"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 2 | 0 | 2 |
| 1996 | 10 | 2 | 12 |
| 1997 | 7 | 3 | 10 |
| 1998 | 5 | 0 | 5 |
| 1999 | 1 | 3 | 4 |
| 2000 | 6 | 0 | 6 |
| 2001 | 2 | 2 | 4 |
| 2002 | 3 | 3 | 6 |
| 2003 | 2 | 2 | 4 |
| 2004 | 1 | 2 | 3 |
| 2005 | 2 | 1 | 3 |
| 2006 | 2 | 2 | 4 |
| 2007 | 1 | 0 | 1 |
| 2008 | 1 | 3 | 4 |
| 2009 | 1 | 1 | 2 |
| 2010 | 0 | 1 | 1 |
| 2011 | 3 | 1 | 4 |
| 2012 | 1 | 1 | 2 |
| 2013 | 1 | 1 | 2 |
| 2014 | 0 | 2 | 2 |
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 1 | 2 |
| 2017 | 0 | 2 | 2 |
| 2018 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
| 2021 | 0 | 1 | 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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Spinocerebellar Ataxia Type 1 protein Ataxin-1 is signaled to DNA damage by ataxia-telangiectasia mutated kinase. Hum Mol Genet. 2021 05 17; 30(8):706-715.
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Longitudinal increases in somatic mosaicism of the expanded CTG repeat in myotonic dystrophy type 1 are associated with variation in age-at-onset. Hum Mol Genet. 2020 08 29; 29(15):2496-2507.
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Loss of Ataxin-1 Potentiates Alzheimer's Pathogenesis by Elevating Cerebral BACE1 Transcription. Cell. 2019 08 22; 178(5):1159-1175.e17.
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The prevalence of CGG repeat expansion mutation in FMR1 gene in the northern Chinese women of reproductive age. BMC Med Genet. 2019 05 16; 20(1):81.
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Analysis of mutational dynamics at the DMPK (CTG)n locus identifies saliva as a suitable DNA sample source for genetic analysis in myotonic dystrophy type 1. PLoS One. 2019; 14(5):e0216407.
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A comprehensive clinical and genetic study in 127 patients with ID in Kinshasa, DR Congo. Am J Med Genet A. 2018 09; 176(9):1897-1909.
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The Initial Symptom and Motor Progression in Spinocerebellar Ataxias. Cerebellum. 2017 06; 16(3):615-622.
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Letter re: Huntington disease reduced penetrance alleles occur at high frequency in the general population. Neurology. 2017 01 17; 88(3):334.
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Clinical and genetic investigation of a Brazilian family with Huntington's disease. Funct Neurol. 2016 Jul-Sep; 31(3):135-42.
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Genome Therapy of Myotonic Dystrophy Type 1 iPS Cells for Development of Autologous Stem Cell Therapy. Mol Ther. 2016 08; 24(8):1378-87.