"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 |
|---|
| 1996 | 1 | 2 | 3 |
| 1997 | 1 | 4 | 5 |
| 1998 | 2 | 3 | 5 |
| 1999 | 0 | 1 | 1 |
| 2000 | 1 | 0 | 1 |
| 2001 | 0 | 2 | 2 |
| 2002 | 0 | 1 | 1 |
| 2003 | 3 | 1 | 4 |
| 2004 | 4 | 1 | 5 |
| 2005 | 4 | 1 | 5 |
| 2006 | 2 | 1 | 3 |
| 2007 | 1 | 1 | 2 |
| 2008 | 1 | 1 | 2 |
| 2009 | 0 | 2 | 2 |
| 2010 | 0 | 2 | 2 |
| 2011 | 0 | 2 | 2 |
| 2012 | 2 | 0 | 2 |
| 2013 | 2 | 1 | 3 |
| 2014 | 0 | 2 | 2 |
| 2015 | 2 | 4 | 6 |
| 2016 | 1 | 6 | 7 |
| 2017 | 5 | 3 | 8 |
| 2018 | 2 | 8 | 10 |
| 2019 | 2 | 4 | 6 |
| 2020 | 1 | 6 | 7 |
| 2021 | 1 | 7 | 8 |
| 2022 | 0 | 3 | 3 |
| 2023 | 3 | 1 | 4 |
| 2024 | 4 | 5 | 9 |
| 2025 | 2 | 5 | 7 |
| 2026 | 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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De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disorders. Nat Commun. 2026 Jan 23; 17(1):1569.
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The utility of ultra-deep RNA sequencing in Mendelian disorder diagnostics. Am J Hum Genet. 2025 Nov 06; 112(11):2578-2590.
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Hidden splice variants in inborn errors of immunity: Uncovering diagnoses and therapeutic targets. J Allergy Clin Immunol. 2025 Dec; 156(6):1477-1488.
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Autoregulation of RPL7B by inhibition of a structural splicing enhancer. Nucleic Acids Res. 2025 Jul 19; 53(14).
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Recurrent de novo variants in the spliceosomal factor CRNKL1 are associated with severe microcephaly and pontocerebellar hypoplasia with seizures. Am J Hum Genet. 2025 Jul 03; 112(7):1722-1732.
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The Masc-PSI complex directly induces male-type doublesex splicing in silkworms. Commun Biol. 2025 Jun 14; 8(1):927.
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A deep intronic founder variant in the SERPINB7 gene causing aberrant splicing is a potential therapeutic target for Nagashima-type palmoplantar keratoderma. J Dermatol Sci. 2025 Aug; 119(2):73-81.
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Clinical validation of RNA sequencing for Mendelian disorder diagnostics. Am J Hum Genet. 2025 Apr 03; 112(4):779-792.
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RNA splicing as a biomarker and phenotypic driver of meningioma DNA-methylation groups. Neuro Oncol. 2024 Dec 05; 26(12):2222-2236.
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Expression levels of core spliceosomal proteins modulate the MBNL-mediated spliceopathy in DM1. Hum Mol Genet. 2024 11 05; 33(21):1873-1886.