"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 | 1 | 1 | 2 |
2006 | 0 | 1 | 1 |
2007 | 0 | 1 | 1 |
2011 | 0 | 2 | 2 |
2012 | 0 | 1 | 1 |
2013 | 0 | 2 | 2 |
2016 | 0 | 1 | 1 |
2018 | 1 | 0 | 1 |
2020 | 0 | 1 | 1 |
2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "RNA Splice Sites" by people in Profiles.
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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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Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome. Clin Epigenetics. 2020 05 11; 12(1):63.
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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.
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Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms. Hum Mol Genet. 2016 06 01; 25(11):2256-2268.
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Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability. Am J Hum Genet. 2013 Jul 11; 93(1):181-90.
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Further genotype-phenotype correlation emerging from two families with PLP1 exon 4 skipping. Clin Genet. 2014 Mar; 85(3):267-72.
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An intronic G run within HIV-1 intron 2 is critical for splicing regulation of vif mRNA. J Virol. 2013 Mar; 87(5):2707-20.
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Functional analysis of splice site mutations in the human hairless (HR) gene using a minigene assay. Br J Dermatol. 2011 Nov; 165(5):1127-32.
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Assembly, disassembly and recycling: the dynamics of exon junction complexes. RNA Biol. 2011 Jan-Feb; 8(1):24-9.
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Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutation. Eur J Paediatr Neurol. 2007 May; 11(3):175-7.