Repetitive Sequences, Nucleic Acid
"Repetitive Sequences, Nucleic Acid" 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.
Sequences of DNA or RNA that occur in multiple copies. There are several types: INTERSPERSED REPETITIVE SEQUENCES are copies of transposable elements (DNA TRANSPOSABLE ELEMENTS or RETROELEMENTS) dispersed throughout the genome. TERMINAL REPEAT SEQUENCES flank both ends of another sequence, for example, the long terminal repeats (LTRs) on RETROVIRUSES. Variations may be direct repeats, those occurring in the same direction, or inverted repeats, those opposite to each other in direction. TANDEM REPEAT SEQUENCES are copies which lie adjacent to each other, direct or inverted (INVERTED REPEAT SEQUENCES).
Descriptor ID |
D012091
|
MeSH Number(s) |
G02.111.570.080.708 G05.360.080.708
|
Concept/Terms |
Selfish DNA- Selfish DNA
- DNAs, Selfish
- Selfish DNAs
- DNA, Selfish
DNA Repetitious Region- DNA Repetitious Region
- DNA Repetitious Regions
- Repetitious Regions, DNA
- Repetitious Region, DNA
Direct Repeat- Direct Repeat
- Direct Repeats
- Repeat, Direct
- Repeats, Direct
Repetitive Region- Repetitive Region
- Repetitive Regions
- Repetitive Sequence
- Repetitive Sequences
Selfish Genes- Selfish Genes
- Gene, Selfish
- Selfish Gene
- Genes, Selfish
|
Below are MeSH descriptors whose meaning is more general than "Repetitive Sequences, Nucleic Acid".
Below are MeSH descriptors whose meaning is more specific than "Repetitive Sequences, Nucleic Acid".
This graph shows the total number of publications written about "Repetitive Sequences, Nucleic Acid" by people in this website by year, and whether "Repetitive Sequences, Nucleic Acid" was a major or minor topic of these publications.
View timeline visualization
Year | Major Topic | Minor Topic | Total |
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1995 | 14 | 26 | 40 |
1996 | 6 | 23 | 29 |
1997 | 9 | 20 | 29 |
1998 | 4 | 32 | 36 |
1999 | 3 | 11 | 14 |
2000 | 3 | 6 | 9 |
2001 | 2 | 9 | 11 |
2002 | 3 | 12 | 15 |
2003 | 4 | 5 | 9 |
2004 | 7 | 8 | 15 |
2005 | 0 | 11 | 11 |
2006 | 4 | 6 | 10 |
2007 | 4 | 5 | 9 |
2008 | 1 | 6 | 7 |
2009 | 1 | 5 | 6 |
2010 | 6 | 14 | 20 |
2011 | 7 | 7 | 14 |
2012 | 5 | 10 | 15 |
2013 | 2 | 8 | 10 |
2014 | 2 | 10 | 12 |
2015 | 1 | 5 | 6 |
2016 | 0 | 5 | 5 |
2017 | 2 | 5 | 7 |
2018 | 0 | 4 | 4 |
2019 | 3 | 4 | 7 |
2020 | 1 | 4 | 5 |
2021 | 2 | 4 | 6 |
2022 | 1 | 3 | 4 |
2023 | 0 | 1 | 1 |
2025 | 0 | 1 | 1 |
Below are the most recent publications written about "Repetitive Sequences, Nucleic Acid" by people in Profiles.
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PhpCNF-Y transcription factor infiltrates heterochromatin to generate cryptic intron-containing transcripts crucial for small RNA production. Nat Commun. 2025 Jan 02; 16(1):268.
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The fidelity of transcription in human cells. Proc Natl Acad Sci U S A. 2023 01 31; 120(5):e2210038120.
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SVDSS: structural variation discovery in hard-to-call genomic regions using sample-specific strings from accurate long reads. Nat Methods. 2023 04; 20(4):550-558.
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Fast and accurate mapping of long reads to complete genome assemblies with VerityMap. Genome Res. 2022 Nov-Dec; 32(11-12):2107-2118.
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Leafy and weedy seadragon genomes connect genic and repetitive DNA features to the extravagant biology of syngnathid fishes. Proc Natl Acad Sci U S A. 2022 06 28; 119(26):e2119602119.
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Complete genomic and epigenetic maps of human centromeres. Science. 2022 04; 376(6588):eabl4178.
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piRNAQuest V.2: an updated resource for searching through the piRNAome of multiple species. RNA Biol. 2022; 19(1):12-25.
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Estimating repeat spectra and genome length from low-coverage genome skims with RESPECT. PLoS Comput Biol. 2021 11; 17(11):e1009449.
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Diploid genomic architecture of Nitzschia inconspicua, an elite biomass production diatom. Sci Rep. 2021 08 02; 11(1):15592.
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Central 22q11.2 deletion (LCR22 B-D) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of CRKL haploinsufficiency in the pathogenesis of 22q11.2 deletion syndrome. Am J Med Genet A. 2021 10; 185(10):3042-3047.