Intron mis-splicing: no alternative?

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.

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.

Who cites it

23 citing papers in PubMed.

1. A Method to Quantitatively Examine Heat Stress-Induced Alternative Splicing in Plants by RNA-Seq and RT-PCR.Methods in molecular biology (Clifton, N.J.) · 2024
   Article
2. The Expanding Role of Alternative Splicing in Vascular Smooth Muscle Cell Plasticity.International journal of molecular sciences · 2021
   Review
3. Intron Retention as a Mode for RNA-Seq Data Analysis.Frontiers in genetics · 2020
   Review
4. Novel homozygous ataxia‑telangiectasia (A‑T) mutated gene mutation identified in a Chinese pedigree with A‑T.Molecular medicine reports · 2019
   Article
5. The Y Chromosome Modulates Splicing and Sex-Biased Intron Retention Rates inGenetics · 2018
   Article
6. Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly.Cell · 2018
   Article
7. Transcriptional-Readthrough RNAs Reflect the Phenomenon of "A Gene Contains Gene(s)" or "Gene(s) within a Gene" in the Human Genome, and Thus Are Not Chimeric RNAs.Genes · 2018
   Review
8. Genetic predisposition to ischaemic stroke byOncotarget · 2017
   Article
9. Deep intronic mutations and human disease.Human genetics · 2017
   Review
10. Cancer cell international · 2017
    Article
11. Hypothesis: Artifacts, Including Spurious Chimeric RNAs with a Short Homologous Sequence, Caused by Consecutive Reverse Transcriptions and Endogenous Random Primers.Journal of Cancer · 2015
    Review
12. Associations of Polymorphisms in MTHFR Gene with the Risk of Age-Related Cataract in Chinese Han Population: A Genotype-Phenotype Analysis.PloS one · 2015
    Article
13. Risk-Association of DNMT1 Gene Polymorphisms with Coronary Artery Disease in Chinese Han Population.International journal of molecular sciences · 2014
    Article
14. Origin of spliceosomal introns and alternative splicing.Cold Spring Harbor perspectives in biology · 2014
    Article
15. Integrin α3β1 controls mRNA splicing that determines Cox-2 mRNA stability in breast cancer cells.Journal of cell science · 2014
    Article
16. An interactive association of advanced glycation end-product receptor gene four common polymorphisms with coronary artery disease in northeastern Han Chinese.PloS one · 2013
    Article
17. Characterization of NOL7 gene point mutations, promoter methylation, and protein expression in cervical cancer.International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists · 2012
    Article
18. Transcriptome profiling using single-molecule direct RNA sequencing.Methods in molecular biology (Clifton, N.J.) · 2011
    Article
19. Detection and analysis of alternative splicing in Yarrowia lipolytica reveal structural constraints facilitating nonsense-mediated decay of intron-retaining transcripts.Genome biology · 2010
    Article
20. Complex selection on 5' splice sites in intron-rich organisms.Genome research · 2009
    Article

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

Authors and funding

2 authors.

Funding

Abstract

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