Evidence map›Paper›PMID 26493705›Full record

ReviewSeminars in cell & developmental biology2015

Non-coding functions of alternative pre-mRNA splicing in development.

Stefan Mockenhaupt, Eugene V Makeyev

Open access · hybridAbstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

44 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
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  6. mRNA Transcript Variants Expressed in Mammalian Cells.International journal of molecular sciences · 2025
    Review
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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 2 countries.

Stefan MockenhauptSchool of Biological Sciences, Nanyang Technological University, Singapore 637551, Singapore.
Eugene V MakeyevSchool of Biological Sciences, Nanyang Technological University, Singapore 637551, Singapore; MRC Centre for Developmental Neurobiology, King's College London, London SE1 1UL, UK. Electronic address: eugene.makeyev@kcl.ac.uk.
Nanyang Technological University · SG

Funding

Biotechnology and Biological Sciences Research Council BB/M001199/1
6 · The paper itself

Abstract

A majority of messenger RNA precursors (pre-mRNAs) in the higher eukaryotes undergo alternative splicing to generate more than one mature product. By targeting the open reading frame region this process increases diversity of protein isoforms beyond the nominal coding capacity of the genome. However, alternative splicing also frequently controls output levels and spatiotemporal features of cellular and organismal gene expression programs. Here we discuss how these non-coding functions of alternative splicing contribute to development through regulation of mRNA stability, translational efficiency and cellular localization.

Indexed as

Alternative SplicingGene Expression Regulation, DevelopmentalAnimalsEvolution, MolecularHumansModels, GeneticMorphogenesisProtein BiosynthesisRNA PrecursorsRNA StabilityRNA PrecursorsAlternative pre-mRNA splicingDevelopmentmRNA localizationmRNA stabilityTranslational regulation

Identifiers

PMID26493705
PMCPMC4683092
OpenAlexW2159172506

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.