Evidence map›Paper›PMID 24472232›Full record

ArticleLongevity & healthspan2012

From cellular senescence to age-associated diseases: the miRNA connection.

Elisabeth Schraml, Johannes Grillari

Open access · hybridAbstract read
In one paragraph

Article in Longevity & healthspan, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Genomic Instability and Epigenetic Changes during Aging.International journal of molecular sciences · 2023
    Review
  5. Mango (Antioxidants (Basel, Switzerland) · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. A step-by-step microRNA guide to cancer development and metastasis.Cellular oncology (Dordrecht, Netherlands) · 2017
    Review
  11. The Immortal Senescence.Methods in molecular biology (Clifton, N.J.) · 2017
    Review
  12. Review
  13. Review
  14. Article
  15. miRNA control of tissue repair and regeneration.The American journal of pathology · 2015
    Review
  16. Review
  17. Absence of mutation in miR-34a gene in a Chinese longevity population.Dong wu xue yan jiu = Zoological research · 2015
    Article
  18. Article
  19. Article
  20. Review
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.

Elisabeth Schraml
Johannes GrillariDepartment of Biotechnology, BOKU VIBT University of Natural Resources and Life Sciences, Vienna, Austria. johannes.grillari@boku.ac.at.
BOKU University · AT

Funding

Austrian Science Fund FWF P 24498
6 · The paper itself

Abstract

Cellular senescence has evolved from an in-vitro model system to study aging in vitro to a multifaceted phenomenon of in-vivo importance as senescent cells in vivo have been identified and their removal delays the onset of age-associated diseases in a mouse model system. From the large emerging class of non-coding RNAs, miRNAs have only recently been functionally implied in the regulatory networks that are modified during the aging process. Here we summarize examples of similarities between the differential expression of miRNAs during senescence and age-associated diseases and suggest that these similarities might emphasize the importance of senescence for the pathogenesis of age-associated diseases. Understanding such a connection on the level of miRNAs might offer valuable opportunities for designing novel diagnostic and therapeutic strategies.

Identifiers

PMID24472232
PMCPMC3922944
OpenAlexW2165783010

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.