"RNA Splicing Factors" 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.
RNA-binding proteins that facilitate or inhibit RNA SPLICING.
Descriptor ID |
D000072260
|
MeSH Number(s) |
D12.776.157.725.829 D12.776.664.962.829
|
Concept/Terms |
RNA Splicing Factors- RNA Splicing Factors
- Factors, RNA Splicing
- Splicing Factors, RNA
- Splicing Factors
- Factors, Splicing
|
Below are MeSH descriptors whose meaning is more general than "RNA Splicing Factors".
Below are MeSH descriptors whose meaning is more specific than "RNA Splicing Factors".
This graph shows the total number of publications written about "RNA Splicing Factors" by people in this website by year, and whether "RNA Splicing Factors" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2013 | 0 | 4 | 4 |
2015 | 0 | 1 | 1 |
2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "RNA Splicing Factors" by people in Profiles.
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Ecd promotes U5 snRNP maturation and Prp8 stability. Nucleic Acids Res. 2021 02 22; 49(3):1688-1707.
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Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy. Epilepsia. 2015 Sep; 56(9):e129-33.
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RBFOX1 and RBFOX3 mutations in rolandic epilepsy. PLoS One. 2013; 8(9):e73323.
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Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3. Nat Genet. 2013 Aug; 45(8):933-6.
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Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndrome. Hum Genet. 2013 Aug; 132(8):885-98.
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Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy. Epilepsia. 2013 Feb; 54(2):265-71.