"RNA Splice Sites" 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.
Nucleotide sequences located at the ends of EXONS and recognized in pre-messenger RNA by SPLICEOSOMES. They are joined during the RNA SPLICING reaction, forming the junctions between exons.
Descriptor ID |
D022821
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MeSH Number(s) |
D13.444.735.544.550 G02.111.570.080.689.687.490 G05.360.080.689.687.490 G05.360.340.024.340.137.800
|
Concept/Terms |
Cryptic Splice Sites- Cryptic Splice Sites
- Cryptic Splice Site
- Splice Site, Cryptic
- Splice Sites, Cryptic
Splice Donor Site- Splice Donor Site
- Donor Site, Splice
- Donor Sites, Splice
- Splice Donor Sites
- 5' Splice Site
- 5' Splice Sites
- Splice Site, 5'
- Splice Sites, 5'
Alternative Splice Sites- Alternative Splice Sites
- Alternative Splice Site
- Splice Site, Alternative
- Splice Sites, Alternative
Splice Acceptor Site- Splice Acceptor Site
- Acceptor Site, Splice
- Acceptor Sites, Splice
- Splice Acceptor Sites
- 3' Splice Site
- 3' Splice Sites
- Splice Site, 3'
- Splice Sites, 3'
|
Below are MeSH descriptors whose meaning is more general than "RNA Splice Sites".
Below are MeSH descriptors whose meaning is more specific than "RNA Splice Sites".
This graph shows the total number of publications written about "RNA Splice Sites" by people in this website by year, and whether "RNA Splice Sites" 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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2004 | 0 | 1 | 1 |
2006 | 1 | 1 | 2 |
2007 | 0 | 1 | 1 |
2012 | 0 | 2 | 2 |
2013 | 1 | 0 | 1 |
2017 | 0 | 1 | 1 |
2019 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "RNA Splice Sites" by people in Profiles.
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Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice. PLoS Genet. 2019 05; 15(5):e1008130.
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A regulated PNUTS mRNA to lncRNA splice switch mediates EMT and tumour progression. Nat Cell Biol. 2017 Sep; 19(9):1105-1115.
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Phosphorylation of the alternative mRNA splicing factor 45 (SPF45) by Clk1 regulates its splice site utilization, cell migration and invasion. Nucleic Acids Res. 2013 May; 41(9):4949-62.
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EuPathDB: the eukaryotic pathogen database. Nucleic Acids Res. 2013 Jan; 41(Database issue):D684-91.
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Mitogen-activated protein kinase phosphorylation of splicing factor 45 (SPF45) regulates SPF45 alternative splicing site utilization, proliferation, and cell adhesion. Mol Cell Biol. 2012 Jul; 32(14):2880-93.
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Global analysis of exon creation versus loss and the role of alternative splicing in 17 vertebrate genomes. RNA. 2007 May; 13(5):661-70.
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The ASAP II database: analysis and comparative genomics of alternative splicing in 15 animal species. Nucleic Acids Res. 2007 Jan; 35(Database issue):D93-8.
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Recessive arrhythmogenic right ventricular dysplasia due to novel cryptic splice mutation in PKP2. Hum Mutat. 2006 Nov; 27(11):1157.
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Evidence for a subpopulation of conserved alternative splicing events under selection pressure for protein reading frame preservation. Nucleic Acids Res. 2004; 32(4):1261-9.
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MYH9 spectrum of autosomal-dominant giant platelet syndromes: unexpected association with fibulin-1 variant-D inactivation. Am J Hematol. 2003 Dec; 74(4):254-62.