"DNA 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 increase number of repeats of a genomic, tandemly repeated DNA sequence from one generation to the next.
| Descriptor ID |
D042622
|
| MeSH Number(s) |
G02.111.570.080.708.800.140 G05.360.080.708.800.074 G05.360.340.024.189.220 G05.360.340.024.850.140 G05.365.590.220 G05.558.220
|
| Concept/Terms |
DNA Repeat Expansion- DNA Repeat Expansion
- DNA Repeat Expansions
- Expansion, DNA Repeat
- Expansions, DNA Repeat
- Repeat Expansion, DNA
- Repeat Expansions, DNA
Expanded DNA Repeats- Expanded DNA Repeats
- DNA Repeat, Expanded
- DNA Repeats, Expanded
- Expanded DNA Repeat
- Repeat, Expanded DNA
- Repeats, Expanded DNA
|
Below are MeSH descriptors whose meaning is more general than "DNA Repeat Expansion".
Below are MeSH descriptors whose meaning is more specific than "DNA Repeat Expansion".
This graph shows the total number of publications written about "DNA Repeat Expansion" by people in this website by year, and whether "DNA Repeat Expansion" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 1 | 0 | 1 |
| 2006 | 1 | 1 | 2 |
| 2012 | 1 | 0 | 1 |
| 2014 | 0 | 1 | 1 |
| 2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "DNA Repeat Expansion" by people in Profiles.
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Congenital Central Hypoventilation Syndrome: Neurocognition Already Reduced in Preschool-Aged Children. Chest. 2016 Mar; 149(3):809-15.
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TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions. Acta Neuropathol. 2014 Mar; 127(3):407-18.
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Congenital central hypoventilation syndrome with PHOX2B gene mutation: are we missing the diagnosis? Indian J Pediatr. 2013 Aug; 80(8):688-90.
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Congenital central hypoventilation syndrome: PHOX2B mutations and phenotype. Am J Respir Crit Care Med. 2006 Nov 15; 174(10):1139-44.
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Prevalence of FMR1 repeat expansions in movement disorders. A systematic review. Neuroepidemiology. 2006; 26(3):151-5.
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Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population. JAMA. 2004 Jan 28; 291(4):460-9.