 RNA Splice Sites
"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
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| 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'
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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 UAMS Profiles 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 |
|---|
| 2022 | 0 | 2 | 2 | | 2020 | 1 | 0 | 1 | | 2017 | 2 | 0 | 2 | | 2015 | 2 | 0 | 2 | | 2008 | 1 | 1 | 2 | | 2005 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "RNA Splice Sites" by people in Profiles over the past ten years.
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Edelman WC, Kiianitsa K, Virmani T, Martinez RA, Young JE, Keene CD, Bird TD, Raskind WH, Korvatska O. Reduced gene dosage is a common mechanism of neuropathologies caused by ATP6AP2 splicing mutations. Parkinsonism Relat Disord. 2022 08; 101:31-38.
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Gao Y, Lin KT, Jiang T, Yang Y, Rahman MA, Gong S, Bai J, Wang L, Sun J, Sheng L, Krainer AR, Hua Y. Systematic characterization of short intronic splicing-regulatory elements in SMN2 pre-mRNA. Nucleic Acids Res. 2022 01 25; 50(2):731-749.
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Rahman MA, Krainer AR, Abdel-Wahab O. SnapShot: Splicing Alterations in Cancer. Cell. 2020 01 09; 180(1):208-208.e1.
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Ahsan KB, Masuda A, Rahman MA, Takeda JI, Nazim M, Ohkawara B, Ito M, Ohno K. SRSF1 suppresses selection of intron-distal 5' splice site of DOK7 intron 4 to generate functional full-length Dok-7 protein. Sci Rep. 2017 09 05; 7(1):10446.
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Ipe TS, Lim J, Reyes MA, Ero M, Leveque C, Lewis B, Kain J. An extremely rare splice site mutation in the gene encoding complement factor I in a patient with atypical hemolytic uremic syndrome. J Clin Apher. 2017 Dec; 32(6):584-588.
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Gupta HV, Vengoechea J, Sahaya K, Virmani T. A splice site mutation in ATP6AP2 causes X-linked intellectual disability, epilepsy, and parkinsonism. Parkinsonism Relat Disord. 2015 Dec; 21(12):1473-5.
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Rahman MA, Azuma Y, Nasrin F, Takeda J, Nazim M, Bin Ahsan K, Masuda A, Engel AG, Ohno K. SRSF1 and hnRNP H antagonistically regulate splicing of COLQ exon 16 in a congenital myasthenic syndrome. Sci Rep. 2015 Aug 18; 5:13208.
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