"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 1 | 0 | 1 |
| 2004 | 0 | 2 | 2 |
| 2005 | 3 | 0 | 3 |
| 2006 | 0 | 1 | 1 |
| 2007 | 0 | 2 | 2 |
| 2011 | 1 | 0 | 1 |
| 2012 | 0 | 2 | 2 |
| 2013 | 3 | 4 | 7 |
| 2014 | 1 | 1 | 2 |
| 2015 | 1 | 3 | 4 |
| 2016 | 0 | 1 | 1 |
| 2017 | 2 | 3 | 5 |
| 2018 | 2 | 4 | 6 |
| 2019 | 3 | 5 | 8 |
| 2020 | 1 | 5 | 6 |
| 2021 | 1 | 2 | 3 |
| 2022 | 1 | 1 | 2 |
| 2023 | 0 | 1 | 1 |
| 2024 | 0 | 1 | 1 |
| 2025 | 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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ATXN10 Gene Expansions in Mexican Patients with Ataxia Without Epilepsy. Cerebellum. 2025 Jan 16; 24(2):33.
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Extended haplotype with rs41524547-G defines the ancestral origin of SCA10. Hum Mol Genet. 2024 09 03; 33(18):1567-1574.
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Primary visual cortex pathology in ALS patients with C9ORF72 expansion. Brain Pathol. 2024 Sep; 34(5):e13229.
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Recurrent repeat expansions in human cancer genomes. Nature. 2023 01; 613(7942):96-102.
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Profiling human pathogenic repeat expansion regions by synergistic and multi-level impacts on molecular connections. Hum Genet. 2023 Feb; 142(2):245-274.
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Nucleoporins are degraded via upregulation of ESCRT-III/Vps4 complex in Drosophila models of C9-ALS/FTD. Cell Rep. 2022 09 20; 40(12):111379.
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Comparing loss of balance and functional capacity among patients with SCA2, SCA3 and SCA10. Clin Neurol Neurosurg. 2022 03; 214:107150.
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Reply to: "Cognitive Impairments in Spinocerebellar Ataxia Type 10 and Their Relation to Cortical Thickness". Mov Disord. 2021 12; 36(12):2977.
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C9orf72-derived arginine-containing dipeptide repeats associate with axonal transport machinery and impede microtubule-based motility. Sci Adv. 2021 04; 7(15).
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UPF1 reduces C9orf72 HRE-induced neurotoxicity in the absence of nonsense-mediated decay dysfunction. Cell Rep. 2021 03 30; 34(13):108925.