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 |
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1997 | 0 | 1 | 1 | 1998 | 0 | 1 | 1 | 2000 | 0 | 1 | 1 | 2001 | 1 | 2 | 3 | 2002 | 1 | 1 | 2 | 2003 | 1 | 0 | 1 | 2005 | 1 | 2 | 3 | 2007 | 0 | 1 | 1 | 2009 | 0 | 1 | 1 | 2011 | 1 | 0 | 1 | 2012 | 0 | 1 | 1 | 2014 | 2 | 0 | 2 |
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Below are the most recent publications written about "Microsatellite Repeats" by people in Profiles.
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An HS, Kang HW, Han HS, Park JY, Hong CG, Park J, Myeong JI, An CM. Genetic differences between the wild and hatchery-produced populations of Korean short barbeled grunter (Hapalogenys nitens) determined with microsatellite markers. Genet Mol Res. 2014 Oct 31; 13(4):8901-12.
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An HS, Kim HY, Kim JB, Chang DS, Park KD, Lee JW, Myeong JI, An CM. Genetic characterization of hatchery populations of Korean spotted sea bass (Lateolabrax maculatus) using multiplex polymerase chain reaction assays. Genet Mol Res. 2014 Aug 28; 13(3):6701-15.
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Nissen S, Liang S, Shehktman T, Kelsoe JR. Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, IFT27 and parvalbumin. Am J Med Genet B Neuropsychiatr Genet. 2012 Dec; 159B(8):941-50.
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An HS, Kim EM, Lee JH, Noh JK, An CM, Yoon SJ, Park KD, Myeong JI. Population genetic structure of wild and hatchery black rockfish Sebastes inermis in Korea, assessed using cross-species microsatellite markers. Genet Mol Res. 2011 Oct 13; 10(4):2492-504.
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Messahel B, Williams R, Ridolfi A, A'hern R, Warren W, Tinworth L, Hobson R, Al-Saadi R, Whyman G, Brundler MA, Kelsey A, Sebire N, Jones C, Vujanic G, Pritchard-Jones K. Allele loss at 16q defines poorer prognosis Wilms tumour irrespective of treatment approach in the UKW1-3 clinical trials: a Children's Cancer and Leukaemia Group (CCLG) Study. Eur J Cancer. 2009 Mar; 45(5):819-26.
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Kumar RA, KaraMohamed S, Sudi J, Conrad DF, Brune C, Badner JA, Gilliam TC, Nowak NJ, Cook EH, Dobyns WB, Christian SL. Recurrent 16p11.2 microdeletions in autism. Hum Mol Genet. 2008 Feb 15; 17(4):628-38.
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Geller B, Tillman R, Badner JA, Cook EH. Are the arginine vasopressin V1a receptor microsatellites related to hypersexuality in children with a prepubertal and early adolescent bipolar disorder phenotype? Bipolar Disord. 2005 Dec; 7(6):610-6.
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Ferraren DO, Liu C, Badner JA, Corona W, Rezvani A, Monje VD, Gershon ES, Bonner TI, Detera-Wadleigh SD. Linkage disequilibrium analysis in the LOC93081-KDELC1-BIVM region on 13q in bipolar disorder. Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 05; 133B(1):12-7.
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Sheen VL, Jansen A, Chen MH, Parrini E, Morgan T, Ravenscroft R, Ganesh V, Underwood T, Wiley J, Leventer R, Vaid RR, Ruiz DE, Hutchins GM, Menasha J, Willner J, Geng Y, Gripp KW, Nicholson L, Berry-Kravis E, Bodell A, Apse K, Hill RS, Dubeau F, Andermann F, Barkovich J, Andermann E, Shugart YY, Thomas P, Viri M, Veggiotti P, Robertson S, Guerrini R, Walsh CA. Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome. Neurology. 2005 Jan 25; 64(2):254-62.
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Schulze TG, Chen YS, Badner JA, McInnis MG, DePaulo JR, McMahon FJ. Additional, physically ordered markers increase linkage signal for bipolar disorder on chromosome 18q22. Biol Psychiatry. 2003 Feb 01; 53(3):239-43.
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