11031, Taiwan.
Ming-Ta HsuInstitute of Biochemistry and Molecular Biology, National Yang-Ming University, Taipei, 112, Taiwan.
Yi-Fan ChenThe Ph.D. Program for Translational Medicine, College of Medical Science and Technology, Taipei Medical University, No.250, Wu-Hsing Street, Taipei, 11031, Taiwan. evan.yifan@tmu.edu.tw.ORCID 0000-0002-0793-8769

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAging leads to decreased skeletal muscle function in mammals and is associated with a progressive loss of muscle mass, quality and strength. Age-related muscle loss (sarcopenia) is an important health problem associated with the aged population.

resultsWe investigated the alteration of genome-wide transcription in mouse skeletal muscle tissue (rectus femoris muscle) during aging using a high-throughput sequencing technique. Analysis revealed significant transcriptional changes between skeletal muscles of mice at 3 (young group) and 24 (old group) months of age. Specifically, genes associated with energy metabolism, cell proliferation, muscle myosin isoforms, as well as immune functions were found to be altered. We observed several interesting gene expression changes in the elderly, many of which have not been reported before.

conclusionsThose data expand our understanding of the various compensatory mechanisms that can occur with age, and further will assist in the development of methods to prevent and attenuate adverse outcomes of aging.

Indexed as

Gene Expression RegulationAnimalsCell ProliferationEnergy MetabolismGene Expression ProfilingMaleMiceMuscle, SkeletalSarcopeniaSequence Analysis, RNAAgingCardiac-related genesDefects on differentiationMuscle fibersRNA sequencing analysisSkeletal muscle

Identifiers

PMID30089464
PMCPMC6083496

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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.