"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 |
|---|
| 2004 | 0 | 1 | 1 |
| 2005 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2007 | 0 | 2 | 2 |
| 2008 | 0 | 1 | 1 |
| 2009 | 0 | 3 | 3 |
| 2010 | 0 | 1 | 1 |
| 2011 | 0 | 1 | 1 |
| 2012 | 0 | 2 | 2 |
| 2013 | 0 | 3 | 3 |
| 2014 | 0 | 2 | 2 |
| 2015 | 1 | 1 | 2 |
| 2016 | 0 | 2 | 2 |
| 2017 | 6 | 28 | 34 |
| 2018 | 7 | 22 | 29 |
| 2019 | 1 | 4 | 5 |
| 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Exons" by people in Profiles.
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A novel ACE2 isoform is expressed in human respiratory epithelia and is upregulated in response to interferons and RNA respiratory virus infection. Nat Genet. 2021 02; 53(2):205-214.
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Structural Variability, Expression Profile, and Pharmacogenetic Properties of TMPRSS2 Gene as a Potential Target for COVID-19 Therapy. Genes (Basel). 2020 12 25; 12(1).
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Alternative splicing of ACE2 possibly generates variants that may limit the entry of SARS-CoV-2: a potential therapeutic approach using SSOs. Clin Sci (Lond). 2020 05 29; 134(10):1143-1150.
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A negative screening of rare genetic variants in the ADIPOQ and STATH genes in cystic fibrosis. Pulmonology. 2020 May - Jun; 26(3):138-144.
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LINE-1-Mediated AluYa5 Insertion Underlying Complete Autosomal Recessive IFN-?R1 Deficiency. J Clin Immunol. 2019 10; 39(7):739-742.
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Sequencing of NOTCH1 gene in an Italian population with bicuspid aortic valve: Preliminary results from the GISSI OUTLIERS VAR study. Gene. 2019 Oct 05; 715:143970.
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Is the Idylla EGFR Mutation Assay feasible on archival stained cytological smears? A pilot study. J Clin Pathol. 2019 Sep; 72(9):609-614.
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Association of group-specific component exon 11 polymorphisms with bronchial asthma in children and adolescents. Scand J Immunol. 2019 Mar; 89(3):e12740.
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Identification of a novel loss-of-function mutation of the GLA gene in a Chinese Han family with Fabry disease. BMC Med Genet. 2018 12 27; 19(1):219.
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Comprehensive analysis of HPV infection, EGFR exon 20 mutations and LINE1 hypomethylation as risk factors for malignant transformation of sinonasal-inverted papilloma to squamous cell carcinoma. Int J Cancer. 2019 03 15; 144(6):1313-1320.