 Sequence Tagged Sites
"Sequence Tagged Sites" 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.
Short tracts of DNA sequence that are used as landmarks in GENOME mapping. In most instances, 200 to 500 base pairs of sequence define a Sequence Tagged Site (STS) that is operationally unique in the human genome (i.e., can be specifically detected by the polymerase chain reaction in the presence of all other genomic sequences). The overwhelming advantage of STSs over mapping landmarks defined in other ways is that the means of testing for the presence of a particular STS can be completely described as information in a database.
| Descriptor ID |
D016324
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| MeSH Number(s) |
G05.360.340.024.810
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| Concept/Terms |
Sequence Tagged Sites- Sequence Tagged Sites
- Sequence Tagged Site
- Site, Sequence Tagged
- Sites, Sequence Tagged
- Tagged Site, Sequence
- Tagged Sites, Sequence
- Sequence-Tagged Sites
- Sequence-Tagged Site
- Site, Sequence-Tagged
- Sites, Sequence-Tagged
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Below are MeSH descriptors whose meaning is more general than "Sequence Tagged Sites".
Below are MeSH descriptors whose meaning is more specific than "Sequence Tagged Sites".
This graph shows the total number of publications written about "Sequence Tagged Sites" by people in this website by year, and whether "Sequence Tagged Sites" 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 |
|---|
| 1993 | 1 | 0 | 1 | | 1995 | 0 | 1 | 1 | | 1997 | 0 | 3 | 3 | | 1998 | 0 | 2 | 2 | | 2001 | 0 | 1 | 1 | | 2002 | 0 | 1 | 1 | | 2004 | 0 | 1 | 1 |
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Below are the most recent publications written about "Sequence Tagged Sites" by people in Profiles.
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Rong J, Abbey C, Bowers JE, Brubaker CL, Chang C, Chee PW, Delmonte TA, Ding X, Garza JJ, Marler BS, Park CH, Pierce GJ, Rainey KM, Rastogi VK, Schulze SR, Trolinder NL, Wendel JF, Wilkins TA, Williams-Coplin TD, Wing RA, Wright RJ, Zhao X, Zhu L, Paterson AH. A 3347-locus genetic recombination map of sequence-tagged sites reveals features of genome organization, transmission and evolution of cotton (Gossypium). Genetics. 2004 Jan; 166(1):389-417.
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Konrad D, Bilan PJ, Nawaz Z, Sweeney G, Niu W, Liu Z, Antonescu CN, Rudich A, Klip A. Need for GLUT4 activation to reach maximum effect of insulin-mediated glucose uptake in brown adipocytes isolated from GLUT4myc-expressing mice. Diabetes. 2002 Sep; 51(9):2719-26.
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Montgomery KT, Lee E, Miller A, Lau S, Shim C, Decker J, Chiu D, Emerling S, Sekhon M, Kim R, Lenz J, Han J, Ioshikhes I, Renault B, Marondel I, Yoon SJ, Song K, Murty VV, Scherer S, Yonescu R, Kirsch IR, Ried T, McPherson J, Gibbs R, Kucherlapati R. A high-resolution map of human chromosome 12. Nature. 2001 Feb 15; 409(6822):945-6.
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Totaro A, Roetto A, Rommens JM, Grifa A, Carella M, d'Agruma L, Valentino MA, D'Ambrosio L, Cicilano M, Camaschella C, Franco B, Gasparini P. Generation of a transcription map of a 1 Mbase region containing the HFE gene (6p22). Eur J Hum Genet. 1998 Mar-Apr; 6(2):105-13.
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Csóka AB, Frost GI, Heng HH, Scherer SW, Mohapatra G, Stern R, Csóka TB. The hyaluronidase gene HYAL1 maps to chromosome 3p21.2-p21.3 in human and 9F1-F2 in mouse, a conserved candidate tumor suppressor locus. Genomics. 1998 Feb 15; 48(1):63-70.
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Roux AF, Rommens JM, Read L, Duncan AM, Cox DW. Physical and transcription map in the region 14q24.3: identification of six novel transcripts. Genomics. 1997 Jul 15; 43(2):130-40.
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Piemontese MR, Memeo E, Carella M, Amati P, Chomel JC, Bonneau D, Pilia G, Cao A, Drabkin H, Gemmill R, Rommens J, Zelante L, Gasparini P, Bisceglia L. A YAC contig spanning the blepharophimosis-ptosis-epicanthus inversus syndrome and propionic acidemia loci. Eur J Hum Genet. 1997 May-Jun; 5(3):171-4.
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Perou CM, Perchellet A, Jago T, Pryor R, Kaplan J, Justice MJ. Comparative mapping in the beige-satin region of mouse chromosome 13. Genomics. 1997 Jan 15; 39(2):136-46.
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Torigoe K, Sato S, Kusaba H, Kohno K, Kuwano M, Okumura K, Green ED, Tsui LC, Scherer SW, Schlessinger D, Wada M. A YAC-based contig of 1.5 Mb spanning the human multidrug resistance gene region and delineating the amplification unit in three human multidrug-resistant cell lines. Genome Res. 1995 Oct; 5(3):233-44.
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Pausova Z, Morgan K, Fujiwara TM, Bourdon J, Goltzman D, Hendy GN. Molecular characterization of an intragenic minisatellite (VNTR) polymorphism in the human parathyroid hormone-related peptide gene in chromosome region 12p12.1-p11.2. Genomics. 1993 Jul; 17(1):243-4.
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