 Microsatellite Repeats
"Microsatellite 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.
A variety of simple repeat sequences that are distributed throughout the GENOME. They are characterized by a short repeat unit of 2-8 basepairs that is repeated up to 100 times. They are also known as short tandem repeats (STRs).
| Descriptor ID |
D018895
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| MeSH Number(s) |
G02.111.570.080.708.800.500 G05.360.080.708.800.500 G05.360.340.024.850.500
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| Concept/Terms |
Microsatellite Repeats- Microsatellite Repeats
- Microsatellite Repeat
- Repeat, Microsatellite
- Repeats, Microsatellite
- Simple Sequence Repeats
- Repeat, Simple Sequence
- Repeats, Simple Sequence
- Sequence Repeat, Simple
- Sequence Repeats, Simple
- Simple Sequence Repeat
- Short Tandem Repeats
- Repeat, Short Tandem
- Repeats, Short Tandem
- Short Tandem Repeat
- Tandem Repeat, Short
- Tandem Repeats, Short
- Simple Repetitive Sequence
- Repetitive Sequence, Simple
- Repetitive Sequences, Simple
- Sequence, Simple Repetitive
- Sequences, Simple Repetitive
- Simple Repetitive Sequences
- Microsatellite Markers
- Marker, Microsatellite
- Markers, Microsatellite
- Microsatellite Marker
- Microsatellites
- Microsatellite
Tetranucleotide Repeats- Tetranucleotide Repeats
- Repeat, Tetranucleotide
- Repeats, Tetranucleotide
- Tetranucleotide Repeat
Pentanucleotide Repeats- Pentanucleotide Repeats
- Pentanucleotide Repeat
- Repeat, Pentanucleotide
- Repeats, Pentanucleotide
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Below are MeSH descriptors whose meaning is more general than "Microsatellite Repeats".
Below are MeSH descriptors whose meaning is more specific than "Microsatellite Repeats".
This graph shows the total number of publications written about "Microsatellite Repeats" by people in this website by year, and whether "Microsatellite 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 |
|---|
| 1998 | 1 | 0 | 1 | | 2002 | 0 | 1 | 1 | | 2003 | 1 | 0 | 1 | | 2004 | 1 | 0 | 1 | | 2009 | 0 | 1 | 1 | | 2011 | 1 | 0 | 1 | | 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Microsatellite Repeats" by people in Profiles.
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Jakubosky D, D'Antonio M, Bonder MJ, Smail C, Donovan MKR, Young Greenwald WW, Matsui H, D'Antonio-Chronowska A, Stegle O, Smith EN, Montgomery SB, DeBoever C, Frazer KA. Properties of structural variants and short tandem repeats associated with gene expression and complex traits. Nat Commun. 2020 06 10; 11(1):2927.
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Amankwah EK, Kelemen LE, Wang Q, Song H, Chenevix-Trench G, Beesley J, Webb PM, Pearce CL, Wu AH, Pike MC, Stram DO, Chang-Claude J, Wang-Gohrke S, Ness RB, Goode EL, Cunningham JM, Fridley BL, Vierkant RA, Tworoger SS, Whittemore AS, McGuire V, Sieh W, Gayther SA, Gentry-Maharaj A, Menon U, Ramus SJ, Rossing MA, Doherty JA, Goodman MT, Carney ME, Lurie G, Wilkens LR, Kj?r SK, H?gdall E, Cramer DW, Terry KL, Garcia-Closas M, Yang H, Lissowska J, Anton-Culver H, Ziogas A, Schildkraut JM, Berchuck A, Pharoah PD. Prostate cancer susceptibility polymorphism rs2660753 is not associated with invasive ovarian cancer. Cancer Epidemiol Biomarkers Prev. 2011 May; 20(5):1028-31.
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Rule AD, Fridley BL, Hunt SC, Asmann Y, Boerwinkle E, Pankow JS, Mosley TH, Turner ST. Genome-wide linkage analysis for uric acid in families enriched for hypertension. Nephrol Dial Transplant. 2009 Aug; 24(8):2414-20.
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Grundberg E, Br?ndstr?m H, Ribom EL, Ljunggren O, Mallmin H, Kindmark A. Genetic variation in the human vitamin D receptor is associated with muscle strength, fat mass and body weight in Swedish women. Eur J Endocrinol. 2004 Mar; 150(3):323-8.
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Grundberg E, Br?ndstr?m H, Ribom EL, Ljunggren O, Kindmark A, Mallmin H. A poly adenosine repeat in the human vitamin D receptor gene is associated with bone mineral density in young Swedish women. Calcif Tissue Int. 2003 Nov; 73(5):455-62.
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Reunanen K, Finnil? S, Laaksonen M, Sumelahti ML, Wikstr?m J, Pastinen T, Kuokkanen S, Saarela J, Uimari P, Ruutiainen J, Ilonen J, Peltonen L, Tienari PJ. Chromosome 19q13 and multiple sclerosis susceptibility in Finland: a linkage and two-stage association study. J Neuroimmunol. 2002 May; 126(1-2):134-42.
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Butler MG, Bittel D, Talebizadeh Z. Prader-Willi syndrome and a deletion/duplication within the 15q11-q13 region. J Med Genet. 2002 Mar; 39(3):202-4.
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Tienari PJ, Kuokkanen S, Pastinen T, Wikstr?m J, Sajantila A, Sandberg-Wollheim M, Palo J, Peltonen L. Golli-MBP gene in multiple sclerosis susceptibility. J Neuroimmunol. 1998 Jan; 81(1-2):158-67.
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DeSilva U, D'Arcangelo G, Braden VV, Chen J, Miao GG, Curran T, Green ED. The human reelin gene: isolation, sequencing, and mapping on chromosome 7. Genome Res. 1997 Feb; 7(2):157-64.
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