"Trinucleotide Repeats" 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.
Microsatellite repeats consisting of three nucleotides dispersed in the euchromatic arms of chromosomes.
| Descriptor ID |
D018911
|
| MeSH Number(s) |
G02.111.570.080.708.800.500.850 G05.360.080.708.800.500.850 G05.360.340.024.850.500.850
|
| Concept/Terms |
Trinucleotide Repeats- Trinucleotide Repeats
- Repeat, Trinucleotide
- Repeats, Trinucleotide
- Trinucleotide Repeat
- Triplet Repeats
- Repeat, Triplet
- Repeats, Triplet
- Triplet Repeat
|
Below are MeSH descriptors whose meaning is more general than "Trinucleotide Repeats".
Below are MeSH descriptors whose meaning is more specific than "Trinucleotide Repeats".
This graph shows the total number of publications written about "Trinucleotide Repeats" by people in this website by year, and whether "Trinucleotide Repeats" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 0 | 1 | 1 |
| 2015 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Trinucleotide Repeats" by people in Profiles.
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The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population. Am J Med Genet B Neuropsychiatr Genet. 2018 04; 177(3):346-357.
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Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype. Am J Med Genet B Neuropsychiatr Genet. 2015 Oct; 168(7):573-85.
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Huntington's disease confirmed by genetic testing in five African families. Mov Disord. 1998 Jul; 13(4):726-30.