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.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 7 | 24 | 31 |
| 1995 | 19 | 24 | 43 |
| 1996 | 9 | 13 | 22 |
| 1997 | 5 | 9 | 14 |
| 1998 | 2 | 7 | 9 |
| 1999 | 2 | 5 | 7 |
| 2000 | 1 | 3 | 4 |
| 2001 | 2 | 4 | 6 |
| 2002 | 2 | 7 | 9 |
| 2003 | 0 | 8 | 8 |
| 2004 | 3 | 7 | 10 |
| 2005 | 3 | 9 | 12 |
| 2006 | 0 | 4 | 4 |
| 2007 | 4 | 5 | 9 |
| 2008 | 2 | 3 | 5 |
| 2009 | 1 | 0 | 1 |
| 2010 | 2 | 1 | 3 |
| 2011 | 1 | 3 | 4 |
| 2012 | 1 | 2 | 3 |
| 2014 | 1 | 2 | 3 |
| 2015 | 1 | 1 | 2 |
| 2016 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
| 2019 | 1 | 1 | 2 |
| 2020 | 0 | 1 | 1 |
| 2021 | 2 | 0 | 2 |
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Below are the most recent publications written about "Repetitive Sequences, Nucleic Acid" by people in Profiles.
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Comparison of Whole Genome Sequencing and Repetitive Element PCR for Multidrug-Resistant Pseudomonas aeruginosa Strain Typing. J Mol Diagn. 2022 02; 24(2):158-166.
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Draft Genome Assemblies and Annotations of Agrypnia vestita Walker, and Hesperophylax magnus Banks Reveal Substantial Repetitive Element Expansion in Tube Case-Making Caddisflies (Insecta: Trichoptera). Genome Biol Evol. 2021 03 01; 13(3).
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Principles of RNA processing from analysis of enhanced CLIP maps for 150 RNA binding proteins. Genome Biol. 2020 04 06; 21(1):90.
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Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndrome. Hum Mutat. 2020 01; 41(1):150-168.
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Repeat-associated non-AUG (RAN) translation mechanisms are running into focus for GGGGCC-repeat associated ALS/FTD. Prog Neurobiol. 2019 12; 183:101697.
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De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-Progressive Neurocognitive Syndrome. Am J Hum Genet. 2019 03 07; 104(3):542-552.
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Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line. Genome Res. 2018 08; 28(8):1126-1135.
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Genetic and Genomic Characterization of 462 Melanoma Patient-Derived Xenografts, Tumor Biopsies, and Cell Lines. Cell Rep. 2017 Nov 14; 21(7):1936-1952.
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The nature of mutations induced by replication?transcription collisions. Nature. 2016 07 07; 535(7610):178-81.
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Mechanisms underlying structural variant formation in genomic disorders. Nat Rev Genet. 2016 Apr; 17(4):224-38.