 AT Rich Sequence
"AT Rich Sequence" 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 nucleic acid sequence that contains an above average number of ADENINE and THYMINE bases.
| Descriptor ID |
D020856
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| MeSH Number(s) |
G02.111.570.080.040 G05.360.080.040
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| Concept/Terms |
AT Rich Sequence- AT Rich Sequence
- AT Rich Sequences
- Sequence, AT Rich
- Sequences, AT Rich
- AT Rich Region
- AT Rich Regions
- Region, AT Rich
- Regions, AT Rich
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Below are MeSH descriptors whose meaning is more general than "AT Rich Sequence".
Below are MeSH descriptors whose meaning is more specific than "AT Rich Sequence".
This graph shows the total number of publications written about "AT Rich Sequence" by people in this website by year, and whether "AT Rich Sequence" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 1 | 0 | 1 | | 2005 | 1 | 0 | 1 | | 2010 | 0 | 2 | 2 |
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Below are the most recent publications written about "AT Rich Sequence" by people in Profiles.
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Long C, Grueter CE, Song K, Qin S, Qi X, Kong YM, Shelton JM, Richardson JA, Zhang CL, Bassel-Duby R, Olson EN. Ataxia and Purkinje cell degeneration in mice lacking the CAMTA1 transcription factor. Proc Natl Acad Sci U S A. 2014 Aug 05; 111(31):11521-6.
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Sheridan MB, Kato T, Haldeman-Englert C, Jalali GR, Milunsky JM, Zou Y, Klaes R, Gimelli G, Gimelli S, Gemmill RM, Drabkin HA, Hacker AM, Brown J, Tomkins D, Shaikh TH, Kurahashi H, Zackai EH, Emanuel BS. A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21). Am J Hum Genet. 2010 Aug 13; 87(2):209-18.
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Hittinger CT, Hesselberth JR. Nucleosome patterning evolution: steady aim despite moving targets. Mol Syst Biol. 2010 May 11; 6:376.
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Inagaki H, Ohye T, Kogo H, Yamada K, Kowa H, Shaikh TH, Emanuel BS, Kurahashi H. Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates. Hum Mutat. 2005 Oct; 26(4):332-42.
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Nimmakayalu MA, Gotter AL, Shaikh TH, Emanuel BS. A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22). Hum Mol Genet. 2003 Nov 01; 12(21):2817-25.
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