"Codon" 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 set of three nucleotides in a protein coding sequence that specifies individual amino acids or a termination signal (CODON, TERMINATOR). Most codons are universal, but some organisms do not produce the transfer RNAs (RNA, TRANSFER) complementary to all codons. These codons are referred to as unassigned codons (CODONS, NONSENSE).
| Descriptor ID |
D003062
|
| MeSH Number(s) |
D13.444.735.544.355 G05.360.335.355 G05.360.340.024.340.137.190
|
| Concept/Terms |
Sense Codon- Sense Codon
- Codons, Sense
- Sense Codons
- Codon, Sense
|
Below are MeSH descriptors whose meaning is more general than "Codon".
Below are MeSH descriptors whose meaning is more specific than "Codon".
This graph shows the total number of publications written about "Codon" by people in this website by year, and whether "Codon" 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 |
|---|
| 1995 | 0 | 2 | 2 |
| 1997 | 1 | 1 | 2 |
| 1998 | 1 | 2 | 3 |
| 1999 | 0 | 2 | 2 |
| 2000 | 1 | 1 | 2 |
| 2001 | 0 | 1 | 1 |
| 2005 | 0 | 1 | 1 |
| 2006 | 0 | 2 | 2 |
| 2010 | 1 | 0 | 1 |
| 2013 | 0 | 1 | 1 |
| 2016 | 0 | 1 | 1 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Codon" by people in Profiles.
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The recurrent postzygotic pathogenic variant p.Glu47Lys in RHOA causes a novel recognizable neuroectodermal phenotype. Hum Mutat. 2020 03; 41(3):591-599.
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The K153Del PRPH2 mutation differentially impacts photoreceptor structure and function. Hum Mol Genet. 2016 08 15; 25(16):3500-3514.
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A TRPC1 protein-dependent pathway regulates osteoclast formation and function. J Biol Chem. 2013 Aug 02; 288(31):22219-32.
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Biochemical analysis of phenotypic diversity associated with mutations in codon 244 of the retinal degeneration slow gene. Biochemistry. 2010 Feb 09; 49(5):905-11.
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Spatial covariation of mutation and nonsynonymous substitution rates in vertebrate mitochondrial genomes. Mol Biol Evol. 2006 Aug; 23(8):1516-24.
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Variations in the association of papillomavirus E2 proteins with mitotic chromosomes. Proc Natl Acad Sci U S A. 2006 Jan 24; 103(4):1047-52.
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First sequenced mitochondrial genome from the phylum Acanthocephala (Leptorhynchoides thecatus) and its phylogenetic position within Metazoa. J Mol Evol. 2005 Jun; 60(6):706-15.
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Characterization of a general stabilizer element that blocks deadenylation-dependent mRNA decay. J Biol Chem. 2001 Aug 17; 276(33):30995-1003.
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The case for the involvement of the Upf3p in programmed -1 ribosomal frameshifting. RNA. 2000 Dec; 6(12):1685-6.
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Emergence of HIV-1 variants containing codon insertions and deletions in the beta3-beta4 hairpin loop domain of reverse transcriptase. Immunol Lett. 2000 Oct 03; 74(2):173-5.