"Coiled Bodies" 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.
A distinct subnuclear domain enriched in splicesomal snRNPs (RIBONUCLEOPROTEINS, SMALL NUCLEAR) and p80-coilin.
Descriptor ID |
D020541
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MeSH Number(s) |
A11.284.430.106.279.345.195
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Concept/Terms |
Coiled Bodies- Coiled Bodies
- Bodies, Coiled
- Body, Coiled
- Coiled Body
- Accessory Bodies of Cajal
- Cajal Accessory Bodies
|
Below are MeSH descriptors whose meaning is more general than "Coiled Bodies".
Below are MeSH descriptors whose meaning is more specific than "Coiled Bodies".
This graph shows the total number of publications written about "Coiled Bodies" by people in this website by year, and whether "Coiled Bodies" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2000 | 1 | 0 | 1 |
2003 | 1 | 1 | 2 |
2006 | 0 | 1 | 1 |
2013 | 0 | 1 | 1 |
2014 | 1 | 0 | 1 |
2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Coiled Bodies" by people in Profiles.
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Composition-dependent thermodynamics of intracellular phase separation. Nature. 2020 05; 581(7807):209-214.
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Human cells lacking coilin and Cajal bodies are proficient in telomerase assembly, trafficking and telomere maintenance. Nucleic Acids Res. 2015 Jan; 43(1):385-95.
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Disease mutant analysis identifies a new function of DAXX in telomerase regulation and telomere maintenance. J Cell Sci. 2015 Jan 15; 128(2):331-41.
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Fam118B, a newly identified component of Cajal bodies, is required for Cajal body formation, snRNP biogenesis and cell viability. J Cell Sci. 2014 May 01; 127(Pt 9):2029-39.
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Whole-genome screening identifies proteins localized to distinct nuclear bodies. J Cell Biol. 2013 Oct 14; 203(1):149-64.
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DNA methyltransferases control telomere length and telomere recombination in mammalian cells. Nat Cell Biol. 2006 Apr; 8(4):416-24.
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The cyclin E/Cdk2 substrate p220(NPAT) is required for S-phase entry, histone gene expression, and Cajal body maintenance in human somatic cells. Mol Cell Biol. 2003 Dec; 23(23):8586-600.
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The cyclin E/Cdk2 substrate and Cajal body component p220(NPAT) activates histone transcription through a novel LisH-like domain. Mol Cell Biol. 2003 May; 23(10):3669-80.
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Cell cycle-regulated phosphorylation of p220(NPAT) by cyclin E/Cdk2 in Cajal bodies promotes histone gene transcription. Genes Dev. 2000 Sep 15; 14(18):2298-313.