"Thymine" 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.
One of four constituent bases of DNA.
| Descriptor ID |
D013941
|
| MeSH Number(s) |
D03.383.742.698.875.899
|
| Concept/Terms |
Thymine- Thymine
- 5-Methyluracil
- 5 Methyluracil
|
Below are MeSH descriptors whose meaning is more general than "Thymine".
Below are MeSH descriptors whose meaning is more specific than "Thymine".
This graph shows the total number of publications written about "Thymine" by people in this website by year, and whether "Thymine" 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 |
|---|
| 2001 | 0 | 1 | 1 |
| 2003 | 0 | 2 | 2 |
| 2008 | 1 | 1 | 2 |
To return to the timeline,
click here.
Below are the most recent publications written about "Thymine" by people in Profiles.
-
Lahoud G, Arar K, Hou YM, Gamper H. RecA-mediated strand invasion of DNA by oligonucleotides substituted with 2-aminoadenine and 2-thiothymine. Nucleic Acids Res. 2008 Dec; 36(21):6806-15.
-
Goteiner D, Ashmen R, Lehrman N, Janal MN, Eskin B. Presence and significance of interleukin-1 polymorphism in patients who present with acute coronary syndrome, angina, and chronic periodontitis: an epidemiologic pilot study. J Periodontol. 2008 Jan; 79(1):138-43.
-
McGuire JM, Gana JA, Petcherskaia M, Kirk KE. Protein binding to expanded telomere repeats in Tetrahymena thermophila. J Eukaryot Microbiol. 2003 Sep-Oct; 50(5):341-8.
-
Park H, Davidson E, King MP. The pathogenic A3243G mutation in human mitochondrial tRNALeu(UUR) decreases the efficiency of aminoacylation. Biochemistry. 2003 Feb 04; 42(4):958-64.
-
Frisch R, Singleton KR, Moses PA, Gonzalez IL, Carango P, Marks HG, Funanage VL. Effect of triplet repeat expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophy. Mol Genet Metab. 2001 Sep-Oct; 74(1-2):281-91.