"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.
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Year | Major Topic | Minor Topic | Total |
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2002 | 0 | 1 | 1 |
2004 | 1 | 2 | 3 |
2005 | 0 | 1 | 1 |
2009 | 0 | 1 | 1 |
2012 | 0 | 2 | 2 |
2013 | 0 | 1 | 1 |
2016 | 0 | 1 | 1 |
2017 | 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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Model-based genome-wide determination of RNA chain elongation rates in Escherichia coli. Sci Rep. 2017 12 08; 7(1):17213.
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Fatal Lymphoproliferative Disease in Two Siblings Lacking Functional FAAP24. J Clin Immunol. 2016 10; 36(7):684-92.
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A realistic model under which the genetic code is optimal. J Mol Evol. 2013 Oct; 77(4):170-84.
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Mutation-based growth charts for SEDC and other COL2A1 related dysplasias. Am J Med Genet C Semin Med Genet. 2012 Aug 15; 160C(3):205-16.
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Chaperones divide yeast proteins into classes of expression level and evolutionary rate. Genome Biol Evol. 2012; 4(5):618-25.
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Severe nemaline myopathy associated with consecutive mutations E74D and H75Y on a single ACTA1 allele. Neuromuscul Disord. 2009 Jul; 19(7):481-4.
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Gene expression levels influence amino acid usage and evolutionary rates in endosymbiotic bacteria. Gene. 2005 Jun 06; 352:109-17.
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Tissue dependent co-segregation of the novel pathogenic G12276A mitochondrial tRNALeu(CUN) mutation with the A185G D-loop polymorphism. J Med Genet. 2004 Dec; 41(12):e124.
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NQO1 C609T polymorphism in distinct entities of pediatric hematologic neoplasms. Haematologica. 2004 Dec; 89(12):1492-7.