"Exons" 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 parts of a transcript of a split GENE remaining after the INTRONS are removed. They are spliced together to become a MESSENGER RNA or other functional RNA.
| Descriptor ID |
D005091
|
| MeSH Number(s) |
G05.360.340.024.340.137.232
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Exons".
Below are MeSH descriptors whose meaning is more specific than "Exons".
This graph shows the total number of publications written about "Exons" by people in this website by year, and whether "Exons" 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 |
|---|
| 1994 | 2 | 16 | 18 |
| 1995 | 4 | 23 | 27 |
| 1996 | 6 | 27 | 33 |
| 1997 | 2 | 24 | 26 |
| 1998 | 7 | 20 | 27 |
| 1999 | 4 | 26 | 30 |
| 2000 | 4 | 36 | 40 |
| 2001 | 4 | 32 | 36 |
| 2002 | 2 | 23 | 25 |
| 2003 | 2 | 26 | 28 |
| 2004 | 7 | 27 | 34 |
| 2005 | 3 | 35 | 38 |
| 2006 | 2 | 24 | 26 |
| 2007 | 3 | 16 | 19 |
| 2008 | 1 | 25 | 26 |
| 2009 | 5 | 22 | 27 |
| 2010 | 5 | 18 | 23 |
| 2011 | 7 | 21 | 28 |
| 2012 | 2 | 22 | 24 |
| 2013 | 7 | 23 | 30 |
| 2014 | 4 | 13 | 17 |
| 2015 | 0 | 19 | 19 |
| 2016 | 5 | 22 | 27 |
| 2017 | 4 | 8 | 12 |
| 2018 | 2 | 12 | 14 |
| 2019 | 2 | 6 | 8 |
| 2020 | 1 | 12 | 13 |
| 2021 | 4 | 3 | 7 |
| 2022 | 0 | 9 | 9 |
| 2023 | 0 | 10 | 10 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Exons" by people in Profiles.
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MATR3 pathogenic variants differentially impair its cryptic splicing repression function. FEBS Lett. 2024 Feb; 598(4):415-436.
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Speg interactions that regulate the stability of excitation-contraction coupling protein complexes in triads and dyads. Commun Biol. 2023 09 14; 6(1):942.
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Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants. Genetics. 2023 08 09; 224(4).
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Progressive osseous heteroplasia in a 5-year-old boy with a novel mutation in exon 2 of GNAS: a case presentation and literature review. BMC Musculoskelet Disord. 2023 Mar 31; 24(1):247.
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A CRISPR/Cas9-engineered mouse carrying a conditional knockout allele for the early growth response-1 transcription factor. Genesis. 2023 07; 61(3-4):e23515.
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Poziotinib in Treatment-Naive NSCLC Harboring HER2 Exon 20 Mutations: ZENITH20-4, A Multicenter, Multicohort, Open-Label, Phase 2 Trial (Cohort 4). J Thorac Oncol. 2023 08; 18(8):1031-1041.
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Alternative splicing mediates the compensatory upregulation of MBNL2 upon MBNL1 loss-of-function. Nucleic Acids Res. 2023 02 22; 51(3):1245-1259.
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A Rare PDGFRA Exon 15 Germline Mutation Identified in a Patient With Phenotypic Manifestations Concerning for GIST-Plus Syndrome: A Case Report and Review of Literature. Int J Surg Pathol. 2023 Sep; 31(6):1139-1145.
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Alternative polyadenylation alters protein dosage by switching between intronic and 3'UTR sites. Sci Adv. 2023 02 17; 9(7):eade4814.
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Clinicopathologic characteristics of myeloproliferative neoplasms with JAK2 exon 12 mutation. Leuk Res. 2023 04; 127:107033.