"Base Pairing" 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.
Pairing of purine and pyrimidine bases by HYDROGEN BONDING in double-stranded DNA or RNA.
| Descriptor ID |
D020029
|
| MeSH Number(s) |
G02.111.570.820.486.100 G02.111.611.500 G05.360.580.100
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Base Pairing".
Below are MeSH descriptors whose meaning is more specific than "Base Pairing".
This graph shows the total number of publications written about "Base Pairing" by people in this website by year, and whether "Base Pairing" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 0 | 2 | 2 |
| 2004 | 0 | 2 | 2 |
| 2006 | 0 | 1 | 1 |
| 2013 | 0 | 1 | 1 |
| 2016 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Base Pairing" by people in Profiles.
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HIF1a-AS1 is a DNA:DNA:RNA triplex-forming lncRNA interacting with the HUSH complex. Nat Commun. 2022 Nov 02; 13(1):6563.
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Isolation and genome-wide characterization of cellular DNA:RNA triplex structures. Nucleic Acids Res. 2019 03 18; 47(5):2306-2321.
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TT-seq maps the human transient transcriptome. Science. 2016 Jun 03; 352(6290):1225-8.
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Use of domesticated pigs by Mesolithic hunter-gatherers in northwestern Europe. Nat Commun. 2013; 4:2348.
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Highly specific gene silencing by artificial microRNAs in Arabidopsis. Plant Cell. 2006 May; 18(5):1121-33.
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Minimal conditions for exonization of intronic sequences: 5' splice site formation in alu exons. Mol Cell. 2004 Apr 23; 14(2):221-31.
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Using the lambdaN peptide to tether proteins to RNAs. Methods Mol Biol. 2004; 257:135-54.
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Mating and pathogenic development of the Smut fungus Ustilago maydis are regulated by one mitogen-activated protein kinase cascade. Eukaryot Cell. 2003 Dec; 2(6):1187-99.
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Leigh Syndrome with COX deficiency and SURF1 gene mutations: MR imaging findings. AJNR Am J Neuroradiol. 2003 Jun-Jul; 24(6):1188-91.
MeSH information
