Evidence map›Paper›PMID 34573439›Full record

ReviewGenes2021

Alternative Splicing in Cardiovascular Disease-A Survey of Recent Findings.

Ena Hasimbegovic, Victor Schweiger, Nina Kastner, Andreas Spannbauer, Denise Traxler, Dominika Lukovic, Mariann Gyöngyösi, Julia Mester-Tonczar

Open access · goldAbstract readReview
In one paragraph

Review in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.8field-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

33 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  15. Article
  16. RNA-Binding Proteins in Cardiomyopathies.Journal of cardiovascular development and disease · 2024
    Review
  17. Hypertrophic cardiomyopathy inThe journal of cardiovascular aging · 2024
    Article
  18. Review
  19. Article
  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

8 authors at 1 institution in 1 country.

Ena HasimbegovicDivision of Cardiology, Department of Internal Medcine II, Medical University of Vienna, A-1090 Vienna, Austria.
Victor SchweigerDivision of Cardiology, Department of Internal Medcine II, Medical University of Vienna, A-1090 Vienna, Austria.
Nina KastnerDivision of Cardiology, Department of Internal Medcine II, Medical University of Vienna, A-1090 Vienna, Austria.ORCID 0000-0002-1576-9029
Andreas SpannbauerDivision of Cardiology, Department of Internal Medcine II, Medical University of Vienna, A-1090 Vienna, Austria.ORCID 0000-0002-9819-0361
Denise TraxlerDivision of Cardiology, Department of Internal Medcine II, Medical University of Vienna, A-1090 Vienna, Austria.
Dominika LukovicDivision of Cardiology, Department of Internal Medcine II, Medical University of Vienna, A-1090 Vienna, Austria.
Mariann GyöngyösiDivision of Cardiology, Department of Internal Medcine II, Medical University of Vienna, A-1090 Vienna, Austria.ORCID 0000-0002-7083-2107
Julia Mester-TonczarDivision of Cardiology, Department of Internal Medcine II, Medical University of Vienna, A-1090 Vienna, Austria.ORCID 0000-0003-1426-6670
Medical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alternative splicing, a driver of posttranscriptional variance, differs from canonical splicing by arranging the introns and exons of an immature pre-mRNA transcript in a multitude of different ways. Although alternative splicing was discovered almost half a century ago, estimates of the proportion of genes that undergo alternative splicing have risen drastically over the last two decades. Deep sequencing methods and novel bioinformatic algorithms have led to new insights into the prevalence of spliced variants, tissue-specific splicing patterns and the significance of alternative splicing in development and disease. Thus far, the role of alternative splicing has been uncovered in areas ranging from heart development, the response to myocardial infarction to cardiac structural disease. Circular RNAs, a product of alternative back-splicing, were initially discovered in 1976, but landmark publications have only recently identified their regulatory role, tissue-specific expression, and transcriptomic abundance, spurring a renewed interest in the topic. The aim of this review is to provide a brief insight into some of the available findings on the role of alternative splicing in cardiovascular disease, with a focus on atherosclerosis, myocardial infarction, heart failure, dilated cardiomyopathy and circular RNAs in myocardial infarction.

Indexed as

Alternative SplicingAnimalsCardiovascular DiseasesHumansProteinsRNA, CircularProteinsRNA, Circularalternative splicingatherosclerosiscircular RNAsdilated cardiomyopathyheart failuremyocardial infarction

Identifiers

PMID34573439
PMCPMC8469243
OpenAlexW3199157075

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.