Evidence map›Paper›PMID 29769273›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2018

Genome-Wide Posttranscriptional Dysregulation by MicroRNAs in Human Asthma as Revealed by Frac-seq.

Rocio T Martinez-Nunez, Hitasha Rupani, Manuela Platé, Mahesan Niranjan, Rachel C Chambers, Peter H Howarth, Tilman Sanchez-Elsner

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Review
  3. Association of theBiology of sport · 2024
    Article
  4. The RNA binding proteinsFrontiers in cell and developmental biology · 2023
    Article
  5. Review
  6. Article
  7. Article
  8. The AI for Scientific Discovery NetworkPatterns (New York, N.Y.) · 2021
    Review
  9. MicroRNA Targets for Asthma Therapy.Advances in experimental medicine and biology · 2021
    Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. 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

7 authors.

Rocio T Martinez-NunezSchool of Immunology and Microbial Sciences, Medical Research Council and Asthma UK Centre in Allergic Mechanisms of Asthma, King's College London, London SE19RT, United Kingdom; rocio.martinez_nunez@kcl.ac.uk.ORCID 0000-0003-2507-4738
Hitasha RupaniClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, United Kingdom.
Manuela PlatéCentre for Inflammation and Tissue Repair, Department of Respiratory Medicine, Rayne Institute, University College London, London WC1E 6JF, United Kingdom; and.ORCID 0000-0002-9957-0681
Mahesan NiranjanSchool of Electronics and Computer Science, University of Southampton, Southampton SO17 1BJ, United Kingdom.ORCID 0000-0001-7021-140X
Rachel C ChambersCentre for Inflammation and Tissue Repair, Department of Respiratory Medicine, Rayne Institute, University College London, London WC1E 6JF, United Kingdom; and.ORCID 0000-0003-1370-9417
Peter H HowarthClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, United Kingdom.
Tilman Sanchez-ElsnerClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, United Kingdom.ORCID 0000-0003-1915-2410

Funding

Medical Research Council G0800649Medical Research Council G0800766Medical Research Council G0900453Medical Research Council MR/K001035/1
6 · The paper itself

Abstract

MicroRNAs are small noncoding RNAs that inhibit gene expression posttranscriptionally, implicated in virtually all biological processes. Although the effect of individual microRNAs is generally studied, the genome-wide role of multiple microRNAs is less investigated. We assessed paired genome-wide expression of microRNAs with total (cytoplasmic) and translational (polyribosome-bound) mRNA levels employing subcellular fractionation and RNA sequencing (Frac-seq) in human primary bronchoepithelium from healthy controls and severe asthmatics. Severe asthma is a chronic inflammatory disease of the airways characterized by poor response to therapy. We found genes (i.e., isoforms of a gene) and mRNA isoforms differentially expressed in asthma, with novel inflammatory and structural pathophysiological mechanisms related to bronchoepithelium disclosed solely by polyribosome-bound mRNAs (e.g.,

Indexed as

AdolescentAdultAgedAlternative SplicingAsthmaBase SequenceEpithelial CellsFemaleGene Expression RegulationHumansMaleMicroRNAsMiddle AgedRespiratory MucosaRNA IsoformsRNA, MessengerMicroRNAsRNA IsoformsRNA, Messenger

Identifiers

PMID29769273
PMCPMC6013048

What OpenQuestion holds

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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.