"RNA Splicing" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The ultimate exclusion of nonsense sequences or intervening sequences (introns) before the final RNA transcript is sent to the cytoplasm.
Descriptor ID |
D012326
|
MeSH Number(s) |
G02.111.760.700 G03.839.700 G05.308.700.700
|
Concept/Terms |
RNA Splicing- RNA Splicing
- Splicing, RNA
- RNA Splicings
- Splicings, RNA
|
Below are MeSH descriptors whose meaning is more general than "RNA Splicing".
Below are MeSH descriptors whose meaning is more specific than "RNA Splicing".
This graph shows the total number of publications written about "RNA Splicing" by people in this website by year, and whether "RNA Splicing" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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2001 | 1 | 0 | 1 |
2003 | 1 | 0 | 1 |
2005 | 1 | 0 | 1 |
2007 | 1 | 0 | 1 |
2009 | 1 | 0 | 1 |
2010 | 0 | 1 | 1 |
2011 | 1 | 0 | 1 |
2012 | 2 | 3 | 5 |
2013 | 0 | 3 | 3 |
2014 | 1 | 1 | 2 |
2015 | 3 | 1 | 4 |
2016 | 4 | 5 | 9 |
2017 | 2 | 3 | 5 |
2018 | 0 | 2 | 2 |
2019 | 1 | 0 | 1 |
2020 | 3 | 1 | 4 |
2021 | 2 | 1 | 3 |
2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "RNA Splicing" by people in Profiles.
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Exon junction complex-associated multi-adapter RNPS1 nucleates splicing regulatory complexes to maintain transcriptome surveillance. Nucleic Acids Res. 2022 06 10; 50(10):5899-5918.
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A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome. Clin Genet. 2021 10; 100(4):486-488.
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An identical-by-descent novel splice-donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese families. Ann Hum Genet. 2021 09; 85(5):186-195.
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Ecd promotes U5 snRNP maturation and Prp8 stability. Nucleic Acids Res. 2021 02 22; 49(3):1688-1707.
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Anything but Ordinary - Emerging Splicing Mechanisms in Eukaryotic Gene Regulation. Trends Genet. 2021 04; 37(4):355-372.
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Apparent Missense Variant in COL7A1 Causes a Severe Form of Recessive Dystrophic Epidermolysis Bullosa via Effects on Splicing. Acta Derm Venereol. 2020 Sep 30; 100(16):adv00275.
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CASC3 promotes transcriptome-wide activation of nonsense-mediated decay by the exon junction complex. Nucleic Acids Res. 2020 09 04; 48(15):8626-8644.
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A Day in the Life of the Exon Junction Complex. Biomolecules. 2020 06 05; 10(6).
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SON haploinsufficiency causes impaired pre-mRNA splicing of CAKUT genes and heterogeneous renal?phenotypes. Kidney Int. 2019 06; 95(6):1494-1504.
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Exon Junction Complexes Suppress Spurious Splice Sites to Safeguard Transcriptome Integrity. Mol Cell. 2018 11 01; 72(3):482-495.e7.