"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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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 1 | 0 | 1 |
| 2005 | 0 | 1 | 1 |
| 2007 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Trinucleotide Repeats" by people in Profiles.
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Butland SL, Devon RS, Huang Y, Mead CL, Meynert AM, Neal SJ, Lee SS, Wilkinson A, Yang GS, Yuen MM, Hayden MR, Holt RA, Leavitt BR, Ouellette BF. CAG-encoded polyglutamine length polymorphism in the human genome. BMC Genomics. 2007 May 22; 8:126.
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Missirlis PI, Mead CL, Butland SL, Ouellette BF, Devon RS, Leavitt BR, Holt RA. Satellog: a database for the identification and prioritization of satellite repeats in disease association studies. BMC Bioinformatics. 2005 Jun 10; 6:145.
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Kittles RA, Young D, Weinrich S, Hudson J, Argyropoulos G, Ukoli F, Adams-Campbell L, Dunston GM. Extent of linkage disequilibrium between the androgen receptor gene CAG and GGC repeats in human populations: implications for prostate cancer risk. Hum Genet. 2001 Sep; 109(3):253-61.
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Kim JS, Yue Q, Jen JC, Nelson SF, Baloh RW. Familial migraine with vertigo: no mutations found in CACNA1A. Am J Med Genet. 1998 Sep 01; 79(2):148-51.
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Chang L, Ernst T, Osborn D, Seltzer W, Leonido-Yee M, Poland RE. Proton spectroscopy in myotonic dystrophy: correlations with CTG repeats. Arch Neurol. 1998 Mar; 55(3):305-11.
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Yue Q, Jen JC, Nelson SF, Baloh RW. Progressive ataxia due to a missense mutation in a calcium-channel gene. Am J Hum Genet. 1997 Nov; 61(5):1078-87.