Trinucleotide Repeat Expansion
"Trinucleotide Repeat Expansion" 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.
An increased number of contiguous trinucleotide repeats in the DNA sequence from one generation to the next. The presence of these regions is associated with diseases such as FRAGILE X SYNDROME and MYOTONIC DYSTROPHY. Some CHROMOSOME FRAGILE SITES are composed of sequences where trinucleotide repeat expansion occurs.
Descriptor ID |
D019680
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MeSH Number(s) |
G02.111.570.080.708.800.140.865 G02.111.570.080.708.800.500.850.200 G05.360.080.708.800.074.865 G05.360.080.708.800.500.850.200 G05.360.340.024.189.220.865 G05.360.340.024.850.500.850.200 G05.365.590.220.865 G05.558.220.865
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Concept/Terms |
Trinucleotide Repeat Expansion- Trinucleotide Repeat Expansion
- Expansion, Trinucleotide Repeat
- Expansions, Trinucleotide Repeat
- Repeat Expansion, Trinucleotide
- Repeat Expansions, Trinucleotide
- Trinucleotide Repeat Expansions
- Expanded Trinucleotide Repeat
- Expanded Trinucleotide Repeats
- Repeat, Expanded Trinucleotide
- Repeats, Expanded Trinucleotide
- Trinucleotide Repeat, Expanded
- Trinucleotide Repeats, Expanded
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Below are MeSH descriptors whose meaning is more general than "Trinucleotide Repeat Expansion".
Below are MeSH descriptors whose meaning is more specific than "Trinucleotide Repeat Expansion".
This graph shows the total number of publications written about "Trinucleotide Repeat Expansion" by people in this website by year, and whether "Trinucleotide Repeat Expansion" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2008 | 0 | 1 | 1 |
2013 | 0 | 1 | 1 |
2017 | 0 | 2 | 2 |
2018 | 1 | 3 | 4 |
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Below are the most recent publications written about "Trinucleotide Repeat Expansion" by people in Profiles.
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Diastolic heart dysfunction is correlated with CTG repeat length in myotonic dystrophy type 1. Neurol Sci. 2018 Nov; 39(11):1935-1943.
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Non invasive mechanical ventilation in DM1: The strong correlation between lung function, neurological-cognitive function and CTG repeats. Neuromuscul Disord. 2018 10; 28(10):894-895.
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Non invasive mechanical ventilation in DM1: The strong correlation between lung function, neurological-cognitive function and CTG repeats. Neuromuscul Disord. 2018 10; 28(10):894-895.
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When Huntington's disease comes early. Nature. 2018 05; 557(7707):S44-S45.
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Imaging of the thymus in myotonic dystrophy type 1. Neurol Sci. 2018 Feb; 39(2):347-351.
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C9ORF72 and parkinsonism: Weak link, innocent bystander, or central player in neurodegeneration? J Neurol Sci. 2017 07 15; 378:49-51.
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Genetic variations creating microRNA target sites in the FXN 3'-UTR affect frataxin expression in Friedreich ataxia. PLoS One. 2013; 8(1):e54791.
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Molecular and clinical characteristics of myotonic dystrophy type 1 in koreans. Korean J Lab Med. 2008 Dec; 28(6):483-92.